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J. Virol., 03 1997, 2303-2309, Vol 71, No. 3
M Lagranderie, AM Balazuc, B Gicquel and M Gheorghiu
Recombinant live Mycobacterium bovis BCG vectors (rBCG) induce strong
cellular and humoral immune responses against various antigens after either
systemic or oral immunization of mice. Cytotoxic T-lymphocyte (CTL)
responses may contribute to the control of human immunodeficiency virus
(HIV) or simian immunodeficiency virus (SIV) infections whose portal of
entry is the gastrointestinal or genital mucosa. In this study, we
immunized BALB/c mice with a recombinant BCG SIV nef and observed its
behavior in oropharyngeal and target organ lymphoid tissues. The cellular
immune responses, particularly the intestinal intraepithelial and systemic
CTL responses, were investigated. The results showed that rBCG SIV nef
translocated the oropharyngeal mucosa and intestinal epithelium. It
diffused to and persisted in target lymphoid organs. Specific SIV Nef
peptide proliferative responses and cytokine production were observed.
Strong systemic and mucosal CTL responses were induced. In particular, we
demonstrated direct specific anti-Nef CTL in intestinal intraepithelial
CD8beta+ T cells. These findings provide evidence that orally administered
rBCG SIV nef may contribute to local defenses against viral invasion.
Therefore, rBCG SIV nef could be a candidate vaccine to protect against SIV
infection and may be used to develop an oral rBCG HIV nef vaccine.
Copyright © 1997, American Society for Microbiology
Oral immunization with recombinant Mycobacterium bovis BCG simian immunodeficiency virus nef induces local and systemic cytotoxic T- lymphocyte responses in mice
Laboratoire du BCG, Institut Pasteur, Paris, France.
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