Dunne D W, Richardson B A, Jones F M, Clark M, Thorne K J, Butterworth A E
Division of Microbiology, University of Cambridge, UK.
Parasite Immunol. 1993 Mar;15(3):181-5. doi: 10.1111/j.1365-3024.1993.tb00598.x.
We report the use of a matched set of mice/human chimaeric antibodies, directed against the 5-iodo-4-hydroxyl-3-nitrophenacetyl (NIP) hapten, to investigate the roles of different human isotypes in antibody-mediated eosinophil-dependent killing of schistosomula. The chimaeric antibodies consist of mouse VH, VL and CL regions with human gamma 1, gamma 2, gamma 3 (2 allotypes), gamma 4, alpha 2, mu or epsilon CH regions and were used in in vitro assays with human eosinophils and NIP-coated S. mansoni schistosomula. Some anti-NIP isotypes mediated high levels of killing, which was specific for NIP-coated larvae, and we suggest that these antibodies will be a valuable tool for studies on the role of antibody isotypes in anti-schistosome immune effector mechanisms. In particular, this method directly demonstrated, for the first time, that IgA is highly effective in mediating the killing of metazoan parasites by human eosinophils.
我们报告了使用一组针对5-碘-4-羟基-3-硝基苯乙酰(NIP)半抗原的匹配小鼠/人嵌合抗体,以研究不同人同种型在抗体介导的嗜酸性粒细胞依赖性杀伤血吸虫幼虫中的作用。嵌合抗体由小鼠VH、VL和CL区域与人γ1、γ2、γ3(2种同种异型)、γ4、α2、μ或ε CH区域组成,并用于与人嗜酸性粒细胞和NIP包被的曼氏血吸虫幼虫的体外试验。一些抗NIP同种型介导高水平的杀伤,这对NIP包被的幼虫具有特异性,并且我们认为这些抗体将是研究抗体同种型在抗血吸虫免疫效应机制中作用的有价值工具。特别是,该方法首次直接证明IgA在介导人嗜酸性粒细胞杀伤后生动物寄生虫方面非常有效。