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I类主要组织相容性复合体(MHC)分子而非其他小鼠基因决定了细胞毒性T细胞对流感抗原表位的识别。

Class I MHC molecules rather than other mouse genes dictate influenza epitope recognition by cytotoxic T cells.

作者信息

Taylor P M, Davey J, Howland K, Rothbard J B, Askonas B A

机构信息

National Institute for Medical Research, London, England.

出版信息

Immunogenetics. 1987;26(4-5):267-72. doi: 10.1007/BF00346521.

Abstract

Influenza nucleoprotein (NP) is an important target antigen for influenza A virus cross-reactive cytotoxic T cells (Tc). Here we examine the NP epitope recognized by cloned and polyclonal BALB/c Tc and the genetics of this recognition pattern. We can define NP residues 147-161 as the epitope seen in conjunction with Kd, the only H-2d class I responder allele for NP restriction. H-2d/H-2b F1 mice (C57BL X DBA/2) primed by influenza infection lyse only H-2d target cells treated with peptide 147-161 while H-2b targets are recognized only after treatment with NP residues 365-379 (previously found to be recognized by Db restricted Tc cells). Tc cell recognition of NP peptide 147-161 is entirely dictated by expression of Kd and not by other B10 or C3H background genes of congenic mice. Restriction of a unique NP sequence by each responder class I major histocompatibility complex (MHC) allele suggests that antigen and class I MHC interact for Tc recognition.

摘要

流感核蛋白(NP)是甲型流感病毒交叉反应性细胞毒性T细胞(Tc)的重要靶抗原。在此,我们研究了克隆的和多克隆的BALB/c Tc所识别的NP表位以及这种识别模式的遗传学特征。我们可以将NP的147 - 161位氨基酸残基定义为与Kd结合时所见的表位,Kd是NP限制性反应中唯一的H-2d I类应答等位基因。经流感感染致敏的H-2d/H-2b F1小鼠(C57BL×DBA/2)仅裂解用147 - 161肽处理过的H-2d靶细胞,而H-2b靶细胞只有在用NP的365 - 379位氨基酸残基(先前发现可被Db限制性Tc细胞识别)处理后才能被识别。Tc细胞对NP肽147 - 161的识别完全由Kd的表达决定,而非由同基因小鼠的其他B10或C3H背景基因决定。每个应答性I类主要组织相容性复合体(MHC)等位基因对独特NP序列的限制性表明,抗原与I类MHC相互作用以实现Tc识别。

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