Uracz W
Department of Clinical Immunology, Copernicus Medical School, Cracow.
Folia Biol (Praha). 1988;34(6):356-71.
Anti-Iatk monoclonal antibodies (mAbs) were found to inhibit syngeneic mixed lymphocyte reaction (SMLR) of mice with k and a haplotypes (H-2k and H-2a) of the major histocompatibility complex (MHC) by acting on responder T cells but not stimulator cells. Only the early phase of SMLR was inhibited by anti-Iat mAbs. The inhibitory effect was due to the blocking of autoreactive T cells but not induction of suppressor lymphocytes. Cross-linking of Iat epitopes induced T cell proliferation of k haplotype strain. The inhibitory pattern of SMLR by four anti-Iat mAbs varied among different strains of mice. The inhibitory pattern seemed to depend on MHC and unidentified non-MHC background genes possessed by stimulator cells, suggesting that the shape of the MHC recognition site must have different conformation depending on both MHC and non-MHC gene products recognized. However, the inhibitory pattern of SMLR by anti-Iat mAbs of strains which differ at the I-J locus: B10.A(5R) and B10.A(3R) was dependent on the genotype of stimulator cells. The same was observed in B10.S(9R) and B10.HTT strains. The inhibitory activity of anti-Iat mAbs was entirely directed against responder T cells and was not passively carried out by the stimulators. It was concluded that Iat epitopes are I region controlled determinants that are utilized by T cells as receptors for self Ia antigens. It is suggested that anti-Iat mAbs react with an idiotype on the receptor(s) for Ia or I-J, or possibly a "receptor" for these receptors.
抗Iat单克隆抗体(mAbs)被发现可通过作用于应答T细胞而非刺激细胞来抑制具有主要组织相容性复合体(MHC)的k和a单倍型(H-2k和H-2a)小鼠的同基因混合淋巴细胞反应(SMLR)。抗Iat mAbs仅抑制SMLR的早期阶段。抑制作用是由于阻断了自身反应性T细胞,而非诱导抑制性淋巴细胞。Iat表位的交联诱导了k单倍型品系的T细胞增殖。四种抗Iat mAbs对SMLR的抑制模式在不同小鼠品系中有所不同。抑制模式似乎取决于刺激细胞所拥有的MHC和未确定的非MHC背景基因,这表明MHC识别位点的形状必定因所识别的MHC和非MHC基因产物而具有不同的构象。然而,在I-J位点不同的品系:B10.A(5R)和B10.A(3R)中,抗Iat mAbs对SMLR的抑制模式取决于刺激细胞的基因型。在B10.S(9R)和B10.HTT品系中也观察到了同样的情况。抗Iat mAbs的抑制活性完全针对应答T细胞,而非由刺激细胞被动执行。得出的结论是,Iat表位是I区控制的决定簇,T细胞将其用作自身Ia抗原的受体。有人提出,抗Iat mAbs与Ia或I-J受体上的独特型反应,或者可能与这些受体的“受体”反应。