Mawas C, Sasportes M, Charmot D, Christen Y, Dausset J
Clin Exp Immunol. 1975 Apr;20(1):83-92.
Cell-mediated lympholysis (CML) in eighteen patients suffering from primary immune deficiencies was studied. Fourteen of these patients had the variable type. Mixed lymphocyte response (MLR) and CML were clearly found to be independent: as well as two groups of patients in whom the two functions were either both normal or both deficient, two other groups were found in whom they were definitely separate. In one group MLR and T-cell mitogen responses were normal but no CML occurred against allogenic lymphocytes, and in the other cytotoxic effectors were generated normally but MLR and T-cell mitogen responses were very much lower than normal. These results show that the functions are independent, and are compatible with the theory that more than one subpopulation of T cells is involved. Neither the MLR or T-cell mitogen responses of these patients can predict their ability to generate cytotoxic effectors.
对18例原发性免疫缺陷患者的细胞介导淋巴细胞溶解(CML)进行了研究。其中14例患者为可变型。混合淋巴细胞反应(MLR)和CML明显是独立的:除了两组患者这两种功能均正常或均缺陷外,还发现另外两组患者这两种功能明显分离。一组患者的MLR和T细胞丝裂原反应正常,但对同种异体淋巴细胞不发生CML,另一组患者正常产生细胞毒性效应细胞,但MLR和T细胞丝裂原反应远低于正常水平。这些结果表明这些功能是独立的,并且与涉及不止一个T细胞亚群的理论相符。这些患者的MLR或T细胞丝裂原反应均不能预测其产生细胞毒性效应细胞的能力。