Related Experiment Video
Updated: Oct 8, 2025

Induction of Ocular Surface Inflammation and Collection of Involved Tissues
Published on: August 4, 2022
Immune-Related Oral, Otologic, and Ocular Adverse Events
Nagham Al-Zubidi1, J Cody Page1, Dan S Gombos1
1Department of Head and Neck Surgery, Division of Surgery, University of Texas MD Anderson Cancer Center, Houston, TX, USA.
Abstract:
Emerging immunotherapeutic agents, including immune checkpoint inhibitors targeting cytotoxic T-lymphocyte-associated antigen-4 (CTLA-4), programmed cell death protein 1 (PD-1), and programmed cell death protein ligand 1 (PD-L1), have revolutionized cancer treatment. The first immune checkpoint inhibitor (ICI) ipilimumab, an anti-CTLA-4, was approved in 2011. Since then, the US Food and Drug Administration (FDA) has approved more than half a dozen immune checkpoint inhibitors to treat various malignancies. These agents are part of a broader class of chemotherapy agents termed immunotherapy, which selectively target different steps in the immune response cascade to upregulate the body's normal response to cancer. While the effects of traditional chemotherapy are well known, the toxicity profile of emerging immune therapies is not fully elucidated. They have been associated with atypical side effects labeled collectively as immune-related adverse events (irAEs).
Insights
New immunotherapies like immune checkpoint inhibitors (ICIs) offer novel cancer treatments by harnessing the immune system. However, these advanced therapies can cause unique immune-related adverse events (irAEs) not seen with traditional chemotherapy.
Area of Science:
- Oncology
- Immunology
- Pharmacology
Background:
- Immune checkpoint inhibitors (ICIs) targeting CTLA-4, PD-1, and PD-L1 have transformed cancer therapy.
- The first ICI, ipilimumab (anti-CTLA-4), gained FDA approval in 2011, paving the way for numerous other approvals.
- Immunotherapy agents selectively modulate the immune response to fight cancer, representing a significant advancement over traditional chemotherapy.
Purpose of the Study:
- To review the revolutionary impact of emerging immunotherapeutic agents in cancer treatment.
- To highlight the distinct toxicity profiles associated with these novel therapies.
- To introduce the concept and collective term for these unique side effects: immune-related adverse events (irAEs).
Main Methods:
- Literature review of FDA-approved immune checkpoint inhibitors.
- Analysis of the mechanism of action for immunotherapies.
- Examination of the known and emerging toxicity profiles of ICIs.
Main Results:
- Several immune checkpoint inhibitors targeting CTLA-4, PD-1, and PD-L1 are now FDA-approved for various cancers.
- These agents represent a class of immunotherapy that enhances the body's anti-cancer immune response.
- Unlike traditional chemotherapy, ICIs are associated with a distinct set of side effects known as immune-related adverse events (irAEs).
Conclusions:
- Immune checkpoint inhibitors have significantly advanced cancer treatment paradigms.
- Understanding the unique toxicity profile, including irAEs, is crucial for managing patients on immunotherapy.
- Further research is needed to fully elucidate the long-term effects and management strategies for irAEs.
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