Mawas C, Charmot D, Comoy A, Sasportes M
Eur J Immunol. 1977 Jan;7(1):11-5. doi: 10.1002/eji.1830070104.
The lectins phytohemagglutinin, pokeweed mitogen and concanavalin A used at their optimal mitogenic concentration, or human lymphocytes activated by the same mitogens, were found to suppress the in vitro generation of cytotoxic effectors when added to a cell-mediated lympholysis (CML) mixture during the first 48 h of culture. The data suggest that the suppressive mechanism is mediated to a greater extent by an allogeneic interaction between lectin-activated cells and the allogeneic cells present in the CML mixture than by suppressor cells induced by the lectin. Since partial suppression was observed with supernatants of activated lymphocytes cultured for 18 h with allogeneic stimulating cells (but not activated lymphocytes alone), a soluble mediator may be involved in the suppressive mechanism. The mechanism of suppression therefore may be identical to the preemption phenomenon recently described in primary and secondary CML.
发现以最佳促有丝分裂浓度使用的植物血凝素、商陆有丝分裂原和刀豆球蛋白A凝集素,或由相同有丝分裂原激活的人淋巴细胞,在培养的最初48小时内添加到细胞介导的淋巴细胞溶解(CML)混合物中时,会抑制体外细胞毒性效应细胞的产生。数据表明,抑制机制在更大程度上是由凝集素激活的细胞与CML混合物中存在的同种异体细胞之间的同种异体相互作用介导的,而不是由凝集素诱导的抑制细胞介导的。由于用同种异体刺激细胞培养18小时的活化淋巴细胞的上清液(但不是单独的活化淋巴细胞)观察到部分抑制,可溶性介质可能参与了抑制机制。因此,抑制机制可能与最近在原发性和继发性CML中描述的抢先现象相同。