Recent Scientific Development of HIV Vaccine and HIV Prevention Strategies

A special issue of Vaccines (ISSN 2076-393X). This special issue belongs to the section "HIV Vaccines".

Deadline for manuscript submissions: closed (15 November 2023) | Viewed by 1966

Special Issue Editors


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Guest Editor
Department of Pharmacology, All India Institute of Medical Sciences, Jodhpur, India
Interests: respiratory; HIV; HIV vaccines; tuberculosis

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Guest Editor
Department of Immunology and Nano-Medicine, Herbert Wertheim College of Medicine, Florida International University, Miami, FL 33199, USA
Interests: immunology; nano-medicine; HIV/AIDS
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Special Issue Information

Dear Colleagues,

The past few years have witnessed many promising advances in HIV prevention strategies involving preexposure prophylaxis approaches. Despite the tremendous efforts to develop a successful human immunodeficiency virus (HIV) vaccine, the quest for a safe and effective HIV vaccine seems to be remarkably long. An effective vaccine is needed to stop the continuing spread of HIV worldwide. A number of unique characteristics of the biology of HIV infections make the creation of an HIV vaccine particularly challenging. Together with other HIV prevention approaches, preventive and therapeutic HIV vaccines will be invaluable tools in bringing the epidemic to an end.

This Special Issue is open to any subject area related to “HIV Vaccine and HIV Prevention Strategies”. We invite research employing quantitative and qualitative methods as well as contributions featuring under-researched populations.

Dr. Jaykaran Charan
Dr. Nagesh Kolishetti
Guest Editors

Manuscript Submission Information

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Keywords

  • HIV
  • HIV vaccine
  • HIV prevention

Published Papers (1 paper)

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Research

19 pages, 3049 KiB  
Article
Subclinical Atherosclerosis Is Associated with Discrepancies in BAFF and APRIL Levels and Altered Breg Potential of Precursor-like Marginal Zone B-Cells in Long-Term HIV Treated Individuals
by Matheus Aranguren, Kim Doyon-Laliberté, Mohamed El-Far, Carl Chartrand-Lefebvre, Jean-Pierre Routy, Jean-Guy Barril, Benoît Trottier, Cécile Tremblay, Madeleine Durand, Johanne Poudrier and Michel Roger
Vaccines 2023, 11(1), 81; https://doi.org/10.3390/vaccines11010081 - 30 Dec 2022
Cited by 2 | Viewed by 1610
Abstract
Chronic inflammation persists in people living with HIV (PLHIV) despite antiretrovial therapy (ART) and is involved in their premature development of cardiovascular diseases (CVD) such as atherosclerosis. We have previously reported that an excess of “B-cell activating factor” (BAFF), an important molecule for [...] Read more.
Chronic inflammation persists in people living with HIV (PLHIV) despite antiretrovial therapy (ART) and is involved in their premature development of cardiovascular diseases (CVD) such as atherosclerosis. We have previously reported that an excess of “B-cell activating factor” (BAFF), an important molecule for the selection and activation of first-line Marginal Zone (MZ) B-cell populations, is associated with deregulations of precursor-like MZ (MZp), whose potent B-cell regulatory (Breg) capacities are altered in PLHIV, early on and despite 1–2 years of ART. Based on these observations, and growing evidence that MZ populations are involved in atherosclerosis control, we designed a cross sectional study to explore the associations between BAFF and its analogue “A proliferation-inducing ligand” (APRIL) with subclinical CVD in long-time-treated individuals of the Canadian HIV and Aging Cohort Study (CHACS) imaging sub-study group. We also characterized the Breg profile of MZp from the blood of these individuals. Results were correlated with the total volume of atherosclerotic plaques (TPV) and with CVD risk factors and biomarkers. TPV was measured using cardiac computerised tomography angiography, and presence of CVD was defined as TPV > 0. We report that blood levels of BAFF are elevated and correlate positively with CVD and its risk factors in PLHIV from the CHACS, in contrast to APRIL levels, which correlate negatively with these factors. The expression levels of Breg markers such as NR4A3, CD39, CD73 and CD83 are significantly lower in PLHIV when compared to those of HIV-uninfected controls. In vitro experiments show that APRIL upregulates the expression of Breg markers by blood MZp from HIV-uninfected individuals, while this modulation is dampened by the addition of recombinant BAFF. Altogether, our observations suggest that strategies viewed to modulate levels of BAFF and/or APRIL could eventually represent a potential treatment target for CVD in PLHIV. Full article
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