Hurtrel B, Lagrange P H
Ann Immunol (Paris). 1978 Jul-Sep;129 C(5):653-68.
Mice injected intravenously (IV) or subcutaneously (SC) with living Candida albicans developed subsequently delayed-type hypersensitivity (DTH) which was measured in vivo by the footpad test after injection of 10(6) heat killed C. albicans (HKC.a.). Compared to systemic injections, SC immunizations with living C.a. gave higher levels of DTH, and lethality was absent. Subcutaneous injections of hundred time more doses of HKC.a. were also able to produce in normal mice a DTH reaction elicited with HKC.a. or with C.a. soluble extracts, but not with candidine. Intraperitoneal injections of varying doses of HKC.a. or subcutaneous injections of varying doses of C.a. soluble extracts failed to produce significant DTH. High levels of sensitization can be induced by using cyclophosphamide or BCG or both pretreatment before immunization, which seems to indicate immunomodulating factors for induction or expression of DTH in normal mice after injections of HKC.a. Kinetics of the local reaction elicited with HKC.a. fulfull usual criteria of DTH in actively immunized mice after CY pretreatment or not, and in passively immunized mice after systemic or local transfer of spleen cells from actively immune donors. Serum from same group of donors was unable to transfer DTH.
静脉内(IV)或皮下(SC)注射活白色念珠菌的小鼠随后出现迟发型超敏反应(DTH),在注射10(6) 热灭活白色念珠菌(HKC.a.)后通过足垫试验在体内进行测量。与全身注射相比,皮下注射活白色念珠菌产生的DTH水平更高,且无致死性。皮下注射剂量高出100倍的HKC.a. 也能够在正常小鼠中产生由HKC.a. 或白色念珠菌可溶性提取物引发的DTH反应,但不能由念珠菌素引发。腹腔注射不同剂量的HKC.a. 或皮下注射不同剂量的白色念珠菌可溶性提取物均未能产生显著的DTH。在免疫前使用环磷酰胺或卡介苗或两者进行预处理可诱导高水平的致敏,这似乎表明在注射HKC.a. 后正常小鼠中诱导或表达DTH的免疫调节因子。HKC.a. 引发的局部反应动力学符合CY预处理或未预处理的主动免疫小鼠以及主动免疫供体的脾细胞经全身或局部转移后的被动免疫小鼠中DTH的通常标准。同一组供体的血清无法传递DTH。