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Published on: May 2, 2025
Immune checkpoint inhibitors in infectious disease
Hannah A D King1, Sharon R Lewin1,2,3
1Department of Infectious Diseases, The University of Melbourne at The Peter Doherty Institute for Infection and Immunity, Melbourne, Victoria, Australia.
Immune checkpoint blockade, particularly targeting programmed cell death 1 (PD-1), shows promise for treating chronic infections like HIV. Anti-PD-1 therapy can restore exhausted immune cells and reverse HIV latency, offering new treatment avenues.
Area of Science:
- Immunology
- Infectious Diseases
- Oncology
Background:
- Immune checkpoint blockade (ICB) has revolutionized cancer immunotherapy.
- ICB is now being explored for chronic viral infections, including HIV and hepatitis B.
- Immune checkpoints regulate T cell responses and are implicated in infectious disease pathology.
Purpose of the Study:
- To discuss the role of immune checkpoints in infectious diseases.
- To explore the potential of ICB, specifically anti-programmed cell death 1 (PD-1), in managing HIV.
- To highlight research on anti-PD-1's impact on HIV latency, T cell function, and persistence.
Main Methods:
- Review of studies on immune checkpoint function and blockade in viral infections.
- Analysis of research investigating anti-PD-1's effects on HIV-specific T cells and viral latency.
- Examination of in vivo studies of anti-PD-1 and anti-CTLA-4 in people with HIV on antiretroviral therapy (ART).
Main Results:
- Anti-PD-1 therapy can restore function to exhausted HIV-specific T cells.
- Anti-PD-1 has the potential to reverse HIV latency, a persistent viral reservoir.
- Studies show ICB impacts the establishment, maintenance, and reversal of HIV latency.
Conclusions:
- Immune checkpoint blockade, particularly anti-PD-1, is a promising strategy for durable immune-mediated control of HIV.
- Further research is needed to evaluate anti-PD-1 in people with HIV on ART without cancer and in combination therapies.
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