Lehner T, Brines R, Jones T, Avery J
Clin Exp Immunol. 1984 Nov;58(2):410-9.
Murine I-J gene products have been found in T suppressor cells (SC) and factors, macrophages and contrasuppressor cells (CSC). However, a human counterpart of the murine I-J has not been reported. As there is strong evidence that some murine anti-Ia antisera cross-react with human Ia antigens, the possibility was tested that mouse anti-I-J antibodies might cross-react with corresponding human class II determinants. Indeed, this revealed that three anti-I-J monoclonal antibodies (MoAb) and two antisera tested react with human mononuclear cells and that a significantly greater proportion of T8+ than T4+ cells or monocytes (Mo) react with the I-J antibodies. This was corroborated by autoradiography with significant inhibition of 125I-SA (streptococcal antigen) binding to T8+ cells but not to Mo by the MoAb or antisera to murine I-J. Functional reconstitution experiments of T4+ helper cells with the SA binding and presenting T8+ Vicia villosa adherent cells (VV-AC) and assessment of specific antibody forming cells to SA suggest that the antigen presenting function of this T8+ subset can be significantly inhibited by killing with the MoAb to I-J and complement. Furthermore, the subset of T8+ VV-AC also functions as CSC, for killing with MoAb to I-J and complement significantly inhibited the contrasuppressor function. This is consistent with the presence of I-J gene products in murine CSC. However, similar treatment of T8+ VV-NAC (non-adherent cells) or monocytes (Mo) failed to affect the suppressor or accessory helper function of these cells, respectively. Phenotypic characterization, inhibition of 125I-SA binding and reconstitution experiments for helper and suppressor functions, suggest that a subset of T8+ antigen binding, presenting and CSC may express determinants cross-reacting with murine I-J molecules.
在小鼠的抑制性T细胞(SC)及其因子、巨噬细胞和抗抑制性细胞(CSC)中已发现小鼠I-J基因产物。然而,尚未报道与小鼠I-J相对应的人类基因产物。由于有强有力的证据表明一些小鼠抗Ia抗血清可与人Ia抗原发生交叉反应,因此对小鼠抗I-J抗体是否可能与人相应的II类决定簇发生交叉反应进行了检测。实际上,这表明所检测的三种抗I-J单克隆抗体(MoAb)和两种抗血清可与人单核细胞发生反应,并且与I-J抗体发生反应的T8 +细胞比例明显高于T4 +细胞或单核细胞(Mo)。用小鼠I-J的MoAb或抗血清进行放射自显影得到了证实,其对125I-SA(链球菌抗原)与T8 +细胞的结合有显著抑制作用,但对单核细胞则无此作用。用结合并呈递SA的T8 +野豌豆黏附细胞(VV-AC)对T4 +辅助性T细胞进行功能重建实验,并评估针对SA的特异性抗体形成细胞,结果表明,用抗I-J的MoAb和补体杀伤该T8 +亚群可显著抑制其抗原呈递功能。此外,T8 + VV-AC亚群还具有抗抑制性细胞功能,因为用抗I-J的MoAb和补体杀伤可显著抑制其抗抑制功能。这与小鼠抗抑制性细胞中存在I-J基因产物是一致的。然而,对T8 + VV-NAC(非黏附细胞)或单核细胞(Mo)进行类似处理,分别未能影响这些细胞的抑制或辅助辅助功能。表型特征分析、对125I-SA结合的抑制作用以及辅助和抑制功能的重建实验表明,T8 +抗原结合、呈递和抗抑制性细胞的一个亚群可能表达与小鼠I-J分子发生交叉反应的决定簇。