Inhibition of HIV replication in vitro by clinical immunosuppressants and chemotherapeutic agents.

Cell Biosci

National Center for Biodefense and Infectious Diseases, Department of Molecular and Microbiology, George Mason University, 10900, University Boulevard, Manassas, VA, USA.

Published: May 2013

AI Article Synopsis

  • Recent studies indicate that allogeneic bone marrow transplantation could lead to a functional cure for HIV-1, but the role of accompanying treatments remains unclear.
  • Our research shows that immunosuppressants, like mycophenolic acid and cyclosporine, along with the chemotherapy agent cytarabine, effectively inhibit HIV-1 replication in laboratory settings.
  • These findings suggest that combining these drugs might not only fight HIV directly but also impact the stability of HIV reservoirs, warranting further research on their therapeutic potential in patients.

Article Abstract

Background: Recent studies have suggested that a functional cure for HIV-1 infection, purportedly resultant from allogeneic bone marrow transplantation, may be possible. Additionally, the first such patient was treated with whole-body irradiation, immunosuppressants, and the chemotherapeutic, cytarabine. However, the precise role of the coinciding medical interventions in diminishing detectable HIV reservoirs remains unstudied.

Findings: In this article, we demonstrate that the immunosuppressants, mycophenolic acid and cyclosporine, and the chemotherapeutic, cytarabine, are potent antiretroviral agents at clinically relevant dosages. These drugs strongly inhibit HIV-1 replication in a GFP indicator T cell line and peripheral blood mononuclear cells (PBMC).

Conclusions: Our study suggests that certain clinical immunosuppressants and chemotherapeutic agents may act combinatorially to inhibit HIV infection. Additionally, chemotherapy-mediated cytotoxicity may also affect the stability of viral reservoirs. Thus, further study is needed to examine potential therapeutic value of these interventions in patients.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3680316PMC
http://dx.doi.org/10.1186/2045-3701-3-22DOI Listing

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