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CD303 (BDCA-2) - a potential novel target for therapy in hematologic malignancies
Nathaniel R Wilson1, Laura Bover2, Marina Konopleva3
1Department of Internal Medicine, The University of Texas Health Science Center at Houston, Houston, TX, USA.
Leukemia & Lymphoma
|September 6, 2021
Summary
Plasmacytoid dendritic cells (pDCs) are key in immunity and cancer. CD303, a pDC marker, shows promise for treating various disorders, including rare blood cancers like blastic plasmacytoid dendritic cell neoplasm (BPDCN).
Area of Science:
- Immunology
- Hematology
- Oncology
Background:
- Plasmacytoid dendritic cells (pDCs) are crucial immunoregulatory cells involved in inflammatory, viral, and malignant conditions.
- Malignant pDC proliferation defines blastic plasmacytoid dendritic cell neoplasm (BPDCN) and pDC-acute myelogenous leukemia (pDC-AML).
- Current therapies targeting CD123 have shown success but relapsed/refractory BPDCN remains challenging.
Purpose of the Study:
- To review the role of CD303, a specific marker of human pDCs, in benign and malignant conditions.
- To explore the potential of CD303-directed therapies for pDC-related disorders.
Main Methods:
- Comprehensive literature review of studies involving CD303 in various diseases.
- Analysis of CD303's function in antigen presentation and immune tolerance.
Main Results:
- CD303 is a specific surface marker for human pDCs.
- Preclinical studies and some clinical trials (e.g., cutaneous lupus erythematosus) show potential for CD303-targeted monoclonal antibodies.
- CD303's involvement in antigen presentation and immune tolerance is highlighted.
Conclusions:
- CD303 represents a promising therapeutic target for pDC-related malignancies like BPDCN and pDC-AML.
- Further investigation into CD303-directed therapies may offer new treatment options for patients with limited alternatives.
- CD303's role extends beyond malignancy, with potential applications in other CD303-expressing conditions.

