Zimecki M, Kapp J A
Institute of Immunology and Experimental Therapy, Polish Academy of Sciences, Wrocław.
Arch Immunol Ther Exp (Warsz). 1994;42(5-6):349-53.
We demonstrate that peritoneal B cells have a much higher ability to present antigen to antigen-specific T cell lines than splenic B cells. Presentation of antigen by B cells is abrogated or drastically reduced after removal of Lyb-5+ cells from the population of splenic or peritoneal B cells. Peritoneal B cells, precultured for 7 days prior to the antigen presentation assay, retain their antigen presenting cell (APC) function. Enrichment for CD5+ cells in the peritoneal B cell population results in a more effective antigen presentation. Lastly, stimulation of B cells via CD5 antigen, by treatment of cells with anti-CD5 antibodies or cross-linking of CD5 receptors, enhances APC function of these cells. The results indicate, both indirectly and directly, that CD5+ B cells play a predominant role in the presentation of conventional antigens to antigen-specific T cells.
我们证明,与脾B细胞相比,腹膜B细胞向抗原特异性T细胞系呈递抗原的能力要高得多。从脾或腹膜B细胞群体中去除Lyb-5+细胞后,B细胞的抗原呈递被消除或显著降低。在抗原呈递试验前预培养7天的腹膜B细胞保留了其抗原呈递细胞(APC)功能。腹膜B细胞群体中CD5+细胞的富集导致更有效的抗原呈递。最后,通过用抗CD5抗体处理细胞或使CD5受体交联,经由CD5抗原刺激B细胞,可增强这些细胞的APC功能。结果间接和直接地表明,CD5+B细胞在向抗原特异性T细胞呈递传统抗原中起主要作用。