不适合移植的大 B 细胞淋巴瘤二线使用 axicabtagene ciloleucel:ALYCANTE 最终分析
Second-line axicabtagene ciloleucel in large B-cell lymphoma ineligible for transplantation: ALYCANTE final analysis.
CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:EBV-induced T-cell responses in EBV-specific and nonspecific cancers.
EBV-induced T-cell responses in EBV-specific and nonspecific cancers.
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Epstein-Barr病毒(EBV)是一种普遍存在的人类肿瘤病毒,与多种恶性肿瘤相关,包括B细胞淋巴瘤、NK/T细胞淋巴瘤及上皮癌。EBV感染口咽部B淋巴细胞和上皮细胞,并在记忆B细胞中建立持续感染。在病毒与宿主保持平衡的情况下,大多数人因T细胞免疫终身监视EBV而不出现症状;持续感染期间,血液中可维持高频率、稳定的记忆性抗EBV T细胞库。T细胞免疫受损者更可能发生危及生命的淋巴增殖性疾病,凸显T细胞在维持EBV-宿主平衡中的关键作用。近期研究发现,EBV蛋白LMP1可在B细胞中针对多种肿瘤相关抗原(TAA)诱发强效T细胞应答。
此外,研究人员也在EBV无关癌症中发现EBV特异性T细胞,引发了关于其抗肿瘤免疫作用的疑问。本文综述EBV相关癌症中的T细胞应答,纳入病毒潜伏模式、宿主免疫状态及人白细胞抗原(HLA)易感性等可能影响免疫结局的因素;讨论EBV诱导的TAA特异性T细胞应答,并探讨EBV特异性T细胞亚群在肿瘤微环境中的潜在作用;同时介绍利用EBV抗原的T细胞免疫治疗策略,包括EBV特异性T细胞和TCR工程化T细胞。
最后,讨论T细胞在EBV感染及相关疾病中的作用,以阐明EBV与T细胞免疫之间的整体相互作用。
Epstein-Barr virus (EBV) is a ubiquitous human tumor virus associated with various malignancies, including B-lymphoma, NK and T-lymphoma, and epithelial carcinoma. It infects B lymphocytes and epithelial cells within the oropharynx and establishes persistent infection in memory B cells. With a balanced virus-host interaction, most individuals carry EBV asymptomatically because of the lifelong surveillance by T cell immunity against EBV.
A stable anti-EBV T cell repertoire is maintained in memory at high frequency in the blood throughout persistent EBV infection. Patients with impaired T cell immunity are more likely to develop life-threatening lymphoproliferative disorders, highlighting the critical role of T cells in achieving the EBV-host balance. Recent studies reveal that the EBV protein, LMP1, triggers robust T-cell responses against multiple tumor-associated antigens (TAAs) in B cells.
Additionally, EBV-specific T cells have been identified in EBV-unrelated cancers, raising questions about their role in antitumor immunity.
Herein, we summarize T-cell responses in EBV-related cancers, considering latency patterns, host immune status, and factors like human leukocyte antigen (HLA) susceptibility, which may affect immune outcomes.
We discuss EBV-induced TAA-specific T cell responses and explore the potential roles of EBV-specific T cell subsets in tumor microenvironments.
We also describe T-cell immunotherapy strategies that harness EBV antigens, ranging from EBV-specific T cells to T cell receptor-engineered T cells. Lastly, we discuss the involvement of T-cells in EBV infection and associated diseases, aiming to elucidate the comprehensive interplay between EBV and T-cell immunity.
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