Article
In vivo decrease in the expression of complement receptor 2 on B-cells in HIV infection.
Department of Pediatrics, Rush-Presbyterian-St Luke's Medical Center, Chicago, Illinois 60612.
AIDS (impact factor:
6.24).
02/1993;
7(1):37-41.
pp.37-41
Source: PubMed
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Citations (0)
- Cited In (2)
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Article: B Cells of HIV-1–Infected Patients Bind Virions through Cd21–Complement Interactions and Transmit Infectious Virus to Activated T Cells
[show abstract] [hide abstract]
ABSTRACT: The impact of HIV-associated immunopathogenesis on B cells has been largely associated with indirect consequences of viral replication. This study demonstrates that HIV interacts directly with B cells in both lymphoid tissues and peripheral blood. B cells isolated from lymph node and peripheral blood mononuclear cells (PBMCs) of 4 and 23 chronically infected patients, respectively, demonstrated similar capacities to pass virus to activated HIV-negative PBMCs when compared with CD4+ cells from the same patients. However, in contrast to T cells, virus associated with B cells was surface bound, as shown by its sensitivity to pronase and the staining pattern revealed by in situ amplification of HIV-1 RNA. Cell sorting and ligand displacing approaches established that CD21 was the HIV-binding receptor on B cells, and that this association was mediated through complement-opsonized virus. These B cells were also found to express significantly lower levels of CD21 compared with HIV-negative individuals, suggesting a direct perturbing effect of HIV on B cells. These findings suggest that B cells, although they themselves are not readily infected by HIV, are similar to follicular dendritic cells in their capacity to serve as extracellular reservoirs for HIV-1. Furthermore, B cells possess the added capability of circulating in peripheral blood and migrating through tissues where they can potentially interact with and pass virus to T cells.Journal of Experimental Medicine 09/2000; 192(5):637-646. · 13.85 Impact Factor -
Article: B cells of HIV-1-infected patients bind virions through CD21-complement interactions and transmit infectious virus to activated T cells.
[show abstract] [hide abstract]
ABSTRACT: The impact of HIV-associated immunopathogenesis on B cells has been largely associated with indirect consequences of viral replication. This study demonstrates that HIV interacts directly with B cells in both lymphoid tissues and peripheral blood. B cells isolated from lymph node and peripheral blood mononuclear cells (PBMCs) of 4 and 23 chronically infected patients, respectively, demonstrated similar capacities to pass virus to activated HIV-negative PBMCs when compared with CD4(+) cells from the same patients. However, in contrast to T cells, virus associated with B cells was surface bound, as shown by its sensitivity to pronase and the staining pattern revealed by in situ amplification of HIV-1 RNA. Cell sorting and ligand displacing approaches established that CD21 was the HIV-binding receptor on B cells, and that this association was mediated through complement-opsonized virus. These B cells were also found to express significantly lower levels of CD21 compared with HIV-negative individuals, suggesting a direct perturbing effect of HIV on B cells. These findings suggest that B cells, although they themselves are not readily infected by HIV, are similar to follicular dendritic cells in their capacity to serve as extracellular reservoirs for HIV-1. Furthermore, B cells possess the added capability of circulating in peripheral blood and migrating through tissues where they can potentially interact with and pass virus to T cells.Journal of Experimental Medicine 10/2000; 192(5):637-46. · 13.85 Impact Factor
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Keywords
additional markers
age-matched control donors
AIDS-related complex
asymptomatic patients
B-cell dysfunction
B-cells
C3d/Epstein-Barr virus receptor
CD20+ B-cells
CD20+ cells co-expressing CR2
CD4+ T-cell percentage
certain immunizations
CR2 expression
Cross-sectional study
Decreased expression
HIV-seropositive patients
percentage co-expression
percentage expression
receptor 2
standard antigen designation
two-color flow cytometric assay