Abstract
Despite the success and ongoing promise of monoclonal antibody–targeted immune checkpoint inhibitor immunotherapy of advanced malignancies, in particular, antibodies directed against CTLA-4 and PD-1/PD-L1, the development of immune-related adverse events (irAEs) remains a constraint of this type of therapy. Although rarely fatal, the occurrence of irAEs may necessitate discontinuation of immunotherapy, as well as administration of corticosteroids or other immunosuppressive therapies that may not only compromise efficacy but also predispose for development of opportunistic infection. Clearly, retention of efficacy of immune checkpoint–targeted therapies with concurrent attenuation of immune-mediated toxicity represents a formidable challenge. In this context, the current brief review examines mechanistic relationships between these events, as well as recent insights into immunopathogenesis, and strategies which may contribute to resolving this issue. These sections are preceded by brief overviews of the discovery and functions of CTLA-4 and PD-1, as well as the chronology of the development of immunotherapeutic monoclonal antibodies which target these immune checkpoint inhibitors.
| Original language | English |
|---|---|
| Pages (from-to) | 6111-6117 |
| Number of pages | 7 |
| Journal | Supportive Care in Cancer |
| Volume | 28 |
| Issue number | 12 |
| DOIs | |
| State | Published - Dec 2020 |
Keywords
- Cytotoxic T-lymphocyte-associated protein 4 (CTLA-4)
- Ipilimumab
- Microbiome
- Nivolumab
- Programmed cell death protein 1 (PD-1)
- Regulatory T lymphocytes (Tregs)
Fingerprint
Dive into the research topics of 'Cancer immunotherapy–related adverse events: causes and challenges'. Together they form a unique fingerprint.Cite this
- APA
- Author
- BIBTEX
- Harvard
- Standard
- RIS
- Vancouver