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Early Viral Entry Assays for the Identification and Evaluation of Antiviral Compounds
Published on: October 29, 2015
Novel strategies to eliminate persistent viral infections
Marianne M Martinic1, Matthias G von Herrath
1La Jolla Institute for Allergy and Immunology, La Jolla, California 92037, USA.
Abstract:
Infection with viruses that have the capacity to modulate or evade the immune response can result in persistence, which can lead to a variety of chronic problems including neoplasia, immunosuppression, autoimmune-like syndromes, and selective organ failure. Recently, two promising new treatment approaches that target either the inhibitory receptor programmed cell death 1 (PD-1) or neutralize interleukin-10 (IL-10) during chronic viral infection have been described. We discuss how future combination therapies can be used to inhibit viral synthesis as well as strengthen the antiviral response without increasing immunopathology or the development of autoimmune disease.
Insights
Chronic viral infections can cause serious health issues. New therapies targeting programmed cell death 1 (PD-1) and interleukin-10 (IL-10) show promise for future combination treatments to control viral load and immune response.
Area of Science:
- Immunology
- Virology
- Oncology
Background:
- Viral infections can persist by evading immune responses, leading to chronic conditions like cancer and organ failure.
- Effective treatments for chronic viral infections remain a significant challenge in medicine.
Purpose of the Study:
- To review emerging therapeutic strategies for chronic viral infections.
- To explore the potential of combination therapies targeting immune checkpoints and cytokines.
Main Methods:
- Review of recent scientific literature on viral immune evasion and therapeutic targets.
- Analysis of novel treatment approaches including programmed cell death 1 (PD-1) inhibition and interleukin-10 (IL-10) neutralization.
Main Results:
- Targeting PD-1 or neutralizing IL-10 are promising strategies for managing chronic viral infections.
- These approaches offer potential to control viral replication and modulate immune responses.
Conclusions:
- Combination therapies inhibiting viral synthesis and enhancing antiviral immunity are feasible.
- Future strategies aim to balance viral clearance with prevention of immunopathology and autoimmune disease.
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