Bick P H, Johnson A G
Scand J Immunol. 1977;6(11):1133-44. doi: 10.1111/j.1365-3083.1977.tb00352.x.
In vitro exposure of mouse thymocytes to complexes of polyadenylic:polyuridylic acid (poly A:U) effected, within 6 h, the release of soluble factor(s) capable of nonspecifically enhancing IgM and IgG plaque-forming cells (PFCs) in in vitro primary and secondary spleen cell responses to burro erythrocytes. Poly A:U stimulation was, most likely, polyclonal, since production of soluble factor(s) occurred in the absence of antigen and in serum-free culture media. Poly A:U-induced soluble factor(s) were not capable of substituting for T cells but were dependent on T cells for the expression of PFC enhancement. These data support the hypothesis that the mechanism of poly A:U's adjuvant action is polyclonal stimulation of T cells, causing early induction and release of nonspecific, soluble PFC-enhancing factor(s).
聚尿苷酸(poly A:U)复合物中,6小时内即可产生可溶性因子,该因子能够在体外对驴红细胞的初次和二次脾细胞反应中,非特异性增强IgM和IgG空斑形成细胞(PFC)。由于可溶性因子的产生发生在无抗原和无血清培养基中,因此poly A:U刺激很可能是多克隆的。poly A:U诱导的可溶性因子不能替代T细胞,但PFC增强作用的表达依赖于T细胞。这些数据支持了以下假设:poly A:U的佐剂作用机制是对T细胞的多克隆刺激,导致非特异性可溶性PFC增强因子的早期诱导和释放。