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CD47: a promising target for immunotherapy in relapsed/refractory malignant lymphoma
Shuzhen Xiong1, Ningning Yue1, Shuni Zhang1
1Department of Hematology, Lanzhou University Second Hospital, Lanzhou, China.
Leukemia & Lymphoma
|April 29, 2026
Summary
CD47 blockade enhances cancer immunotherapy by enabling macrophage phagocytosis and disrupting tumor signaling. This review explores CD47
Area of Science:
- Oncology
- Immunology
- Molecular Biology
Background:
- CD47 is an immune checkpoint molecule mediating tumor immune escape via the 'don't eat me' signal.
- Elevated CD47 expression in lymphoma correlates with poor prognosis and varied subtype expression.
- CD47 blockade is a promising cancer immunotherapy target.
Purpose of the Study:
- To review the therapeutic potential of CD47 blockade in lymphoma.
- To analyze CD47 expression, mechanisms of action, and clinical challenges.
- To guide future clinical applications of CD47-targeting strategies.
Main Methods:
- Literature review integrating evidence on CD47 expression and mechanisms in lymphoma.
- Analysis of CD47 blockade's dual effects on immune cells and tumor signaling pathways.
- Assessment of current clinical challenges and emerging therapeutic strategies.
Main Results:
- CD47 blockade enhances macrophage phagocytosis via the CD47/SIRPα pathway, promoting tumor clearance.
- CD47 inhibition also disrupts thrombospondin-1 (TSP-1) and integrin signaling, yielding multifaceted anti-tumor effects.
- Clinical challenges include off-target toxicity and transient responses, necessitating novel approaches.
Conclusions:
- CD47 blockade demonstrates significant therapeutic potential in lymphoma by overcoming immune evasion.
- Combining CD47 inhibition with other therapies or gene editing may overcome resistance.
- Further research and clinical strategies are needed to optimize CD47-targeting therapies for lymphoma treatment.
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