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HIV gp120-specific cell-mediated immune responses in mice after oral immunization with recombinant Salmonella.

TitleHIV gp120-specific cell-mediated immune responses in mice after oral immunization with recombinant Salmonella.
Publication TypeJournal Article
Year of Publication1995
AuthorsBerggren, RE, Wunderlich, A, Ziegler, E, Schleicher, M, Duke, RC, Looney, D, Fang, FC
JournalJ Acquir Immune Defic Syndr Hum Retrovirol
Volume10
Issue5
Pagination489-95
Date Published1995 Dec 15
ISSN1077-9450
KeywordsAdministration, Oral, AIDS Vaccines, Animals, Antibodies, Bacterial, Base Sequence, DNA Primers, Enzyme-Linked Immunosorbent Assay, Female, HIV Antibodies, HIV Envelope Protein gp120, HIV Infections, HIV-1, Immunity, Cellular, Immunization, Intestinal Mucosa, Lymphocyte Activation, Male, Mice, Mice, Inbred BALB C, Molecular Sequence Data, Plasmids, Salmonella typhimurium, T-Lymphocytes, Vaccines, Synthetic
Abstract

Salmonella is of great interest as a potential human immunodeficiency virus vaccine vector because of its ability to elicit potent mucosal and systemic immune responses when administered orally. To determine whether such a vaccine could elicit an immune response in mice, plasmids expressing HIV gp120-LAI were introduced into attenuated S. typhimurium. Three serial doses of 10(10) recombinant organisms were administered orally to BALB/c mice at 2-week intervals. Immunized mice but not control mice demonstrated proliferative T cell responses to gp120-LAI, comparable in magnitude to the proliferative responses to Salmonella antigens. Immunized mice had detectable serum and intestinal Salmonella-specific IgA and serum Salmonella-specific IgG. However, no gp120-specific antibody was detected in either serum or intestinal washes. These results indicate that live recombinant Salmonella-based vaccine constructs can induce HIV-specific cellular immune responses in vivo.

Alternate JournalJ. Acquir. Immune Defic. Syndr. Hum. Retrovirol.
PubMed ID8548327
Grant List1K08AI01248-01 / AI / NIAID NIH HHS / United States
AI-07447-02 / AI / NIAID NIH HHS / United States
AI-32463-03 / AI / NIAID NIH HHS / United States