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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
1
|
pubmed:dateCreated |
1999-3-22
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pubmed:abstractText |
An IgG2a monoclonal antibody (Mab) directed against glycoprotein D of herpes simplex virus 2 (HSV-2) was compared with an IgA heavy chain Mab switch variant to investigate the effect of isotype for topical immunoprotection of the murine vagina. The IgA Mab, a mixture of monomeric and polymeric IgA, was indistinguishable from its IgG parent in an in vitro HSV-2 neutralization assay. When these class switched Mabs were delivered to the mouse vagina, we also found no significant difference between the IgG and IgA for preventing vaginal transmission of HSV-2 infection. The implications of these results for active and passive immunization strategies against vaginal transmission of genital herpes infections are discussed.
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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 |
Oct
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pubmed:issn |
0165-0378
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
40
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
93-101
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pubmed:dateRevised |
2006-11-15
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pubmed:meshHeading |
pubmed-meshheading:9862259-Administration, Topical,
pubmed-meshheading:9862259-Animals,
pubmed-meshheading:9862259-Antibodies, Monoclonal,
pubmed-meshheading:9862259-Antibodies, Viral,
pubmed-meshheading:9862259-Antigenic Variation,
pubmed-meshheading:9862259-Female,
pubmed-meshheading:9862259-Herpes Genitalis,
pubmed-meshheading:9862259-Herpesvirus 2, Human,
pubmed-meshheading:9862259-Humans,
pubmed-meshheading:9862259-Immunization, Passive,
pubmed-meshheading:9862259-Immunoglobulin A,
pubmed-meshheading:9862259-Immunoglobulin Class Switching,
pubmed-meshheading:9862259-Immunoglobulin G,
pubmed-meshheading:9862259-Mice,
pubmed-meshheading:9862259-Vagina
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pubmed:year |
1998
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pubmed:articleTitle |
Comparison of an anti-HSV-2 monoclonal IgG and its IgA switch variant for topical immunoprotection of the mouse vagina.
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pubmed:affiliation |
Department of Biophysics, The Johns Hopkins University, Baltimore, MD 21218, USA.
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pubmed:publicationType |
Journal Article,
Comparative Study
|