McCalmon R T, Kubo R T, Grey H M
J Immunol. 1975 Jun;114(6):1766-70.
The effect of anti-beta2-microglobulin (beta2m) on the mixed lymphocyte reaction (MLR), and an antigen-induced proliferative response was studied. Anti-beta2m IgG and Fab' fragments completely inhibited the MLR. Preincubation of stimulator or responder cells with anti-beta2m suggested that the major effect of anti-beta2m may be on the responder cell population. A clear-cut effect on responder cells was demonstrated by showing that anti-beta2m completely inhibited a MLR in which the stimulator population was a beta2m negative lymphoblastoid cell line. Anti-beta2m also inhibited PPD-induced proliferation of sensitized lymphocytes. The kinetics of this inhibition indicated that anti-beta2m added within the first 18 hr of stimulation was effective in inhibiting the proliferative response. These data are discussed in light of the hypothesis that beta2m may be a subunit of an antigen receptor on T cells.
研究了抗β2微球蛋白(β2m)对混合淋巴细胞反应(MLR)以及抗原诱导的增殖反应的影响。抗β2m IgG和Fab'片段完全抑制了MLR。用抗β2m对刺激细胞或反应细胞进行预孵育表明,抗β2m的主要作用可能在于反应细胞群体。通过显示抗β2m完全抑制了刺激群体为β2m阴性淋巴母细胞系的MLR,证明了其对反应细胞有明确的作用。抗β2m也抑制了PPD诱导的致敏淋巴细胞增殖。这种抑制的动力学表明,在刺激的最初18小时内加入抗β2m可有效抑制增殖反应。根据β2m可能是T细胞上抗原受体亚基的假说对这些数据进行了讨论。