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Published on: November 12, 2019
Targeting CD47 as a therapeutic strategy: A common bridge in the therapy of COVID-19-related cancers
Milad Zandi1, Maryam Shafaati2, Mohammad Shenagari3
1Department of Virology, School of Public Health, Tehran University of Medical Sciences, Tehran, Iran.
Abstract:
Macrophages are essential mediators of innate immunity. Non-self-cells resist phagocytosis through the expression of the checkpoint molecule CD47. CD47, as the integrin-associated protein, is overexpressed on tumor and SARS-CoV-2-infected cells as a potential surface biomarker for immune surveillance evasion. CD47-signal-regulating protein alpha (SIRPα) interaction is a promising innate immunotarget. Previous findings based on monoclonal antibodies (mAbs) or fusion proteins that block CD47 or SIRPα have been developed in cancer research. While CD47 efficacy in infectious diseases, especially severe COVID-19 studies, is lacking, focus on macrophage-mediated immunotherapy that increases "eat me" signals in combination therapy with mAbs is optimistic. This integrin-related protein can be as a potential target to therapy for COVID-19. Here, we concentrate on the role of the CD47 signaling pathway as a novel therapeutic strategy for COVID-19-associated cancer treatment.
Insights
CD47, an immune checkpoint protein, is overexpressed on cancer and SARS-CoV-2 infected cells. Targeting the CD47-SIRPα pathway offers a novel immunotherapy strategy for COVID-19 and associated cancers.
Area of Science:
- Immunology
- Oncology
- Virology
Background:
- Macrophages are key innate immune cells.
- CD47 acts as a "don't eat me" signal, preventing phagocytosis by macrophages.
- Tumor cells and SARS-CoV-2 infected cells overexpress CD47 to evade immune surveillance.
Purpose of the Study:
- To explore the CD47 signaling pathway as a therapeutic target.
- To investigate the potential of CD47-based immunotherapy for COVID-19 and associated cancers.
Main Methods:
- Review of existing research on CD47 blockade in cancer immunotherapy.
- Analysis of CD47's role in SARS-CoV-2 infection and immune evasion.
- Focus on macrophage-mediated immunotherapy and combination strategies.
Main Results:
- CD47 blockade using monoclonal antibodies (mAbs) or fusion proteins shows promise in cancer research.
- CD47 overexpression is a potential biomarker for immune evasion in both cancer and COVID-19.
- Combining CD47-targeted therapies with macrophage activation may enhance immune responses.
Conclusions:
- The CD47-SIRPα axis is a viable target for innate immunotherapy.
- Targeting CD47 presents a novel therapeutic strategy for COVID-19-associated cancers.
- Further research into CD47-based combination therapies is warranted for infectious diseases and cancer.
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