| Literature DB >> 9125572 |
C Abou-Zeid1, M P Gares, J Inwald, R Janssen, Y Zhang, D B Young, C Hetzel, J R Lamb, S L Baldwin, I M Orme, V Yeremeev, B V Nikonenko, A S Apt.
Abstract
A 19-kDa lipoprotein from Mycobacterium tuberculosis was expressed as a recombinant antigen in the nonpathogenic mycobacterial host strain M. vaccae. Immunization of mice with the recombinant M. vaccae resulted in induction of a strong type 1 immune response to the 19-kDa antigen, characterized by immunoglobulin G2a (IgG2a) antibodies and gamma interferon (IFN-gamma) production by splenocytes. Immunization with the same antigen in incomplete Freund's adjuvant induced a strong IgG1 response with only low levels of IFN-gamma. Subsequent intravenous and aerosol challenges of immunized mice with virulent M. tuberculosis demonstrated no evidence of protection associated with the response to the 19-kDa antigen; in fact, the presence of the recombinant 19-kDa antigen abrogated the limited protection conferred by M. vaccae (vector control). The recombinant M. vaccae system is a convenient approach to induction of type 1 responses to M. tuberculosis antigens. However, the unexpected reduction in protective efficacy of M. vaccae expressing the 19-kDa antigen highlights the complexity of testing recombinant subunit vaccines and the need for a better understanding of the immune mechanisms required for effective vaccination against tuberculosis.Entities:
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Year: 1997 PMID: 9125572 PMCID: PMC175231 DOI: 10.1128/iai.65.5.1856-1862.1997
Source DB: PubMed Journal: Infect Immun ISSN: 0019-9567 Impact factor: 3.441