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癌症的细胞毒性T淋巴细胞疗法与肿瘤逃逸机制

Cytotoxic T lymphocyte therapy of cancer and tumor escape mechanisms.

作者信息

Melief C J, Kast W M

机构信息

Division of Immunology, The Netherlands Cancer Institute, Amsterdam.

出版信息

Semin Cancer Biol. 1991 Oct;2(5):347-54.

PMID:1773050
Abstract

In animal models complete and permanent eradication of tumors can be achieved by adoptive transfer of tumor specific T cells, combined with interleukin 2. The most active cells are CD8+ cytotoxic T lymphocytes (CTL), which recognize peptides of 8-10 amino acids in length, bound to the antigen presenting groove of MHC class I molecules. In the case of virus-induced tumors these peptides are processed from viral proteins. Potentially immunogenic human tumors include melanoma and renal cell carcinoma in addition to the virus-associated cancers Burkitt's lymphoma and cervical carcinoma. The potential of CTL therapy of human cancer needs to be tested with cloned tumor cells. Remedies to over-come poor immunogenicity and evasion by tumor cells of CTL mediated-destruction are discussed.

摘要

在动物模型中,通过过继转移肿瘤特异性T细胞并联合白细胞介素2,可实现肿瘤的完全和永久性根除。最活跃的细胞是CD8 + 细胞毒性T淋巴细胞(CTL),它们识别长度为8 - 10个氨基酸的肽段,这些肽段与MHC I类分子的抗原呈递槽结合。对于病毒诱导的肿瘤,这些肽段由病毒蛋白加工而成。除了与病毒相关的癌症(伯基特淋巴瘤和宫颈癌)外,潜在具有免疫原性的人类肿瘤还包括黑色素瘤和肾细胞癌。人类癌症的CTL疗法潜力需要用克隆的肿瘤细胞进行测试。文中还讨论了克服肿瘤细胞免疫原性差以及逃避CTL介导破坏的补救措施。

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