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
[21]   c-Kit - A hematopoietic cell essential receptor tyrosine kinase [J].
Edling, Charlotte E. ;
Hallberg, Bengt .
INTERNATIONAL JOURNAL OF BIOCHEMISTRY & CELL BIOLOGY, 2007, 39 (11) :1995-1998
[22]   Targeting c-kit in the therapy of mast cell disorders: Current update [J].
El-Agamy, Dina S. .
EUROPEAN JOURNAL OF PHARMACOLOGY, 2012, 690 (1-3) :1-3
[23]  
Esnault S, 2002, ARCH IMMUNOL THER EX, V50, P121
[24]   A survival Kit for pancreatic beta cells: stem cell factor and c-Kit receptor tyrosine kinase [J].
Feng, Zhi-Chao ;
Riopel, Matthew ;
Popell, Alex ;
Wang, Rennian .
DIABETOLOGIA, 2015, 58 (04) :654-665
[25]   Mast Cell Activation Syndrome: A Review [J].
Frieri, Marianne ;
Patel, Reenal ;
Celestin, Jocelyn .
CURRENT ALLERGY AND ASTHMA REPORTS, 2013, 13 (01) :27-32
[26]   Bidirectional Mast Cell-Eosinophil Interactions in Inflammatory Disorders and Cancer [J].
Galdiero, Maria Rosaria ;
Varricchi, Gilda ;
Seaf, Mansour ;
Marone, Giancarlo ;
Levi-Schaffer, Francesca ;
Marone, Gianni .
FRONTIERS IN MEDICINE, 2017, 4
[27]   Regulation of Mast Cell Responses in Health and Disease [J].
Gilfillan, Alasdair M. ;
Beaven, Michael A. .
CRITICAL REVIEWS IN IMMUNOLOGY, 2011, 31 (06) :475-529
[28]   Systemic mast cell activation disease: the role of molecular genetic alterations in pathogenesis, heritability and diagnostics [J].
Haenisch, Britta ;
Noethen, Markus M. ;
Molderings, Gerhard J. .
IMMUNOLOGY, 2012, 137 (03) :197-205
[29]   Kit and FCεRI mediate unique and convergent signals for release of inflammatory mediators from human mast cells [J].
Hundley, TR ;
Gilfillan, AM ;
Tkaczyk, C ;
Andrade, MV ;
Metcalfe, DD ;
Beaven, MA .
BLOOD, 2004, 104 (08) :2410-2417
[30]   Omalizumab in the treatment of adult patients with mastocytosis: A systematic review [J].
Jendoubi, Fatma ;
Gaudenzio, Nicolas ;
Gallini, Adeline ;
Negretto, Mathilde ;
Paul, Carle ;
Livideanu, Cristina .
CLINICAL AND EXPERIMENTAL ALLERGY, 2020, 50 (06) :654-661