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Updated: Mar 8, 2026

Identifying PD-1/PD-L1 Inhibitors with Surface Plasmon Resonance Technology
Published on: May 2, 2025
Anti-PD-1/PD-L1 therapy for infectious diseases: learning from the cancer paradigm
Martin Rao1, Davide Valentini2, Ernest Dodoo3
1Division of Therapeutic Immunology (TIM), Department of Laboratory Medicine (LABMED), Karolinska Institutet, Stockholm, Sweden.
Objectives:
Immune checkpoint pathways regulate optimal host immune responses against transformed cells, induce immunological memory, and limit tissue pathology. Conversely, aberrant immune checkpoint activity signifies a poor prognosis in cancer and infectious diseases. Host-directed therapy (HDT) via immune checkpoint blockade has revolutionized cancer treatment with therapeutic implications for chronic infections, thus laying the foundation for this review.
Methods:
Online literature searches were performed via PubMed, PubMed Central, and Google using the keywords "immune checkpoint inhibition"; "host-directed therapy"; "T cell exhaustion"; "cancer immunotherapy"; "anti-PD-1 therapy"; "anti-PD-L1 therapy"; "chronic infections"; "antigen-specific cells"; "tuberculosis"; "malaria"; "viral infections"; "human immunodeficiency virus"; "hepatitis B virus"; "hepatitis C virus"; "cytomegalovirus" and "Epstein-Barr virus". Search results were filtered based on relevance to the topics covered in this review.
Results:
The use of monoclonal antibodies directed against the antigen-experienced T-cell marker programmed cell death 1 (PD-1) and its ligand PD-L1 in the context of chronic infectious diseases is reviewed. The potential pitfalls and precautions, based on clinical experience from treating patients with cancer with PD-1/PD-L1 pathway inhibitors, are also described.
Conclusions:
Anti-PD-1/PD-L1 therapy holds promise as adjunctive therapy for chronic infectious diseases such as tuberculosis and HIV, and must therefore be tested in randomized clinical trials.
Insights
Immune checkpoint inhibitors, like anti-programmed cell death 1 (PD-1) and anti-PD-L1 therapies, show promise for treating chronic infections. Further clinical trials are needed to confirm their efficacy and safety in infectious diseases.
Area of Science:
- Immunology
- Oncology
- Infectious Diseases
Background:
- Immune checkpoint pathways are crucial for regulating immune responses and preventing autoimmunity.
- Aberrant immune checkpoint activity is linked to poor outcomes in cancer and chronic infections.
- Host-directed therapy (HDT) using immune checkpoint blockade has transformed cancer treatment.
Purpose of the Study:
- To review the application of anti-PD-1 and anti-PD-L1 therapies in chronic infectious diseases.
- To discuss potential challenges and safety considerations based on cancer treatment experiences.
Main Methods:
- Literature searches were conducted using PubMed, PubMed Central, and Google.
- Keywords included immune checkpoint inhibition, HDT, T cell exhaustion, cancer immunotherapy, anti-PD-1, anti-PD-L1, and specific chronic infections.
- Search results were filtered for relevance.
Main Results:
- Monoclonal antibodies targeting the PD-1/PD-L1 pathway are being explored for chronic infections.
- Clinical insights from cancer immunotherapy with PD-1/PD-L1 inhibitors offer valuable lessons.
- Potential pitfalls and precautions for using these therapies in infectious diseases are outlined.
Conclusions:
- Anti-PD-1/PD-L1 therapy presents a promising adjunctive treatment strategy for chronic infections like tuberculosis and HIV.
- Randomized clinical trials are essential to validate the effectiveness and safety of these therapies in infectious disease contexts.
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