Tewari R P, Sharma D K, Mathur A
J Infect Dis. 1978 Nov;138(5):605-13. doi: 10.1093/infdis/138.5.605.
The lymphoid cells responsible for protective immunity to histoplasmosis were characterized. Adoptive transfer of spleen and peritoneal cells treated with antiserum to theta-antigen from mice immunized with ribosomes or live yeast cells of Histoplasma capsulatum abrogated the ability of these cells to protect the syngeneic recipients, whereas treatment of lymphoid cells with antiserum to IgG did not affect the immunity. Prior removal of glass-adhering cells from spleen and peritoneal cell suspensions did not alter their protective activity. Treatment with mitomycin C, an antimitotic agent, ablated the capacity of immune lymphocytes to protect the syngeneic recipients. These results indicate that the immune spleen and peritoneal cells that confer immunity to histoplasmosis are thymus-dependent (T) lymphocytes and that their active proliferation in the recipients is necessary for expression of the protective immunity. Furthermore, the immunity elicited by immunization with histoplasma ribosomes and live yeast cells is mediated by a similar mechanism.
对组织胞浆菌病具有保护性免疫作用的淋巴细胞特性得以明确。用抗θ抗原抗血清处理来自用荚膜组织胞浆菌核糖体或活酵母细胞免疫的小鼠的脾脏和腹膜细胞后进行过继转移,消除了这些细胞保护同基因受体的能力,而用抗IgG抗血清处理淋巴细胞则不影响免疫。事先从脾脏和腹膜细胞悬液中去除玻璃黏附细胞并不改变其保护活性。用抗有丝分裂剂丝裂霉素C处理消除了免疫淋巴细胞保护同基因受体的能力。这些结果表明,赋予组织胞浆菌病免疫的免疫脾脏和腹膜细胞是胸腺依赖性(T)淋巴细胞,并且它们在受体中的活跃增殖对于保护性免疫的表达是必需的。此外,用组织胞浆菌核糖体和活酵母细胞免疫引发的免疫是由类似机制介导的。