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Widespread B cell perturbations in HIV-1 infection afflict naive and marginal zone B cells.
- Source :
-
The Journal of experimental medicine [J Exp Med] 2019 Sep 02; Vol. 216 (9), pp. 2071-2090. Date of Electronic Publication: 2019 Jun 20. - Publication Year :
- 2019
-
Abstract
- Perturbations in B cells are a hallmark of HIV-1 infection. This is signified by increased numbers of exhausted CD21 <superscript>neg</superscript> memory B cells, driven by continuous antigen-specific and bystander activation. Using high-dimensional flow cytometry, we demonstrate that this exhausted phenotype is also prevalent among peripheral antigen-inexperienced naive and marginal zone (MZ) B cells in acute and chronic HIV-1 infection. A substantial fraction of naive and MZ B cells exhibit down-regulated CD21 levels and diminished response to B cell receptor (BCR)-dependent stimulation. Compared with CD21 <superscript>pos</superscript> subsets, the CD21 <superscript>neg</superscript> naive and MZ B cells differ in the expression of chemokine receptors and activation markers. Effective antiretroviral treatment normalizes peripheral naive and MZ B cell populations. Our results emphasize a more widely spread impairment of B cells in HIV-1 infection than previously appreciated, including antigen-inexperienced cells. This highlights the importance of monitoring functional capacities of naive B cells in HIV-1 infection, as exhausted CD21 <superscript>neg</superscript> naive B cells may severely impair induction of novel B cell responses.<br /> (© 2019 Liechti et al.)
- Subjects :
- Algorithms
Antiretroviral Therapy, Highly Active
Apoptosis
B-Lymphocyte Subsets immunology
Biomarkers metabolism
Cell Proliferation
Clonal Anergy
HIV Infections drug therapy
Humans
Lymphocyte Activation immunology
Phenotype
Receptors, Chemokine metabolism
Receptors, Complement 3d metabolism
Receptors, Interleukin-21 metabolism
B-Lymphocytes immunology
HIV Infections immunology
HIV-1 immunology
Subjects
Details
- Language :
- English
- ISSN :
- 1540-9538
- Volume :
- 216
- Issue :
- 9
- Database :
- MEDLINE
- Journal :
- The Journal of experimental medicine
- Publication Type :
- Academic Journal
- Accession number :
- 31221742
- Full Text :
- https://doi.org/10.1084/jem.20181124