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Published on: February 5, 2020
[Immune-related adverse events after immune checkpoints inhibitors in 2019: An update]
T Comont1, J Belliere2, V Sibaud3
1Service de médecine interne et immunopathologie, centre hospitalier universitaire de Toulouse, institut universitaire du cancer de Toulouse Oncopôle, 31100 Toulouse, France; UFR Purpan, université Toulouse III Paul-Sabatier, 31100, Toulouse, France; UMR1037-Inserm, ERL5294 CNRS, centre de recherche en cancérologie de Toulouse, 31100 Toulouse, France.
Abstract:
Use of checkpoint inhibitors to treat cancer was one of the most important revolution these last years and an increasing number of new types of tumors is currently under investigation with these new treatments. However, immune-related adverse events associated with these agents frequently affect various organs, mimicking auto-immune or inflammatory diseases. Some of these effects can be severe, often requiring hospitalization and specialized treatment (immunosuppression). Most known agents are ipilimumab (anti-CTLA-4 antibody) nivolumab and pembrolizumab (anti-PD-1 antibodies). New molecules are now approved or in development as anti-PD-L1 antibodies, anti-LAG-3 or anti-TIM-3 antibodies, increasing the probability and new description of immune-related adverse events. With his experience in auto-immune diseases, the immunologist/internal medicine specialist has an important role in the management of these toxicities. The goal of this review is to focus on the incidence, diagnostic assessment and recommended management of the most relevant immune-related adverse events.
Insights
Checkpoint inhibitors revolutionize cancer treatment but can cause immune-related adverse events. This review details their incidence, diagnosis, and management by specialists.
Area of Science:
- Oncology
- Immunology
- Internal Medicine
Background:
- Checkpoint inhibitors (e.g., ipilimumab, nivolumab, pembrolizumab) represent a significant advancement in cancer therapy.
- These immunotherapies can trigger immune-related adverse events (irAEs) affecting multiple organs, often mimicking autoimmune diseases.
- Emerging agents like anti-PD-L1, anti-LAG-3, and anti-TIM-3 antibodies expand the landscape of irAEs.
Purpose of the Study:
- To review the incidence, diagnostic assessment, and management strategies for key immune-related adverse events associated with cancer immunotherapy.
- To highlight the critical role of immunologists and internal medicine specialists in managing these toxicities.
Main Methods:
- Literature review focusing on immune-related adverse events from checkpoint inhibitor therapy.
- Analysis of reported incidence, diagnostic criteria, and treatment guidelines for irAEs.
- Synthesis of information on established and novel immunotherapeutic agents.
Main Results:
- irAEs are a common and potentially severe complication of checkpoint inhibitor therapy.
- These events require careful diagnosis to differentiate from other conditions.
- Management often involves immunosuppressive therapies, necessitating specialist input.
Conclusions:
- Checkpoint inhibitors offer profound anti-cancer benefits but necessitate vigilant monitoring for irAEs.
- Effective management of irAEs relies on early recognition, accurate diagnosis, and timely intervention by specialists.
- Understanding and managing irAEs is crucial for optimizing cancer immunotherapy outcomes.
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