Literature DB >> 25681347

Bone marrow plasma cells are a primary source of serum HIV-1-specific antibodies in chronically infected individuals.

Jairo M Montezuma-Rusca1, Susan Moir2, Lela Kardava1, Clarisa M Buckner1, Aaron Louie1, Leo J Y Kim1, Brian H Santich1, Wei Wang1, Olivia R Fankuchen1, Gabriella Diaz3, Janine R Daub4, Sergio D Rosenzweig5, Tae-Wook Chun1, Yuxing Li6, Raul C Braylan5, Katherine R Calvo5, Anthony S Fauci1.   

Abstract

Several potent and broadly neutralizing Abs to HIV-1 have been isolated recently from peripheral blood B cells of infected individuals, based on prescreening of Ab activity in the serum. However, little is known regarding the cells that make the Abs that circulate in the blood. Accordingly, we investigated the most likely source, the bone marrow, of chronically HIV-1-infected individuals who were not receiving antiretroviral therapy. Increased frequencies of plasma cells, as well as B cell precursors, namely preB-I and preB-II, and decreased frequencies of mature B cells were observed in bone marrow aspirates of these individuals compared with HIV-negative counterparts. Increased frequencies of bone marrow plasma cells are consistent with known hallmarks of HIV-1 infection, namely hypergammaglobulinemia and increased frequencies of peripheral blood plasmablasts. Levels of HIV-1 envelope (Env)-binding and HIV-1-neutralizing Abs were measured in serum, and corresponding frequencies of Ab-secreting or Env-binding cells were measured in the blood (plasmablasts and memory B cells) and in the bone marrow (plasma cells). A strong correlation was observed between serum HIV-1-specific Abs and Env-specific bone marrow-derived plasma cells, but not circulating plasmablasts or memory B cells. These findings demonstrate that, despite HIV-1-induced phenotypic and functional B cell dysregulation in the peripheral blood and secondary lymphoid tissues, bone marrow plasma cells remain a primary source for circulating HIV-1-specific Abs in HIV-1-infected individuals.

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Year:  2015        PMID: 25681347      PMCID: PMC4355319          DOI: 10.4049/jimmunol.1402424

Source DB:  PubMed          Journal:  J Immunol        ISSN: 0022-1767            Impact factor:   5.422


  48 in total

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