Augmentation of Stimulator of Interferon Genes–Induced Type I Interferon Production in COPA Syndrome-Reference-Cited by-同舟云学术

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Augmentation of Stimulator of Interferon Genes–Induced Type I Interferon Production in COPA Syndrome

Published:2021-11 Issue:11 Volume:73 Page:2105-2115
ISSN:2326-5191
Container-title:Arthritis & Rheumatology
language:en
Short-container-title:Arthritis Rheumatol

Author:

Kato Takashi¹^ORCID,Yamamoto Masaki²,Honda Yoshitaka³^ORCID,Orimo Takashi⁴,Sasaki Izumi¹^ORCID,Murakami Kohei⁵^ORCID,Hemmi Hiroaki⁶,Fukuda‐Ohta Yuri¹,Isono Kyoichi¹,Takayama Saki²,Nakamura Hidenori²,Otsuki Yoshiro²,Miyamoto Toshiaki²,Takita Junko⁷,Yasumi Takahiro⁷,Nishikomori Ryuta⁸^ORCID,Matsubayashi Tadashi²,Izawa Kazushi⁷,Kaisho Tsuneyasu¹^ORCID

Affiliation:

1. Wakayama Medical University Wakayama Japan

2. Seirei Hamamatsu General Hospital Hamamatsu Japan

3. Institute for the Advanced Study of Human Biology and Kyoto University Kyoto Japan

4. Wakayama Medical University, Wakayama, Japan, and Osaka University Graduate School of Medicine Osaka Japan

5. Okayama University of Science Imabari Japan

6. Wakayama Medical University, Wakayama, Japan, and Okayama University of Science Imabari Japan

7. Kyoto University Graduate School of Medicine Kyoto Japan

8. Kurume University School of Medicine Kurume Japan

Funder

Japan Society for the Promotion of Science

Hokkaido University

Wakayama Medical University

Ishibashi Foundation

Ministry of Health, Labour and Welfare

Ichiro Kanehara Foundation for the Promotion of Medical Sciences and Medical Care

Inamori Foundation

Japan Agency for Medical Research and Development

Uehara Memorial Foundation

Takeda Science Foundation

University of Tokyo

Publisher

Wiley

Subject

Immunology,Rheumatology,Immunology and Allergy

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/art.41790

Reference38 articles.

1. COPA mutations impair ER‐Golgi transport and cause hereditary autoimmune‐mediated lung disease and arthritis [letter];Watkin LB;Nat Genet,2015

2. Copa syndrome: a novel autosomal dominant immune dysregulatory disease [review];Vece TJ;J Clin Immunol,2016

3. COPA syndrome in an Icelandic family caused by a recurrent missense mutation in COPA;Jensson BO;BMC Med Genet,2017

4. Imaging findings of Copa syndrome in a 12‐year‐old boy;Noorelahi R;Pediatr Radiol,2018

5. An unprecedented COPA gene mutation in two patients in the same family: comparative clinical analysis of newly reported patients with other known COPA gene mutations [review];Patwardhan A;Pediatr Rheumatol Online J,2019

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1. Human life within a narrow range: The lethal ups and downs of type I interferons;Science Immunology;2024-07-05

2. Pharmacological potential of cyclic nucleotide signaling in immunity;Pharmacology & Therapeutics;2024-06

3. ER: a critical hub for STING signaling regulation;Trends in Cell Biology;2024-02

4. Single-molecule localization microscopy reveals STING clustering at the trans-Golgi network through palmitoylation-dependent accumulation of cholesterol;Nature Communications;2024-01-11

5. Heterozygous mutations in the C-terminal domain of COPA underlie a complex autoinﬂammatory syndrome;Journal of Clinical Investigation;2024-01-04

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