Dynamics of memory B-cell populations in blood, lymph nodes, and bone marrow during antiretroviral therapy and envelope boosting in simian immunodeficiency virus SIVmac251-infected rhesus macaques. 2012

Thorsten Demberg, and Egidio Brocca-Cofano, and Peng Xiao, and David Venzon, and Diego Vargas-Inchaustegui, and Eun Mi Lee, and Irene Kalisz, and V S Kalyanaraman, and Janet Dipasquale, and Katherine McKinnon, and Marjorie Robert-Guroff
Vaccine Branch, National Cancer Institute, Bethesda, Maryland, USA.

Human immunodeficiency virus (HIV)/simian immunodeficiency virus (SIV) infection causes B-cell dysregulation and the loss of memory B cells in peripheral blood mononuclear cells (PBMC). These effects are not completely reversed by antiretroviral treatment (ART). To further elucidate B-cell changes during chronic SIV infection and treatment, we investigated memory B-cell subpopulations and plasma cells/plasmablasts (PC/PB) in blood, bone marrow, and lymph nodes of rhesus macaques during ART and upon release from ART. Macaques previously immunized with SIV recombinants and the gp120 protein were included to assess the effects of prior vaccination. ART was administered for 11 weeks, with or without gp120 boosting at week 9. Naïve and resting, activated, and tissue-like memory B cells and PC/PB were evaluated by flow cytometry. Antibody-secreting cells (ASC) and serum antibody titers were assessed. No lasting changes in B-cell memory subpopulations occurred in bone marrow and lymph nodes, but significant decreases in numbers of activated memory B cells and increases in numbers of tissue-like memory B cells persisted in PBMC. Macaque PC/PB were found to be either CD27(+) or CD27(-) and therefore were defined as CD19(+) CD38(hi) CD138(+). The numbers of these PC/PB were transiently increased in both PBMC and bone marrow following gp120 boosting of the unvaccinated and vaccinated macaque groups. Similarly, ASC numbers in PBMC and bone marrow of the two macaque groups also transiently increased following envelope boosting. Nevertheless, serum binding titers against SIVgp120 remained unchanged. Thus, even during chronic SIV infection, B cells respond to antigen, but long-term memory does not develop, perhaps due to germinal center destruction. Earlier and/or prolonged treatment to allow the generation of virus-specific long-term memory B cells should benefit ART/therapeutic vaccination regimens.

UI MeSH Term Description Entries
D007156 Immunologic Memory The altered state of immunologic responsiveness resulting from initial contact with antigen, which enables the individual to produce antibodies more rapidly and in greater quantity in response to secondary antigenic stimulus. Immune Memory,Immunological Memory,Memory, Immunologic,Immune Memories,Immunologic Memories,Immunological Memories,Memory, Immune,Memory, Immunological
D008198 Lymph Nodes They are oval or bean shaped bodies (1 - 30 mm in diameter) located along the lymphatic system. Lymph Node,Node, Lymph,Nodes, Lymph
D008253 Macaca mulatta A species of the genus MACACA inhabiting India, China, and other parts of Asia. The species is used extensively in biomedical research and adapts very well to living with humans. Chinese Rhesus Macaques,Macaca mulatta lasiota,Monkey, Rhesus,Rhesus Monkey,Rhesus Macaque,Chinese Rhesus Macaque,Macaca mulatta lasiotas,Macaque, Rhesus,Rhesus Macaque, Chinese,Rhesus Macaques,Rhesus Macaques, Chinese,Rhesus Monkeys
D008297 Male Males
D008562 Membrane Glycoproteins Glycoproteins found on the membrane or surface of cells. Cell Surface Glycoproteins,Surface Glycoproteins,Cell Surface Glycoprotein,Membrane Glycoprotein,Surface Glycoprotein,Glycoprotein, Cell Surface,Glycoprotein, Membrane,Glycoprotein, Surface,Glycoproteins, Cell Surface,Glycoproteins, Membrane,Glycoproteins, Surface,Surface Glycoprotein, Cell,Surface Glycoproteins, Cell
D010950 Plasma Cells Specialized forms of antibody-producing B-LYMPHOCYTES. They synthesize and secrete immunoglobulin. They are found only in lymphoid organs and at sites of immune responses and normally do not circulate in the blood or lymph. (Rosen et al., Dictionary of Immunology, 1989, p169 & Abbas et al., Cellular and Molecular Immunology, 2d ed, p20) Plasmacytes,Cell, Plasma,Cells, Plasma,Plasma Cell,Plasmacyte
D001854 Bone Marrow Cells Cells contained in the bone marrow including fat cells (see ADIPOCYTES); STROMAL CELLS; MEGAKARYOCYTES; and the immediate precursors of most blood cells. Bone Marrow Cell,Cell, Bone Marrow,Cells, Bone Marrow,Marrow Cell, Bone,Marrow Cells, Bone
D005434 Flow Cytometry Technique using an instrument system for making, processing, and displaying one or more measurements on individual cells obtained from a cell suspension. Cells are usually stained with one or more fluorescent dyes specific to cell components of interest, e.g., DNA, and fluorescence of each cell is measured as it rapidly transverses the excitation beam (laser or mercury arc lamp). Fluorescence provides a quantitative measure of various biochemical and biophysical properties of the cell, as well as a basis for cell sorting. Other measurable optical parameters include light absorption and light scattering, the latter being applicable to the measurement of cell size, shape, density, granularity, and stain uptake. Cytofluorometry, Flow,Cytometry, Flow,Flow Microfluorimetry,Fluorescence-Activated Cell Sorting,Microfluorometry, Flow,Cell Sorting, Fluorescence-Activated,Cell Sortings, Fluorescence-Activated,Cytofluorometries, Flow,Cytometries, Flow,Flow Cytofluorometries,Flow Cytofluorometry,Flow Cytometries,Flow Microfluorometries,Flow Microfluorometry,Fluorescence Activated Cell Sorting,Fluorescence-Activated Cell Sortings,Microfluorimetry, Flow,Microfluorometries, Flow,Sorting, Fluorescence-Activated Cell,Sortings, Fluorescence-Activated Cell
D000704 Analysis of Variance A statistical technique that isolates and assesses the contributions of categorical independent variables to variation in the mean of a continuous dependent variable. ANOVA,Analysis, Variance,Variance Analysis,Analyses, Variance,Variance Analyses
D000818 Animals Unicellular or multicellular, heterotrophic organisms, that have sensation and the power of voluntary movement. Under the older five kingdom paradigm, Animalia was one of the kingdoms. Under the modern three domain model, Animalia represents one of the many groups in the domain EUKARYOTA. Animal,Metazoa,Animalia

Related Publications

Thorsten Demberg, and Egidio Brocca-Cofano, and Peng Xiao, and David Venzon, and Diego Vargas-Inchaustegui, and Eun Mi Lee, and Irene Kalisz, and V S Kalyanaraman, and Janet Dipasquale, and Katherine McKinnon, and Marjorie Robert-Guroff
April 2013, Journal of virology,
Thorsten Demberg, and Egidio Brocca-Cofano, and Peng Xiao, and David Venzon, and Diego Vargas-Inchaustegui, and Eun Mi Lee, and Irene Kalisz, and V S Kalyanaraman, and Janet Dipasquale, and Katherine McKinnon, and Marjorie Robert-Guroff
May 2022, The Journal of clinical investigation,
Thorsten Demberg, and Egidio Brocca-Cofano, and Peng Xiao, and David Venzon, and Diego Vargas-Inchaustegui, and Eun Mi Lee, and Irene Kalisz, and V S Kalyanaraman, and Janet Dipasquale, and Katherine McKinnon, and Marjorie Robert-Guroff
August 2016, Journal of virology,
Thorsten Demberg, and Egidio Brocca-Cofano, and Peng Xiao, and David Venzon, and Diego Vargas-Inchaustegui, and Eun Mi Lee, and Irene Kalisz, and V S Kalyanaraman, and Janet Dipasquale, and Katherine McKinnon, and Marjorie Robert-Guroff
October 2020, Journal of virology,
Thorsten Demberg, and Egidio Brocca-Cofano, and Peng Xiao, and David Venzon, and Diego Vargas-Inchaustegui, and Eun Mi Lee, and Irene Kalisz, and V S Kalyanaraman, and Janet Dipasquale, and Katherine McKinnon, and Marjorie Robert-Guroff
September 2000, Veterinary pathology,
Thorsten Demberg, and Egidio Brocca-Cofano, and Peng Xiao, and David Venzon, and Diego Vargas-Inchaustegui, and Eun Mi Lee, and Irene Kalisz, and V S Kalyanaraman, and Janet Dipasquale, and Katherine McKinnon, and Marjorie Robert-Guroff
December 2021, AIDS (London, England),
Thorsten Demberg, and Egidio Brocca-Cofano, and Peng Xiao, and David Venzon, and Diego Vargas-Inchaustegui, and Eun Mi Lee, and Irene Kalisz, and V S Kalyanaraman, and Janet Dipasquale, and Katherine McKinnon, and Marjorie Robert-Guroff
December 2007, Journal of virology,
Thorsten Demberg, and Egidio Brocca-Cofano, and Peng Xiao, and David Venzon, and Diego Vargas-Inchaustegui, and Eun Mi Lee, and Irene Kalisz, and V S Kalyanaraman, and Janet Dipasquale, and Katherine McKinnon, and Marjorie Robert-Guroff
June 2007, Journal of virology,
Thorsten Demberg, and Egidio Brocca-Cofano, and Peng Xiao, and David Venzon, and Diego Vargas-Inchaustegui, and Eun Mi Lee, and Irene Kalisz, and V S Kalyanaraman, and Janet Dipasquale, and Katherine McKinnon, and Marjorie Robert-Guroff
January 2018, PloS one,
Thorsten Demberg, and Egidio Brocca-Cofano, and Peng Xiao, and David Venzon, and Diego Vargas-Inchaustegui, and Eun Mi Lee, and Irene Kalisz, and V S Kalyanaraman, and Janet Dipasquale, and Katherine McKinnon, and Marjorie Robert-Guroff
February 2016, AIDS research and human retroviruses,
Copied contents to your clipboard!