Source:http://linkedlifedata.com/resource/pubmed/id/15087226
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
1-2
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pubmed:dateCreated |
2004-4-16
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pubmed:abstractText |
In the interest of better understanding the role of human memory B cells in protection against disease, we developed an assay to quantitate antigen-specific memory B cells in human blood. This assay utilizes a 6-day polyclonal stimulation of PBMC followed by an antigen-specific ELISPOT for the detection of memory B cells that have differentiated into antibody secreting cells (ASC) in vitro. We have used this assay to demonstrate that the anthrax vaccine (AVA; BioThrax) elicits a substantial population of protective-antigen (PA) specific memory B cells, and these B cells satisfy the canonical surface phenotype of human memory B cells: CD19(+)CD20(+)Ig(+)CD27(+). These anti-PA antigen-specific memory B cells are IgG(+) and represent up to 2% of circulating IgG(+) B cells. Furthermore, these results confirm that vaccine-elicited memory B cells reside in the CD27(+) B cell population. This ELISPOT-based system has been designed in a generalized manner, such that the assay can be rapidly adapted to detect human antigen-specific memory B cells of any given specificity. This method should be useful for quantitatively assessing the potency of vaccines and the longevity of B cell immunological memory to various vaccines or infectious diseases.
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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/Anthrax Vaccines,
http://linkedlifedata.com/resource/pubmed/chemical/Antibodies, Bacterial,
http://linkedlifedata.com/resource/pubmed/chemical/Antigens, Bacterial,
http://linkedlifedata.com/resource/pubmed/chemical/Bacterial Toxins,
http://linkedlifedata.com/resource/pubmed/chemical/Epitopes, B-Lymphocyte,
http://linkedlifedata.com/resource/pubmed/chemical/Pokeweed Mitogens,
http://linkedlifedata.com/resource/pubmed/chemical/anthrax toxin
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pubmed:status |
MEDLINE
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pubmed:month |
Mar
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pubmed:issn |
0022-1759
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
286
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
111-22
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pubmed:dateRevised |
2006-11-15
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pubmed:meshHeading |
pubmed-meshheading:15087226-Anthrax Vaccines,
pubmed-meshheading:15087226-Antibodies, Bacterial,
pubmed-meshheading:15087226-Antigens, Bacterial,
pubmed-meshheading:15087226-B-Lymphocytes,
pubmed-meshheading:15087226-Bacterial Toxins,
pubmed-meshheading:15087226-Epitopes, B-Lymphocyte,
pubmed-meshheading:15087226-Flow Cytometry,
pubmed-meshheading:15087226-Humans,
pubmed-meshheading:15087226-Immunoenzyme Techniques,
pubmed-meshheading:15087226-Immunologic Memory,
pubmed-meshheading:15087226-Immunomagnetic Separation,
pubmed-meshheading:15087226-Immunophenotyping,
pubmed-meshheading:15087226-Pokeweed Mitogens,
pubmed-meshheading:15087226-Sensitivity and Specificity,
pubmed-meshheading:15087226-Staphylococcus aureus
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pubmed:year |
2004
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pubmed:articleTitle |
Tracking human antigen-specific memory B cells: a sensitive and generalized ELISPOT system.
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pubmed:affiliation |
Emory Vaccine Center and Department of Microbiology and Immunology, Emory University School of Medicine, 1510 Clifton Road, Rm G-211, Atlanta, GA 30322, USA. shane@liai.org
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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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