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在 HLA(A、B)相合的无关个体中通过计划性免疫对纯化链球菌抗原的母细胞转化进行血清学抑制。

Serological inhibition of blast transformation to purified streptococcal antigens by planned immunization in HLA (A,B) compatible unrelated individuals.

作者信息

Greenberg L J, Chopky R L, Noreen H, Gray E D, Yunis E J, Ferrara G B

出版信息

Vox Sang. 1978;34(3):136-42. doi: 10.1111/j.1423-0410.1978.tb02455.x.

Abstract

Sera obtained from planned immunizations between unrelated donors and recipients, identical or compatible at HLA-A and B, were assessed for their capacity to alter the in vitro response of a test panel of lymphocytes to PHA and a purified streptococcal antigen (PAS). In the case of PHA, no serum effects were apparent. The response to PAS, however, significantly inhibited by two sera. When tested for their complement-dependent cytotoxicity on enriched populations of T and B lymphocytes, none of the sera manifested cytotoxicity against T cells nor did serological inhibition correlate with the capacity to lyze B cells. The data suggest that inhibition of the PSA response is mediated by blocking antibodies specific for a subset of lymphocytes, possibly T cells. While the precise mechanism governing the response to PSA is not known, the data are compatible with the idea that an HLA-linked Ir gene, expressed on a subset of T lymphocytes, controls immune responsiveness to PSA.

摘要

从无关供体和受体之间的计划免疫中获得的血清,在HLA - A和B位点相同或相容,评估其改变一组测试淋巴细胞对植物血凝素(PHA)和纯化链球菌抗原(PAS)的体外反应的能力。对于PHA,未观察到明显的血清效应。然而,对PAS的反应被两种血清显著抑制。当测试它们对富集的T和B淋巴细胞群体的补体依赖性细胞毒性时,没有一种血清表现出对T细胞的细胞毒性,血清学抑制也与裂解B细胞的能力无关。数据表明,对PAS反应的抑制是由针对淋巴细胞亚群(可能是T细胞)的阻断抗体介导的。虽然控制对PAS反应的精确机制尚不清楚,但这些数据与以下观点一致,即在T淋巴细胞亚群上表达的HLA连锁免疫反应基因控制对PAS的免疫反应性。

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