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Predicate | Object |
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rdf:type | |
lifeskim:mentions |
umls-concept:C0017968,
umls-concept:C0019704,
umls-concept:C0020971,
umls-concept:C0026724,
umls-concept:C0026809,
umls-concept:C0086022,
umls-concept:C0178602,
umls-concept:C0205171,
umls-concept:C0205263,
umls-concept:C0205373,
umls-concept:C0442027,
umls-concept:C0442335,
umls-concept:C0871261,
umls-concept:C1704632,
umls-concept:C1705099,
umls-concept:C1706817,
umls-concept:C2911692
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pubmed:issue |
14
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pubmed:dateCreated |
1997-10-28
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pubmed:abstractText |
Previous studies from our group showed that a Salmonella-HIV vector vaccine that expressed recombinant HIV-1 envelope protein gp120 stably in the vector cytoplasm elicited type 1 helper T cell (Th1) responses to gp120. Despite the promise of such vaccines, a major limitation in their use was that multiple immunizations were required to elicit even small responses. For this reason, we sought a modified vector configuration that would induce more potent gp120-specific T cell responses exhibiting a broader spectrum of effector functions after a single inoculation. In this article we describe the construction and immunogenicity of a Salmonella-HIV vector that displays a truncated derivative of HIV-1(IIIB) envelope in the periplasm of the vector. A single oral dose of this Salmonella vector, called H683(pW58-asd+), generated a gp120-specific proliferation response in the spleen 14 days after immunization. In agreement with our previous findings, the gp120-specific splenic CD4+ T cells elicited by H683(pW58-asd+) displayed a Th1 phenotype; however, gp120-specific splenic CD4+ Th2 cells were also evident. In addition, this strain induced strong gp120-specific IgA antibody-secreting cell (ASC) responses in the intestinal lamina propria and mesenteric lymph nodes. As many as 2% of the total lamina propria and mesenteric lymph node IgA ASCs were found to be specific for gp120 28 days after a single oral dose of H683(pW57-asd+). Because the proliferative response following a single dose of H683(pW58-asd+) was comparable to that seen previously after three doses of an analogous construct expressing recombinant gp120 in the cytoplasm, these observations suggest that Salmonella-vectored secreted HIV-1 antigens elicit higher T cell responses than their cytoplasmically bound analogs.
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pubmed:grant | |
pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:month |
Sep
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pubmed:issn |
0889-2229
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:day |
20
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pubmed:volume |
13
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
1187-94
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pubmed:dateRevised |
2007-11-14
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pubmed:meshHeading |
pubmed-meshheading:9310285-Administration, Oral,
pubmed-meshheading:9310285-Animals,
pubmed-meshheading:9310285-CD4-Positive T-Lymphocytes,
pubmed-meshheading:9310285-Cloning, Molecular,
pubmed-meshheading:9310285-Female,
pubmed-meshheading:9310285-Genetic Vectors,
pubmed-meshheading:9310285-HIV,
pubmed-meshheading:9310285-HIV Envelope Protein gp120,
pubmed-meshheading:9310285-Immunity, Mucosal,
pubmed-meshheading:9310285-Immunization,
pubmed-meshheading:9310285-Lymphocyte Activation,
pubmed-meshheading:9310285-Mice,
pubmed-meshheading:9310285-Recombinant Proteins,
pubmed-meshheading:9310285-Salmonella typhimurium,
pubmed-meshheading:9310285-Spleen
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pubmed:year |
1997
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pubmed:articleTitle |
Induction of mucosal and systemic responses against human immunodeficiency virus type 1 glycoprotein 120 in mice after oral immunization with a single dose of a Salmonella-HIV vector.
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pubmed:affiliation |
Division of Infectious Diseases and Gastroenterology, School of Medicine, Johns Hopkins University, Baltimore, Maryland 21202, USA.
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pubmed:publicationType |
Journal Article,
Research Support, U.S. Gov't, P.H.S.,
Research Support, Non-U.S. Gov't
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