首页> 美国卫生研究院文献>The Journal of Experimental Medicine >Multiple class I and class II major histocompatibility complex allospecificities are generated with T cell receptor variable (V) domains created by a single Ti beta V gene family
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Multiple class I and class II major histocompatibility complex allospecificities are generated with T cell receptor variable (V) domains created by a single Ti beta V gene family

机译:使用单个Ti beta V基因家族创建的T细胞受体可变(V)域产生多个I类和II类主要组织相容性复合物异源特异性

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摘要

10 alloreactive cytotoxic T lymphocytes using REX Ti beta variable region (V) gene segments in formation of their antigen/major histocompatibility complex (MHC) T3-Ti receptor were selected, cloned, and characterized in an effort to examine the extent of receptor diversity created by this one V gene family. Multiple and distinct class II as well as class I allospecificities were generated from the formation of different Ti beta V domains. Five allospecificities were directed at various class I epitopes whereas the other five were directed at class II MHC gene products. The following conclusions were drawn: (a) Ti beta V genes do not segregate into those that encode class I and those that encode class II allospecificities; and (b) there is no restriction on the Ti beta V gene pool available to T4+ vs. T8+ T lymphocytes.
机译:选择,克隆并表征了10个使用REX Tiβ可变区(V)基因片段形成其抗原/主要组织相容性复合体(MHC)T3-Ti受体的同种异体反应性细胞毒性T淋巴细胞,并对其进行了表征,以检验产生的受体多样性的程度通过这个一个V基因家族。通过形成不同的TiβV结构域,产生了多种不同的II类以及I类同种异体。五种同种异性针对各种I类表位,而其他五种针对II类MHC基因产物。得出以下结论:(a)TiβV基因没有分离为编码I类和II类同种异体的基因; (b)对T4 +与T8 + T淋巴细胞可用的Ti beta V基因库没有限制。

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