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抑制细胞对肿瘤免疫反应的调节:成年胸腺切除后的消除

Suppressor cell regulation of immune response to tumors: abrogation by adult thymectomy.

作者信息

Reinisch C L, Andrew S L, Schlossman S F

出版信息

Proc Natl Acad Sci U S A. 1977 Jul;74(7):2989-92. doi: 10.1073/pnas.74.7.2989.

Abstract

The regulatory role of the adult thymus on the appearance of cytotoxic and suppressor T cells (thymus-derived lymphocytes) to allogeneic and autochthonous virus-induced tumors in mice was investigated. It was demonstrated that C57BL/6 mice challenged with allogeneic P815 mastocytoma cells and complete Freund's adjuvant failed to develop cytotoxic cells but instead developed suppressor T cells which inhibited cytotoxic T cell function. Further, adjuvant-induced suppressor cells prevented the primary in vitro induction of cytotoxic T cells to P815 mastocytoma cells. In contrast, adult thymectomized animals, when challenged with adjuvant and allogeneic cells, had a normal cytotoxic response in vivo and their cells could not inhibit the generation of cytotoxic T cells in vitro. These studies suggested that the intact adult thymus was necessary for the induction of suppressor cells. Moreover, suppressor cells regulated cytotoxic T cell activity both in vivo and in vitro. Further, it was shown that adjuvant could prevent the normal immune response to virus-induced tumors. BALB/c mice treated with murine sarcoma virus developed tumors which reached a maximal size by day 14 and then regressed. Sham thymectomized animals treated with virus and complete Freund's adjuvant to generate suppressor cells died from progressive tumor growth. In contrast, thymectomized animals similarly treated had normal regression of tumor and survived. These studies lead to the conclusion that the adult thymus may regulate immune responsiveness by the export of suppressor T cells which regulate other T cell responses to both allogeneic and tumor antigens.

摘要

研究了成年胸腺对小鼠细胞毒性T细胞和抑制性T细胞(胸腺来源的淋巴细胞)针对同种异体和自身病毒诱导肿瘤出现的调节作用。结果表明,用同种异体P815肥大细胞瘤细胞和完全弗氏佐剂攻击的C57BL/6小鼠未能产生细胞毒性细胞,反而产生了抑制性T细胞,这些抑制性T细胞抑制了细胞毒性T细胞的功能。此外,佐剂诱导的抑制性细胞阻止了体外对P815肥大细胞瘤细胞的细胞毒性T细胞的初次诱导。相反,成年胸腺切除的动物在用佐剂和同种异体细胞攻击时,体内有正常的细胞毒性反应,其细胞在体外不能抑制细胞毒性T细胞的产生。这些研究表明,完整的成年胸腺对于抑制性细胞的诱导是必要的。此外,抑制性细胞在体内和体外均调节细胞毒性T细胞的活性。进一步研究表明,佐剂可阻止对病毒诱导肿瘤的正常免疫反应。用鼠肉瘤病毒处理的BALB/c小鼠发生肿瘤,到第14天达到最大尺寸,然后消退。用病毒和完全弗氏佐剂处理以产生抑制性细胞的假胸腺切除动物死于肿瘤的进行性生长。相反,同样处理的胸腺切除动物肿瘤正常消退并存活。这些研究得出结论,成年胸腺可能通过输出抑制性T细胞来调节免疫反应性,这些抑制性T细胞调节其他T细胞对同种异体和肿瘤抗原的反应。

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