Thorsby E, Ferrone S, Nousiainen H, Hirschberg H
Tissue Antigens. 1983 Feb;21(2):148-58. doi: 10.1111/j.1399-0039.1983.tb00382.x.
The specificity of the inhibitory activity of anti HLA-DR antisera on the proliferative response of human T cells to soluble antigens has been recently challenged. Furthermore, there are conflicting reports about the effect of antisera to the stimulatory antigen. Therefore, we investigated the inhibitory activity of different antisera on the proliferative response of T lymphocytes from sensitized donors to the antigens HSV and PPD. Alloantisera to DR specificities shared between antigen presenting cells (APC) and T cells displayed a strong inhibitory activity: alloantisera to HLA-DR specificities expressed only by APC or the T cell donor displayed lower or no inhibitory activity. Monoclonal antibodies to monomorphic determinants of HLA-DR molecules were inhibitory, but only when used at a high concentration. Antisera to HLA-ABC molecules and to HSV displayed little if any inhibition. These findings provide further evidence that the HLA-DR molecules as such in the APC membrane, which were also present during initial sensitization, are restriction elements for T cells.
抗HLA - DR抗血清对人T细胞对可溶性抗原增殖反应的抑制活性的特异性最近受到了挑战。此外,关于抗血清对刺激抗原作用的报道相互矛盾。因此,我们研究了不同抗血清对致敏供体T淋巴细胞对HSV和PPD抗原增殖反应的抑制活性。抗原呈递细胞(APC)和T细胞之间共有的DR特异性同种抗血清表现出强烈的抑制活性:仅由APC或T细胞供体表达的HLA - DR特异性同种抗血清表现出较低或无抑制活性。针对HLA - DR分子单态决定簇的单克隆抗体具有抑制作用,但仅在高浓度使用时才有效。抗HLA - ABC分子和抗HSV的抗血清几乎没有抑制作用。这些发现进一步证明,APC膜上的HLA - DR分子本身,在初次致敏时也存在,是T细胞的限制元件。