Irwin M J, Heath W R, Sherman L A
Department of Immunology, Scripps Clinic and Research Foundation, La Jolla, California 92037.
J Exp Med. 1989 Oct 1;170(4):1091-101. doi: 10.1084/jem.170.4.1091.
As compared with the vigorous T cell response normally observed against allogeneic MHC molecules, T cells recognize xenogeneic MHC molecules poorly. To define structural features of the MHC molecule important for such species-specific recognition, HLA-A2(A2)-specific murine CTL were examined for their recognition of transfected cell lines expressing the class I molecules A2 or A2/H-2Kb(A2/Kb). A2/Kb is a chimeric molecule consisting of the alpha 1 and alpha 2 domains of A2 and the alpha 3, transmembrane, and cytoplasmic regions of Kb. The majority of CTL clones showed enhanced recognition of transfected cell lines expressing this chimeric molecule. Enhanced recognition was shown to correlate with sensitivity of the CTL clones to inhibition by anti-CD8 antibody. These results suggested that CD8 may interact with class I in a species-specific manner, and that suboptimal CD8 interaction with the alpha 3 domain of xenogeneic molecules may be an important contribution to poor xenoreactivity. This conclusion was supported by the capacity of A2/Kb, but not A2 human cell transfectants, to induce a primary in vitro CTL xenoresponse specific for A2.
与通常观察到的针对同种异体MHC分子的强烈T细胞反应相比,T细胞对异种MHC分子的识别较差。为了确定对这种物种特异性识别重要的MHC分子的结构特征,研究了HLA-A2(A2)特异性鼠CTL对表达I类分子A2或A2/H-2Kb(A2/Kb)的转染细胞系的识别。A2/Kb是一种嵌合分子,由A2的α1和α2结构域以及Kb的α3、跨膜和细胞质区域组成。大多数CTL克隆对表达这种嵌合分子的转染细胞系的识别增强。已证明增强的识别与CTL克隆对抗CD8抗体抑制的敏感性相关。这些结果表明,CD8可能以物种特异性方式与I类分子相互作用,并且CD8与异种分子α3结构域的次优相互作用可能是异种反应性差的一个重要原因。A2/Kb而非A2人细胞转染体诱导针对A2的原发性体外CTL异种反应的能力支持了这一结论。