Interleukin-17A released from intestinal γδT cells induces cytokine storm in mice with severe dengue

Author:

Kurosu Takeshi1,Okuzaki Daisuke2ORCID,Sakai Yusuke1,Kadi Mohamad Al3ORCID,Phanthanawiboon Supranee4,Ami Yasusi1,Shimojima Masayuki5,Yoshikawa Tomoki1,Fukushi Shuetsu1,Nagata Noriyo1,Suzuki Tadaki1,Kamimura Daisuke6,Murakami Masaaki6,Ebihara Hideki1,Saijo Masayuki1ORCID

Affiliation:

1. National Institute of Infectious Diseases

2. Single Cell Genomics, Human immunology, WPI Immunology Frontier Research Center, Osaka University

3. IFReC, Osaka University

4. Faculty of Medicine, Khon Kaen University, Khon Kaen, Thailand

5. Department of Virology I, National Institute of Infectious Diseases

6. Institute for Genetic Medicine, Graduate School of Medicine, Hokkaido University

Abstract

Abstract Blockade of TNF-α signaling protects mice from lethal infection with dengue virus (DENV); however, what causes cytokine storm or how TNF-α aggravates the disease remains unknown. Here, we performed transcriptome analysis of the liver and small intestine samples collected chronologically from DENV-3 P12/08-infected IFN-α/β and γ receptor knockout (IFN-α/β/γRKO) mice in the presence/absence of blockade of TNF-α Ab signaling. We found that TNF-α induced production of IL-17A by small intestinal γδT cells, regulated production of other cytokines such as IL-6 cooperatively with TNF-α, and played a crucial role in mortality. Also, neutrophil-derived matrix metalloprotease-8 was identified as an effector molecule causing vascular leakage. Blockade of TNF-α or IL-17A signaling strongly inhibited nuclear translocation of NF-κB p65 in stroma-like cells and epithelial cells, and prevented induction of IL-6. These findings enable us to better understand cytokine storm associated with severe dengue, and may facilitate development of new therapeutic strategies.

Publisher

Research Square Platform LLC

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