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次要组织相容性抗原的遗传起源。

The genetic origin of minor histocompatibility antigens.

作者信息

Roopenian D C, Christianson G J, Davis A P, Zuberi A R, Mobraaten L E

机构信息

Jackson Laboratory, Bar Harbor, ME 04609.

出版信息

Immunogenetics. 1993;38(2):131-40. doi: 10.1007/BF00190900.

Abstract

The purpose of this study was to elucidate the genetic origin of minor histocompatibility (H) antigens. Toward this end common inbred mouse strains, distinct subspecies, and species of the subgenus Mus were examined for expression of various minor H antigens. These antigens were encoded by the classical minor H loci H-3 and H-4 or by newly identified minor H antigens detected as a consequence of mutation. Both minor H antigens that stimulate MHC class I-restricted cytotoxic T cells (Tc) and antigens that stimulate MHC class II-restricted helper T cells (Th) were monitored. The results suggested that strains of distinct ancestry commonly express identical or cross-reactive antigens. Moreover, a correlation between the lack of expression of minor H antigens and ancestral heritage was observed. To address whether the antigens found on unrelated strains were allelic with the sensitizing minor H antigens or a consequence of antigen cross-reactivity, classical genetic segregation analysis was carried out. Even in distinct subspecies and species, the minor H antigens always mapped to the site of the appropriate minor H locus. Together the results suggest: 1) minor H antigen sequences are evolutionarily stable in that their pace of antigenic change is slow enough to predate subspeciation and speciation; 2) the minor H antigens originated in the inbred strains as a consequence of a rare polymorphism or loss mutation carried in a founder mouse stock that caused the mouse to perceive the wild-type protein as foreign; 3) there is a remarkable lack of antigenic cross-reactivity between the defined minor H antigens and other gene products.

摘要

本研究的目的是阐明次要组织相容性(H)抗原的遗传起源。为此,我们检测了常见的近交系小鼠品系、不同的亚种以及小家鼠亚属的物种中各种次要H抗原的表达情况。这些抗原由经典的次要H基因座H-3和H-4编码,或者由因突变而新发现的次要H抗原编码。我们监测了刺激MHC I类限制性细胞毒性T细胞(Tc)的次要H抗原以及刺激MHC II类限制性辅助性T细胞(Th)的抗原。结果表明,不同祖先的品系通常表达相同或交叉反应的抗原。此外,还观察到次要H抗原表达缺失与祖先遗传之间的相关性。为了确定在不相关品系上发现的抗原与致敏次要H抗原是等位基因关系还是抗原交叉反应的结果,我们进行了经典的遗传分离分析。即使在不同的亚种和物种中,次要H抗原总是定位于相应次要H基因座的位置。综合这些结果表明:1)次要H抗原序列在进化上是稳定的,因为它们的抗原变化速度足够慢,早于亚种形成和物种形成;2)次要H抗原起源于近交系,是由于奠基小鼠群体中携带的罕见多态性或缺失突变,导致小鼠将野生型蛋白视为外来蛋白;3)在已定义的次要H抗原与其他基因产物之间,抗原交叉反应明显缺乏。

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