Sprent J, Schaefer M
Department of Immunology, Research Institute of Scripps Clinic, La Jolla, CA 92037.
Int Immunol. 1989;1(5):517-25. doi: 10.1093/intimm/1.5.517.
Information was sought on the antigen-presenting cells (APC) required for stimulating primary mixed-lymphocyte reactions (MLR) by unprimed Lyt-2+ cells in the absence of added lymphokines. Like L3T4+ cells, Lyt-2+ cells gave very high MLR in response to H-2-different dendritic cells (DC). Surprisingly, high MLR were also elicited by thioglycollate-induced peritoneal exudate cells (PEC), including Ia- PEC; these cells were non-immunogenic for L3T4+ cells. Since PEC consisted almost entirely of macrophages (M phi), the data suggest that at least two different cell types, DC and M phi, can express APC function for unprimed Lyt-2+ cells. Since resident peritoneal M phi and in vitro cultured PEC were poorly immunogenic, the APC function of M phi might be limited to a subset of these cells, e.g. to immature M phi.
在不添加淋巴因子的情况下,研究了未致敏的Lyt-2⁺细胞刺激原发性混合淋巴细胞反应(MLR)所需的抗原呈递细胞(APC)。与L3T4⁺细胞一样,Lyt-2⁺细胞对H-2不同的树突状细胞(DC)产生非常高的MLR。令人惊讶的是,包括Ia⁻PEC在内的巯基乙酸诱导的腹腔渗出细胞(PEC)也能引发高MLR;这些细胞对L3T4⁺细胞无免疫原性。由于PEC几乎完全由巨噬细胞(M phi)组成,数据表明至少两种不同的细胞类型,即DC和M phi,可对未致敏的Lyt-2⁺细胞发挥APC功能。由于驻留腹腔M phi和体外培养的PEC免疫原性较差,M phi的APC功能可能仅限于这些细胞的一个亚群,例如未成熟的M phi。