MIF and CD74 as Emerging Biomarkers for Immune Checkpoint Blockade Therapy
Year: 2024
Type: review
Abstract: Immune checkpoint blockade (ICB) therapy is used to treat a wide range of cancers; however, some patients are at risk of developing treatment resistance and/or immune-related adverse events (irAEs). Thus, there is a great need for the identification of reliable predictive biomarkers for response and toxicity. The cytokine MIF (macrophage migration inhibitory factor) and its cognate receptor CD74 are intimately connected with cancer progression and have previously been proposed as prognostic biomarkers for patient outcome in various cancers, including solid tumors such as malignant melanoma. Here, we assess their potential as predictive biomarkers for response to ICB therapy and irAE development. We provide a brief overview of their function and roles in the context of cancer and autoimmune disease. We also review the evidence showing that MIF and CD74 may be of use as predictive biomarkers of patient response to ICB therapy and irAE development. We also highlight that careful consideration is required when assessing the potential of serum MIF levels as a biomarker due to its reported circadian expression in human plasma. Finally, we suggest future directions for the establishment of MIF and CD74 as predictive biomarkers for ICB therapy and irAE development to guide further research in this field.
Source: Cancers
Language: English
Subfield: Immunology
Field: Immunology and Microbiology
Domain: Life Sciences
Open Access status: gold
Estimated APC paid: $3,296
Funders: U.S. Department of Defense, American Cancer Society, U.S. Department of Veterans Affairs, Office of Research and Development, Oregon Health and Science University, National Institutes of Health, National Cancer Institute, National Institute of Allergy and Infectious Diseases, National Institute of Neurological Disorders and Stroke, Cancer Early Detection Advanced Research Center, Knight Cancer Institute, Oregon Health and Science University
Awards: G1786676759, G1997890062, G2040153736, Development of DRα1-MOG-35-55 for treatment of DR2 negative MS subjects, G2222850937, G2369920607, G2906302043, G4007725361, G4119534169, G5850682332, G6532925016, G7596729856, G7724147662, G783262747, G8126816323, G8829522369, Yale SPORE in Skin Cancer
OpenAlex ID: W4396674061
