Fathman C G, Collavo D, Davies S, Nabholz M
J Immunol. 1977 Apr;118(4):1232-8.
We have examined the kinetics and specificity of secondary in vitro mixed lymphocyte reactions (MLR). With limited numbers of primed responder cells (PRC) in the presence of "excess antigen" it was possible to obtain proliferative responses that were proportional to the number of PRC initially placed in culture. The responding cells, after an initial lag period, seem to grow exponentially until day 3 of culture. The responses of PRC (with the strain combinations and culture conditions described in this report) seemed to be directed toward stimulator cell determinants whose expression was determined by genes in the I region of the MHC. In one case, the relevant incompatibilities could be further restricted to the I-A region. Although PRC responded best to stimulator cells sharing the I region with the priming stimulator cell, apparent cross-reactivity could be observed by restimulating PRC with stimulator cells that did not carry the MHC haplotype of the priming stimulator cell. The rate of proliferation (measured as 3H-thymidine incorporation) in these apparent cross-reactions was reproducible and comparable to the rate observed in response to the priming stimulator cell. It was possible, therefore, to estimate the proportion of PRC that reacted in the presence of third party stimulator cells compared to the response of these PRC to the priming stimulator cells. We have estimated that the response of A (B6) PRC against H-2d and H-2s haplotype stimulator cells is about half of the response of these PRC to H-2b, the priming stimulator cell.
我们已经研究了体外二次混合淋巴细胞反应(MLR)的动力学和特异性。在“过量抗原”存在的情况下,使用有限数量的致敏应答细胞(PRC),有可能获得与最初接种到培养物中的PRC数量成比例的增殖反应。应答细胞在最初的延迟期后,似乎呈指数增长,直到培养的第3天。PRC的反应(在本报告中描述的菌株组合和培养条件下)似乎针对刺激细胞决定簇,其表达由MHC的I区基因决定。在一种情况下,相关的不相容性可进一步局限于I-A区。尽管PRC对与致敏刺激细胞共享I区的刺激细胞反应最佳,但通过用不携带致敏刺激细胞MHC单倍型的刺激细胞重新刺激PRC,可以观察到明显的交叉反应。在这些明显的交叉反应中,增殖率(以3H-胸腺嘧啶核苷掺入量衡量)是可重复的,并且与对致敏刺激细胞反应中观察到的速率相当。因此,有可能估计在第三方刺激细胞存在下反应的PRC比例与这些PRC对致敏刺激细胞反应的比例。我们估计,A(B6)PRC对H-2d和H-2s单倍型刺激细胞的反应约为这些PRC对致敏刺激细胞H-2b反应的一半。