Hilburger M E, Zwilling B S
Department of Microbiology, College of Biological Sciences, Ohio State University, Columbus 43210.
Clin Exp Immunol. 1994 May;96(2):225-9. doi: 10.1111/j.1365-2249.1994.tb06546.x.
We have compared the antigen-presenting capacity of macrophages from congenic BALB/c.Bcgr and BALB/c.Bcgs mice that differentially express MHC class II glycoproteins. Several different criteria were used to evaluate the presentation of a protein antigen, ovalbumin (OVA), including limiting the concentration of antigen or the numbers of macrophages, and using both native OVA and OVA peptide 323-339. No differences in the capacity of macrophages from Bcgr and Bcgs mice to present antigen to a OVA-specific T cell hybridoma were found. Splenic macrophages from BCG-infected congenic mice also induced an equivalent amount of IL-2 production by the T cell hybridoma. The relationship of these findings to other differences that have been attributed to Bcg are discussed.
我们比较了同基因BALB/c.Bcgr和BALB/c.Bcgs小鼠中巨噬细胞的抗原呈递能力,这两种小鼠差异表达MHC II类糖蛋白。使用了几种不同的标准来评估蛋白质抗原卵清蛋白(OVA)的呈递情况,包括限制抗原浓度或巨噬细胞数量,并使用天然OVA和OVA肽323-339。未发现Bcgr和Bcgs小鼠的巨噬细胞将抗原呈递给OVA特异性T细胞杂交瘤的能力存在差异。来自卡介苗感染的同基因小鼠的脾巨噬细胞也诱导T细胞杂交瘤产生等量的白细胞介素-2。讨论了这些发现与归因于Bcg的其他差异之间的关系。