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主要组织相容性复合体在调节巨噬细胞 - 淋巴细胞相互作用中的作用。

The role of the major histocompatibility complex in the regulation of macrophage-T lymphocyte interaction.

作者信息

Shevach E M

出版信息

J Invest Dermatol. 1980 May;74(5):289-91. doi: 10.1111/1523-1747.ep12543471.

Abstract

The proliferative response of guinea pig T lymphocytes which have been primed in vivo can only be induced by antigen-pulsed syngeneic macrophages. The development of techniques to prime T lymphocytes in vitro has allowed us to demonstrate that the genetic restriction on the interaction of the macrophage and T lymphocyte is regulated by the Ia antigens of the macrophage used during the initial sensitization step. Following removal of alloreactive cells, T cells can be sensitized to antigen-treated allogeneic macrophages. It thus appears likely that T cells do not recognize antigen per se, but can only be sensitized to antigen-modified membrane components or to complexes of antigen combined with certain membrane molecules. We postulate that the Ia antigens themselves are the products of the immune response genes and function in both macrophages and B lymphocytes as antigen recognition structures.

摘要

在体内已被致敏的豚鼠T淋巴细胞的增殖反应,只能由经抗原脉冲处理的同基因巨噬细胞诱导。体外致敏T淋巴细胞技术的发展,使我们能够证明巨噬细胞与T淋巴细胞相互作用的遗传限制,是由初始致敏步骤中所用巨噬细胞的Ia抗原调节的。去除同种反应性细胞后,T细胞可被抗原处理的同种异体巨噬细胞致敏。因此,T细胞似乎本身并不识别抗原,而只能被抗原修饰的膜成分或与某些膜分子结合的抗原复合物致敏。我们推测,Ia抗原本身是免疫反应基因的产物,在巨噬细胞和B淋巴细胞中均作为抗原识别结构发挥作用。

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