Farr A G, Dorf M E, Unanue E R
Proc Natl Acad Sci U S A. 1977 Aug;74(8):3542-6. doi: 10.1073/pnas.74.8.3542.
In this study we show that T cells from mice infected with Listeria monocytogenes can interact in vitro with normal macrophages to produce a number of soluble mediators, including lymphostimulatory molecules. One of these molecules was a 15,000-dalton protein mitogenic for thymocytes. Generation of mitogenic activity was essentially completed by the first 24 hr of culture and did not require the addition of Listeria antigens. Production of mitogenic protein required contact between the lymphocytes and macrophages, because it did not occur when the two cells were separated by a cell-impermeable membrane. Optimal production of mitogenic protein occurred only when the lymphocytes and macrophages shared homologous I-A regions of the major histocompatibility complex. Once generated, the mitogenic protein did not display histocompatibility restriction and could stimulate allogeneic as well as syngeneic thymocytes. Strains of mice with the C57 background responded poorly to mitogenic protein even though those strains were capable of producing it. We conclude that an early stage in T cell immunity to Listeria involves an intimate association with macrophages regulated by the H-2 complex.
在本研究中,我们发现感染单核细胞增生李斯特菌的小鼠的T细胞可在体外与正常巨噬细胞相互作用,产生多种可溶性介质,包括淋巴细胞刺激分子。其中一种分子是对胸腺细胞有促有丝分裂作用的15,000道尔顿蛋白质。促有丝分裂活性在培养的最初24小时基本完成,且不需要添加李斯特菌抗原。促有丝分裂蛋白的产生需要淋巴细胞与巨噬细胞接触,因为当两个细胞被细胞不可渗透的膜隔开时不会发生。促有丝分裂蛋白的最佳产生仅在淋巴细胞和巨噬细胞共享主要组织相容性复合体的同源I-A区域时才会出现。一旦产生,促有丝分裂蛋白不表现出组织相容性限制,并且可以刺激同种异体以及同基因胸腺细胞。具有C57背景的小鼠品系对促有丝分裂蛋白反应不佳,尽管这些品系能够产生它。我们得出结论,T细胞对李斯特菌免疫的早期阶段涉及与由H-2复合体调节的巨噬细胞的密切关联。