Expression, characterization and therapeutic efficacy of chimeric Fab of anti-idiotypic antibody NP30 against Schistosoma japonicum

► A human–mouse chimeric Fab of monoclonal anti-idiotypic antibody NP30 (chFab-NP30) against Schistosoma japonicum was constructed and expressed in E. coli. ► The purified chFab-NP30 inhibited the binding of parent NP30 to sera from schistosomiasis patients in a dose-dependent manner. ► Administrati...

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Published inActa tropica Vol. 118; no. 2; pp. 159 - 164
Main Authors Xu, Jing, Zhu, Xiao-Juan, Li, Yu-Hua, Dai, Yang, Zhu, Yin-Chang, Zheng, Jiang, Feng, Zhen-Qing, Guan, Xiao-Hong
Format Journal Article
LanguageEnglish
Published Oxford Elsevier B.V 01.05.2011
Elsevier
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Summary:► A human–mouse chimeric Fab of monoclonal anti-idiotypic antibody NP30 (chFab-NP30) against Schistosoma japonicum was constructed and expressed in E. coli. ► The purified chFab-NP30 inhibited the binding of parent NP30 to sera from schistosomiasis patients in a dose-dependent manner. ► Administration of the chimeric Fab in vivo increased the survival rate, reduced egg burdens and ameliorated organ pathology of mice with acute schistosomiasis. ► chFab-NP30 is a promising candidate to be used as a specific and efficient recombinant antibody against acute schistosomiasis japonica. The murine monoclonal anti-idiotypic antibody NP30 is a promising therapeutic antibody against Schistosoma japonicum. However, the immunogenicity of murine NP30 limits its further study and application in humans. Here the chimeric Fab of NP30 (chFab-NP30) comprising the variable regions of murine NP30 and constant regions of human antibody was assembled. chFab-NP30 was expressed and purified as a soluble and functional protein. Administration of chFab-NP30 in vivo increased the survival rate, reduced egg burdens and ameliorated organ pathology of mice with acute schistosomiasis. Our study indicated that chFab-NP30 is a promising candidate to be used as a specific and efficient recombinant antibody against acute schistosomiasis japonica. Further studies on function mechanism of chFab-NP30 needs to be carried out in the future.
Bibliography:http://dx.doi.org/10.1016/j.actatropica.2011.01.006
ObjectType-Article-1
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ISSN:0001-706X
1873-6254
DOI:10.1016/j.actatropica.2011.01.006