Thomas D W, Shevach E M
J Exp Med. 1976 Nov 2;144(5):1263-73. doi: 10.1084/jem.144.5.1263.
In order to analyze the genetic factors involved in the regulation of macrophage-T-cells interaction we have developed an in vitro primary response to soluble protein antigens in which nonimmune guinea pig T cells can be sensitized and subsequently challenged in tissue culture with antigen-pulsed macrophages. Antigen-specific T-cell activation, as measured by increased DNA synthesis, occurred when syngeneic antigen-pulsed macrophages were used for both initial sensitization and secondary challenge. No T-cell activation occurred when allogeneic antigen-pulsed macrophages were used for secondary challenge of cells primed when syngeneic macrophages. When allogeneic antigen-pulsed macrophages were used in both primary and secondary cultures it was difficult to assess antigen-specific stimulation due to the substantial mixed leukocyte reaction. However, when T cells from F1 animals were primed with parental antigen-pulsed macrophages they responded only to the parental macrophages used for initial sensitization but not to those of the other parent. These results are discussed with respect to T-cell recognition of a complex antigenic determinant which may include I-region gene products.
为了分析参与巨噬细胞 - T细胞相互作用调节的遗传因素,我们开发了一种针对可溶性蛋白抗原的体外初级反应,其中非免疫豚鼠T细胞可以被致敏,随后在组织培养中用抗原脉冲巨噬细胞进行攻击。当同基因抗原脉冲巨噬细胞用于初始致敏和二次攻击时,通过增加的DNA合成来测量的抗原特异性T细胞活化发生。当同种异体抗原脉冲巨噬细胞用于同基因巨噬细胞致敏的细胞的二次攻击时,没有发生T细胞活化。当同种异体抗原脉冲巨噬细胞用于原代和二次培养时,由于大量的混合白细胞反应,难以评估抗原特异性刺激。然而,当来自F1动物的T细胞用亲本抗原脉冲巨噬细胞致敏时,它们仅对用于初始致敏的亲本巨噬细胞有反应,而对另一亲本的巨噬细胞没有反应。就可能包括I区基因产物的复杂抗原决定簇的T细胞识别而言,对这些结果进行了讨论。