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II类同种异体抗原参与小鼠体内K/D区域不同的甲状腺移植排斥反应的调节。

Participation of class II alloantigens in in vivo regulation of K/D region disparate thyroid graft rejection in mice.

作者信息

Isakov N, Bach F H

出版信息

J Immunol. 1985 Jun;134(6):3580-5.

PMID:2859332
Abstract

Class I and II molecules preferentially activate cytotoxic T cells and helper T cells, respectively, in primary in vitro alloactivation of T lymphocytes. Collaboration between these subpopulations leads to an efficient anti-class I specific cytotoxic response. We tested whether the presence of class II, in addition to class I, alloantigens on thyroid allografts in vivo induces augmentation of anti-class I antigen immune response and leads to rejection of K/D region disparate grafts which otherwise would have been accepted. Different pairs of K or D region disparate mouse strains were selected in which transplantation across a class I antigen disparity alone resulted in long-term graft acceptance. In some pairs of mouse strains, co-transplantation of recipient mice with a second thyroid graft sharing the K/D region of the first, but additionally expressing an allo class II molecule, led to accelerated K/D region disparate thyroid graft rejection. Transplantation of thyroid allografts expressing both class II and I alloantigens did not induce increased host anti-class I antigen cytotoxic response, or affect the frequency of specific precursor cytotoxic T cells. In one pair of congenic mouse strains, acute rejection of K/D region disparate thyroid grafts occurred in the absence of class II alloantigen stimulation; in other strains, co-transplantation of class I and II alloantigen disparate thyroid allografts was not sufficient to induce K/D region disparate graft rejection. The results thus demonstrate that a class II alloantigen on a thyroid graft may augment the rejection response directed against the graft class I alloantigens. The class II alloantigen stimulation was not always essential or sufficient for induction of class I antigen disparate thyroid graft rejection, and was dependent on the specific I region and/or K/D region gene allele.

摘要

在T淋巴细胞的初次体外同种异体激活中,I类和II类分子分别优先激活细胞毒性T细胞和辅助性T细胞。这些亚群之间的协作导致高效的抗I类特异性细胞毒性反应。我们测试了在体内甲状腺同种异体移植中,除了I类同种异体抗原外,II类同种异体抗原的存在是否会诱导抗I类抗原免疫反应增强,并导致K/D区域不同的移植物被排斥,否则这些移植物本可被接受。选择了不同的K或D区域不同的小鼠品系对,其中仅跨越I类抗原差异进行移植会导致移植物长期存活。在某些小鼠品系对中,将受体小鼠与第二个甲状腺移植物共同移植,该移植物与第一个移植物共享K/D区域,但额外表达一种同种II类分子,导致K/D区域不同的甲状腺移植物排斥加速。表达II类和I类同种异体抗原的甲状腺同种异体移植并未诱导宿主抗I类抗原细胞毒性反应增加,也未影响特异性前体细胞毒性T细胞的频率。在一对同源小鼠品系中,在没有II类同种异体抗原刺激的情况下发生了K/D区域不同的甲状腺移植物急性排斥;在其他品系中,I类和II类同种异体抗原不同的甲状腺同种异体移植共同移植不足以诱导K/D区域不同的移植物排斥。因此,结果表明甲状腺移植物上的II类同种异体抗原可能增强针对移植物I类同种异体抗原的排斥反应。II类同种异体抗原刺激对于诱导I类抗原不同的甲状腺移植物排斥并不总是必需的或充分的,并且取决于特定的I区域和/或K/D区域基因等位基因。

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