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在针对PHA-P诱导的外周血单个核细胞增殖的HLA I类抗原单态和多态决定簇的单克隆抗体抑制中,单核细胞不起作用。

Lack of a role of monocytes in the inhibition by monoclonal antibodies to monomorphic and polymorphic determinants of HLA class I antigens of PHA-P-induced peripheral blood mononuclear cell proliferation.

作者信息

De Felice M, Turco M C, Corbo L, Carandente Giarrusso P, Lamberti A, Valerio G, Temponi M, Costanzo F, Ferrone S, Venuta S

机构信息

Istituto di Oncologia Clinica e Sperimentale, Facoltà di Medicina e Chirurgia di Catanzaro, Università di Reggio Calabria, Italy.

出版信息

Cell Immunol. 1989 Aug;122(1):164-77. doi: 10.1016/0008-8749(89)90157-3.

Abstract

This study aimed at characterizing the mechanism(s) underlying the regulatory role of distinct determinants of HLA Class I antigens in PHA-P-induced T cell proliferation and the involvement of monocytes in this phenomenon. The anti-HLA-A2,A28 monoclonal antibodies (MoAb) CR11-351, the MoAb Q6/64 to a determinant restricted to the gene products of the I antigens HLA-B locus, and the MoAb CR10-215 and W6/32 to distinct monomorphic determinants of HLA Class I antigens were found to inhibit PHA-P-induced peripheral blood mononuclear cell (PBMC) proliferation in a dose-dependent fashion. The inhibition is specific and reflects neither inhibition of PHA-P binding to cells nor a toxic effect of the anti-HLA Class I MoAb. The latter differed in the concentration required to induce inhibition, in the influence of the concentration of PHA-P used as mitogen, in the differential effect on the donors used as a source of PBMC, and/or in the requirement of the Fc portion to induce inhibition. At variance with the information in the literature, the inhibitory effect of anti-HLA Class I MoAb on PHA-P-induced PBMC proliferation neither reflected their interaction with accessory cells nor was mediated by suppressor factors released by monocytes stimulated with PHA-P in the presence of anti-HLA Class I MoAb. Therefore, the regulatory role of HLA Class I antigens in T cell proliferation is not likely to be mediated by monocytes and/or factors released from them, but may reflect an involvement of these molecules in T cell activation pathways.

摘要

本研究旨在阐明HLA I类抗原不同决定簇在PHA - P诱导的T细胞增殖中发挥调节作用的机制,以及单核细胞在此现象中的参与情况。抗HLA - A2、A28单克隆抗体(MoAb)CR11 - 351、针对I抗原HLA - B基因座产物限制性决定簇的MoAb Q6/64,以及针对HLA I类抗原不同单态决定簇的MoAb CR10 - 215和W6/32,均被发现以剂量依赖性方式抑制PHA - P诱导的外周血单个核细胞(PBMC)增殖。这种抑制具有特异性,既不反映对PHA - P与细胞结合的抑制,也不反映抗HLA I类MoAb的毒性作用。后者在诱导抑制所需的浓度、用作促有丝分裂原的PHA - P浓度的影响、对用作PBMC来源的供体的不同效应,和/或诱导抑制对Fc部分的需求方面存在差异。与文献中的信息不同,抗HLA I类MoAb对PHA - P诱导的PBMC增殖的抑制作用既不反映它们与辅助细胞的相互作用,也不是由在抗HLA I类MoAb存在下PHA - P刺激的单核细胞释放的抑制因子介导的。因此,HLA I类抗原在T细胞增殖中的调节作用不太可能由单核细胞和/或它们释放的因子介导,而可能反映这些分子参与了T细胞激活途径。

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