Zobrazeno 1 - 10 of 31 pro vyhledávání: '"Kohei, Yokose"'
1
Akademický článek
Interferon-γ induces interleukin-6 production by neutrophils via the Janus kinase (JAK)-signal transducer and activator of transcription (STAT) pathway
Autor: Shuhei Yoshida, Shunya Yamada, Kohei Yokose, Haruki Matsumoto, Yuya Fujita, Tomoyuki Asano, Naoki Matsuoka, Jumpei Temmoku, Shuzo Sato, Makiko Yoshiro-Furuya, Hiroshi Watanabe, Kiyoshi Migita
Publikováno v: BMC Research Notes, Vol 14, Iss 1, Pp 1-7 (2021)
Abstract Objective Interferon-gamma (IFN-γ) is overexpressed in rheumatoid synovium and thought to be involved in the pathogenesis of rheumatoid arthritis (RA). In this study, we examined our hypothesis that IFN-γ activates innate immune cells and
Externí odkaz: https://doaj.org/article/7423a7e241de4144a22ca45e34e3bfae
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2
Akademický článek
Case Report: Coexistence of Multiple Myeloma and Auricular Chondritis in VEXAS Syndrome
Autor: Haruki Matsumoto, Yuya Fujita, Masahiko Fukatsu, Takayuki Ikezoe, Kohei Yokose, Tomoyuki Asano, Naomi Tsuchida, Ayaka Maeda, Shuhei Yoshida, Honami Hashimoto, Jumpei Temmoku, Naoki Matsuoka, Makiko Yashiro-Furuya, Shuzo Sato, Mai Murakami, Hidenori Sato, Chiharu Sakuma, Kazumasa Kawashima, Norshalena Shakespear, Yuri Uchiyama, Hiroshi Watanabe, Yohei Kirino, Naomichi Matsumoto, Kiyoshi Migita
Publikováno v: Frontiers in Immunology, Vol 13 (2022)
Vacuoles, E1 enzyme, X-linked, autoinflammatory, somatic (VEXAS) syndrome is an inflammatory disorder caused by somatic UBA1 variants, which are sometimes associated with hematological disorders, including myelodysplastic syndrome (MDS). VEXAS syndro
Externí odkaz: https://doaj.org/article/15ad25200ddd42caba1dc7f8ef5088a2
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3
Akademický článek
Association between inflammatory cytokines and immune–checkpoint molecule in rheumatoid arthritis
Autor: Haruki Matsumoto, Yuya Fujita, Tomoyuki Asano, Naoki Matsuoka, Jumpei Temmoku, Shuzo Sato, Makiko Yashiro–Furuya, Kohei Yokose, Shuhei Yoshida, Eiji Suzuki, Toru Yago, Hiroshi Watanabe, Atsushi Kawakami, Kiyoshi Migita
Publikováno v: PLoS ONE, Vol 16, Iss 11 (2021)
Background Anti-citrullinated peptide antibodies (ACPA) and inflammatory cytokines play important roles in the development of rheumatoid arthritis (RA). T cell immunoglobulin and mucin–domain containing–3 (TIM–3) is an immune-checkpoint molecul
Externí odkaz: https://doaj.org/article/5146651f887140efad76d4db9c829101
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5
Total Hip Joint Replacement in a Patient with Colchicine-Resistant Familial Mediterranean Fever under Canakinumab Treatment
Autor: Haruki Matsumoto, Hironori Ohashi, Yuya Fujita, Shuhei Yoshida, Kohei Yokose, Jumpei Temmoku, Naoki Matsuoka, Yumetaka Shinden, Keigo Kusano, Tatsuru Sonobe, Yohei Nakamoto, Makiko Yashiro-Furuya, Tomoyuki Asano, Shuzo Sato, Eiji Suzuki, Toru Yago, Hiroshi Watanabe, Kiyoshi Migita
Publikováno v: The Tohoku Journal of Experimental Medicine. 256:169-174
Familial Mediterranean fever (FMF) is a hereditary autoinflammatory disease characterized by recurrent episodes of fever and serositis. Periodic febrile attack can be managed with biologic medication in colchicine-resistant FMF patients, however, no
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::594c6f893a12ce588ff048f922838828
https://doi.org/10.1620/tjem.256.169
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8
Adult-Onset Still’s Disease Complicated by Immunoglobulin A Vasculitis and anti-CCP Antibody-Positive Arthritis
Autor: Yuya Fujita, Shuzo Sato, Haruki Matsumoto, Jumpei Temmoku, Makiko Yashiro-Furuya, Naoki Matsuoka, Tomoyuki Asano, Kohei Yokose, Shuhei Yoshida, Mikio Ohtsuka, Hiroshi Watanabe, Kiyoshi Migita
Publikováno v: The Tohoku Journal of Experimental Medicine. 255:297-301
A 38-year-old male was admitted to our hospital for arthralgia, fever, skin rash, and purpura. He was diagnosed as having adult-onset Still's disease (AOSD) based on Yamaguchi's criteria. Skin biopsy revealed immunoglobulin A (IgA) vasculitis. He was
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0bb54f7fb4f9f20ede718aa94d63e6c3
https://doi.org/10.1620/tjem.255.297
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9
Immunoglobulin A Vasculitis in a Japanese Patient with Complete Familial Mediterranean Fever Carrying MEFV Exon 10 Mutation
Autor: Shuzo Sato, Jun Wada, Naoki Matsuoka, Tomomi Sasajima, Hiroshi Watanabe, Kiyoshi Migita, Kohei Yokose, Tomohiro Suzuki, Yutaka Ejiri, Tomoyuki Asano, Jumpei Temmoku, Makiko Yashiro-Furuya, Haruki Matsumoto, Shuhei Yoshida, Yuya Fujita, Toru Yago
Publikováno v: The Tohoku Journal of Experimental Medicine. 255:157-162
Immunoglobulin A (IgA) vasculitis is a systemic small-vessel vasculitis involving the skin, kidney, joints, and gastrointestinal tract. Familial Mediterranean fever (FMF) is the most common autoinflammatory disease characterized by periodic fever, pe
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::e94b9eae1a646696cab35939f0a9947d
https://doi.org/10.1620/tjem.255.157
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10
Association between inflammatory cytokines and immune–checkpoint molecule in rheumatoid arthritis
Autor: Yuya Fujita, Atsushi Kawakami, Haruki Matsumoto, Shuhei Yoshida, Jumpei Temmoku, Tomoyuki Asano, Shuzo Sato, Kohei Yokose, Eiji Suzuki, Toru Yago, Naoki Matsuoka, Makiko Yashiro-Furuya, Kiyoshi Migita, Hiroshi Watanabe
Publikováno v: PLoS ONE
PLoS ONE, Vol 16, Iss 11, p e0260254 (2021)
PLoS ONE, Vol 16, Iss 11 (2021)
BackgroundRheumatoid arthritis (RA) is a heterogeneous inflammatory disease. Both anti-citrullinated peptide antibodies (ACPA) and inflammatory cytokines play an important role in the development of RA. The aim of this study was to investigate the as
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::75c8c22712cf6588543689c78f9377d1
http://europepmc.org/articles/PMC8601500
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