Ghosh A K, Dasgupta S, Ghose A C
Department of Microbiology, Bose Institute, Kankurgachi, Calcutta, India.
Clin Diagn Lab Immunol. 1995 May;2(3):291-6. doi: 10.1128/cdli.2.3.291-296.1995.
Antileishmanial antibody responses in the sera of Indian kala-azar (KA) and post-KA dermal leishmaniasis (PKADL) patients were analyzed by enzyme-linked immunosorbent assay (ELISA) and immunoblot experiments using immunoglobulin G (IgG) class- and subclass-specific reagents. All sera showed antileishmanial reactivities in IgG ELISA which followed the order IgG1 > IgG2 > IgG3, with very little IgG4. Immunoblot analysis with IgG class-specific reagents revealed variable patterns of reactivity by KA and PKADL sera, although certain common bands around the 60- to 63-kDa regions were discernible. Sera from antimony-unresponsive KA cases, on the other hand, strongly recognized two bands at around 20 to 22 kDa, in addition to other bands in the high-molecular-mass region. Further analysis showed that the 28-kDa band was preferentially recognized by the IgG2 isotype, while 20- to 22-kDa and 60- to 63-kDa bands were recognized by the IgG1 isotype. Antibodies belonging to the IgG3 isotype reacted to antigens primarily in the region of 14 to 34 kDa and persisted in patients even several months after cure. Immunoblot studies also revealed the presence of a nonspecific band which arose as a result of binding between a 66-kDa leishmanial antigen and streptavidin. Finally, the results presented in this study suggest that certain leishmanial antigens preferentially stimulate the synthesis of a particular IgG subclass(es), depending on the nature of such antigens or their epitopes.
采用酶联免疫吸附测定(ELISA)和免疫印迹实验,使用免疫球蛋白G(IgG)类和亚类特异性试剂,分析了印度黑热病(KA)患者和黑热病后皮肤利什曼病(PKADL)患者血清中的抗利什曼原虫抗体反应。所有血清在IgG ELISA中均显示出抗利什曼原虫反应性,其顺序为IgG1>IgG2>IgG3,IgG4含量极少。用IgG类特异性试剂进行的免疫印迹分析显示,KA和PKADL血清的反应模式各不相同,尽管在60至63 kDa区域周围可识别出某些共同条带。另一方面,对锑无反应的KA病例的血清,除了高分子质量区域的其他条带外,还强烈识别出两条约20至22 kDa的条带。进一步分析表明,28 kDa条带优先被IgG2同种型识别,而20至22 kDa和60至63 kDa条带被IgG1同种型识别。属于IgG3同种型的抗体主要与14至34 kDa区域的抗原发生反应,并且在患者治愈后数月仍持续存在。免疫印迹研究还揭示了一条非特异性条带的存在,它是由66 kDa利什曼原虫抗原与链霉抗生物素蛋白之间的结合产生的。最后,本研究结果表明,某些利什曼原虫抗原根据此类抗原或其表位的性质,优先刺激特定IgG亚类的合成。