東京科学大学 · 医歯学総合研究科 · 教授

研究关键词原発性免疫不全症・X連鎖無ガンマグロブリン血症・血球貪食性リンパ組織球症・XIAP欠損症・Griscelli症候群2型・XLP1リンパ増殖性疾患・EBER flow FISH・自己炎症性疾患造血細胞移植・IKZF1ハプロ不全

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• Sagawa H, Hirata K, Katayama S, Shibata H, Toyofuku E, Kaneko S, Katata Y, Takezawa Y, Uematsu M, Onishi I, Yamazaki Y, Hattori T, Yamamoto M, Shimizu M, Imai K, Yasumi T, Morio T, Yokota T, Sasahara Y, Kanegane H. . Two Cases of CLIPPERS-like Syndrome Sharing a Hypomorphic UNC13D Variant. J Clin Immunol. 2026.03; 46 (1): ( PubMed , DOI )2026
• Wakatsuki R, Nishimura M, Tomomasa D, Takahashi S, Suzuki K, Kawaguchi K, Saura R, Inoue S, Takeuchi I, Arai K, Sugiyama M, Narishige Y, Oshima A, Tsumura M, Okada S, Hoshino A, Takagi M, Kanegane H. . Rapid flow cytometric diagnosis of XIAP deficiency. Pediatr Allergy Immunol. 2026.01; 37 (1): e70284. ( PubMed , DOI )2026
• Nishimura A, Uppuluri R, Raj R, Swaminathan VV, Cheng Y, Abu-Arja RF, Fu B, Laberko A, Albert MH, Hauck F, Bucciol G, Bigley V, Elcombe S, Kharya G, Pronk CJH, Wehr C, Neven B, Warnatz K, Meyts I, Morio T, Gennery AR, Kanegane H.. Correction to: An international survey of allogeneic hematopoietic cell transplantation for X-linked agammaglobulinemia. J Clin Immunol. 2026.01; 46 (1): 11. ( PubMed , DOI )2026
• Tanaka T, Sugawara A, Yasuoka R, Sakaguchi K, Natsume O, Haga K, Maruta Y, Kobayashi A, Sato T, Saito E, Minakawa S, Hirata Y, Shibata H, Yasumi T, Shimizu M, Kanegane H, Kudo K, Fukuda M, Teui K.. Functional characterization of Griscelli syndrome type 2 sine albinism in Japanese patients. J Hum Immun. 2026.07; 2 (4): e20250270. ( PubMed , DOI )2026