Zobrazeno 1 - 10
of 181
pro vyhledávání: '"Naotomo, Kambe"'
Publikováno v:
Allergology International, Vol 72, Iss 3, Pp 385-393 (2023)
Cryopyrin-associated periodic syndromes (CAPS) and Schnitzler syndrome (SchS) are autoinflammatory diseases that present with urticaria-like rashes. CAPS is characterized by periodic or persistent systemic inflammation caused by the dysfunction of th
Externí odkaz:
https://doaj.org/article/6a2159e259004afb80a0f46f6b31c4f2
Autor:
Riko Takimoto-Ito, Naotomo Kambe, Toshiaki Kogame, Takashi Nomura, Kazushi Izawa, Tomoyasu Jo, Yasuhiro Kazuma, Hajime Yoshifuji, Yuya Tabuchi, Hiroyasu Abe, Mayuko Yamamoto, Kimiko Nakajima, Ozumi Tomita, Yosuke Yagi, Kazumoto Katagiri, Yuki Matsuzaka, Yohei Takeuchi, Miho Hatanaka, Takuro Kanekura, Sora Takeuchi, Takafumi Kadono, Yuya Fujita, Kiyoshi Migita, Takahiro Fujino, Takahiko Akagi, Tomoyuki Mukai, Tohru Nagano, Mitsuhiro Kawano, Hayato Kimura, Yukari Okubo, Akimichi Morita, Michihiro Hide, Takahiro Satoh, Akihiko Asahina, Nobuo Kanazawa, Kenji Kabashima
Publikováno v:
Allergology International, Vol 72, Iss 2, Pp 297-305 (2023)
Background: Schnitzler syndrome is a rare disorder with chronic urticaria, and there is no report summarizing the current status in Japan. Methods: A nationwide survey of major dermatology departments in Japan was conducted in 2019. We further perfor
Externí odkaz:
https://doaj.org/article/1bff97464e6d4ad49cae826f877c0cf6
Publikováno v:
Pediatric Rheumatology Online Journal, Vol 20, Iss 1, Pp 1-9 (2022)
Abstract Background Blau syndrome (BS) is a rare autoinflammatory disorder with NOD2 gain-of-function mutation and characterized by autoactivation of the NFκB pathway. Classically considered a disease of high penetrance, reports on NOD2 mutations un
Externí odkaz:
https://doaj.org/article/c6d8581b54654273bee52f6d8e1d78f2
Publikováno v:
Frontiers in Immunology, Vol 14 (2023)
IntroductionBlau syndrome is a rare autosomal dominant autoinflammatory granulomatous disease caused by a mutation in the NOD2 gene. It is characterized by a clinical trial of granulomatous dermatitis, arthritis, and uveitis. Tofacitinib is a pan Jan
Externí odkaz:
https://doaj.org/article/63e22e968a1540e1a1ce71ed3631fbbe
Autor:
Kaori Takezawa, Ikuko Ueda‐Hayakawa, Akihiro Tanaka, Yonsu Son, Fumikazu Yamazaki, Naotomo Kambe, Hiroyuki Okamoto, Manabu Fujimoto
Publikováno v:
Journal of Cutaneous Immunology and Allergy, Vol 5, Iss 3, Pp 88-93 (2022)
Abstract Dermatomyositis (DM) is a systemic disease characterized by chronic inflammation in the skin and muscle. A variety of myositis‐specific autoantibodies (MSAs) are detected in patients with DM. These antibodies are associated with unique cli
Externí odkaz:
https://doaj.org/article/29c93efeae694f749a12ebf738d380e1
Autor:
Naotomo Kambe
Publikováno v:
Allergology International, Vol 72, Iss 3, Pp 357-358 (2023)
Externí odkaz:
https://doaj.org/article/d891f9cd137b4dfba2aaeae824de3a89
Autor:
Izumi Kishimoto, Ni Ma, Riko Takimoto-Ito, Chisa Nakashima, Atsushi Otsuka, Andrew F. Walls, Hideaki Tanizaki, Naotomo Kambe
Publikováno v:
Frontiers in Immunology, Vol 13 (2022)
A decrease in the number of basophils in the peripheral blood, or basopenia, has been noted, reflecting the activity of chronic spontaneous urticaria (CSU). Infiltration of basophils into the skin has also been reported, but the mechanism of basopeni
Externí odkaz:
https://doaj.org/article/b4930095276f4e2fb74236f35942b1db
Autor:
Takayuki Miyamoto, Yoshitaka Honda, Kazushi Izawa, Nobuo Kanazawa, Saori Kadowaki, Hidenori Ohnishi, Masakazu Fujimoto, Naotomo Kambe, Naoya Kase, Takeshi Shiba, Yasuo Nakagishi, Shuji Akizuki, Kosaku Murakami, Masahiro Bamba, Yutaka Nishida, Ayano Inui, Tomoo Fujisawa, Daisuke Nishida, Naomi Iwata, Yoshikazu Otsubo, Shingo Ishimori, Momoko Nishikori, Kiminobu Tanizawa, Tomoyuki Nakamura, Takeshi Ueda, Yoko Ohwada, Yu Tsuyusaki, Masaki Shimizu, Takasuke Ebato, Kousho Iwao, Akiharu Kubo, Toshinao Kawai, Tadashi Matsubayashi, Tatsuhiko Miyazaki, Tomohiro Kanayama, Masahiko Nishitani-Isa, Hiroshi Nihira, Junya Abe, Takayuki Tanaka, Eitaro Hiejima, Satoshi Okada, Osamu Ohara, Megumu K. Saito, Junko Takita, Ryuta Nishikomori, Takahiro Yasumi
Publikováno v:
Frontiers in Immunology, Vol 13 (2022)
PurposeUpregulation of type I interferon (IFN) signaling has been increasingly detected in inflammatory diseases. Recently, upregulation of the IFN signature has been suggested as a potential biomarker of IFN-driven inflammatory diseases. Yet, it rem
Externí odkaz:
https://doaj.org/article/5700023cf0774dc68dac5c83825a3a61
Autor:
Tomoko Matsuda, Naotomo Kambe, Riko Takimoto-Ito, Yoko Ueki, Satoshi Nakamizo, Megumu K. Saito, Syuji Takei, Nobuo Kanazawa
Publikováno v:
Frontiers in Immunology, Vol 13 (2022)
Blau syndrome is a systemic autoinflammatory granulomatous disease caused by mutations in the nucleotide-binding oligomerization domain 2 (NOD2) gene. NOD2 is an intracellular pathogen recognition receptor. Upon binding to muramyl dipeptide (MDP), NO
Externí odkaz:
https://doaj.org/article/2533f05b4c0b415c9e65a5d3e36ccc1b
Publikováno v:
Frontiers in Immunology, Vol 13 (2022)
Urticaria is a symptom of acute skin allergies that is not clearly understood, but mast cell histamine is hypothesized to cause swelling and itching. Omalizumab, an anti-human IgE antibody that traps IgE and prevents its binding to high-affinity IgE
Externí odkaz:
https://doaj.org/article/805635eb9c36447b9326d5c4360a9896