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与小鼠Mls基因座相关的一种新的同种抗原系统。

A new alloantigenic system associated with the Mls locus in the mouse.

作者信息

Tonkonogy S L, Winn H J

出版信息

J Immunol. 1976 Mar;116(3):835-41.

PMID:56400
Abstract

An antiserum prepared by injecting C3H/HeJ mice with CBA/J tissue has been shown to react with cell surface components that are not part of any previously described system of serologically detectable alloantigens. The antiserum, which is designated AST-101, acts selectively in cytotoxic tests carried out with lymphoid cells, killing B cells, but not T cells. Phagocytic cells found in peritoneal exudates are also killed by AST-101 and complement in vitro; the sensitivity of other cell types has not been determined. Strain distribution does not indicate any association of the AST-101 system with H-2, Ly, or Thy systems; genetic analysis reveals close linkage with the mouse minor MLC-stimulating (Mls) locus. Serologic analysis also points to a close association between antigens reactive with AST-101 and the products of the Mls genes.

摘要

通过向C3H/HeJ小鼠注射CBA/J组织制备的抗血清已被证明能与细胞表面成分发生反应,这些成分不属于任何先前描述的血清学可检测同种异体抗原系统。这种抗血清被命名为AST - 101,在用淋巴细胞进行的细胞毒性试验中具有选择性作用,能杀死B细胞,但不杀死T细胞。在腹膜渗出物中发现的吞噬细胞在体外也会被AST - 101和补体杀死;其他细胞类型的敏感性尚未确定。品系分布表明AST - 101系统与H - 2、Ly或Thy系统没有任何关联;遗传分析显示与小鼠次要混合淋巴细胞刺激(Mls)位点紧密连锁。血清学分析也表明与AST - 101反应的抗原与Mls基因产物之间存在密切关联。

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