Breard J M, Friedman S M, Chess L
Ann Immunol (Paris). 1977 Jan-Mar;128(1-2):145-7.
Human peripheral blood B lymphocytes, isolated by Sephadex G-200 anti-Fab column chromatography, were non specifically induced by either pokeweed mitogen (PWM) or soluble products of antigen stimulated T cells, to differenciate into plaque directed against human Ia-like antigens (anti-p 23-30) inhibited the differenciation of B cells into antibody forming cells. Thus, while PWM induced proliferation was only mildly reduced by anti-p 23-30, the PWM induced PFC response was totally abrogated. Conversely, the antiserum abolished both the proliferative and the PFC responses generated by products of activated T cells. Using both Ouchterlony plates and co-precipitation techniques, we were unable to detect p 23-30 molecules on the active products present in the T cells supernatants. These data suggest that the inhibitory effects are secondary to interaction of the antiserum with B cells determinants.
通过葡聚糖G - 200抗Fab柱层析分离得到的人外周血B淋巴细胞,可被商陆有丝分裂原(PWM)或抗原刺激的T细胞可溶性产物非特异性诱导,分化为针对人Ia样抗原的空斑形成细胞(抗p 23 - 30),该物质抑制B细胞分化为抗体形成细胞。因此,虽然抗p 23 - 30仅轻微降低PWM诱导的增殖,但PWM诱导的PFC反应完全被消除。相反,该抗血清消除了活化T细胞产物产生的增殖反应和PFC反应。使用双向免疫扩散板和共沉淀技术,我们无法在T细胞上清液中的活性产物上检测到p 23 - 30分子。这些数据表明,抑制作用是抗血清与B细胞决定簇相互作用的继发效应。