Germain R N, Mayer S V, Mescher M F
J Immunol. 1982 Jan;128(1):506-11.
A model system has been developed for exploring the requirements for activation of T cells by subcellular forms of Ia alloantigen. Lymph node cells from mice recently primed subcutaneously with viable allogeneic cells show strong proliferative responses in vitro to membrane preparations derived from cells bearing the appropriate I-region-encoded glycoproteins. This stimulation shows kinetics characteristic of a secondary response, with a peak at 24 to 48 hr. Primary responses to alloantigen-bearing membranes are weak or absent under these conditions. The predominant cell type involved in the secondary response is the Lyt-1+ T lymphocyte, and the major antigenic stimulus is the I-A subregion-encoded Ia glycoprotein. Syngeneic Ia+ accessory cells do not appear necessary for activation to occur. Detergent solubilized reconstituted membrane vesicles also will stimulate primed T lymphocytes to respond by proliferation. The applications of this approach to the study of T cell recognition of antigen and the role of nonspecific lymphokines in T cell triggering are discussed.
已开发出一种模型系统,用于探索亚细胞形式的Ia同种异体抗原激活T细胞的条件。近期经皮下注射活的同种异体细胞致敏的小鼠淋巴结细胞,在体外对来源于携带适当I区编码糖蛋白的细胞的膜制剂表现出强烈的增殖反应。这种刺激呈现出二次反应的动力学特征,在24至48小时达到峰值。在这些条件下,对携带同种异体抗原的膜的初次反应很弱或不存在。参与二次反应的主要细胞类型是Lyt-1+ T淋巴细胞,主要的抗原刺激是I-A亚区编码的Ia糖蛋白。同基因Ia+辅助细胞似乎并非激活所必需。经去污剂溶解的重组膜囊泡也能刺激致敏的T淋巴细胞通过增殖作出反应。本文讨论了该方法在T细胞对抗原的识别研究以及非特异性淋巴细胞因子在T细胞触发中的作用研究中的应用。