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Review Article Open Access
Volume 2 | Issue 1 | DOI: https://doi.org/10.46439/allergy.2.017

Modulation of type 2 inflammation by sensing immunomodulatory RNA in house dust mite and viruses

  • 1Department of Clinical Laboratory Sciences, College of Applied Medical Sciences, Al Jouf University, Sakaka, Saudi Arabia
  • 2Department of Microbiology, Immunology and Molecular Genetics, Long School of Medicine, University of Texas Health San Antonio, TX, USA
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Corresponding Author

Xiao-Dong Li, lix8@uthscsa.edu or Xiao-Dong.Li@outlook.com

Received Date: October 21, 2020

Accepted Date: April 07, 2021

Abstract

The incidence of allergic diseases has been increasing over the past few decades worldwide. Although allergic reactions are often characterized by an overzealous Th2 inflammatory response, the underlying mechanisms remain poorly defined. House dust mite (HDM) is one of the most common indoor allergens that cause allergic diseases such as asthma. Recent studies suggest that innate immunity activated by HDM allergens is critical for driving the development of a polarized type 2 response. HDM harbors not only allergic protein antigens, but also non-protein microbial products, e.g., LPS or dsRNA, which can trigger innate immune responses that either promote a type 2 inflammatory phenotype or suppress a severe type 2 immunopathologies in mice, respectively. In this review, we discuss how the innate sensing of immunomodulatory RNA in HDM allergens and viruses modulates type 2 inflammatory responses. 

Keywords

Allergen immunotherapy, Dermatophagoides pteronyssinus, Dermatophagoides farina, Double-stranded RNA, Group 2 innate lymphoid cells, House dust mite, Toll-like receptor 3, Type 2 inflammation

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