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Myeloid-derived suppressor cells: Implication in myeloid malignancies and immunotherapy.
Kapor, Suncica; Radojkovic, Milica; Santibanez, Juan F.
Afiliación
  • Kapor S; Department of Hematology, Clinical, and Hospital Center "Dr. Dragisa Misovic-Dedinje,", Heroja Milana Tepica 1, Belgrade 11020, Serbia.
  • Radojkovic M; Department of Hematology, Clinical, and Hospital Center "Dr. Dragisa Misovic-Dedinje,", Heroja Milana Tepica 1, Belgrade 11020, Serbia; Faculty of Medicine, University of Belgrade, Dr. Subotica Starijeg 8, Belgrade 11000, Serbia.
  • Santibanez JF; Molecular Oncology group, Institute for Medical Research, National Institute of the Republic of Serbia, University of Belgrade, Dr. Subotica 4, POB 102, Belgrade 11129, Serbia; Centro Integrativo de Biología y Química Aplicada (CIBQA), Universidad Bernardo O Higgins, General Gana 1780, Santiago 8370854, Chile. Electronic address: jfsantibanez@imi.bg.ac.rs.
Acta Histochem ; 126(5-7): 152183, 2024 Jul 18.
Article en En | MEDLINE | ID: mdl-39029317
ABSTRACT
Myeloid malignancies stem from a modified hematopoietic stem cell and predominantly include acute myeloid leukemia, myelodysplastic neoplasms, myeloproliferative malignancies, and chronic myelomonocytic leukemia. Myeloid-derived suppressor cells (MDSCs) exhibit immunoregulatory properties by governing the innate and adaptive immune systems, creating a permissive and supportive environment for neoplasm growth. This review examines the key characteristics of MDSCs in myeloid malignancies, highlighting that an increased MDSC count corresponds to heightened immunosuppressive capabilities, fostering an immune-tolerant neoplasm microenvironment. Also, this review analyzes and describes the potential of combined cancer therapies, focusing on targeting MDSC generation, expansion, and their inherent immunosuppressive activities to enhance the efficacy of current cancer immunotherapies. A comprehensive understanding of the implications of myeloid malignancies may enhance the exploration of immunotherapeutic strategies for their potential application.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Acta Histochem Año: 2024 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Acta Histochem Año: 2024 Tipo del documento: Article
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