HOMEPRODUCTSCOMPANYCONTACTFAQResearchDictionaryPharmaSign Up FREE or Login

Double negative T cells mediate Lag3-dependent antigen-specific protection in allergic asthma.

Abstract
Allergic asthma is an inflammatory disorder of the airway without satisfactory traditional therapies capable of controlling the underlying pathology. New approaches that can overcome the detrimental effects of immune dysregulation are thus desirable. Here we adoptively transfer ovalbumin (OVA) peptide-primed CD4-CD8- double negative T (DNT) cells intravenously into a mouse model of OVA-induced allergic asthma to find that OVA-induced airway hyperresponsiveness, lung inflammation, mucus production and OVA-specific IgG/IgE production are significantly suppressed. The immunosuppressive function of the OVA-specific DNT cells is dependent on the inhibition of CD11b+ dendritic cell function, T follicular helper cell proliferation, and IL-21 production. Mechanistically, Lag3 contributes to MHC-II antigen recognition and trogocytosis, thereby modulating the antigen-specific immune regulation by DNT cells. The effectiveness of ex vivo-generated allergen-specific DNT cells in alleviating airway inflammation thus supports the potential utilization of DNT cell-based therapy for the treatment of allergic asthma.
AuthorsDan Tian, Lu Yang, Song Wang, Yanbing Zhu, Wen Shi, Chunpan Zhang, Hua Jin, Yue Tian, Hufeng Xu, Guangyong Sun, Kai Liu, Zhongtao Zhang, Dong Zhang
JournalNature communications (Nat Commun) Vol. 10 Issue 1 Pg. 4246 (09 18 2019) ISSN: 2041-1723 [Electronic] England
PMID31534137 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
Chemical References
  • Allergens
  • Antigens, CD
  • Histocompatibility Antigens Class II
  • Immunoglobulin G
  • Interleukins
  • Immunoglobulin E
  • Ovalbumin
  • interleukin-21
  • Lymphocyte Activation Gene 3 Protein
  • Lag3 protein, mouse
Topics
  • Adoptive Transfer
  • Allergens (immunology)
  • Animals
  • Antigens, CD (metabolism)
  • Asthma (chemically induced, immunology, physiopathology, therapy)
  • Bronchial Hyperreactivity (chemically induced, immunology, therapy)
  • Dendritic Cells (immunology)
  • Disease Models, Animal
  • Histocompatibility Antigens Class II
  • Immunoglobulin E (biosynthesis)
  • Immunoglobulin G (biosynthesis)
  • Interleukins (biosynthesis)
  • Male
  • Mice
  • Mice, Inbred BALB C
  • Mice, Inbred C57BL
  • Mice, Knockout
  • Ovalbumin
  • T-Lymphocytes, Regulatory (immunology, transplantation)
  • Th2 Cells (immunology)
  • Lymphocyte Activation Gene 3 Protein

Join CureHunter, for free Research Interface BASIC access!

Take advantage of free CureHunter research engine access to explore the best drug and treatment options for any disease. Find out why thousands of doctors, pharma researchers and patient activists around the world use CureHunter every day.
Realize the full power of the drug-disease research graph!


Choose Username:
Email:
Password:
Verify Password:
Enter Code Shown: