A fully human anti-c-Kit monoclonal antibody 2G4 inhibits proliferation and degranulation of human mast cells

被引:6
作者
Kim, Kwang-Hyeok [1 ]
Kim, Jin-Ock [1 ]
Park, Sang Gyu [1 ]
机构
[1] Ajou Univ, Coll Pharm, 206 World Cup Ro, Suwon 16499, Gyeonggi Do, South Korea
关键词
Mast cell; Mast cell disease; Allergy; c-Kit; Monoclonal antibody; FC-EPSILON-RI; ACTIVATION DISEASE; RECEPTOR; OMALIZUMAB; ANGIOGENESIS; PATHOGENESIS; EOSINOPHILS; EXPRESSION; SURVIVAL; ASTHMA;
D O I
10.1007/s11010-022-04557-3
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Given that mast cells are pivotal contributors to allergic diseases, various allergy treatments have been developed to inhibit them. Omalizumab, an anti-immunoglobulin E antibody, is a representative therapy that can alleviate allergy symptoms by inhibiting mast cell degranulation. However, omalizumab cannot reduce the proliferation and accumulation of mast cells, which is a fundamental cause of allergic diseases. c-Kit is essential for the proliferation, survival, and differentiation of mast cells. Excessive c-Kit activation triggers various mast cell diseases, such as asthma, chronic spontaneous urticaria, and mastocytosis. Herein, we generated 2G4, an anti-c-Kit antibody, to develop a therapeutic agent for mast cell diseases. The therapeutic efficacy of 2G4 antibody was evaluated in LAD2, a human mast cell line. 2G4 antibody completely inhibited c-Kit signaling by blocking the binding of stem cell factor, known as the c-Kit ligand. Inhibition of c-Kit signaling led to the suppression of proliferation, migration, and degranulation in LAD2 cells. Moreover, 2G4 antibody suppressed the secretion of pro-inflammatory cytokines, including granulocyte-macrophage colony-stimulating factor, vascular endothelial growth factor, C-C motif chemokine ligand 2, brain-derived neurotrophic factor, and complement component C5/C5a, which can exacerbate allergy symptoms. Taken together, these results suggest that 2G4 antibody has potential as a novel therapeutic agent for mast cell diseases.
引用
收藏
页码:861 / 873
页数:13
相关论文
共 70 条
[11]   The mast cell and allergic diseases: role in pathogenesis and implications for therapy [J].
Brown, J. M. ;
Wilson, T. M. ;
Metcalfe, D. D. .
CLINICAL AND EXPERIMENTAL ALLERGY, 2008, 38 (01) :4-18
[12]   Stem cell factor-induced airway hyperreactivity in allergic and normal mice [J].
Campbell, E ;
Hogaboam, C ;
Lincoln, P ;
Lukacs, NW .
AMERICAN JOURNAL OF PATHOLOGY, 1999, 154 (04) :1259-1265
[13]   Controlling Mast Cell Activation and Homeostasis: Work Influenced by Bill Paul That Continues Today [J].
Caslin, Heather L. ;
Kiwanuka, Kasalina N. ;
Haque, Tamara T. ;
Taruselli, Marcela T. ;
MacKnight, H. Patrick ;
Paranjape, Anuya ;
Ryan, John J. .
FRONTIERS IN IMMUNOLOGY, 2018, 9
[14]   Mastocytosis- a mutated KIT receptor induced myeloproliferative disorder [J].
Chatterjee, Anindya ;
Ghosh, Joydeep ;
Kapur, Reuben .
ONCOTARGET, 2015, 6 (21) :18250-18264
[15]   Functional Deregulation of KIT Link to Mast Cell Proliferative Diseases and Other Neoplasms [J].
Cruse, Glenn ;
Metcalfe, Dean D. ;
Olivera, Ana .
IMMUNOLOGY AND ALLERGY CLINICS OF NORTH AMERICA, 2014, 34 (02) :219-+
[16]   Soluble Kit receptor blocks stem cell factor bioactivity in vitro [J].
Dahlen, DD ;
Lin, NL ;
Liu, YC ;
Broudy, VC .
LEUKEMIA RESEARCH, 2001, 25 (05) :413-421
[17]   KIT signaling is dispensable for human mast cell progenitor development [J].
Dahlin, Joakim S. ;
Ekoff, Maria ;
Grootens, Jennine ;
Lof, Liza ;
Amini, Rose-Marie ;
Hagberg, Hans ;
Ungerstedt, Johanna S. ;
Olsson-Stromberg, Ulla ;
Nilsson, Gunnar .
BLOOD, 2017, 130 (16) :1785-1794
[18]   Monocyte Chemoattractant Protein-1 (MCP-1): An Overview [J].
Deshmane, Satish L. ;
Kremlev, Sergey ;
Amini, Shohreh ;
Sawaya, Bassel E. .
JOURNAL OF INTERFERON AND CYTOKINE RESEARCH, 2009, 29 (06) :313-326
[19]   Eosinophil activation of fibroblasts from chronic allergen-induced disease utilizes stem cell factor for phenotypic changes [J].
Dolgachev, Vladislav ;
Berlin, Aaron A. ;
Lukacs, Nicholas W. .
AMERICAN JOURNAL OF PATHOLOGY, 2008, 172 (01) :68-76
[20]   Omalizumab [J].
Easthope, S ;
Jarvis, B .
DRUGS, 2001, 61 (02) :253-260