The USP7-STAT3-granzyme-Par-1 axis regulates allergic inflammation by promoting differentiation of IL-5-producing Th2 cells

被引:9
作者
Kumagai, Jin [1 ,2 ]
Kiuchi, Masahiro [1 ]
Kokubo, Kota [1 ]
Yagyu, Hiroyuki [1 ]
Nemoto, Masahiro [1 ]
Tsuji, Kaori [1 ]
Nagahata, Ken [1 ,3 ]
Sasaki, Atsushi [1 ]
Hishiya, Takahisa [1 ]
Onoue, Miki [1 ]
Shinmi, Rie [1 ]
Sonobe, Yuri [1 ]
Iinuma, Tomohisa [4 ]
Yonekura, Syuji [4 ]
Shinga, Jun [5 ]
Hanazawa, Toyoyuki [4 ]
Koseki, Haruhiko [6 ]
Nakayama, Toshinori [1 ]
Yokote, Koutaro [2 ]
Hirahara, Kiyoshi [1 ,7 ]
机构
[1] Chiba Univ, Grad Sch Med, Dept Immunol, Chiba 2608670, Japan
[2] Chiba Univ, Grad Sch Med, Dept Endocrinol Hematol & Gerontol, Chiba 2608670, Japan
[3] Sapporo Med Univ, Dept Rheumatol, Sapporo 0608556, Japan
[4] Chiba Univ, Grad Sch Med, Dept Otorhinolaryngol Head & Neck Surg, Chiba 2608670, Japan
[5] RIKEN, Ctr Integrat Med Sci, Lab Immunotherapy, Yokohama, Kanagawa 2300045, Japan
[6] Chiba Univ, Grad Sch Med, Dept Cellular & Mol Med, Chiba 2608670, Japan
[7] Chiba Univ, Synergy Inst Futurist Mucosal Vaccine Res & Dev, Chiba 2608670, Japan
关键词
pathogenic Th2; ubiquitin specific protease 7 (USP7); granzyme; signal transducers and activators of transcription (STAT)3; asthma; intractable allergic disease; TRANSCRIPTION; GRANZYMES; HAUSP; INHIBITION; EXPRESSION; APOPTOSIS; FATE; IL-4; P53;
D O I
10.1073/pnas.2302903120
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Uncontrolled type 2 immunity by type 2 helper T (Th2) cells causes intractable allergic diseases; however, whether the interaction of CD4+ T cells shapes the pathophysiology of allergic diseases remains unclear. We identified a subset of Th2 cells that produced the serine proteases granzyme A and B early in differentiation. Granzymes cleave protease- activated receptor (Par) -1 and induce phosphorylation of p38 mitogen- activated protein kinase (MAPK), resulting in the enhanced production of IL -5 and IL -13 in both mouse and human Th2 cells. Ubiquitin- specific protease 7 (USP7) regulates IL- 4- induced phosphorylation of STAT3, resulting in granzyme production during Th2 cell differentiation. Genetic deletion of Usp7 or Gzma and pharmacological blockade of granzyme B ameliorated allergic airway inflammation. Furthermore, PAR -1+ and granzyme+ Th2 cells were colocalized in nasal polyps from patients with eosinophilic chronic rhinosinusitis. Thus, the USP7- STAT3- granzymes-Par-1 pathway is a potential therapeutic target for intractable allergic diseases.
引用
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页数:12
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