Yamamoto Y, Onoue K
J Immunol. 1979 Mar;122(3):942-8.
Histocompatibility-linked restriction of macrophage-T lymphocyte interaction in antigen-induced MIF production by sensitized lymphocytes was examined, by using combinations of inbred strain 2, strain 13, and JY-1 guinea pigs. The effective interaction of the antigen-bearing macrophages with the immune T lymphocytes was observed when the donor of the antigen-bearing macrophages and that of the immune lymphocytes shared Ia antigens of the major histocompatibility complex. Identities of B antigens and S antigens were not important for this cooperation. It was further demonstrated that the previously reported soluble factor derived from LPS-stimulated peritoneal adherent cells (macrophages) could help antigenic activation of the immune lymphocytes across the strain barrier provided a small number of macrophages (0.01%) from syngeneic strain were present. These results show that the presence of macrophages is absolutely required to present antigen to immune T lymphocytes in a genetically restricted manner and the soluble factor from macrophages appears to give a nonspecific effect on the lymphocyte activation in addition to or in collaboration with antigenic stimulation.
通过使用近交系2、13系和JY-1豚鼠的组合,研究了在致敏淋巴细胞抗原诱导的巨噬细胞移动抑制因子(MIF)产生过程中巨噬细胞与T淋巴细胞相互作用的组织相容性连锁限制。当携带抗原的巨噬细胞供体和免疫淋巴细胞供体共享主要组织相容性复合体的Ia抗原时,观察到携带抗原的巨噬细胞与免疫T淋巴细胞的有效相互作用。B抗原和S抗原的一致性对这种合作并不重要。进一步证明,先前报道的源自脂多糖刺激的腹腔黏附细胞(巨噬细胞)的可溶性因子,只要存在少量同基因系的巨噬细胞(0.01%),就可以帮助免疫淋巴细胞跨品系屏障进行抗原激活。这些结果表明,巨噬细胞的存在是绝对必要的,以便以基因限制的方式将抗原呈递给免疫T淋巴细胞,并且巨噬细胞的可溶性因子除了与抗原刺激协同作用外,似乎还对淋巴细胞激活产生非特异性作用。