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调节性T细胞的精细特异性。II. 在一个遗传性无反应小鼠品系中,抑制性T细胞和辅助性T细胞由鸡卵清溶菌酶的不同区域诱导产生。

Fine specificity of regulatory T cells. II. Suppressor and helper T cells are induced by different regions of hen egg-white lysozyme in a genetically nonresponder mouse strain.

作者信息

Adorini L, Harvey M A, Miller A, Sercarz E E

出版信息

J Exp Med. 1979 Aug 1;150(2):293-306. doi: 10.1084/jem.150.2.293.

Abstract

We have examined the ability of two purified peptide fragments derived from hen (chicken) egg-white lysozyme (HEL); N-terminal, Co-terminal peptide (a.a. 1--17:cys 6--cys 127:120--129) and mixed disulfide LII peptide (LII) (a.a. 13--105) to induce antigen-specific suppression or help in B10 (H-2b) nonresponder and B10.A (H-2a) responder mice. An anti-HEL primary in vitro antibody response can be obtained in either strain by stimulation with HEL coupled to erythrocytes (RBC). Preimmunization with HEL-complete Freund's adjuvant-(CFA) or N-C-CFA-induced suppression of the anti-HEL PFC response to HEL-RBC in spleen cell cultures from B10 mice, whereas helper activity was demonstrated in cultures from B10.A mice similarly immunized. LII-CFA priming elicited helper cells in both C57BL/10 Sn (B10) and B10.A/SgSn (B10.A) mice. The genetic nonresponsiveness of B10 mice to HEL can therefore be attributed to the activation of suppressor T cells by a limited portion of the molecule (e.g., N-C) which prevent the potential response directed against other epitopes on the same molecule (e.g., LII). One manifestation of major histocompatibility complex gene activity appears to be the intramolecular selection of different antigenic determinants leading to activation of functionally different T-cell subpopulations.

摘要

我们检测了源自鸡卵清溶菌酶(HEL)的两个纯化肽片段的能力;N端、C端肽(氨基酸1-17:半胱氨酸6-半胱氨酸127:120-129)和混合二硫键LII肽(LII)(氨基酸13-105),以诱导B10(H-2b)无反应小鼠和B10.A(H-2a)有反应小鼠产生抗原特异性抑制或辅助作用。通过用与红细胞(RBC)偶联的HEL刺激,在任一品系中均可获得抗HEL体外初次抗体反应。用HEL-完全弗氏佐剂-(CFA)或N-C-CFA预免疫可抑制B10小鼠脾细胞培养物中对HEL-RBC的抗HEL PFC反应,而在同样免疫的B10.A小鼠的培养物中则显示出辅助活性。LII-CFA预激发在C57BL/10 Sn(B10)和B10.A/SgSn(B10.A)小鼠中均引发了辅助性细胞。因此,B10小鼠对HEL的遗传无反应性可归因于分子的有限部分(例如N-C)激活了抑制性T细胞,这阻止了针对同一分子上其他表位(例如LII)的潜在反应。主要组织相容性复合体基因活性的一种表现似乎是不同抗原决定簇的分子内选择,导致功能不同的T细胞亚群被激活。

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