首页> 美国卫生研究院文献>The Journal of Experimental Medicine >Major histocompatibility complex-restricted self recognition. A monoclonal anti-I-Ak reagent blocks helper T cell recognition of self major histocompatibility complex determinants
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Major histocompatibility complex-restricted self recognition. A monoclonal anti-I-Ak reagent blocks helper T cell recognition of self major histocompatibility complex determinants

机译:主要组织相容性复杂的自我识别。单克隆抗I-Ak试剂可阻断辅助T细胞对自身主要组织相容性复合物决定簇的识别

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摘要

The functional role of cell surface Ia antigens has been studied for in vitro antibody responses, using as a probe the ability of anti-Ia reagents to inhibit these responses. A hybridoma monoclonal anti-Ia reagent specific for a product of I-Ak (Ia.17) profoundly inhibited in vitro antibody responses to TNP-KLH by spleen cells of the I-Ak but not I-Ab haplotype. This inhibition by anti-I-Ak product, but not by interaction with T or B cell product, in spite of the fact that functional B cells as well as accessory cells could be shown to express the determinant detected by this hybridoma reagent. These results suggest that the Ia expressed by accessory cells in of unique functional importance in these responses. To further characterize the function of Ia antigens in this response system, the mechanism of anti- I-Ak inhibition was determined. The inhibition resulting from interaction of anti-I-Ak with accessory cell Ia was not mediated by nonspecific suppressor cells, nor was there nonspecific interference with accessory cell function as a result of the binding of anti-Ia antibody. The relationship between anti-Ia inhibition and T helper cell recognition of self determinations on accessory cells was analyzed using T cells from radiation bone marrow chimeras. It was demonstrated that (B10 X B10.A)F1 leads to B10 (F1 leads to B10) chimera T cells were able to cooperate with B10 (H-2b and I-Ab) but not B10.A (H-2a and I-Ak) accessory cells for responses to TNP-KLH; F1 leads to B10.A T cells were able to cooperate with B10.A but not B10 accessory cells; and both chimera populations were able to cooperate with (B10 X B10.A)F1 (F1) accessory cells. Monoclonal anti-I-Ak inhibited the cooperation of F1 leads to B10.A T cells with the same F1 accessory cells. Thus, inhibition by anti-I-Ak is dependent upon active helper T cell recognition of I-Ak-encoded determinants expressed on accessory cells. These findings demonstrate that T cells recognize self Ia determinants expressed on accessory cells, and that such recognition is required for the generation of T cell-dependent antibody responses.
机译:已经研究了细胞表面Ia抗原在体外抗体应答中的功能性作用,使用抗Ia试剂抑制这些应答的能力作为探针。特异于I-Ak产物的杂交瘤单克隆抗Ia试剂(Ia.17)可以显着抑制I-Ak脾细胞对TNP-KLH的体外抗体反应,但对I-Ab单倍型则没有抑制作用。尽管可以显示功能性B细胞以及辅助细胞均可以表达这种杂交瘤试剂检测到的决定簇,但抗I-Ak产物的抑制作用却不与T细胞或B细胞产物的相互作用抑制。这些结果表明由辅助细胞表达的Ia在这些反应中具有独特的功能重要性。为了进一步表征Ia抗原在该应答系统中的功能,确定了抗I-Ak抑制的机制。由抗I-Ak与辅助细胞Ia相互作用产生的抑制作用不是由非特异性抑制细胞介导的,也不是由于抗Ia抗体的结合而对辅助细胞功能产生了非特异性干扰。使用来自放射骨髓嵌合体的T细胞分析了抗Ia抑制与T辅助细胞自身对辅助细胞的识别之间的关系。已证明(B10 X B10.A)F1导致B10(F1导致B10)嵌合体T细胞能够与B10(H-2b和I-Ab)协同作用,但不能与B10.A(H-2a和I)协同作用-Ak)辅助细胞对TNP-KLH的反应; F1导致B10.A T细胞能够与B10.A协同,但不能与B10辅助细胞协同;并且两个嵌合体种群都能够与(B10 X B10.A)F1(F1)辅助细胞合作。单克隆抗I-Ak抑制F1的协同作用,导致B10.A T细胞具有相同的F1辅助细胞。因此,抗I-Ak的抑制作用取决于对辅助细胞上表达的I-Ak编码决定簇的主动辅助T细胞识别。这些发现证明T细胞识别在辅助细胞上表达的自身Ia决定簇,并且这种识别是产生T细胞依赖性抗体应答所必需的。

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