OX40-OX40L interactions: a promising therapeutic target for allergic diseases?

被引:40
作者
Wang, Yui-Hsi
Liu, Yong-Jun
机构
[1] Univ Texas MD Anderson Canc Ctr, Dept Immunol, Houston, TX 77030 USA
[2] Univ Texas MD Anderson Canc Ctr, Ctr Canc Immunol Res, Houston, TX 77030 USA
[3] Univ Texas Houston, Grad Sch Biomed Sci, Houston, TX USA
关键词
D O I
10.1172/JCI34182
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Recent advances in understanding the cellular and molecular mechanisms of atopy have shed light on potential targets for the development of new therapies for allergic diseases. In this issue of the JCI, Seshasayee et al. provide direct in vivo evidence that OX40 has critical roles in allergic inflammation mediated by thymic stromal lymphopoietin (TSLP) (see the related article beginning on page 3868). Blockade of interactions between OX40 on Th2 cells and OX40 ligand (OX40L) on TSLP-activated DCs using an OX40L-specific monoclonal antibody, inhibited Th2 cell-mediated immune responses in both mouse and nonhuman primate models of allergic inflammation. The results point to potential therapeutic approaches to targeting the cellular and molecular mechanism underlying TSLP-mediated allergic inflammation.
引用
收藏
页码:3655 / 3657
页数:3
相关论文
共 50 条
[1]   THE ROLE OF OX40-OX40L INTERACTIONS IN ATHEROSCLEROSIS PATHOGENESIS [J].
Huang, F. ;
Yao, Y-L. ;
Wang, M. .
DRUGS OF THE FUTURE, 2015, 40 (10) :651-658
[2]   OX40L-OX40 interactions: A possible target for gastrointestinal autoimmune diseases [J].
Mahmood, Tahrin ;
Yang, Ping-Chang .
NORTH AMERICAN JOURNAL OF MEDICAL SCIENCES, 2012, 4 (11) :533-536
[3]   OX40-OX40L Expression in Idiopathic Inflammatory Myopathies [J].
Papadopoulos, Constantinos ;
Terzis, Gerasimos ;
Papadimas, George K. ;
Manta, Panagiota .
ANALYTICAL AND QUANTITATIVE CYTOLOGY AND HISTOLOGY, 2013, 35 (01) :17-26
[4]   The crystal structure of the costimulatory OX40-OX40L complex [J].
Compaan, Deanne M. ;
Hymowitz, Sarah G. .
STRUCTURE, 2006, 14 (08) :1321-1330
[5]   A Narrative Review of the OX40-OX40L Pathway as a Potential Therapeutic Target in Atopic Dermatitis: Focus on Rocatinlimab and Amlitelimab [J].
Abdelhalim, Asaad ;
Yilmaz, Orhan ;
Berair, Mohamed Elshaikh ;
Torres, Tiago .
DERMATOLOGY AND THERAPY, 2024, 14 (12) :3197-3210
[6]   The Role of OX40-OX40L Axis in the Pathogenesis of Atopic Dermatitis [J].
Schettini, Natale ;
Pacetti, Lucrezia ;
Corazza, Monica ;
Borghi, Alessandro .
DERMATITIS, 2025, 36 (01) :28-36
[7]   Research progress in OX40/OX40L in allergic diseases [J].
Song, Rongrong ;
Zhang, Huanlei ;
Liang, Zhuoping .
INTERNATIONAL FORUM OF ALLERGY & RHINOLOGY, 2024, 14 (12) :1921-1928
[8]   Prolongation of allograft survival by artemisinin treatment is associated with blockade of OX40-OX40L [J].
Liu, Lihua ;
Zhao, Juanzhi ;
Li, An ;
Yang, Xuan ;
Sprangers, Ben ;
Li, Shengqiao .
IMMUNOPHARMACOLOGY AND IMMUNOTOXICOLOGY, 2021, 43 (03) :291-298
[9]   Involvement of OX40-OX40L interactions in the intestinal manifestations of the murine acute graft-versus-host disease [J].
Stüber, E ;
Von Freier, A ;
Marinescu, D ;
Fölsch, UR .
GASTROENTEROLOGY, 1998, 115 (05) :1205-1215
[10]   OX40-OX40L Axis in Cutaneous T-Cell Lymphomas: Pathogenic, Prognostic, and Potential Therapeutic Perspectives [J].
Guglielmo, Alba ;
Borghi, Alessandro ;
Zengarini, Corrado ;
Piraccini, Bianca Maria ;
Corazza, Monica ;
Pileri, Alessandro .
BIOMOLECULES, 2025, 15 (05)