Abstract | PURPOSE OF REVIEW: Several recent advances are permitting a detailed examination of the HIV-specific B-cell response. In this review, we summarize these advances and their implications for understanding the response to HIV during chronic infection or in vaccine. RECENT FINDINGS: In HIV-infected patients, aberrant B-cell phenotypes have been associated with diminished humoral responses to other pathogens. HIV-specific B cells are overrepresented in some of these abnormal subsets. Over the past 2 years, flow cytometry-based techniques have been developed to stain HIV-specific B cells. These techniques are permitting a re-examination of frequency, phenotype, and function of HIV-specific B cells. They are also permitting the isolation of HIV-specific B cells in high purity. Immunoglobulin G from sorted HIV-specific B cells is oligoclonal, uses a limited repertoire of immunoglobulin genes, and targets multiple epitopes on Env. SUMMARY: It is likely that the defects found in total B cells in HIV-infected patients also play a role in the poorly effective HIV-specific antibody response. A subset of HIV-infected patients produced broadly neutralizing antibodies. Understanding this antibody response, and the B cells that underlie it, may be critical in efforts to elicit neutralizing antibodies against HIV.
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Authors | Nicole A Doria-Rose, Mark Connors |
Journal | Current opinion in HIV and AIDS
(Curr Opin HIV AIDS)
Vol. 4
Issue 5
Pg. 426-30
(Sep 2009)
ISSN: 1746-6318 [Electronic] United States |
PMID | 20048707
(Publication Type: Journal Article, Review)
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Chemical References |
- AIDS Vaccines
- HIV Antibodies
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Topics |
- AIDS Vaccines
(immunology)
- B-Lymphocytes
(immunology)
- Flow Cytometry
(methods)
- HIV
(immunology)
- HIV Antibodies
(biosynthesis)
- HIV Infections
(immunology)
- Humans
- Lymphocyte Subsets
(immunology)
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