Source:http://linkedlifedata.com/resource/pubmed/id/12683403
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
2
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pubmed:dateCreated |
2003-4-9
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pubmed:abstractText |
Mucosal secretory IgA is considered to have an important role in the prevention of human immunodeficiency virus type 1 (HIV-1) transmission through sexual intercourse. Therefore, substances that induce HIV-1-specific IgA antibody in the genital tract may become promising candidates for prophylactic vaccine against HIV-1 infection. We have previously reported that concanavalin A-immobilized polystyrene nanospheres (Con A-NS) could efficiently capture HIV-1 particles and gp120 antigens on their surface and that intravaginal immunization with inactivated HIV-1-capturing nanospheres (HIV-NS) induced vaginal anti-HIV-1 IgA antibody in mice. In this study, various strategies for immunization with HIV-NS were undertaken to induce HIV-1-specific IgA response in the mouse genital tract. HIV-NS were administered intravaginally, orally, intranasally or intraperitoneally to mice. Progesterone treatment enhanced the anti-HIV-1 IgA response to intravaginal immunization significantly, but intranasal immunization with HIV-NS was more effective compared with other immunization routes in terms of vaginal IgA response. In addition, vaginal washes from intranasally immunized mice were capable of neutralizing HIV-1(IIIB). Thus, application of HIV-NS is a practical approach to promote HIV-1-specific IgA response by the vaginal mucosa in the mouse and intranasal appears to be an effective immunization route in this animal model. Intranasal immunization with HIV-NS should be further pursued for its potential as an HIV-1 prophylactic vaccine.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/AIDS Vaccines,
http://linkedlifedata.com/resource/pubmed/chemical/HIV Antibodies,
http://linkedlifedata.com/resource/pubmed/chemical/HIV Envelope Protein gp120,
http://linkedlifedata.com/resource/pubmed/chemical/Immunoglobulin A, Secretory,
http://linkedlifedata.com/resource/pubmed/chemical/Vaccines, Inactivated
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pubmed:status |
MEDLINE
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pubmed:month |
Feb
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pubmed:issn |
0146-6615
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
69
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
163-72
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pubmed:dateRevised |
2003-11-14
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pubmed:meshHeading |
pubmed-meshheading:12683403-AIDS Vaccines,
pubmed-meshheading:12683403-Administration, Intranasal,
pubmed-meshheading:12683403-Animals,
pubmed-meshheading:12683403-Estrus,
pubmed-meshheading:12683403-Female,
pubmed-meshheading:12683403-HIV Antibodies,
pubmed-meshheading:12683403-HIV Envelope Protein gp120,
pubmed-meshheading:12683403-HIV Infections,
pubmed-meshheading:12683403-HIV-1,
pubmed-meshheading:12683403-Immunity, Mucosal,
pubmed-meshheading:12683403-Immunization,
pubmed-meshheading:12683403-Immunoglobulin A, Secretory,
pubmed-meshheading:12683403-Mice,
pubmed-meshheading:12683403-Microspheres,
pubmed-meshheading:12683403-Mucous Membrane,
pubmed-meshheading:12683403-Neutralization Tests,
pubmed-meshheading:12683403-Vaccines, Inactivated,
pubmed-meshheading:12683403-Vagina
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pubmed:year |
2003
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pubmed:articleTitle |
Mucosal immunization with inactivated HIV-1-capturing nanospheres induces a significant HIV-1-specific vaginal antibody response in mice.
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pubmed:affiliation |
Japan Immunoresearch Laboratories, Takasaki, Gunma, Japan. akagit@jimro.co.jp
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pubmed:publicationType |
Journal Article
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