Gross W L, Rucks A
Clin Exp Immunol. 1983 May;52(2):372-80.
The plaque forming cell (PFC) and proliferative responses of human peripheral blood lymphocytes and highly purified blood B cells induced by pokeweed mitogen (PWM) and group A streptoccocal cell membranes (A-ScM) were compared with the responses triggered by various cell preparations of Klebsiella pneumoniae K 43 (Klebs). The number of PFC was determined by a protein A plaque assay, and lymphoproliferation was measured by 3H-thymidine incorporation. In cell cultures stimulated with PWM and A-ScM, lymphocyte proliferation appeared to be associated with the generation of PFC. Klebs caused development of PFC without measurable prior proliferation. Whereas the response to PWM and A-ScM was absolutely T cell-dependent, highly purified B cells generated PFC when incubated with Klebs. Moreover, restitution of T cells to the B cell fraction did not augment (or diminish) the number of plaques. These studies establish that Klebs cell envelope structures contain a T cell-independent polyclonal B cell activator for human B lymphocytes in a high stage of differentiation. Use of this probe should provide further insight into the cellular interactions involved in the differentiation of antibody forming cells in humans.
将人类外周血淋巴细胞和高度纯化的血液B细胞在商陆丝裂原(PWM)和A组链球菌细胞膜(A-ScM)诱导下的空斑形成细胞(PFC)及增殖反应,与肺炎克雷伯菌K43(Klebs)的各种细胞制剂引发的反应进行了比较。通过蛋白A空斑试验确定PFC的数量,通过³H-胸腺嘧啶核苷掺入法测量淋巴细胞增殖。在用PWM和A-ScM刺激的细胞培养物中,淋巴细胞增殖似乎与PFC的产生相关。Klebs可导致PFC的形成,而之前没有可测量的增殖。虽然对PWM和A-ScM的反应绝对依赖T细胞,但高度纯化的B细胞与Klebs一起孵育时可产生PFC。此外,将T细胞恢复到B细胞组分中并不会增加(或减少)空斑数量。这些研究证实,Klebs细胞包膜结构含有一种针对高分化阶段人类B淋巴细胞的T细胞非依赖性多克隆B细胞激活剂。使用该探针应能进一步深入了解人类抗体形成细胞分化过程中涉及的细胞相互作用。