rdf:type |
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lifeskim:mentions |
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pubmed:issue |
2
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pubmed:dateCreated |
1990-3-27
|
pubmed:abstractText |
Indirect assays for IgM and IgA antibodies often lack sensitivity and specificity due to interference from IgG antibodies. To overcome this problem we have developed a simple procedure using recombinant protein G coupled to agarose beads to remove the interfering IgG. A series of HIV seroconversion panels was tested by IgM and IgA immunoblot after protein G treatment in order to evaluate IgG removal and to study appearance of IgM and IgA antibodies in early HIV infection. Protein G treatment removed 99.9% of the IgG and reduced IgG anti-HIV titers of over 1/100,000 to undetectable levels. Both IgM and IgA HIV antibodies were detected as early in seroconversion as were IgG HIV antibodies. IgA HIV antibodies persisted for a longer period of time, reacted with more HIV proteins, and showed more intense staining than IgM HIV antibodies.
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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
|
pubmed:month |
Feb
|
pubmed:issn |
0022-1759
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pubmed:author |
|
pubmed:issnType |
Print
|
pubmed:day |
9
|
pubmed:volume |
126
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
199-204
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pubmed:dateRevised |
2007-11-15
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pubmed:meshHeading |
pubmed-meshheading:2406346-Bacterial Proteins,
pubmed-meshheading:2406346-Enzyme-Linked Immunosorbent Assay,
pubmed-meshheading:2406346-Evaluation Studies as Topic,
pubmed-meshheading:2406346-HIV Antibodies,
pubmed-meshheading:2406346-HIV Seropositivity,
pubmed-meshheading:2406346-Humans,
pubmed-meshheading:2406346-Immunoblotting,
pubmed-meshheading:2406346-Immunoglobulin A,
pubmed-meshheading:2406346-Immunoglobulin G,
pubmed-meshheading:2406346-Immunoglobulin M,
pubmed-meshheading:2406346-Immunologic Techniques,
pubmed-meshheading:2406346-Recombinant Proteins,
pubmed-meshheading:2406346-Sepharose
|
pubmed:year |
1990
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pubmed:articleTitle |
Detection of IgM and IgA HIV antibodies after removal of IgG with recombinant protein G.
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pubmed:affiliation |
Massachusetts Department of Public Health, State Laboratory Institute, Jamaica Plain 02130.
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pubmed:publicationType |
Journal Article,
Research Support, U.S. Gov't, P.H.S.
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