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自身MHC肽上决定簇层次结构的破坏:对显性决定簇的伴随耐受诱导和对隐蔽自身决定簇的致敏。

Disruption of the determinant hierarchy on a self-MHC peptide: concomitant tolerance induction to the dominant determinant and priming to the cryptic self-determinant.

作者信息

Benichou G, Fedoseyeva E, Olson C A, Geysen H M, McMillan M, Sercarz E E

机构信息

Department of Microbiology and Molecular Genetics, UCLA 90024.

出版信息

Int Immunol. 1994 Jan;6(1):131-8. doi: 10.1093/intimm/6.1.131.

DOI:10.1093/intimm/6.1.131
PMID:7511927
Abstract

The presentation of self-peptides in a self-restricted manner plays a critical role in the complex positive and negative selective process of T cell recognition of self-determinants. The population of determinants comprises (i) a dominant set which is efficiently presented and induces clonal elimination or inactivation of the corresponding autoreactive T cells, and (ii) a cryptic set which is not processed efficiently enough to reach the threshold of presentation to make an impact on the T cell repertoire during thymic selection. Here we have studied a self-MHC peptide, Ld 61-85, which as shown in earlier work was able to induce vigorous T cell proliferation in syngeneic animals. Despite the fact that this peptide as a whole is 'cryptic', the fine specificity of the class II restricted response was complex, in that there were three distinct and overlapping T cell determinants: the dominant determinant, Ld 65-80, flanked by two cryptic determinants, Ld 61-75 and Ld 73-85, all of which compete for stimulating in vivo autoreactive T cell proliferative responses. The hierarchy of these determinants bears an interesting relationship to tolerance. Ld 61-85 or Ld 61-80 priming induces proliferation only to Ld 65-80; likewise, tolerance induction to Ld 61-80 prevents elicitation of a subsequent response to Ld 61-80 or Ld 65-80 in the local lymph nodes. However, in the Ld 61-80 tolerant mice, in vivo challenge with Ld 61-80 induces a strong T cell proliferative response directed towards cryptic Ld 61-75.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

以自身限制的方式呈递自身肽段,在T细胞识别自身抗原决定簇的复杂的阳性和阴性选择过程中起着关键作用。抗原决定簇群体包括:(i)一个优势集,其能被有效呈递并诱导相应自身反应性T细胞的克隆清除或失活;(ii)一个隐蔽集,其加工效率不足以达到呈递阈值,从而在胸腺选择过程中对T细胞库产生影响。在此,我们研究了一种自身MHC肽段,Ld 61 - 85,如先前研究所示,其能够在同基因动物中诱导强烈的T细胞增殖。尽管该肽段整体上是“隐蔽的”,但II类限制性反应的精细特异性却很复杂,因为存在三个不同且重叠的T细胞决定簇:优势决定簇Ld 65 - 80,两侧是两个隐蔽决定簇Ld 61 - 75和Ld 73 - 85,所有这些决定簇都竞争刺激体内自身反应性T细胞增殖反应。这些决定簇的层级关系与耐受性存在有趣的关联。用Ld 61 - 85或Ld 61 - 80预刺激仅诱导对Ld 65 - 80的增殖;同样,对Ld 61 - 80的耐受性诱导可防止在局部淋巴结中引发对Ld 61 - 80或Ld 65 - 80的后续反应。然而,在Ld 61 - 80耐受的小鼠中,用Ld 61 - 80进行体内攻击会诱导针对隐蔽的Ld 61 - 75的强烈T细胞增殖反应。(摘要截短于250字)

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