Please use this identifier to cite or link to this item: http://hdl.handle.net/123456789/803
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dc.contributor.authorPanda, Amulya K; Talwar, GP; Purswani, Shilpi; Vohra, Richa; Pal, Rahul; Lohiya, Nirmal K; Gupta, Jagdish C-
dc.date.accessioned2016-05-04T08:39:01Z-
dc.date.available2016-05-04T08:39:01Z-
dc.date.issued2011-09-
dc.identifier.urihttp://hdl.handle.net/123456789/803-
dc.description.abstractThe objective of this work was to identify a human use-permissible adjuvant to enhance significantly the antibody response to a recombinant anti-hCG vaccine. Previous Phase II efficacy trials in sexually active women have demonstrated the prevention of pregnancy at hCG bioneutralization titers of 50ng/ml or more. Mycobacterium indicus pranii (MIP), a non-pathogenic Mycobacterium employed as an autoclaved suspension in aqueous buffer, significantly increased antibody titers in the FVB strain of mice. Three other genetic strains of mice: SJL, C3H, and C57Bl/6 responded with antibody titers several-fold higher than 50 ng/ml, which is the protective threshold in women, although there were differences in the peak titers attained. In addition, the duration of the antibody response was lengthened. The vaccine hCGβ-LTB, given together with MIP, induces both a Th1 and Th2 response, which is reflected in the production of not only IgG1, but also a high proportion of IgG2a and IgG2b antibodies.en_US
dc.publisherElsevier Ireland Ltden_US
dc.titleMycobacterium indicus pranii is a potent immunomodulator for a recombinant vaccine against human chorionic gonadotropinen_US
dc.keywordGenetic strains of mice, Antibody sub classes, Adjuvanten_US
dc.journalJournal of Reproductive Immunologyen_US
dc.volumeno91en_US
dc.issueno1-2en_US
dc.pages24-30en_US
Appears in Collections:Product Development Cell Unit- II, Publications

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