Strategies to generate functionally normal neutrophils to reduce infection and infection-related mortality in cancer chemotherapy

被引:8
作者
Abdel-Azim, Hisham [1 ]
Sun, Weili [2 ]
Wu, Lingtao [3 ]
机构
[1] Univ Southern Calif, Childrens Hosp Los Angeles, Pediat Hematol Oncol Blood & Marrow Transplantat, Saban Res Inst,Keck Sch Med, 4650 Sunset Blvd, Los Angeles, CA 90027 USA
[2] City Hope Natl Med Ctr, Pediat Hematol Oncol, 1500 E Duarte Rd, Duarte, CA 91010 USA
[3] Therapeut Approaches, Res & Dev, 2712 San Gabriel Blvd, Rosemead, CA 91770 USA
基金
美国国家卫生研究院;
关键词
Neutrophil innate immunity; Granule formation; Partially differentiated neutrophils; Cancer chemotherapy-induced neutropenia; GCSF biologics; Retinoid agonist Am80; COLONY-STIMULATING FACTOR; RETINOIC-ACID-RECEPTOR; ACUTE PROMYELOCYTIC LEUKEMIA; CYCLIN-DEPENDENT KINASE; BINDING-PROTEIN EPSILON; ACUTE MYELOID-LEUKEMIA; BETA(2) LEUKOCYTE INTEGRIN; HEMATOPOIETIC STEM-CELLS; DIFFERENTIATION IN-VITRO; ALPHA-MESSENGER-RNA;
D O I
10.1016/j.pharmthera.2019.107403
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Neutrophils form an essential part of innate immunity against infection. Cancer chemotherapy-induced neutropenia (CCIN) is a condition in which the number of neutrophils in a patient's bloodstream is decreased, leading to increased susceptibility to infection. Granulocyte colony-stimulating factor (GCSF) has been the only approved treatment for CCIN over two decades. To date, CCIN-related infection and mortality remain a significant concern, as neutrophils generated in response to administered GCSF are functionally immature and cannot effectively fight infection. This review summarizes the molecular regulatory mechanisms of neutrophil granulocytic differentiation and innate immunity development, dissects the biology of GCSF in myeloid expansion, highlights the shortcomings of GCSF in CCIN treatment, updates the recent advance of a selective retinoid agonist that promotes neutrophil granulocytic differentiation, and evaluates the benefits of developing GCSF biosimilars to increase access to GCSF biologics versus seeking a new mode to fundamentally advance GCSF therapy for treatment of CCIN. (C) 2019 Elsevier Inc. All rights reserved.
引用
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页数:16
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