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细胞溶解性T淋巴细胞对分离的I类H-2蛋白和流感肽的反应。

Cytolytic T-lymphocyte response to isolated class I H-2 proteins and influenza peptides.

作者信息

Kane K P, Vitiello A, Sherman L A, Mescher M F

机构信息

Division of Membrane Biology, Medical Biology Institute, La Jolla, California 92037.

出版信息

Nature. 1989 Jul 13;340(6229):157-9. doi: 10.1038/340157a0.

Abstract

T cells recognize antigenic peptides in the context of major histocompatibility complex (MHC) proteins. Peptide binding to class II MHC proteins, and T-cell recognition of these complexes at the functional level has been demonstrated. Although considerable evidence suggests that class I-restricted cytotoxic T lymphocytes (CTL) recognize class I-peptide complexes, this has not yet been directly demonstrated. Chen and Parham have recently detected a low level of direct binding of radiolabelled influenza peptides to class I HLA proteins, but the relevance of this binding to T-cell recognition remains uncertain. We report here that purified class I proteins pulsed with influenza peptides can trigger antigen-specific, TCR-mediated degranulation by CTL. Effective pulsing depends on both peptide concentration and time, and can occur within 60 minutes. These results provide strong support for the formation of an antigenic complex that is recognized by CTL in which peptide antigens are bound to isolated class I proteins.

摘要

T细胞在主要组织相容性复合体(MHC)蛋白的背景下识别抗原肽。已证实肽与II类MHC蛋白结合,以及T细胞在功能水平上对这些复合物的识别。尽管大量证据表明I类限制性细胞毒性T淋巴细胞(CTL)识别I类-肽复合物,但这尚未得到直接证实。陈和帕尔哈姆最近检测到放射性标记的流感肽与I类HLA蛋白的低水平直接结合,但这种结合与T细胞识别的相关性仍不确定。我们在此报告,用流感肽脉冲处理的纯化I类蛋白可触发CTL进行抗原特异性、TCR介导的脱颗粒。有效的脉冲处理取决于肽浓度和时间,且可在60分钟内发生。这些结果为形成一种被CTL识别的抗原复合物提供了有力支持,其中肽抗原与分离的I类蛋白结合。

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