Araneo B A, Yowell R L, Sercarz E E
J Immunol. 1979 Sep;123(3):961-7.
A singular responsiveness to HEL was revealed in a peripheral lymphoid compartment of the genetically nonresponsive H-2b mouse. Although i.p. injection of HEL induces suppression and a lack of anti-HEL production, following footpad injection there is an early emergence in the popliteal lymph node (P-LN) of HEL-specific helper activity and plaque-forming cells. Furthermore, the early P-LN transiently expresses one of two T cell types needed for initiation of suppression. Delayed recruitment of the second required cell-type permits the induction of efficient suppression. There is only a short period during which there is concurrent representation of the two T cell subpopulations, and by mixing early and late deficient P-LN T cells, suppression could be established. The general implication of these results is that although a vigorous helper cell potential may exist in a strain nonresponsive to a multideterminant antigen, it can be obscured by a regulatory cell imbalance that results in the manifestation of a generalized Ir gene "defect."
在基因上无反应性的H-2b小鼠的外周淋巴区室中发现了对 HEL 的独特反应性。虽然腹腔注射 HEL 会诱导抑制作用且缺乏抗 HEL 产生,但在足垫注射后,腘窝淋巴结(P-LN)中会早期出现 HEL 特异性辅助活性和噬斑形成细胞。此外,早期的 P-LN 短暂表达启动抑制作用所需的两种 T 细胞类型之一。延迟募集第二种所需的细胞类型可诱导有效的抑制作用。只有在短时间内两种 T 细胞亚群同时存在,并且通过混合早期和晚期缺陷的 P-LN T 细胞,可以建立抑制作用。这些结果的一般含义是,尽管在对多决定簇抗原无反应性的品系中可能存在强大的辅助细胞潜能,但它可能会被调节细胞失衡所掩盖,这种失衡导致了普遍的 Ir 基因“缺陷”的表现。