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Published on: January 5, 2016
B cells and atherosclerosis: A HIV perspective
Laventa M Obare1, Rachel H Bonami2,3,4,5, Amanda C Doran3,4,5,6
1Division of Infectious Diseases, Department of Medicine, Vanderbilt University Medical Center, Nashville, Tennessee, USA.
B cells play a complex role in atherosclerosis, influencing cardiovascular disease (CVD) risk, especially in people with HIV (PLWH). Understanding these roles may lead to new B cell-targeted therapies for CVD.
Area of Science:
- Immunology
- Cardiovascular Science
- Virology
Background:
- Atherosclerosis is a major cause of global cardiovascular disease (CVD), driven by inflammation and lipid metabolism.
- B cells are implicated in atherosclerosis pathogenesis, but their role, particularly in HIV infection, is not fully understood.
- HIV infection is associated with chronic immune activation, potentially impacting B cell function and CVD risk.
Purpose of the Study:
- To review the diverse functions of B cells in atherosclerosis.
- To specifically examine the influence of HIV on B cell roles in atherosclerosis.
- To explore the proatherogenic and antiatherogenic properties of B cells in the context of HIV.
Main Methods:
- Literature review focusing on B cell functions in atherosclerosis.
- Analysis of B cell roles including natural antibody production, antigen presentation, and cytokine/chemokine production.
- Examination of how HIV-associated immune dysregulation affects B cells and CVD risk.
Main Results:
- B cells contribute to atherosclerotic plaque development through natural antibodies targeting modified lipoproteins and cellular debris.
- B cells modulate local and systemic immune responses via antigen presentation and cytokine production.
- HIV may exacerbate CVD risk by altering B cell functions within the atherosclerotic environment.
Conclusions:
- B cells possess both proatherogenic and antiatherogenic properties that influence atherosclerotic plaque development.
- HIV significantly impacts B cell-mediated immune responses, potentially increasing CVD risk in infected individuals.
- Further research into B cell functions in HIV-associated atherosclerosis may yield novel therapeutic targets for CVD prevention.
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