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AbstractA diverse range of viruses have well-established roles as the primary driver of oncogenesis in various haematological malignancies and solid tumours. Indeed, estimates suggest that approximately 1.5 million patients annually are diagnosed with virus-related cancers. The predominant human oncoviruses include Epstein–Barr virus (EBV), Kaposi sarcoma-associated herpesvirus (KSHV), hepatitis B and C viruses (HBV and HCV), human papillomavirus (HPV), human T-lymphotropic virus type 1 (HTLV1), and Merkel cell polyomavirus (MCPyV).
摘要多种病毒在各种血液系统恶性肿瘤和实体瘤中作为肿瘤发生的主要驱动因素具有公认的作用。事实上,估计表明,每年约有150万患者被诊断出患有病毒相关癌症。主要的人类肿瘤病毒包括爱泼斯坦-巴尔病毒(EBV),卡波西肉瘤相关疱疹病毒(KSHV),乙型和丙型肝炎病毒(HBV和HCV),人乳头瘤病毒(HPV),人T淋巴细胞病毒1型(HTLV1)和默克尔细胞多瘤病毒(MCPyV)。
In addition, although not inherently oncogenic, human immunodeficiency virus (HIV) is associated with immunosuppression that contributes to the development of AIDS-defining cancers (specifically, Kaposi sarcoma, aggressive B cell non-Hodgkin lymphoma and cervical cancer). Given that an adaptive T cell-mediated immune response is crucial for the control of viral infections, increasing research is being focused on evaluating virus-specific T cell therapies for the treatment of virus-associated cancers.
此外,人类免疫缺陷病毒(HIV)虽然不是天生致癌的,但与免疫抑制有关,这有助于艾滋病定义癌症(特别是卡波西肉瘤,侵袭性B细胞非霍奇金淋巴瘤和宫颈癌)的发展。鉴于适应性T细胞介导的免疫应答对于控制病毒感染至关重要,越来越多的研究集中在评估用于治疗病毒相关癌症的病毒特异性T细胞疗法。
In this Review, we briefly outline the roles of viruses in the pathogenesis of these malignancies before describing progress to date in the field of virus-specific T cell therapy and evaluating the potential utility of these therapies to treat or possibly even prevent virus-related malignancies.Key points.
在这篇综述中,我们简要概述了病毒在这些恶性肿瘤发病机制中的作用,然后描述了迄今为止在病毒特异性T细胞治疗领域的进展,并评估了这些疗法治疗甚至可能预防病毒相关恶性肿瘤的潜在效用。关键点。
Viruses can contribute to the development of cancer via inflammation, disruption of the cell cycle by viral oncoproteins, direct integration into the genome, and genomic instability and are often required for the proliferation of malignant cells.
病毒可以通过炎症,病毒癌蛋白破坏细胞周期,直接整合到基因组中以及基因组不稳定来促进癌症的发展,并且通常是恶性细胞增殖所必需的。
Virus-specific T cell (VST) therapies have demonstrated a favourable safety profile and can be manufactured from autologous, allogeneic donor and third-party sources.
病毒特异性T细胞(VST)疗法已显示出良好的安全性,可以从自体,同种异体供体和第三方来源制造。
Although historically costly and time-consuming to manufacture, novel rapid manufacturing techniques promise to reduce the costs of and increase accessibility to VST therapies.
尽管历史上制造成本高昂且耗时,但新型快速制造技术有望降低VST疗法的成本并增加其可及性。
VSTs targeting Epstein–Barr virus (EBV) have the most substantial evidence of efficacy, with few adverse events, leading to the first regulatory approval of VSTs for use in oncology practice.
针对爱泼斯坦-巴尔病毒(EBV)的VST具有最实质的疗效证据,几乎没有不良事件,这导致VST首次获得监管部门批准用于肿瘤学实践。
Adoptive cell therapy has not yet achieved success in the treatment of all virus-associated cancers owing to multiple barriers, including the immunosuppressive tumour microenvironment, tumour heterogeneity and viral immune evasion mechanisms.
由于多种障碍,包括免疫抑制性肿瘤微环境,肿瘤异质性和病毒免疫逃避机制,过继性细胞疗法尚未在治疗所有病毒相关癌症方面取得成功。
Combinatorial treatment strategies might expand the clinical utility of VST therapies.
组合治疗策略可能会扩大VST疗法的临床应用。
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Fig. 1: Virus-associated oncogenesis.Fig. 2: Manufacturing of VST therapies.
。图2:VST疗法的制造。
ReferencesPlummer, M. et al. Global burden of cancers attributable to infections in 2012: a synthetic analysis. Lancet Glob. Health 4, e609-16 (2016).Article
参考文献Plummer,M。等人,《2012年感染引起的全球癌症负担:综合分析》。。健康4,e609-16(2016)。文章
PubMed
PubMed
Google Scholar
谷歌学者
Volesky-Avellaneda, K. D. et al. Cancers attributable to infections in the US in 2017: a meta-analysis. JAMA Oncol. 9, 1678–1687 (2023).Article
Volesky-Avellaneda,K.D.等人。2017年美国感染引起的癌症:荟萃分析。JAMA Oncol。91678-1687(2023)。文章
PubMed
PubMed
Google Scholar
谷歌学者
Farrell, P. J. Epstein-Barr virus and cancer. Annu. Rev. Pathol. 14, 29–53 (2019).Article
Farrell,P.J。爱泼斯坦-巴尔病毒与癌症。年。Pathol牧师。14,29-53(2019)。文章
CAS
中科院
PubMed
PubMed
Google Scholar
谷歌学者
Chowdhary, S. et al. Recent updates on viral oncogenesis: available preventive and therapeutic entities. Mol. Pharm. 20, 3698–3740 (2023).Article
Chowdhary,S.等人。病毒肿瘤发生的最新进展:可用的预防和治疗实体。摩尔药理学203698-3740(2023)。文章
CAS
中科院
PubMed
PubMed
PubMed Central
公共医学中心
Google Scholar
谷歌学者
Krump, N. A. & You, J. Molecular mechanisms of viral oncogenesis in humans. Nat. Rev. Microbiol. 16, 684–698 (2018).Article
Krump,N.A。&You,J。人类病毒肿瘤发生的分子机制。自然修订版微生物学。16684-698(2018)。文章
CAS
中科院
PubMed
PubMed
PubMed Central
公共医学中心
Google Scholar
谷歌学者
Skolnik, J. M. & Morrow, M. P. Vaccines for HPV-associated diseases. Mol. Aspects Med. 94, 101224 (2023).Article
Skolnik,J.M。&Morrow,M.P。针对HPV相关疾病的疫苗。Mol.Aspects Med.94101224(2023)。文章
CAS
中科院
PubMed
PubMed
Google Scholar
谷歌学者
Balfour, H. H. Jr., Schmeling, D. O. & Grimm-Geris, J. M. The promise of a prophylactic Epstein-Barr virus vaccine. Pediatr. Res. 87, 345–352 (2020).Article
Balfour,H.H.Jr.,Schmeling,D.O。和Grimm Geris,J.M。预防性爱泼斯坦-巴尔病毒疫苗的前景。儿科。第87345-352号决议(2020年)。文章
CAS
中科院
PubMed
PubMed
Google Scholar
谷歌学者
Cohen, J. I. Vaccine development for Epstein-Barr virus. Adv. Exp. Med. Biol. 1045, 477–493 (2018).Article
Cohen,J.I。爱泼斯坦-巴尔病毒的疫苗开发。高级实验医学生物学。1045477-493(2018)。文章
CAS
中科院
PubMed
PubMed
PubMed Central
公共医学中心
Google Scholar
谷歌学者
Hont, A. B. et al. The generation and application of antigen-specific T cell therapies for cancer and viral-associated disease. Mol. Ther. 30, 2130–2152 (2022).Article
Hont,A.B.等人。针对癌症和病毒相关疾病的抗原特异性T细胞疗法的产生和应用。摩尔热。302130–2152(2022)。文章
CAS
中科院
PubMed
PubMed
PubMed Central
公共医学中心
Google Scholar
谷歌学者
Toner, K. & Bollard, C. M. EBV+ lymphoproliferative diseases: opportunities for leveraging EBV as a therapeutic target. Blood 139, 983–994 (2022).Article
Toner,K。&Bollard,C.M。EBV+淋巴组织增生性疾病:利用EBV作为治疗靶点的机会。血液139983-994(2022)。文章
CAS
中科院
PubMed
PubMed
PubMed Central
公共医学中心
Google Scholar
谷歌学者
Papadopoulou, A., Alvanou, M., Karavalakis, G., Tzannou, I. & Yannaki, E. Pathogen-specific T cells: targeting old enemies and new invaders in transplantation and beyond. Hemasphere 7, e809 (2023).Article
Papadopoulou,A.,Alvanou,M.,Karavalakis,G.,Tzannou,I。&Yannaki,E.病原体特异性T细胞:在移植和其他方面针对旧敌人和新入侵者。Hemasphere 7,e809(2023)。文章
CAS
中科院
PubMed
PubMed
PubMed Central
公共医学中心
Google Scholar
谷歌学者
Martinov, T. & Greenberg, P. D. Targeting driver oncogenes and other public neoantigens using T cell receptor-based cellular therapy. Annu. Rev. Cancer Biol. 7, 331–351 (2023).Article
Martinov,T。&Greenberg,P.D。使用基于T细胞受体的细胞疗法靶向驱动癌基因和其他公共新抗原。年。癌症生物学评论。7331-351(2023)。文章
PubMed
PubMed
PubMed Central
公共医学中心
Google Scholar
谷歌学者
McLaughlin, L. P., Gottschalk, S., Rooney, C. M. & Bollard, C. M. EBV-directed T cell therapeutics for EBV-associated lymphomas. Methods Mol. Biol. 1532, 255–265 (2017).Article
McLaughlin,L.P.,Gottschalk,S.,Rooney,C.M。和Bollard,C.M。EBV导向的T细胞治疗EBV相关淋巴瘤。方法分子生物学。1532255-265(2017)。文章
CAS
中科院
PubMed
PubMed
Google Scholar
谷歌学者
Keam, S. J. Tabelecleucel: first approval. Mol. Diagn. Ther. 27, 425–431 (2023).Article
。分子诊断。他们。27425-431(2023)。文章
CAS
中科院
PubMed
PubMed
Google Scholar
谷歌学者
Keller, M. D. et al. T-cell receptor sequencing demonstrates persistence of virus-specific T cells after antiviral immunotherapy. Br. J. Haematol. 187, 206–218 (2019).Article
Keller,M.D.等人,T细胞受体测序证明抗病毒免疫治疗后病毒特异性T细胞的持久性。Br.J.血液学。187206-218(2019)。文章
CAS
中科院
PubMed
PubMed
PubMed Central
公共医学中心
Google Scholar
谷歌学者
Galati, L., Chiantore, M. V., Marinaro, M. & Di Bonito, P. Human oncogenic viruses: characteristics and prevention strategies-lessons learned from human papillomaviruses. Viruses 16, 416 (2024).Article
Galati,L.,Chiantore,M.V.,Marinaro,M。&Di Bonito,P。人类致癌病毒:特征和预防策略从人乳头瘤病毒中吸取的教训。。文章
CAS
中科院
PubMed
PubMed
PubMed Central
公共医学中心
Google Scholar
谷歌学者
Cesarman, E. et al. Kaposi sarcoma. Nat. Rev. Dis. Prim. 5, 9 (2019).Article
Cesarman,E.等,卡波西肉瘤。国家牧师。普里姆。5.9 (2019).文章
PubMed
PubMed
Google Scholar
谷歌学者
Vasudevan, H. N. & Yom, S. S. Nasopharyngeal carcinoma and its association with epstein-barr virus. Hematol. Oncol. Clin. North Am. 35, 963–971 (2021).Article
Vasudevan,H.N。&Yom,S.S。鼻咽癌及其与爱泼斯坦-巴尔病毒的关系。血液学。Oncol公司。临床。。文章
PubMed
PubMed
Google Scholar
谷歌学者
Cohen, J. I., Bollard, C. M., Khanna, R. & Pittaluga, S. Current understanding of the role of Epstein-Barr virus in lymphomagenesis and therapeutic approaches to EBV-associated lymphomas. Leuk. Lymphoma 49, 27–34 (2008).Article
Cohen,J.I.,Bollard,C.M.,Khanna,R。&Pittaluga,S。目前对爱泼斯坦-巴尔病毒在淋巴瘤发生中的作用以及EBV相关淋巴瘤的治疗方法的理解。白血病。淋巴瘤49,27-34(2008)。文章
CAS
中科院
PubMed
PubMed
PubMed Central
公共医学中心
Google Scholar
谷歌学者
Latour, S. & Fischer, A. Signaling pathways involved in the T-cell-mediated immunity against Epstein-Barr virus: lessons from genetic diseases. Immunol. Rev. 291, 174–189 (2019).Article
Latour,S。&Fischer,A。涉及T细胞介导的针对爱泼斯坦-巴尔病毒的免疫的信号传导途径:遗传疾病的教训。免疫。第291174-189版(2019)。文章
CAS
中科院
PubMed
PubMed
Google Scholar
谷歌学者
Schiller, J. T. & Lowy, D. R. An introduction to virus infections and human cancer. Recent. Results Cancer Res. 217, 1–11 (2021).Article
Schiller,J.T。&Lowy,D.R。病毒感染和人类癌症简介。最近。结果癌症研究217,1-11(2021)。文章
CAS
中科院
PubMed
PubMed
PubMed Central
公共医学中心
Google Scholar
谷歌学者
Qian, Z. et al. HBV integrations reshaping genomic structures promote hepatocellular carcinoma. Gut 73, 1169–1182 (2024).Article
Qian,Z.等。重塑基因组结构的HBV整合促进肝细胞癌。肠道731169-1182(2024)。文章
PubMed
PubMed
Google Scholar
谷歌学者
Jia, Y. et al. HBV DNA polymerase upregulates the transcription of PD-L1 and suppresses T cell activity in hepatocellular carcinoma. J. Transl. Med. 22, 272 (2024).Article
Jia,Y。等人。HBV DNA聚合酶上调PD-L1的转录并抑制肝细胞癌中的T细胞活性。J、 翻译。医学22272(2024)。文章
CAS
中科院
PubMed
PubMed
PubMed Central
公共医学中心
Google Scholar
谷歌学者
Dong, W., Wang, H., Li, M., Li, P. & Ji, S. Virus-induced host genomic remodeling dysregulates gene expression, triggering tumorigenesis. Front. Cell Infect. Microbiol. 14, 1359766 (2024).Article
Dong,W.,Wang,H.,Li,M.,Li,P。&Ji,S。病毒诱导的宿主基因组重塑失调基因表达,引发肿瘤发生。正面。细胞感染。微生物。141359766(2024)。文章
CAS
中科院
PubMed
PubMed
PubMed Central
公共医学中心
Google Scholar
谷歌学者
Zoulim, F., Chen, P. J., Dandri, M., Kennedy, P. & Seeger, C. Hepatitis B virus DNA integration: implications for diagnostics, therapy, and outcome. J. Hepatol. https://doi.org/10.1016/j.jhep.2024.06.037 (2024).Article
Zoulim,F.,Chen,P.J.,Dandri,M.,Kennedy,P。&Seeger,C。乙型肝炎病毒DNA整合:对诊断,治疗和结果的影响。J、 肝病。https://doi.org/10.1016/j.jhep.2024.06.037(2024年)。文章
PubMed
PubMed
Google Scholar
谷歌学者
Vallejo-Ruiz, V., Gutiérrez-Xicotencatl, L., Medina-Contreras, O. & Lizano, M. Molecular aspects of cervical cancer: a pathogenesis update. Front. Oncol. 14, 1356581 (2024).Article
Vallejo-Ruiz,V.,Gutiérrez-Xicotencatl,L.,Medina-Contreras,O。&Lizano,M。宫颈癌的分子方面:发病机制更新。正面。Oncol公司。141356581(2024)。文章
CAS
中科院
PubMed
PubMed
PubMed Central
公共医学中心
Google Scholar
谷歌学者
Li, W. et al. The characteristics of HPV integration in cervical intraepithelial cells. J. Cancer 10, 2783–2787 (2019).Article
Li,W。等。宫颈上皮内细胞中HPV整合的特征。J、 癌症102783-2787(2019)。文章
CAS
中科院
PubMed
PubMed
PubMed Central
公共医学中心
Google Scholar
谷歌学者
Tian, R. et al. Risk stratification of cervical lesions using capture sequencing and machine learning method based on HPV and human integrated genomic profiles. Carcinogenesis 40, 1220–1228 (2019).Article
Tian,R.等人。使用基于HPV和人类整合基因组图谱的捕获测序和机器学习方法对宫颈病变进行风险分层。致癌作用401220-1228(2019)。文章
CAS
中科院
PubMed
PubMed
Google Scholar
谷歌学者
Wang, L. et al. Epstein-Barr virus episome physically interacts with active regions of the host genome in lymphoblastoid cells. J. Virol. 94, e01390-20 (2020).Article
Wang,L。等人。爱泼斯坦-巴尔病毒附加体与淋巴母细胞中宿主基因组的活性区域发生物理相互作用。J、 维罗尔。94,e01390-20(2020)。文章
PubMed
PubMed
PubMed Central
公共医学中心
Google Scholar
谷歌学者
Alcami, A. & Koszinowski, U. H. Viral mechanisms of immune evasion. Trends Microbiol. 8, 410–418 (2000).Article
Alcami,A。&Koszinowski,U.H。免疫逃避的病毒机制。趋势微生物。8410-418(2000)。文章
CAS
中科院
PubMed
PubMed
PubMed Central
公共医学中心
Google Scholar
谷歌学者
Sabourirad, S., Dimitriadis, E. & Mantamadiotis, T. Viruses exploit growth factor mechanisms to achieve augmented pathogenicity and promote tumorigenesis. Arch. Microbiol. 206, 193 (2024).Article
Sabourirad,S.,Dimitriadis,E。&Mantamadiotis,T。病毒利用生长因子机制实现增强的致病性并促进肿瘤发生。拱门。微生物。206193(2024)。文章
CAS
中科院
PubMed
PubMed
PubMed Central
公共医学中心
Google Scholar
谷歌学者
Zhao, B. Epstein-barr virus B cell growth transformation: the nuclear events. Viruses 15, 832 (2023).Article
赵,B。爱泼斯坦-巴尔病毒B细胞生长转化:核事件。病毒15832(2023)。文章
PubMed
PubMed
PubMed Central
公共医学中心
Google Scholar
谷歌学者
Medhat, A., Arzumanyan, A. & Feitelson, M. A. Hepatitis B x antigen (HBx) is an important therapeutic target in the pathogenesis of hepatocellular carcinoma. Oncotarget 12, 2421–2433 (2021).Article
Medhat,A.,Arzumanyan,A。&Feitelson,M.A。乙型肝炎x抗原(HBx)是肝细胞癌发病机制中的重要治疗靶点。Oncotarget 122421–2433(2021)。文章
PubMed
PubMed
PubMed Central
公共医学中心
Google Scholar
谷歌学者
Mittal, S. & Banks, L. Molecular mechanisms underlying human papillomavirus E6 and E7 oncoprotein-induced cell transformation. Mutat. Res. Rev. Mutat. Res. 772, 23–35 (2017).Article
Mittal,S。&Banks,L。人乳头瘤病毒E6和E7癌蛋白诱导细胞转化的分子机制。突变。Res.修订版Mutat。第772、23-35号决议(2017年)。文章
CAS
中科院
PubMed
PubMed
Google Scholar
谷歌学者
Mueller, S. N. & Rouse, B. T. in Clinical Immunology 3rd edn (eds Robert. R. R. et al.) 421–431 (Mosby, 2008).Latour, S. & Winter, S. Inherited immunodeficiencies with high predisposition to Epstein-Barr virus-driven lymphoproliferative diseases. Front. Immunol. 9, 1103 (2018).Article .
Mueller,S.N。和Rouse,B.T.《临床免疫学》第三版(编辑Robert.R.R.等人)421-431(Mosby,2008)。Latour,S。和Winter,S。遗传性免疫缺陷,易患爱泼斯坦-巴尔病毒驱动的淋巴增生性疾病。正面。免疫。91103(2018)。文章。
PubMed
PubMed
PubMed Central
公共医学中心
Google Scholar
谷歌学者
Cohen, J. I. Primary immunodeficiencies associated with EBV disease. Curr. Top. Microbiol. Immunol. 390, 241–265 (2015).CAS
Cohen,J.I。与EBV疾病相关的原发性免疫缺陷。货币。顶部。微生物。免疫。390241-265(2015)。中科院
PubMed
PubMed
PubMed Central
公共医学中心
Google Scholar
谷歌学者
Sacco, K. A., Notarangelo, L. D. & Delmonte, O. M. When to suspect inborn errors of immunity in Epstein-Barr virus-related lymphoproliferative disorders. Clin. Microbiol. Infect. 29, 457–462 (2023).Article
Sacco,K.A.,Notarangelo,L.D。和Delmonte,O.M。何时怀疑爱泼斯坦-巴尔病毒相关淋巴增生性疾病的先天性免疫缺陷。临床。微生物。感染。29457-462(2023)。文章
CAS
中科院
PubMed
PubMed
Google Scholar
谷歌学者
Cohen, J. I. Epstein-Barr virus infection. N. Engl. J. Med. 343, 481–492 (2000).Article
科恩,J.I。爱泼斯坦-巴尔病毒感染。N、 英语。J、 医学34343481-492(2000)。文章
CAS
中科院
PubMed
PubMed
Google Scholar
谷歌学者
Aggarwal, S., Agarwal, P. & Singh, A. K. Human papilloma virus vaccines: a comprehensive narrative review. Cancer Treat. Res. Commun. 37, 100780 (2023).Article
Aggarwal,S.,Agarwal,P。&Singh,A.K。人乳头瘤病毒疫苗:全面的叙述性综述。癌症治疗。公共资源。。文章
PubMed
PubMed
Google Scholar
谷歌学者
Davies, S. I. et al. Robust production of Merkel cell polyomavirus oncogene specific t cells from healthy donors for adoptive transfer. Front. Immunol. 11, 592721 (2020).Article
Davies,S.I.等人。从健康供体中稳定生产Merkel细胞多瘤病毒癌基因特异性t细胞用于过继转移。正面。免疫。11592721(2020)。文章
CAS
中科院
PubMed
PubMed
PubMed Central
公共医学中心
Google Scholar
谷歌学者
Chapuis, A. G. et al. Regression of metastatic Merkel cell carcinoma following transfer of polyomavirus-specific T cells and therapies capable of re-inducing HLA class-I. Cancer Immunol. Res. 2, 27–36 (2014).Article
Chapuis,A.G.等人。转移多瘤病毒特异性T细胞后转移性默克尔细胞癌的消退和能够重新诱导HLA I类的疗法。癌症免疫。第2、27–36号决议(2014年)。文章
CAS
中科院
PubMed
PubMed
Google Scholar
谷歌学者
Mohanty, S. & Harhaj, E. W. Mechanisms of innate immune sensing of HTLV-1 and viral immune evasion. Pathogens 12, 735 (2023).Article
Mohanty,S。&Harhaj,E.W。HTLV-1先天免疫感应和病毒免疫逃避的机制。病原体12735(2023)。文章
CAS
中科院
PubMed
PubMed
PubMed Central
公共医学中心
Google Scholar
谷歌学者
Nagarsheth, N. B. et al. TCR-engineered T cells targeting E7 for patients with metastatic HPV-associated epithelial cancers. Nat. Med. 27, 419–425 (2021).Article
Nagarsheth,N.B.等人,针对转移性HPV相关上皮癌患者靶向E7的TCR工程化T细胞。《自然医学》27419-425(2021)。文章
CAS
中科院
PubMed
PubMed
PubMed Central
公共医学中心
Google Scholar
谷歌学者
Sterner, R. C. & Sterner, R. M. CAR-T cell therapy: current limitations and potential strategies. Blood Cancer J. 11, 69 (2021).Article
Sterner,R.C。和Sterner,R.M。CAR-T细胞疗法:目前的局限性和潜在的策略。血癌J.11,69(2021)。文章
PubMed
PubMed
PubMed Central
公共医学中心
Google Scholar
谷歌学者
Kahan, S. M., Wherry, E. J. & Zajac, A. J. T cell exhaustion during persistent viral infections. Virology 479-480, 180–193 (2015).Article
Kahan,S.M.,Wherry,E.J。&Zajac,A.J。持续病毒感染期间T细胞耗竭。病毒学479-480180-193(2015)。文章
CAS
中科院
PubMed
PubMed
Google Scholar
谷歌学者
Bollard, C. M. et al. Tumor-specific T-cells engineered to overcome tumor immune evasion induce clinical responses in patients with relapsed Hodgkin lymphoma. J. Clin. Oncol. 36, 1128–1139 (2018).Article
Bollard,C.M.等人。为克服肿瘤免疫逃逸而设计的肿瘤特异性T细胞在复发性霍奇金淋巴瘤患者中诱导临床反应。J、 临床。Oncol公司。361128-1139(2018)。文章
CAS
中科院
PubMed
PubMed
PubMed Central
公共医学中心
Google Scholar
谷歌学者
Bell, M. & Gottschalk, S. Engineered cytokine signaling to improve CAR T cell effector function. Front. Immunol. 12, 684642 (2021).Article
Bell,M。&Gottschalk,S。工程化细胞因子信号传导以改善CAR T细胞效应子功能。正面。免疫。12684642(2021)。文章
CAS
中科院
PubMed
PubMed
PubMed Central
公共医学中心
Google Scholar
谷歌学者
Rooney, C. M. et al. Use of gene-modified virus-specific T lymphocytes to control Epstein-Barr-virus-related lymphoproliferation. Lancet 345, 9–13 (1995).Article
Rooney,C.M.等人。使用基因修饰的病毒特异性T淋巴细胞来控制爱泼斯坦-巴尔病毒相关的淋巴增殖。。文章
CAS
中科院
PubMed
PubMed
Google Scholar
谷歌学者
Harris, K. M., Davila, B. J., Bollard, C. M. & Keller, M. D. Virus-specific T cells: current and future use in primary immunodeficiency disorders. J. Allergy Clin. Immunol. Pract. 7, 809–818 (2019).Article
Harris,K.M.,Davila,B.J.,Bollard,C.M。&Keller,M.D。病毒特异性T细胞:目前和未来在原发性免疫缺陷疾病中的应用。J、 过敏临床。免疫。实践。7809-818(2019)。文章
PubMed
PubMed
Google Scholar
谷歌学者
Gustafson, M. P. et al. Emerging frontiers in immuno- and gene therapy for cancer. Cytotherapy 25, 20–32 (2023).Article
Gustafson,M.P.等人。癌症免疫和基因治疗的新兴前沿。细胞疗法25,20-32(2023)。文章
CAS
中科院
PubMed
PubMed
Google Scholar
谷歌学者
Qian, C. et al. Viral-specific T-cell transfer from HSCT donor for the treatment of viral infections or diseases after HSCT. Bone Marrow Transpl. 53, 114–122 (2018).Article
Qian,C.等人。HSCT供体的病毒特异性T细胞转移,用于治疗HSCT后的病毒感染或疾病。骨髓移植。53114-122(2018)。文章
CAS
中科院
Google Scholar
谷歌学者
Wehler, T. C. et al. Rapid identification and sorting of viable virus-reactive CD4+ and CD8+ T cells based on antigen-triggered CD137 expression. J. Immunol. Methods 339, 23–37 (2008).Article
Wehler,T.C.等人。基于抗原触发的CD137表达快速鉴定和分选活病毒反应性CD4+和CD8+T细胞。J、 免疫。方法339,23-37(2008)。文章
CAS
中科院
PubMed
PubMed
Google Scholar
谷歌学者
Frentsch, M. et al. Direct access to CD4+ T cells specific for defined antigens according to CD154 expression. Nat. Med. 11, 1118–1124 (2005).Article
Frentsch,M。等人。根据CD154表达直接获得对确定抗原特异的CD4+T细胞。《自然医学》11118-1124(2005)。文章
CAS
中科院
PubMed
PubMed
Google Scholar
谷歌学者
Thomas, S. et al. Framework engineering to produce dominant T cell receptors with enhanced antigen-specific function. Nat. Commun. 10, 4451 (2019).Article
Thomas,S.等人的框架工程,以产生具有增强的抗原特异性功能的显性T细胞受体。国家公社。104451(2019)。文章
PubMed
PubMed
PubMed Central
公共医学中心
Google Scholar
谷歌学者
Rosenberg, S. A. et al. Use of tumor-infiltrating lymphocytes and interleukin-2 in the immunotherapy of patients with metastatic melanoma. A preliminary report. N. Engl. J. Med. 319, 1676–1680 (1988).Article
Rosenberg,S.A.等人。肿瘤浸润淋巴细胞和白细胞介素-2在转移性黑色素瘤患者免疫治疗中的应用。初步报告。N、 英语。J、 医学3191676-1680(1988)。文章
CAS
中科院
PubMed
PubMed
Google Scholar
谷歌学者
Kazemi, M. H. et al. Tumor-infiltrating lymphocytes for treatment of solid tumors: it takes two to tango? Front. Immunol. 13, 1018962 (2022).Article
Kazemi,M.H.等人。用于治疗实体瘤的肿瘤浸润淋巴细胞:探戈需要两个人?正面。免疫。131018962(2022)。文章
CAS
中科院
PubMed
PubMed
PubMed Central
公共医学中心
Google Scholar
谷歌学者
Stevanovic, S. et al. Complete regression of metastatic cervical cancer after treatment with human papillomavirus-targeted tumor-infiltrating T cells. J. Clin. Oncol. 33, 1543–1550 (2015).Article
Stevanovic,S.等人。用人乳头瘤病毒靶向肿瘤浸润性T细胞治疗后转移性宫颈癌的完全消退。J、 临床。Oncol公司。331543-1550(2015)。文章
CAS
中科院
PubMed
PubMed
PubMed Central
公共医学中心
Google Scholar
谷歌学者
Xie, N. et al. Neoantigens: promising targets for cancer therapy. Signal. Transduct. Target. Ther. 8, 9 (2023).Article
Xie,N.等人。新抗原:癌症治疗的有希望的靶标。。Transduct公司。目标。他们。8,9(2023)。文章
CAS
中科院
PubMed
PubMed
PubMed Central
公共医学中心
Google Scholar
谷歌学者
Munz, C. Redirecting T cells against epstein-barr virus infection and associated oncogenesis. Cells 9, 1400 (2020).Article
Munz,C。重定向T细胞以抵抗爱泼斯坦-巴尔病毒感染和相关的肿瘤发生。细胞91400(2020)。文章
PubMed
PubMed
PubMed Central
公共医学中心
Google Scholar
谷歌学者
Bollard, C. M. et al. Sustained complete responses in patients with lymphoma receiving autologous cytotoxic T lymphocytes targeting Epstein-Barr virus latent membrane proteins. J. Clin. Oncol. 32, 798–808 (2014).Article
。J、 临床。Oncol公司。32798-808(2014)。文章
CAS
中科院
PubMed
PubMed
Google Scholar
谷歌学者
Chua, D. et al. Adoptive transfer of autologous Epstein-Barr virus-specific cytotoxic T cells for nasopharyngeal carcinoma. Int. J. Cancer 94, 73–80 (2001).Article
Chua,D。等人。过继转移自体爱泼斯坦-巴尔病毒特异性细胞毒性T细胞治疗鼻咽癌。Int.J.Cancer 94,73-80(2001)。文章
CAS
中科院
PubMed
PubMed
Google Scholar
谷歌学者
Heslop, H. E., Savoldo, B. & Rooney, C. M. Cellular therapy of Epstein-Barr-virus-associated post-transplant lymphoproliferative disease. Best Pract. Res. Clin. Haematol. 17, 401–413 (2004).Article
Heslop,H.E.,Savoldo,B。&Rooney,C.M。爱泼斯坦-巴尔病毒相关移植后淋巴增生性疾病的细胞治疗。最佳实践。临床研究。血液。17401-413(2004)。文章
CAS
中科院
PubMed
PubMed
Google Scholar
谷歌学者
Lucas, K. G., Small, T. N., Heller, G., Dupont, B. & O’Reilly, R. J. The development of cellular immunity to Epstein-Barr virus after allogeneic bone marrow transplantation. Blood 87, 2594–2603 (1996).Article
。血液872594-2603(1996)。文章
CAS
中科院
PubMed
PubMed
Google Scholar
谷歌学者
Papadopoulos, E. B. et al. Infusions of donor leukocytes to treat Epstein-Barr virus-associated lymphoproliferative disorders after allogeneic bone marrow transplantation. N. Engl. J. Med. 330, 1185–1191 (1994).Article
Papadopoulos,E.B.等人输注供体白细胞治疗异基因骨髓移植后爱泼斯坦-巴尔病毒相关的淋巴组织增生性疾病。N、 英语。J、 医学3301185-1191(1994)。文章
CAS
中科院
PubMed
PubMed
Google Scholar
谷歌学者
Bollard, C. M. & Heslop, H. E. T cells for viral infections after allogeneic hematopoietic stem cell transplant. Blood 127, 3331–3340 (2016).Article
Bollard,C.M。&Heslop,H.E.T细胞用于异基因造血干细胞移植后的病毒感染。血液1273331-3340(2016)。文章
CAS
中科院
PubMed
PubMed
PubMed Central
公共医学中心
Google Scholar
谷歌学者
Doubrovina, E. et al. Adoptive immunotherapy with unselected or EBV-specific T cells for biopsy-proven EBV+ lymphomas after allogeneic hematopoietic cell transplantation. Blood 119, 2644–2656 (2012).Article
Doubrovina,E.等人。异基因造血细胞移植后活检证实的EBV+淋巴瘤的未选择或EBV特异性T细胞过继免疫治疗。血液1192644-2656(2012)。文章
CAS
中科院
PubMed
PubMed
PubMed Central
公共医学中心
Google Scholar
谷歌学者
Heslop, H. E. et al. Long-term outcome of EBV-specific T-cell infusions to prevent or treat EBV-related lymphoproliferative disease in transplant recipients. Blood 115, 925–935 (2010).Article
Heslop,H.E.等人。EBV特异性T细胞输注预防或治疗移植受者EBV相关淋巴组织增生性疾病的长期结果。血液115925-935(2010)。文章
CAS
中科院
PubMed
PubMed
PubMed Central
公共医学中心
Google Scholar
谷歌学者
McLaughlin, L. P. et al. EBV/LMP-specific T cells maintain remissions of T- and B-cell EBV lymphomas after allogeneic bone marrow transplantation. Blood 132, 2351–2361 (2018).Article
McLaughlin,L.P。等人。EBV/LMP特异性T细胞在异基因骨髓移植后维持T细胞和B细胞EBV淋巴瘤的缓解。血液1322351-2361(2018)。文章
CAS
中科院
PubMed
PubMed
PubMed Central
公共医学中心
Google Scholar
谷歌学者
Prockop, S. E. & Vatsayan, A. Epstein-Barr virus lymphoproliferative disease after solid organ transplantation. Cytotherapy 19, 1270–1283 (2017).Article
。细胞疗法191270-1283(2017)。文章
CAS
中科院
PubMed
PubMed
Google Scholar
谷歌学者
Rubinstein, J., Toner, K., Gross, T. & Wistinghausen, B. Diagnosis and management of post-transplant lymphoproliferative disease following solid organ transplantation in children, adolescents, and young adults. Best Pract. Res. Clin. Haematol. 36, 101446 (2023).Article
Rubinstein,J.,Toner,K.,Gross,T。&Wistinghausen,B。儿童,青少年和年轻人实体器官移植后移植后淋巴增生性疾病的诊断和治疗。最佳实践。临床研究。血液。36101446(2023)。文章
PubMed
PubMed
Google Scholar
谷歌学者
Wistinghausen, B., Gross, T. G. & Bollard, C. Post-transplant lymphoproliferative disease in pediatric solid organ transplant recipients. Pediatr. Hematol. Oncol. 30, 520–531 (2013).Article
Wistinghausen,B.,Gross,T.G。&Bollard,C。小儿实体器官移植受者的移植后淋巴增生性疾病。儿科。血液学。Oncol公司。30520-531(2013)。文章
CAS
中科院
PubMed
PubMed
Google Scholar
谷歌学者
Haque, T. et al. Reconstitution of EBV-specific T cell immunity in solid organ transplant recipients. J. Immunol. 160, 6204–6209 (1998).Article
。J、 免疫。1606204-6209(1998)。文章
CAS
中科院
PubMed
PubMed
Google Scholar
谷歌学者
Khanna, R. et al. Activation and adoptive transfer of Epstein-Barr virus-specific cytotoxic T cells in solid organ transplant patients with posttransplant lymphoproliferative disease. Proc. Natl Acad. Sci. USA 96, 10391–10396 (1999).Article
Khanna,R.等人。患有移植后淋巴增生性疾病的实体器官移植患者中爱泼斯坦-巴尔病毒特异性细胞毒性T细胞的激活和过继转移。程序。国家科学院。科学。美国9610391–10396(1999)。文章
CAS
中科院
PubMed
PubMed
PubMed Central
公共医学中心
Google Scholar
谷歌学者
Comoli, P. et al. Treatment of EBV-related post-renal transplant lymphoproliferative disease with a tailored regimen including EBV-specific T cells. Am. J. Transpl. 5, 1415–1422 (2005).Article
Comoli,P。等人。用包括EBV特异性T细胞的定制方案治疗EBV相关的肾移植后淋巴增生性疾病。。51415-1422(2005)。文章
Google Scholar
谷歌学者
Savoldo, B. et al. Treatment of solid organ transplant recipients with autologous Epstein Barr virus-specific cytotoxic T lymphocytes (CTLs). Blood 108, 2942–2949 (2006).Article
Savoldo,B。等人。用自体爱泼斯坦-巴尔病毒特异性细胞毒性T淋巴细胞(CTL)治疗实体器官移植受者。血液1082942-2949(2006)。文章
CAS
中科院
PubMed
PubMed
PubMed Central
公共医学中心
Google Scholar
谷歌学者
Prockop, S. et al. Off-the-shelf EBV-specific T cell immunotherapy for rituximab-refractory EBV-associated lymphoma following transplantation. J. Clin. Invest. 130, 733–747 (2020).Article
Prockop,S.等人。移植后利妥昔单抗难治性EBV相关淋巴瘤的现成EBV特异性T细胞免疫疗法。J、 临床。投资。130733-747(2020)。文章
CAS
中科院
PubMed
PubMed
PubMed Central
公共医学中心
Google Scholar
谷歌学者
Barker, J. N. et al. Successful treatment of EBV-associated posttransplantation lymphoma after cord blood transplantation using third-party EBV-specific cytotoxic T lymphocytes. Blood 116, 5045–5049 (2010).Article
Barker,J.N.等人。使用第三方EBV特异性细胞毒性T淋巴细胞成功治疗脐血移植后EBV相关的移植后淋巴瘤。血液1165045-5049(2010)。文章
CAS
中科院
PubMed
PubMed
PubMed Central
公共医学中心
Google Scholar
谷歌学者
Wistinghausen, B. et al. ANHL1522: durable immunity to EBV post rituximab and third party LMP-specific T-cells: a children’s oncology group study. Blood Adv. 12, 1116–1127 (2024).Article
Wistinghausen,B。等人ANHL1522:利妥昔单抗和第三方LMP特异性T细胞对EBV的持久免疫力:儿童肿瘤学小组研究。血液杂志121116-1127(2024)。文章
Google Scholar
谷歌学者
Bollard, C. M. et al. Complete responses of relapsed lymphoma following genetic modification of tumor-antigen presenting cells and T-lymphocyte transfer. Blood 110, 2838–2845 (2007).Article
Bollard,C.M.等人。肿瘤抗原呈递细胞基因修饰和T淋巴细胞转移后复发淋巴瘤的完全反应。血液1102838-2845(2007)。文章
CAS
中科院
PubMed
PubMed
PubMed Central
公共医学中心
Google Scholar
谷歌学者
Kim, W. S. et al. Autologous EBV-specific T cell treatment results in sustained responses in patients with advanced extranodal NK/T lymphoma: results of a multicenter study. Ann. Hematol. 100, 2529–2539 (2021).Article
Kim,W.S.等人。自体EBV特异性T细胞治疗导致晚期结外NK/T淋巴瘤患者持续反应:一项多中心研究的结果。安。血液学。1002529-2539(2021)。文章
CAS
中科院
PubMed
PubMed
Google Scholar
谷歌学者
Comoli, P. et al. Cell therapy of stage IV nasopharyngeal carcinoma with autologous Epstein-Barr virus-targeted cytotoxic T lymphocytes. J. Clin. Oncol. 23, 8942–8949 (2005).Article
Comoli,P。等人。用自体爱泼斯坦-巴尔病毒靶向的细胞毒性T淋巴细胞治疗IV期鼻咽癌。J、 临床。Oncol公司。238942-8949(2005)。文章
CAS
中科院
PubMed
PubMed
Google Scholar
谷歌学者
Chia, W. K. et al. Adoptive T-cell transfer and chemotherapy in the first-line treatment of metastatic and/or locally recurrent nasopharyngeal carcinoma. Mol. Ther. 22, 132–139 (2014).Article
Chia,W.K.等。过继性T细胞转移和化疗在转移性和/或局部复发性鼻咽癌一线治疗中的应用。摩尔热。22132-139(2014)。文章
CAS
中科院
PubMed
PubMed
Google Scholar
谷歌学者
Secondino, S. et al. Long-lasting responses with chemotherapy followed by T-cell therapy in recurrent or metastatic EBV-related nasopharyngeal carcinoma. Front. Immunol. 14, 1208475 (2023).Article
Secondino,S.等人。复发或转移性EBV相关鼻咽癌的化疗后T细胞治疗的长期反应。正面。免疫。141208475(2023)。文章
CAS
中科院
PubMed
PubMed
PubMed Central
公共医学中心
Google Scholar
谷歌学者
Toh, H. C. et al. 652O Randomized phase III VANCE study: gemcitabine and carboplatin (GC) followed by Epstein Barr virus-specific autologous cytotoxic T lymphocytes (EBV-CTL) versus the same chemotherapy as first-line treatment for advanced nasopharyngeal carcinoma (NPC). Ann. Oncol.
Toh,H.C.等人652O随机III期VANCE研究:吉西他滨和卡铂(GC),然后是爱泼斯坦-巴尔病毒特异性自体细胞毒性T淋巴细胞(EBV-CTL),与一线治疗晚期鼻咽癌(NPC)相同的化疗。安科。
33, S840 (2022).Article .
33,S840(2022)。文章。
Google Scholar
谷歌学者
Haque, T. et al. Allogeneic cytotoxic T-cell therapy for EBV-positive posttransplantation lymphoproliferative disease: results of a phase 2 multicenter clinical trial. Blood 110, 1123–1131 (2007).Article
Haque,T。等人。EBV阳性移植后淋巴增生性疾病的同种异体细胞毒性T细胞疗法:2期多中心临床试验的结果。血液1101123-1131(2007)。文章
CAS
中科院
PubMed
PubMed
Google Scholar
谷歌学者
Keller, M. D. et al. Secondary bone marrow graft loss after third-party virus-specific T cell infusion: case report of a rare complication. Nat. Commun. 15, 2749 (2024).Article
Keller,M.D.等人。第三方病毒特异性T细胞输注后继发性骨髓移植物丢失:罕见并发症的病例报告。国家公社。152749(2024)。文章
CAS
中科院
PubMed
PubMed
PubMed Central
公共医学中心
Google Scholar
谷歌学者
Leen, A. M. et al. Multicenter study of banked third-party virus-specific T cells to treat severe viral infections after hematopoietic stem cell transplantation. Blood 121, 5113–5123 (2013).Article
。血液1215113-5123(2013)。文章
CAS
中科院
PubMed
PubMed
PubMed Central
公共医学中心
Google Scholar
谷歌学者
Tzannou, I. et al. Off-the-shelf virus-specific T cells to treat BK virus, human herpesvirus 6, cytomegalovirus, Epstein-Barr virus, and adenovirus infections after allogeneic hematopoietic stem-cell transplantation. J. Clin. Oncol. 35, 3547–3557 (2017).Article
Tzannou,I。等人。用于治疗异基因造血干细胞移植后BK病毒,人类疱疹病毒6,巨细胞病毒,爱泼斯坦-巴尔病毒和腺病毒感染的现成病毒特异性T细胞。J、 临床。Oncol公司。353547-3557(2017)。文章
CAS
中科院
PubMed
PubMed
PubMed Central
公共医学中心
Google Scholar
谷歌学者
Withers, B. et al. Establishment and operation of a third-party virus-specific T cell bank within an allogeneic stem cell transplant program. Biol. Blood Marrow Transpl. 24, 2433–2442 (2018).Article
Withers,B.等人。在同种异体干细胞移植计划中建立和运营第三方病毒特异性T细胞库。生物骨髓移植。242433-2442(2018)。文章
CAS
中科院
Google Scholar
谷歌学者
Kazi, S. et al. Long-term follow up after third-party viral-specific cytotoxic lymphocytes for immunosuppression- and Epstein-Barr virus-associated lymphoproliferative disease. Haematologica 104, e356–e359 (2019).Article
Kazi,S.等人。第三方病毒特异性细胞毒性淋巴细胞治疗免疫抑制和爱泼斯坦-巴尔病毒相关淋巴增生性疾病的长期随访。。文章
PubMed
PubMed
PubMed Central
公共医学中心
Google Scholar
谷歌学者
Mahadeo, K. M. et al. Tabelecleucel for allogeneic haematopoietic stem-cell or solid organ transplant recipients with Epstein-Barr virus-positive post-transplant lymphoproliferative disease after failure of rituximab or rituximab and chemotherapy (ALLELE): a phase 3, multicentre, open-label trial.
Mahadeo,K.M.等人,Tabelecleucel用于利妥昔单抗或利妥昔单抗和化疗失败后具有爱泼斯坦-巴尔病毒阳性移植后淋巴增生性疾病的同种异体造血干细胞或实体器官移植受者(等位基因):一项3期,多中心,开放标签试验。
Lancet Oncol. 25, 376–387 (2024).Article .
柳叶刀Oncol。。文章。
CAS
中科院
PubMed
PubMed
Google Scholar
谷歌学者
Bonifacius, A. et al. Patient-tailored adoptive immunotherapy with EBV-specific T cells from related and unrelated donors. J. Clin. Invest. 133, e163548 (2023).Article
Bonifacius,A.等人用来自相关和不相关供体的EBV特异性T细胞进行患者定制的过继免疫治疗。J、 临床。投资。133,e163548(2023)。文章
CAS
中科院
PubMed
PubMed
PubMed Central
公共医学中心
Google Scholar
谷歌学者
Bollard, C. M. et al. Adapting a transforming growth factor beta-related tumor protection strategy to enhance antitumor immunity. Blood 99, 3179–3187 (2002).Article
Bollard,C.M.等人采用转化生长因子β相关的肿瘤保护策略来增强抗肿瘤免疫力。血液993179-3187(2002)。文章
CAS
中科院
PubMed
PubMed
Google Scholar
谷歌学者
Foster, A. E. et al. Antitumor activity of EBV-specific T lymphocytes transduced with a dominant negative TGF-beta receptor. J. Immunother. 31, 500–505 (2008).Article
Foster,A.E.等人。用显性负性TGF-β受体转导的EBV特异性T淋巴细胞的抗肿瘤活性。J、 免疫疗法。31500–505(2008)。文章
CAS
中科院
PubMed
PubMed
PubMed Central
公共医学中心
Google Scholar
谷歌学者
Cruz, C. R. et al. Infusion of donor-derived CD19-redirected virus-specific T cells for B-cell malignancies relapsed after allogeneic stem cell transplant: a phase 1 study. Blood 122, 2965–2973 (2013).Article
Cruz,C.R.等人。输注供体来源的CD19重定向病毒特异性T细胞治疗异基因干细胞移植后复发的B细胞恶性肿瘤:1期研究。血液1222965-2973(2013)。文章
CAS
中科院
PubMed
PubMed
PubMed Central
公共医学中心
Google Scholar
谷歌学者
McKenna, M. et al. Real-world evidence of the safety and survival with CD19 CAR-T cell therapy for relapsed/refractory solid organ transplant-related PTLD. Br. J. Haematol. 202, 248–255 (2023).Article
McKenna,M.等人。CD19 CAR-T细胞治疗复发/难治性实体器官移植相关PTLD的安全性和生存率的现实证据。Br.J.血液学。202248–255(2023)。文章
CAS
中科院
PubMed
PubMed
Google Scholar
谷歌学者
Harputluoglu, M. & Carr, B. I. Hepatitis B before and after hepatocellular carcinoma. J. Gastrointest. Cancer 52, 1206–1210 (2021).Article
。J、 胃肠学家。癌症521206-1210(2021)。文章
PubMed
PubMed
Google Scholar
谷歌学者
Thomas, D. L. Global elimination of chronic hepatitis. N. Engl. J. Med. 380, 2041–2050 (2019).Article
Thomas,D.L。全球消除慢性肝炎。N、 英语。J、 医学3802041-2050(2019)。文章
PubMed
PubMed
Google Scholar
谷歌学者
Shen, C., Jiang, X., Li, M. & Luo, Y. Hepatitis virus and hepatocellular carcinoma: recent advances. Cancers 15, 533 (2023).Article
Shen,C.,Jiang,X.,Li,M。&Luo,Y。肝炎病毒和肝细胞癌:最新进展。癌症15533(2023)。文章
CAS
中科院
PubMed
PubMed
PubMed Central
公共医学中心
Google Scholar
谷歌学者
Luna-Cuadros, M. A. et al. Risk of hepatocellular carcinoma after hepatitis C virus cure. World J. Gastroenterol. 28, 96–107 (2022).Article
Luna Cuadros,M.A.等人。丙型肝炎病毒治愈后肝细胞癌的风险。世界J.胃肠病学。28,96-107(2022)。文章
CAS
中科院
PubMed
PubMed
PubMed Central
公共医学中心
Google Scholar
谷歌学者
Finn, R. S. et al. Atezolizumab plus bevacizumab in unresectable hepatocellular carcinoma. N. Engl. J. Med. 382, 1894–1905 (2020).Article
Finn,R.S.等人,Atezolizumab联合贝伐单抗治疗不可切除的肝细胞癌。N、 英语。J、 医学3821994-1905(2020)。文章
CAS
中科院
PubMed
PubMed
Google Scholar
谷歌学者
Tan, A. T. & Bertoletti, A. HBV-HCC treatment with mRNA electroporated HBV-TCR T cells. Immunother. Adv. 2, ltab026 (2022).Article
Tan,A.T。&Bertoletti,A。用mRNA电穿孔的HBV-TCR T细胞治疗HBV-HCC。免疫疗法。Adv.2,ltab026(2022)。文章
PubMed
PubMed
Google Scholar
谷歌学者
Ozer, M., Goksu, S. Y., Akagunduz, B., George, A. & Sahin, I. Adoptive cell therapy in hepatocellular carcinoma: a review of clinical trials. Cancers 15, 1808 (2023).Article
Ozer,M.,Goksu,S.Y.,Akagunduz,B.,George,A。&Sahin,I。肝细胞癌的过继细胞疗法:临床试验综述。癌症151808(2023)。文章
CAS
中科院
PubMed
PubMed
PubMed Central
公共医学中心
Google Scholar
谷歌学者
Bertoletti, A. et al. T cell receptor-therapy in HBV-related hepatocellularcarcinoma. Oncoimmunology 4, e1008354 (2015).Article
Bertoletti,A。等。HBV相关肝细胞癌的T细胞受体治疗。肿瘤免疫学4,e1008354(2015)。文章
PubMed
PubMed
PubMed Central
公共医学中心
Google Scholar
谷歌学者
Bertoletti, A. & Tan, A. T. HBV as a target for CAR or TCR-T cell therapy. Curr. Opin. Immunol. 66, 35–41 (2020).Article
Bertoletti,A。&Tan,A.T。HBV作为CAR或TCR-T细胞治疗的靶标。货币。奥平。免疫。66,35-41(2020)。文章
CAS
中科院
PubMed
PubMed
Google Scholar
谷歌学者
Qasim, W. et al. Immunotherapy of HCC metastases with autologous T cell receptor redirected T cells, targeting HBsAg in a liver transplant patient. J. Hepatol. 62, 486–491 (2015).Article
Qasim,W。等人。用自体T细胞受体重定向T细胞对HCC转移进行免疫治疗,靶向肝移植患者的HBsAg。J、 肝病。。文章
CAS
中科院
PubMed
PubMed
Google Scholar
谷歌学者
Tan, A. T. et al. Use of expression profiles of HBV-DNA integrated into genomes of hepatocellular carcinoma cells to select T cells for immunotherapy. Gastroenterology 156, 1862–1876.e9 (2019).Article
Tan,A.T.等人。利用整合到肝细胞癌细胞基因组中的HBV-DNA表达谱来选择用于免疫治疗的T细胞。胃肠病学1561862-1876.e9(2019)。文章
CAS
中科院
PubMed
PubMed
Google Scholar
谷歌学者
Meng, F. et al. Immunotherapy of HBV-related advanced hepatocellular carcinoma with short-term HBV-specific TCR expressed T cells: results of dose escalation, phase I trial. Hepatol. Int. 15, 1402–1412 (2021).Article
Meng,F。等人。用短期HBV特异性TCR表达的T细胞免疫治疗HBV相关的晚期肝细胞癌:剂量递增的结果,I期试验。肝病。内景151402-1412(2021)。文章
PubMed
PubMed
Google Scholar
谷歌学者
Yang, F. et al. Messenger RNA electroporated hepatitis B virus (HBV) antigen-specific T cell receptor (TCR) redirected T cell therapy is well-tolerated in patients with recurrent HBV-related hepatocellular carcinoma post-liver transplantation: results from a phase I trial. Hepatol. Int.
Yang,F。等人。信使RNA电穿孔乙型肝炎病毒(HBV)抗原特异性T细胞受体(TCR)重定向T细胞治疗在肝移植后复发性HBV相关肝细胞癌患者中具有良好的耐受性:I期试验的结果。肝病。内景。
17, 850–859 (2023).Article .
17850-859(2023)。文章。
PubMed
PubMed
Google Scholar
谷歌学者
Bohne, F. et al. T cells redirected against hepatitis B virus surface proteins eliminate infected hepatocytes. Gastroenterology 134, 239–247 (2008).Article
Bohne,F。等人。针对乙型肝炎病毒表面蛋白重定向的T细胞消除了感染的肝细胞。胃肠病学134239-247(2008)。文章
CAS
中科院
PubMed
PubMed
Google Scholar
谷歌学者
Malagón, T., Franco, E. L., Tejada, R. & Vaccarella, S. Epidemiology of HPV-associated cancers past, present and future: towards prevention and elimination. Nat. Rev. Clin. Oncol. 21, 522–538 (2024).Article
Malagón,T.,Franco,E.L.,Tejada,R。&Vaccarella,S。HPV相关癌症的流行病学过去,现在和未来:预防和消除。国家修订临床。Oncol公司。21522-538(2024)。文章
PubMed
PubMed
Google Scholar
谷歌学者
Doran, S. L. et al. T-cell receptor gene therapy for human papillomavirus-associated epithelial cancers: a first-in-human, phase I/II study. J. Clin. Oncol. 37, 2759–2768 (2019).Article
Doran,S.L.等人,《人乳头瘤病毒相关上皮癌的T细胞受体基因治疗:人类第一次I/II期研究》。J、 临床。Oncol公司。372759-2768(2019)。文章
CAS
中科院
PubMed
PubMed
PubMed Central
公共医学中心
Google Scholar
谷歌学者
Eskander, R. N. & Tewari, K. S. Immunotherapy: an evolving paradigm in the treatment of advanced cervical cancer. Clin. Ther. 37, 20–38 (2015).Article
Eskander,R.N。&Tewari,K.S。免疫疗法:治疗晚期宫颈癌的不断发展的范例。临床。他们。37,20-38(2015)。文章
CAS
中科院
PubMed
PubMed
Google Scholar
谷歌学者
Huang, H. et al. Phase I study of adjuvant immunotherapy with autologous tumor-infiltrating lymphocytes in locally advanced cervical cancer. J. Clin. Invest. 132, e157726 (2022).Article
Huang,H.等。局部晚期宫颈癌自体肿瘤浸润淋巴细胞辅助免疫治疗的I期研究。J、 临床。投资。132,e157726(2022)。文章
CAS
中科院
PubMed
PubMed
PubMed Central
公共医学中心
Google Scholar
谷歌学者
Liu, W., MacDonald, M. & You, J. Merkel cell polyomavirus infection and Merkel cell carcinoma. Curr. Opin. Virol. 20, 20–27 (2016).Article
Liu,W.,MacDonald,M。&You,J。Merkel细胞多瘤病毒感染和Merkel细胞癌。货币。奥平。维罗尔。20,20-27(2016)。文章
CAS
中科院
PubMed
PubMed
PubMed Central
公共医学中心
Google Scholar
谷歌学者
Veatch, J. et al. Merkel polyoma virus specific T-cell receptor transgenic T-cell therapy in PD-1 inhibitor refractory Merkel cell carcinoma. J. Clin. Oncol. 40, 9549 (2022).Article
Veatch,J.等。Merkel多瘤病毒特异性T细胞受体转基因T细胞治疗PD-1抑制剂难治性Merkel细胞癌。J、 临床。Oncol公司。409549(2022)。文章
Google Scholar
谷歌学者
Bangham, C. R. M. HTLV-1 persistence and the oncogenesis of adult T-cell leukemia/lymphoma. Blood 141, 2299–2306 (2023).CAS
Bangham,C.R.M。HTLV-1持久性和成人T细胞白血病/淋巴瘤的肿瘤发生。血液1412299-2306(2023)。中科院
PubMed
PubMed
PubMed Central
公共医学中心
Google Scholar
谷歌学者
Sampaio, G. C. L. et al. Human T cell lymphotropic virus type 1 global prevalence associated with the human development index: systematic review with meta-analysis. AIDS Res. Hum. Retroviruses 39, 145–165 (2023).Article
Sampaio,G.C.L.等人。与人类发展指数相关的人类T细胞嗜淋巴细胞病毒1型全球流行率:荟萃分析的系统评价。AIDS Res.Hum。逆转录病毒39145-165(2023)。文章
CAS
中科院
PubMed
PubMed
Google Scholar
谷歌学者
Gessain, A. & Cassar, O. Epidemiological aspects and world distribution of HTLV-1 infection. Front. Microbiol. 3, 388 (2012).Article
Gessain,A。&Cassar,O。HTLV-1感染的流行病学方面和世界分布。正面。微生物。3388(2012)。文章
PubMed
PubMed
PubMed Central
公共医学中心
Google Scholar
谷歌学者
Shimoyama, M. Diagnostic criteria and classification of clinical subtypes of adult T-cell leukaemia-lymphoma. A report from the Lymphoma Study Group (1984-87). Br. J. Haematol. 79, 428–437 (1991).Article
Shimoyama,M。成人T细胞白血病淋巴瘤临床亚型的诊断标准和分类。淋巴瘤研究小组(1984-87)的报告。Br.J.血液学。。文章
CAS
中科院
PubMed
PubMed
Google Scholar
谷歌学者
Bangham, C. R. & Osame, M. Cellular immune response to HTLV-1. Oncogene 24, 6035–6046 (2005).Article
Bangham,C.R。和Osame,M。对HTLV-1的细胞免疫应答。癌基因246035-6046(2005)。文章
CAS
中科院
PubMed
PubMed
Google Scholar
谷歌学者
Hishizawa, M. et al. Transplantation of allogeneic hematopoietic stem cells for adult T-cell leukemia: a nationwide retrospective study. Blood 116, 1369–1376 (2010).Article
Hishizawa,M.等人。异基因造血干细胞移植治疗成人T细胞白血病:一项全国性回顾性研究。血液1161369-1376(2010)。文章
CAS
中科院
PubMed
PubMed
Google Scholar
谷歌学者
Bazarbachi, A. H. et al. Outcome of stem cell transplantation in HTLV-1-associated North American adult T-cell leukemia/lymphoma. Clin. Hematol. Int. 5, 78–91 (2023).Article
。临床。血液学。内景5,78-91(2023)。文章
PubMed
PubMed
PubMed Central
公共医学中心
Google Scholar
谷歌学者
Harashima, N. et al. Graft-versus-Tax response in adult T-cell leukemia patients after hematopoietic stem cell transplantation. Cancer Res. 64, 391–399 (2004).Article
Harashima,N。等人。造血干细胞移植后成人T细胞白血病患者的移植物抗税反应。癌症研究64391-399(2004)。文章
CAS
中科院
PubMed
PubMed
Google Scholar
谷歌学者
Harashima, N. et al. Identification of two new HLA-A*1101-restricted tax epitopes recognized by cytotoxic T lymphocytes in an adult T-cell leukemia patient after hematopoietic stem cell transplantation. J. Virol. 79, 10088–10092 (2005).Article
Harashima,N。等人。造血干细胞移植后成人T细胞白血病患者中细胞毒性T淋巴细胞识别的两个新的HLA-A*1101限制性tax表位的鉴定。J、 维罗尔。7910088–10092(2005)。文章
CAS
中科院
PubMed
PubMed
PubMed Central
公共医学中心
Google Scholar
谷歌学者
Suehiro, Y. et al. Clinical outcomes of a novel therapeutic vaccine with Tax peptide-pulsed dendritic cells for adult T cell leukaemia/lymphoma in a pilot study. Br. J. Haematol. 169, 356–367 (2015).Article
Suehiro,Y.等人。在一项初步研究中,用Tax肽脉冲树突状细胞治疗成人T细胞白血病/淋巴瘤的新型治疗性疫苗的临床结果。Br.J.血液学。169356-367(2015)。文章
CAS
中科院
PubMed
PubMed
Google Scholar
谷歌学者
Kannagi, M. et al. Maintenance of long remission in adult T-cell leukemia by Tax-targeted vaccine: a hope for disease-preventive therapy. Cancer Sci. 110, 849–857 (2019).Article
Kannagi,M.等人。通过Tax靶向疫苗维持成人T细胞白血病的长期缓解:疾病预防治疗的希望。癌症科学。110849-857(2019)。文章
CAS
中科院
PubMed
PubMed
PubMed Central
公共医学中心
Google Scholar
谷歌学者
Suehiro, Y. Tax-targeted dendritic cell vaccine therapy for long-term remission of adult T-cell leukemia-lymphoma [Japanese]. Rinsho Ketsueki 64, 670–677 (2023).PubMed
Suehiro,Y。Tax靶向树突状细胞疫苗治疗成人T细胞白血病淋巴瘤的长期缓解[日本]。Rinsho Ketsueki 64670–677(2023)。PubMed出版社
Google Scholar
谷歌学者
Takeda, S. et al. Genetic and epigenetic inactivation of tax gene in adult T-cell leukemia cells. Int. J. Cancer 109, 559–567 (2004).Article
Takeda,S.等人。成人T细胞白血病细胞中tax基因的遗传和表观遗传失活。《国际癌症杂志》109559-567(2004)。文章
CAS
中科院
PubMed
PubMed
Google Scholar
谷歌学者
Miura, M. et al. Kinetics of HTLV-1 reactivation from latency quantified by single-molecule RNA FISH and stochastic modelling. PLoS Pathog. 15, e1008164 (2019).Article
Miura,M.等人。通过单分子RNA FISH和随机建模定量的潜伏期HTLV-1再激活的动力学。PLoS Pathog。15,e1008164(2019)。文章
PubMed
PubMed
PubMed Central
公共医学中心
Google Scholar
谷歌学者
Gaudray, G. et al. The complementary strand of the human T-cell leukemia virus type 1 RNA genome encodes a bZIP transcription factor that down-regulates viral transcription. J. Virol. 76, 12813–12822 (2002).Article
人类T细胞白血病病毒1型RNA基因组的互补链编码一种下调病毒转录的bZIP转录因子。J、 维罗尔。7612813-12822(2002)。文章
CAS
中科院
PubMed
PubMed
PubMed Central
公共医学中心
Google Scholar
谷歌学者
Chang, Y. et al. Identification of herpesvirus-like DNA sequences in AIDS-associated Kaposi’s sarcoma. Science 266, 1865–1869 (1994).Article
Chang,Y.等人。艾滋病相关卡波西肉瘤中疱疹病毒样DNA序列的鉴定。科学2661865-1869(1994)。文章
CAS
中科院
PubMed
PubMed
Google Scholar
谷歌学者
Cesarman, E., Chang, Y., Moore, P. S., Said, J. W. & Knowles, D. M. Kaposi’s sarcoma-associated herpesvirus-like DNA sequences in AIDS-related body-cavity-based lymphomas. N. Engl. J. Med. 332, 1186–1191 (1995).Article
Cesarman,E.,Chang,Y.,Moore,P.S.,Said,J.W.&Knowles,D.M.Kaposi的肉瘤相关疱疹病毒样DNA序列在艾滋病相关的体腔淋巴瘤中。N、 英语。J、 医学杂志3321186-1191(1995)。文章
CAS
中科院
PubMed
PubMed
Google Scholar
谷歌学者
Soulier, J. et al. Kaposi’s sarcoma-associated herpesvirus-like DNA sequences in multicentric Castleman’s disease. Blood 86, 1276–1280 (1995).Article
Soulier,J。等人。多中心Castleman病中与Kaposi肉瘤相关的疱疹病毒样DNA序列。血液861276-1280(1995)。文章
CAS
中科院
PubMed
PubMed
Google Scholar
谷歌学者
Broussard, G. & Damania, B. KSHV: immune modulation and immunotherapy. Front. Immunol. 10, 3084 (2019).Article
Broussard,G。&Damania,B。KSHV:免疫调节和免疫治疗。正面。免疫。。文章
CAS
中科院
PubMed
PubMed
Google Scholar
谷歌学者
Goncalves, P. H., Uldrick, T. S. & Yarchoan, R. HIV-associated Kaposi sarcoma and related diseases. AIDS 31, 1903–1916 (2017).Article
Goncalves,P.H.,Uldrick,T.S。&Yarchoan,R。HIV相关的卡波西肉瘤和相关疾病。艾滋病311903-1916(2017)。文章
PubMed
PubMed
Google Scholar
谷歌学者
Bihl, F. et al. Cellular immune responses and disease control in acute AIDS-associated Kaposi’s sarcoma. AIDS 23, 1918–1922 (2009).Article
Bihl,F。等人。急性艾滋病相关卡波西肉瘤的细胞免疫反应和疾病控制。艾滋病231918-1922(2009)。文章
PubMed
PubMed
Google Scholar
谷歌学者
Naimo, E., Zischke, J. & Schulz, T. F. Recent advances in developing treatments of Kaposi’s sarcoma herpesvirus-related diseases. Viruses 13, 1797 (2021).Article
Naimo,E.,Zischke,J。&Schulz,T.F。开发卡波西肉瘤疱疹病毒相关疾病治疗的最新进展。病毒131797(2021)。文章
CAS
中科院
PubMed
PubMed
PubMed Central
公共医学中心
Google Scholar
谷歌学者
Keller, M. D. et al. Antiviral cellular therapy for enhancing T-cell reconstitution before or after hematopoietic stem cell transplantation (ACES): a two-arm, open label phase II interventional trial of pediatric patients with risk factor assessment. Nat. Commun. 15, 3258 (2024).Article .
Keller,M.D.等人。造血干细胞移植(ACES)前后增强T细胞重建的抗病毒细胞疗法:一项针对儿科患者的双臂开放标签II期介入试验,并进行危险因素评估。国家公社。153258(2024)。文章。
CAS
中科院
PubMed
PubMed
PubMed Central
公共医学中心
Google Scholar
谷歌学者
Gay, C. L. et al. The effects of human immunodeficiency virus type 1 (HIV-1) antigen-expanded specific T-cell therapy and vorinostat on persistent HIV-1 infection in people with HIV on antiretroviral therapy. J. Infect. Dis. 229, 743–752 (2024).Article
Gay,C.L.等人。人类免疫缺陷病毒1型(HIV-1)抗原扩展特异性T细胞疗法和伏立诺他对抗逆转录病毒疗法的HIV感染者持续感染HIV-1的影响。J、 感染。Dis。229743-752(2024)。文章
PubMed
PubMed
Google Scholar
谷歌学者
Bekker, L.-G. et al. HIV infection. Nat. Rev. Dis. Prim. 9, 42 (2023).Article
Bekker,L.-G.等人,《艾滋病毒感染》。纳特牧师说。普里姆。9、42(2023年)。文章
PubMed
PubMed
Google Scholar
谷歌学者
Grulich, A. E., van Leeuwen, M. T., Falster, M. O. & Vajdic, C. M. Incidence of cancers in people with HIV/AIDS compared with immunosuppressed transplant recipients: a meta-analysis. Lancet 370, 59–67 (2007).Article
Grulich,A.E.,van Leeuwen,M.T.,Falster,M.O。&Vajdic,C.M。与免疫抑制移植受者相比,艾滋病毒/艾滋病患者的癌症发病率:荟萃分析。柳叶刀370,59-67(2007)。文章
PubMed
PubMed
Google Scholar
谷歌学者
Yarchoan, R. & Uldrick, T. S. HIV-associated cancers and related diseases. N. Engl. J. Med. 378, 2145 (2018).Article
Yarchoan,R。&Uldrick,T.S。HIV相关癌症和相关疾病。N、 英语。J、 医学杂志3782145(2018)。文章
PubMed
PubMed
Google Scholar
谷歌学者
Morlat, P. et al. Causes of death among HIV-infected patients in France in 2010 (national survey): trends since 2000. AIDS 28, 1181–1191 (2014).Article
Morlat,P.等人,《2010年法国艾滋病毒感染者死亡原因(全国调查):2000年以来的趋势》。艾滋病281181-1191(2014)。文章
PubMed
PubMed
Google Scholar
谷歌学者
Kim, Y. et al. Trends of cause of death among human immunodeficiency virus patients and the impact of low CD4 counts on diagnosis to death: a retrospective cohort study. J. Korean Med. Sci. 35, e355 (2020).Article
Kim,Y.等人。人类免疫缺陷病毒患者死亡原因的趋势以及低CD4计数对死亡诊断的影响:一项回顾性队列研究。J、 韩国医学科学。35,e355(2020)。文章
PubMed
PubMed
PubMed Central
公共医学中心
Google Scholar
谷歌学者
Walker, R. E. et al. Long-term in vivo survival of receptor-modified syngeneic T cells in patients with human immunodeficiency virus infection. Blood 96, 467–474 (2000).CAS
Walker,R.E.等人。人类免疫缺陷病毒感染患者受体修饰的同基因T细胞的长期体内存活。血液96467-474(2000)。中科院
PubMed
PubMed
Google Scholar
谷歌学者
Mitsuyasu, R. T. et al. Prolonged survival and tissue trafficking following adoptive transfer of CD4ζ gene-modified autologous CD4+ and CD8+ T cells in human immunodeficiency virus-infected subjects. Blood 96, 785–793 (2000).Article
Mitsuyasu,R.T.等人在人类免疫缺陷病毒感染的受试者中过继转移CD4ζ基因修饰的自体CD4+和CD8+T细胞后,延长了生存期和组织运输。血液96785-793(2000)。文章
CAS
中科院
PubMed
PubMed
Google Scholar
谷歌学者
Van Gulck, E. et al. mRNA-based dendritic cell vaccination induces potent antiviral T-cell responses in HIV-1-infected patients. AIDS 26, F1–12 (2012).Article
Van Gulck,E。等人。基于mRNA的树突状细胞疫苗接种在HIV-1感染患者中诱导有效的抗病毒T细胞应答。艾滋病26,F1-12(2012)。文章
PubMed
PubMed
Google Scholar
谷歌学者
Allard, S. D. et al. A phase I/IIa immunotherapy trial of HIV-1-infected patients with Tat, Rev and Nef expressing dendritic cells followed by treatment interruption. Clin. Immunol. 142, 252–268 (2012).Article
Allard,S.D.等人,一项针对HIV-1感染患者的I/IIa期免疫治疗试验,该患者表达Tat,Rev和Nef的树突状细胞,随后中断治疗。临床。免疫。142252-268(2012)。文章
CAS
中科院
PubMed
PubMed
Google Scholar
谷歌学者
Sung, J. A. et al. HIV-specific, ex vivo expanded T cell therapy: feasibility, safety, and efficacy in ART-suppressed HIV-infected individuals. Mol. Ther. 26, 2496–2506 (2018).Article
Sung,J.A.等人。HIV特异性体外扩增T细胞疗法:ART抑制HIV感染者的可行性,安全性和有效性。摩尔热。262496-2506(2018)。文章
CAS
中科院
PubMed
PubMed
PubMed Central
公共医学中心
Google Scholar
谷歌学者
Hutter, G. et al. Long-term control of HIV by CCR5 Delta32/Delta32 stem-cell transplantation. N. Engl. J. Med. 360, 692–698 (2009).Article
Hutter,G。等人。通过CCR5 Delta32/Delta32干细胞移植长期控制HIV。N、 英语。J、 医学360692-698(2009)。文章
PubMed
PubMed
Google Scholar
谷歌学者
Gupta, R. K. et al. HIV-1 remission following CCR5Δ32/Δ32 haematopoietic stem-cell transplantation. Nature 568, 244–248 (2019).Article
Gupta,R.K.等人,CCR5Δ32/Δ32造血干细胞移植后HIV-1缓解。自然568244-248(2019)。文章
CAS
中科院
PubMed
PubMed
PubMed Central
公共医学中心
Google Scholar
谷歌学者
Jensen, B. O. et al. In-depth virological and immunological characterization of HIV-1 cure after CCR5Δ32/Δ32 allogeneic hematopoietic stem cell transplantation. Nat. Med. 29, 583–587 (2023).Article
Jensen,B.O.等人。CCR5Δ32/Δ32异基因造血干细胞移植后HIV-1治愈的深入病毒学和免疫学表征。《自然医学》29583-587(2023)。文章
CAS
中科院
PubMed
PubMed
PubMed Central
公共医学中心
Google Scholar
谷歌学者
Hsu, J. et al. HIV-1 remission and possible cure in a woman after haplo-cord blood transplant. Cell 186, 1115–1126.e8 (2023).Article
Hsu,J。等人。单倍体脐带血移植后女性的HIV-1缓解和可能的治愈。细胞1861115-1126.e8(2023)。文章
CAS
中科院
PubMed
PubMed
PubMed Central
公共医学中心
Google Scholar
谷歌学者
Dickter, J. K. et al. HIV-1 remission after allogeneic hematopoietic-cell transplantation. N. Engl. J. Med. 390, 669–671 (2024).Article
Dickter,J.K.等人。异基因造血细胞移植后HIV-1缓解。N、 英语。J、 医学杂志390669-671(2024)。文章
PubMed
PubMed
Google Scholar
谷歌学者
Xu, L. et al. CRISPR-edited stem cells in a patient with HIV and acute lymphocytic leukemia. N. Engl. J. Med. 381, 1240–1247 (2019).Article
Xu,L.等人,CRISPR编辑了HIV和急性淋巴细胞白血病患者的干细胞。N、 英语。J、 医学3811240-1247(2019)。文章
CAS
中科院
PubMed
PubMed
Google Scholar
谷歌学者
Sáez-Cirión, A. et al. Absence of viral rebound for 18 months without antiretrovirals after allogeneic hematopoietic stem cell transplantation with wild-type CCR5 donor cells to treat a biphenotypic sarcoma. ias2023.org, https://programme.ias2023.org/Abstract/Abstract/?abstractid=5819 (2023).Ondondo, B.
。ias2023.org,https://programme.ias2023.org/Abstract/Abstract/?abstractid=5819(2023年)。昂东多,B。
et al. Novel conserved-region T-cell mosaic vaccine with high global HIV-1 coverage is recognized by protective responses in untreated infection. Mol. Ther. 24, 832–842 (2016).Article .
具有高全球HIV-1覆盖率的新型保守区T细胞镶嵌疫苗在未经治疗的感染中具有保护性反应。摩尔热。24832-842(2016)。文章。
CAS
中科院
PubMed
PubMed
PubMed Central
公共医学中心
Google Scholar
谷歌学者
Patel, S. et al. HIV-specific T cells can be generated against non-escaped T cell epitopes with a GMP-compliant manufacturing platform. Mol. Ther. Methods Clin. Dev. 16, 11–20 (2020).Article
Patel,S。等人。通过符合GMP的制造平台,可以针对未逃逸的T细胞表位产生HIV特异性T细胞。摩尔热。方法临床。发展16,11-20(2020)。文章
CAS
中科院
PubMed
PubMed
Google Scholar
谷歌学者
Conarty, J. P. & Wieland, A. The tumor-specific immune landscape in HPV+ head and neck cancer.Viruses 15, 1296 (2023).Article
Conarty,J.P。&Wieland,A。HPV+头颈癌中的肿瘤特异性免疫景观。病毒151296(2023)。文章
CAS
中科院
PubMed
PubMed
PubMed Central
公共医学中心
Google Scholar
谷歌学者
Xue, R. et al. Liver tumour immune microenvironment subtypes and neutrophil heterogeneity. Nature 612, 141–147 (2022).Article
薛,R。等。肝肿瘤免疫微环境亚型和中性粒细胞异质性。自然612141-147(2022)。文章
CAS
中科院
PubMed
PubMed
Google Scholar
谷歌学者
Verma, N. K. et al. Obstacles for T-lymphocytes in the tumour microenvironment: therapeutic challenges, advances and opportunities beyond immune checkpoint. EBioMedicine 83, 104216 (2022).Article
Verma,N.K.等人,《肿瘤微环境中T淋巴细胞的障碍:免疫检查点之外的治疗挑战,进展和机遇》。EBioMedicine 83104216(2022)。文章
CAS
中科院
PubMed
PubMed
PubMed Central
公共医学中心
Google Scholar
谷歌学者
Shah, N. N. & Fry, T. J. Mechanisms of resistance to CAR T cell therapy. Nat. Rev. Clin. Oncol. 16, 372–385 (2019).CAS
Shah,N.N。&Fry,T.J。对CAR T细胞疗法的抗性机制。国家修订临床。Oncol公司。16372-385(2019)。中科院
PubMed
PubMed
PubMed Central
公共医学中心
Google Scholar
谷歌学者
Rossetti, R. et al. Combination of genetically engineered T cells and immune checkpoint blockade for the treatment of cancer. Immunother. Adv. 2, ltac005 (2022).Article
Rossetti,R。等人。基因工程T细胞和免疫检查点阻断的组合用于治疗癌症。免疫疗法。Adv.2,ltac005(2022)。文章
PubMed
PubMed
PubMed Central
公共医学中心
Google Scholar
谷歌学者
Siu, L. L. et al. Tabelecleucel in combination with pembrolizumab (Pembro) in platinum-pretreated, recurrent/metastatic Epstein-Barr virus (EBV)-positive nasopharyngeal carcinoma (EBV+NPC). J. Clin. Oncol. 37, TPS6092 (2019).Article
Siu,L。L。等人Tabelecleucel联合pembrolizumab(Pembro)治疗铂类预处理的复发/转移性爱泼斯坦-巴尔病毒(EBV)阳性鼻咽癌(EBV+NPC)。J、 临床。Oncol公司。37,TPS6092(2019)。文章
Google Scholar
谷歌学者
Park, J., Thomas, S. & Munster, P. N. Epigenetic modulation with histone deacetylase inhibitors in combination with immunotherapy. Epigenomics 7, 641–652 (2015).Article
Park,J.,Thomas,S。&Munster,P.N。用组蛋白脱乙酰酶抑制剂结合免疫疗法进行表观遗传调节。表观基因组学7641-652(2015)。文章
CAS
中科院
PubMed
PubMed
Google Scholar
谷歌学者
Ghosh, S. K., Perrine, S. P., Williams, R. M. & Faller, D. V. Histone deacetylase inhibitors are potent inducers of gene expression in latent EBV and sensitize lymphoma cells to nucleoside antiviral agents. Blood 119, 1008–1017 (2012).Article
Ghosh,S.K.,Perrine,S.P.,Williams,R.M。&Faller,D.V。组蛋白脱乙酰酶抑制剂是潜伏EBV中基因表达的有效诱导剂,并使淋巴瘤细胞对核苷抗病毒药物敏感。血液1191008-1017(2012)。文章
CAS
中科院
PubMed
PubMed
PubMed Central
公共医学中心
Google Scholar
谷歌学者
Lam, S. et al. Broadly-specific cytotoxic T cells targeting multiple HIV antigens are expanded from HIV+ patients: implications for immunotherapy. Mol. Ther. 23, 387–395 (2015).Article
Lam,S.等人。针对多种HIV抗原的广泛特异性细胞毒性T细胞从HIV+患者中扩增出来:对免疫治疗的影响。摩尔热。23387-395(2015)。文章
CAS
中科院
PubMed
PubMed
Google Scholar
谷歌学者
Lee, P. H., Keller, M. D., Hanley, P. J. & Bollard, C. M. Virus-specific T cell therapies for HIV: lessons learned from hematopoietic stem cell transplantation. Front. Cell Infect. Microbiol. 10, 298 (2020).Article
Lee,P.H.,Keller,M.D.,Hanley,P.J。&Bollard,C.M。针对HIV的病毒特异性T细胞疗法:从造血干细胞移植中吸取的教训。正面。细胞感染。微生物。。文章
CAS
中科院
PubMed
PubMed
PubMed Central
公共医学中心
Google Scholar
谷歌学者
Lam, S. & Bollard, C. T-cell therapies for HIV. Immunotherapy 5, 407–414 (2013).Article
Lam,S。&Bollard,C。HIV的T细胞疗法。免疫疗法5407-414(2013)。文章
CAS
中科院
PubMed
PubMed
Google Scholar
谷歌学者
Zhang, J., Guo, Y., Fang, H., Guo, X. & Zhao, L. Oncolytic virus oHSV2 combined with PD-1/PD-L1 inhibitors exert antitumor activity by mediating CD4+ T and CD8+ T cell infiltration in the lymphoma tumor microenvironment. Autoimmunity 56, 2259126 (2023).Article
Zhang,J.,Guo,Y.,Fang,H.,Guo,X。&Zhao,L。溶瘤病毒oHSV2与PD-1/PD-L1抑制剂联合通过介导CD4+T和CD8+T细胞浸润发挥抗肿瘤活性淋巴瘤肿瘤微环境。自身免疫562259126(2023)。文章
PubMed
PubMed
Google Scholar
谷歌学者
Bollard, C. M. et al. Cytotoxic T lymphocyte therapy for Epstein-Barr virus+ Hodgkin’s disease. J. Exp. Med. 200, 1623–1633 (2004).Article
Bollard,C.M.等人。细胞毒性T淋巴细胞治疗爱泼斯坦-巴尔病毒+霍奇金病。J、 实验医学2001623-1633(2004)。文章
CAS
中科院
PubMed
PubMed
PubMed Central
公共医学中心
Google Scholar
谷歌学者
Gallot, G. et al. T-cell therapy using a bank of EBV-specific cytotoxic T cells: lessons from a phase I/II feasibility and safety study. J. Immunother. 37, 170–179 (2014).Article
Gallot,G。等人。使用EBV特异性细胞毒性T细胞库的T细胞疗法:I/II期可行性和安全性研究的经验教训。J、 免疫疗法。。文章
CAS
中科院
PubMed
PubMed
Google Scholar
谷歌学者
Haque, T. et al. Treatment of Epstein-Barr-virus-positive post-transplantation lymphoproliferative disease with partly HLA-matched allogeneic cytotoxic T cells. Lancet 360, 436–442 (2002).Article
。柳叶刀360436-442(2002)。文章
PubMed
PubMed
Google Scholar
谷歌学者
Vickers, M. A. et al. Establishment and operation of a good manufacturing practice-compliant allogeneic Epstein-Barr virus (EBV)-specific cytotoxic cell bank for the treatment of EBV-associated lymphoproliferative disease. Br. J. Haematol. 167, 402–410 (2014).Article
Vickers,M.A.等人。建立和运行符合良好生产规范的同种异体爱泼斯坦-巴尔病毒(EBV)特异性细胞毒性细胞库,用于治疗EBV相关的淋巴增生性疾病。Br.J.血液学。167402-410(2014)。文章
PubMed
PubMed
PubMed Central
公共医学中心
Google Scholar
谷歌学者
Pfeiffer, T. et al. Posoleucel, an allogeneic, off-the-shelf multivirus-specific T-cell therapy, for the treatment of refractory viral infections in the post-HCT setting. Clin. Cancer Res. 29, 324–330 (2023).Article
Pfeiffer,T。等人,Posoleucel,一种同种异体,现成的多病毒特异性T细胞疗法,用于治疗HCT后难治性病毒感染。临床。癌症研究29324-330(2023)。文章
CAS
中科院
PubMed
PubMed
PubMed Central
公共医学中心
Google Scholar
谷歌学者
Louis, C. U. et al. Enhancing the in vivo expansion of adoptively transferred EBV-specific CTL with lymphodepleting CD45 monoclonal antibodies in NPC patients. Blood 113, 2442–2450 (2009).Article
Louis,C.U.等人,用淋巴消耗性CD45单克隆抗体增强NPC患者过继转移的EBV特异性CTL的体内扩增。血液1132442-2450(2009)。文章
CAS
中科院
PubMed
PubMed
PubMed Central
公共医学中心
Google Scholar
谷歌学者
Huang, J. et al. Epstein-Barr virus-specific adoptive immunotherapy for recurrent, metastatic nasopharyngeal carcinoma. Cancer 123, 2642–2650 (2017).Article
Huang,J.等。复发转移性鼻咽癌的爱泼斯坦-巴尔病毒特异性过继免疫治疗。癌症1232642-2650(2017)。文章
CAS
中科院
PubMed
PubMed
Google Scholar
谷歌学者
Download referencesAcknowledgementsThe work of the authors is supported by the US National Institutes of Health National Cancer Institute (Award Numbers 5P01 CA148600-09 and 1P01 CA225618-01A1 to C.M.B.); a Leukaemia and Lymphoma Society Translational Research Program award (to C.M.B.); and a Hyundai Hope on Wheels Scholar Grant (to K.T.).Author informationAuthors and AffiliationsCenter for Cancer and Immunology Research, Children’s National Hospital, Washington, DC, USAKeri Toner, Chase D.
下载参考文献致谢作者的工作得到了美国国立卫生研究院国家癌症研究所的支持(授予C.M.B.的奖项编号5P01 CA148600-09和1P01 CA225618-01A1);白血病和淋巴瘤协会转化研究计划奖(授予C.M.B.);以及现代希望车轮奖学金(授予K.T.)。作者信息作者和附属机构癌症和免疫学研究中心,华盛顿特区儿童国立医院,USAKeri Toner,Chase D。
McCann & Catherine M. BollardDepartment of Paediatrics, The George Washington University School of Medicine and Health Sciences, Washington, DC, USAKeri Toner, Chase D. McCann & Catherine M. BollardAuthorsKeri TonerView author publicationsYou can also search for this author in.
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PubMed Google ScholarContributionsK.T. and C.D.M. researched data for the article. All authors contributed substantially to discussions of content, wrote the article, and reviewed and/or edited the manuscript before submission.Corresponding authorCorrespondence to
。T、 和C.D.M.研究了文章的数据。所有作者都对内容的讨论做出了重大贡献,撰写了文章,并在提交前审查和/或编辑了稿件。对应作者对应
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凯瑟琳·M·博拉德。道德宣言
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C.M.B. is on the Board of Directors of Cabaletta Bio and is a scientific co-founder and scientific advisory board member of Catamaran Bio, holds stock in Repertoire Immune Medicines and Neximmune, and serves on the data and safety monitoring board of Swedish Orphan Biovitrum (Sobi). The other authors declare no competing interests..
C、 M.B.是Cabaletta Bio的董事会成员,是双体船Bio的科学联合创始人和科学顾问委员会成员,持有免疫药物和Neximune的股票,并担任瑞典孤儿生物数据和安全监测委员会(Sobi)的成员。其他作者声明没有利益冲突。。
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Nature Reviews Clinical Oncology thanks B. Eiz-Vesper, who co-reviewed with A. Bonifacius; A. Bertoletti; and the other, anonymous, reviewer(s) for their contribution to the peer review of this work.
自然评论临床肿瘤学感谢B.Eiz Vesper,他与A.Bonifacius共同审查;A、 贝托莱蒂;另一位匿名审稿人对这项工作的同行评审做出了贡献。
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