Abstract | BACKGROUND: METHODS: In vivo, the role of GITRL in modulating house dust mite (HDM)-induced asthma was assessed in adeno-associated virus (AAV)-shGITRL mice. In vitro, the role of GITRL expression by DCs was evaluated in LV-shGITRL bone marrow dendritic cells (BMDCs) under HDM stimulation. And the direct effect of GITRL was observed by stimulating splenocytes with GITRL protein. The effect of regulating GITRL on CD4+ T cell differentiation was detected. Further, GITRL mRNA in the peripheral blood of asthmatic children was tested. RESULTS: GITRL was significantly increased in HDM-challenged mice. In GITRL knockdown mice, allergen-induced airway inflammation, serum total IgE levels and airway hyperresponsiveness (AHR) were reduced. In vitro, GITRL expression on BMDCs was increased after HDM stimulation. Further, knocking down GITRL on DCs partially restored the balance of Th1/Th2 and Th17/Treg cells. Moreover, GITRL stimulation in vitro inhibited Treg cell differentiation and promoted Th2 and Th17 cell differentiation. Similarly, GITRL mRNA expression was increased in the peripheral blood from asthmatic children. CONCLUSIONS: This study identified a novel role for GITRL expressed by DCs as a positive regulator of CD4+ T cells responses in asthma, which implicates that GITRL inhibitors may be a potential immunotherapy for asthma.
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Authors | Yaping Wang, Kou Liao, Bo Liu, Chao Niu, Wenjing Zou, Lili Yang, Ting Wang, Daiyin Tian, Zhengxiu Luo, Jihong Dai, Qubei Li, Enmei Liu, Caihui Gong, Zhou Fu, Ying Li, Fengxia Ding |
Journal | Respiratory research
(Respir Res)
Vol. 22
Issue 1
Pg. 46
(Feb 08 2021)
ISSN: 1465-993X [Electronic] England |
PMID | 33557842
(Publication Type: Journal Article)
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Chemical References |
- Tnfsf18 protein, mouse
- Tumor Necrosis Factors
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Topics |
- Animals
- Asthma
(blood, metabolism)
- CD4-Positive T-Lymphocytes
(metabolism)
- Cell Differentiation
(physiology)
- Child
- Coculture Techniques
- Dendritic Cells
(metabolism)
- Female
- Humans
- Mice
- Mice, Inbred C57BL
- Pyroglyphidae
- Respiratory Hypersensitivity
(blood, metabolism)
- Tumor Necrosis Factors
(biosynthesis, blood)
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