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左旋咪唑对T细胞介导免疫的增强作用。

Potentiation of T-cell mediated immunity by levamisole.

作者信息

Renoux G, Renoux M, Teller M N, McMahon S, Guillaumin J M

出版信息

Clin Exp Immunol. 1976 Aug;25(2):288-96.

Abstract

Cell-mediated immunity is a requirement for recognition and elimination of cells and for prevention or treatment of a variety of diseases. Therefore, the development of a product potentially active in increasing immunity involves its testing in assays specific for cell-mediated immunity. The effectiveness of a single administration of levamisole was demonstrated in the rejection of isografts in a male to female C57BL/6 system, and on the enhancement of levels of the delayed type hypersensitivity (DTH) to sheep red cells (SRBC). Indeed, in five on nine tests, an injection of 25 mg/kg of levamisole to female recipients either on the day of grafting or 7 days after grafting resulted in a RT50% rejection time of 25 days, compared with 46 days in untreated controls. Levamisole administered at the time of immunization with various doses of SRBC elicited earlier, higher and more sustained DTH levels than in untreated controls. Such induction of T-cell activation was accompanied by a switch on anti-SRBC antibodies from IgM to IgG. These findings confirm and extend data evidencing the ability of levamisole to recruit and activate T cells for an increased or restored cell-mediated immunity.

摘要

细胞介导的免疫对于识别和清除细胞以及预防或治疗多种疾病至关重要。因此,开发一种可能具有增强免疫力活性的产品需要在针对细胞介导免疫的检测中进行测试。单次给予左旋咪唑的有效性在雄性到雌性C57BL/6系统中同种异体移植的排斥反应以及对绵羊红细胞(SRBC)迟发型超敏反应(DTH)水平的增强中得到了证明。事实上,在九项测试中的五项中,在移植当天或移植后7天向雌性受体注射25mg/kg的左旋咪唑,导致RT50%排斥时间为25天,而未治疗的对照组为46天。在用不同剂量的SRBC免疫时给予左旋咪唑,比未治疗的对照组引发更早、更高且更持久的DTH水平。这种T细胞激活的诱导伴随着抗SRBC抗体从IgM向IgG的转换。这些发现证实并扩展了证明左旋咪唑能够募集和激活T细胞以增强或恢复细胞介导免疫能力的数据。

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