Personnel Information

写真a

IMAI Kohsuke


Job title

Visiting Lecturer

Homepage URL

http://www.tmd.ac.jp/med/ped/

Research Areas, Keywords

Primary immunodeficiency

Graduating School 【 display / non-display

  • Tokyo Medical and Dental University, Faculty of Medicine, 1992.03, Graduated

Graduate School 【 display / non-display

  • Tokyo Medical and Dental University, Graduate School, Division of Medical Sciences, Doctor's Course, 1999.03, Completed

Campus Career 【 display / non-display

  • 1992.06
    -
    1992.08
    Tokyo Medical and Dental University, (Old Organization)Medical Hospital, Hospital Departments, Department of Pediatrics, Maternal and Woman's Medicine, Pediatrics, Trainee Resident
  • 1994.02
    -
    1994.03
    Tokyo Medical and Dental University, (Old Organization)Medical Hospital, Hospital Departments, Department of Pediatrics, Maternal and Woman's Medicine, Pediatrics, Senior Resident
  • 1999.04
    -
    2000.09
    Tokyo Medical and Dental University, (Old Organization)Medical Hospital, Hospital Departments, Department of Pediatrics, Maternal and Woman's Medicine, Pediatrics, Senior Resident
  • 2011.04
    -
    2014.03
    Tokyo Medical and Dental University, Graduate School of Medical and Dental Sciences, Endowed Departments, Associate Professor
  • 2014.04
    -
    2022.03
    Tokyo Medical and Dental University, Graduate School of Medical and Dental Sciences, Endowed Departments, Department of Pediatrics, Perinatal and Maternal Medicine, Associate Professor
  • 2022.05
    -
    2023.04
    Tokyo Medical and Dental University, Graduate School of Medical and Dental Sciences, Medical and Dental Sciences, Division of Bio-Environmental Response, Department of Pediatrics and Developmental Biology, Visiting Lecturer
  • 2023.05
     
     
    Tokyo Medical and Dental University, Graduate School of Medical and Dental Sciences, Biomedical Sciences and Engineering, Division of Biomedical Laboratory Sciences, Department of Molecular Microbiology, Visiting Lecturer
  • 2023.06
    -
    Now
    Tokyo Medical and Dental University, Graduate School of Medical and Dental Sciences, Medical and Dental Sciences, Division of Bio-Environmental Response, Department of Pediatrics and Developmental Biology, Visiting Lecturer

▼display all

External Career 【 display / non-display

  • 2001.07
    -
    2004.07
    , Project Researcher
  • 2006.04
    -
    2008.09
    , Junior Associate Professor
  • 2008.10
    -
    2011.07
    , Associate Professor
  • 2011.08
    -
    2022.03
    , Visiting Lecturer
  • 2022.04
    -
    Now
    , Professor

Academic Activity 【 display / non-display

  • 2012
    -
    2015
    Mid-Winter Seminar Tutor
  • 2012
    -
    2018
    Pediatric international

Research Areas 【 display / non-display

  • Medical biochemistry

  • Embryonic medicine and pediatrics

  • Immunology

Qualification Acquired 【 display / non-display

  • Doctor

 

Research Theme 【 display / non-display

  • Establishment of newborn screening of primary immunodeficiency (PID) in Japan, 2004.08 - Now

  • Understanding the molecular mechanism of immunoglobulin class switch recombination and antibody production through the genetic analysis of the causative gene of hyper-IgM syndrome, combined immunodeficiency, CVID and B cell deficiency, 2001.07 - Now

  • Genetic diagnosis and clinical database construction of the PID patients, 1994.04 - Now

  • Hematopoietic stem cell transplantation and gene therapy for PID, 1994.04 - Now

Published Papers & Misc 【 display / non-display

  1. Akira Nishimura, Yuki Aoki, Yasuyoshi Ishiwata, Takuya Ichimura, Junichi Ueyama, Yuta Kawahara, Takahiro Tomoda, Maiko Inoue, Kazuaki Matsumoto, Kento Inoue, Haruka Hiroki, Shintaro Ono, Motoi Yamashita, Tsubasa Okano, Mari Tanaka-Kubota, Miho Ashiarai, Satoshi Miyamoto, Reiji Miyawaki, Chika Yamagishi, Mari Tezuka, Teppei Okawa, Akihiro Hoshino, Akifumi Endo, Masato Yasuhara, Takahiro Kamiya, Noriko Mitsuiki, Toshiaki Ono, Takeshi Isoda, Masakatsu Yanagimachi, Daisuke Tomizawa, Masayuki Nagasawa, Shuki Mizutani, Michiko Kajiwara, Masatoshi Takagi, Hirokazu Kanegane, Kohsuke Imai, Tomohiro Morio. Hematopoietic Cell Transplantation with Reduced Intensity Conditioning Using Fludarabine/Busulfan or Fludarabine/Melphalan for Primary Immunodeficiency Diseases. J Clin Immunol. 2021.07; 41 (5): 944-957. ( PubMed, DOI )

  2. Masatoshi Takagi, Chihiro Tomoyasu, Junko Yamanaka, Takayuki Hamabata, Takeshi Isoda, Takako Miyamura, Kohsuke Imai. Immunological assessment of a patient with infant acute lymphoblastic leukemia. Pediatr Int. 2024.01; 66 (1): e15738. ( PubMed, DOI )

  3. Motoi Yamashita, Masae Kuroha, Yuko Kinowawki, Nao Kashiwagi, Kotaro Watanabe, Mika Nagase, Daiki Niizato, Noriko Mitsuiki, Takeshi Isoda, Takahiro Kamiya, Atsuko Arisaka, Motoki Inaji, Kenichi Ohashi, Kohsuke Imai, Hirokazu Kanegane, Tomohiro Morio, Masatoshi Takagi. A SAMD5-SASH1 fusion in solitary infantile myofibromatosis. Pediatr Blood Cancer. 2023.03; e30278. ( PubMed, DOI )

  4. Dan Tomomasa, Takeshi Isoda, Noriko Mitsuiki, Kento Inoue, Akira Nishimura, Kazuhiro Uda, Toru Uchiyama, Motoi Yamashita, Takahiro Kamiya, Akifumi Endo, Masatoshi Takagi, Kohsuke Imai, Michiko Kajiwara, Morton J Cowan, Tomohiro Morio, Hirokazu Kanegane. Successful TCRαβ/CD19-Depleted Hematopoietic Cell Transplantation for a Patient With Artemis Deficiency. J Pediatr Hematol Oncol. 2023.02; ( PubMed, DOI )

  5. Aoi Morishita, Tzu-Wen Yeh, Kouki Tomari, Mihoko Furuichi, Kenichi Kashimada, Tomohiro Morio, Masatoshi Takagi, Kohsuke Imai. Transient immune deficiency accompanied with homozygous CBL rare variant. Pediatr Int. 2022.12; e15439. ( PubMed, DOI )

  6. Qian Zhang, Daniela Matuozzo, Jérémie Le Pen, Danyel Lee, Leen Moens, Takaki Asano, Jonathan Bohlen, Zhiyong Liu, Marcela Moncada-Velez, Yasemin Kendir-Demirkol, Huie Jing, Lucy Bizien, Astrid Marchal, Hassan Abolhassani, Selket Delafontaine, Giorgia Bucciol, , Gulsum Ical Bayhan, Sevgi Keles, Ayca Kiykim, Selda Hancerli, Filomeen Haerynck, Benoit Florkin, Nevin Hatipoglu, Tayfun Ozcelik, Guillaume Morelle, Mayana Zatz, Lisa F P Ng, David Chien Lye, Barnaby Edward Young, Yee-Sin Leo, Clifton L Dalgard, Richard P Lifton, Laurent Renia, Isabelle Meyts, Emmanuelle Jouanguy, Lennart Hammarström, Qiang Pan-Hammarström, Bertrand Boisson, Paul Bastard, Helen C Su, Stéphanie Boisson-Dupuis, Laurent Abel, Charles M Rice, Shen-Ying Zhang, Aurélie Cobat, Jean-Laurent Casanova. Recessive inborn errors of type I IFN immunity in children with COVID-19 pneumonia. J Exp Med. 2022.08; 219 (8): ( PubMed, DOI )

  7. Tessa Mollie Campbell, Zhiyong Liu, Qian Zhang, Marcela Moncada-Velez, Laura E Covill, Peng Zhang, Ilad Alavi Darazam, Paul Bastard, Lucy Bizien, Giorgia Bucciol, Sara Lind Enoksson, Emmanuelle Jouanguy, Şemsi Nur Karabela, Taushif Khan, Yasemin Kendir-Demirkol, Andres Augusto Arias, Davood Mansouri, Per Marits, Nico Marr, Isabelle Migeotte, Leen Moens, Tayfun Ozcelik, Isabelle Pellier, Anton Sendel, Mohammad Shahrooei, C I Edvard Smith, Isabelle Vandernoot, Karen Willekens, , Peter Bergman, Laurent Abel, Aurélie Cobat, Jean-Laurent Casanova, Isabelle Meyts, Yenan T Bryceson. Respiratory viral infections in otherwise healthy humans with inherited IRF7 deficiency. J Exp Med. 2022.07; 219 (7): ( PubMed, DOI )

  8. Akira Nishimura, Satoshi Miyamoto, Kohsuke Imai, Tomohiro Morio. Conditioning regimens for inborn errors of immunity: current perspectives and future strategies. Int J Hematol. 2022.07; 116 (1): 7-15. ( PubMed, DOI )

  9. Adela Escudero, Masatoshi Takagi, Franziska Auer, Ulrike Anne Friedrich, Satoshi Miyamoto, Atsushi Ogawa, Kohsuke Imai, Barbara Pascual, María Vela, Polina Stepensky, Layal Yasin, Sarah Elitzur, Arndt Borkhardt, Antonio Pérez-Martínez, Julia Hauer. Clinical and immunophenotypic characteristics of familial leukemia predisposition caused by PAX5 germline variants. Leukemia. 2022.07; ( PubMed, DOI )

  10. Shohei Eto, Yoko Nukui, Miyuki Tsumura, Yu Nakagama, Kenichi Kashimada, Yoko Mizoguchi, Takanori Utsumi, Maki Taniguchi, Fumiaki Sakura, Kosuke Noma, Yusuke Yoshida, Shinichiro Ohshimo, Shintaro Nagashima, Keisuke Okamoto, Akifumi Endo, Kohsuke Imai, Hirokazu Kanegane, Hidenori Ohnishi, Shintaro Hirata, Eiji Sugiyama, Nobuaki Shime, Masanori Ito, Hiroki Ohge, Yasutoshi Kido, Paul Bastard, Jean-Laurent Casanova, Osamu Ohara, Junko Tanaka, Tomohiro Morio, Satoshi Okada. Neutralizing Type I Interferon Autoantibodies in Japanese Patients with Severe COVID-19. J Clin Immunol. 2022.06; ( PubMed, DOI )

  11. Tomoko Niwano, Tadashi Hosoya, Saori Kadowaki, Etsushi Toyofuku, Takuya Naruto, Masaki Shimizu, Hidenori Ohnishi, Ryuji Koike, Tomohiro Morio, Kohsuke Imai, Masayuki Yoshida, Shinsuke Yasuda. An adult case of suspected A20 haploinsufficiency mimicking polyarteritis nodosa. Rheumatology (Oxford). 2022.05; ( PubMed, DOI )

  12. Shohei Eto, Yoko Nukui, Miyuki Tsumura, Yu Nakagama, Kenichi Kashimada, Yoko Mizoguchi, Takanori Utsumi, Maki Taniguchi, Fumiaki Sakura, Kosuke Noma, Yusuke Yoshida, Shinichiro Ohshimo, Shintaro Nagashima, Keisuke Okamoto, Akifumi Endo, Kohsuke Imai, Hirokazu Kanegane, Hidenori Ohnishi, Shintaro Hirata, Eiji Sugiyama, Nobuaki Shime, Masanori Ito, Hiroki Ohge, Yasutoshi Kido, Paul Bastard, Jean-Laurent Casanova, Junko Tanaka, Tomohiro Morio, Satoshi Okada. Neutralizing Type I Interferon Autoantibodies in Japanese Patients With Severe COVID-19. Res Sq. 2022.03; ( PubMed, DOI )

  13. Egg D, Rump IC, Mitsuiki N, Rojas-Restrepo J, Maccari ME, Schwab C, Gabrysch A, Warnatz K, Goldacker S, Patiño V, Wolff D, Okada S, Hayakawa S, Shikama Y, Kanda K, Imai K, Sotomatsu M, Kuwashima M, Kamiya T, Morio T, Matsumoto K, Mori T, Yoshimoto Y, Dybedal I, Kanariou M, Kucuk ZY, Chapdelaine H, Petruzelkova L, Lorenz HM, Sullivan KE, Heimall J, Moutschen M, Litzman J, Recher M, Albert MH, Hauck F, Seneviratne S, Schmid JP, Kolios A, Unglik G, Klemann C, Snapper S, Giulino-Roth L, Svaton M, Platt CD, Hambleton S, Neth O, Gosse G, Reinsch S, Holzinger D, Kim YJ, Bakhtiar S, Atschekzei F, Schmidt R, Sogkas G, Chandrakasan S, Rae W, Derfalvi B, Marquart HV, Ozen A, Kiykim A, Karakoc-Aydiner E, Králíčková P, de Bree G, Kiritsi D, Seidel MG, Kobbe R, Dantzer J, Alsina L, Armangue T, Lougaris V, Agyeman P, Nyström S, Buchbinder D, Arkwright PD, Grimbacher B.. Therapeutic options for CTLA-4 insufficiency. J Allergy Clin Immunol. 2022.02; 149 (2): 736-746. ( PubMed, DOI )

  14. Kay Tanita, Yoshiki Kawamura, Hiroki Miura, Noriko Mitsuiki, Takahiro Tomoda, Kento Inoue, Akihiro Iguchi, Masafumi Yamada, Taro Yoshida, Hideki Muramatsu, Norimasa Tada, Toshihiro Matsui, Motohiro Kato, Katsuhide Eguchi, Masataka Ishimura, Shouichi Ohga, Kohsuke Imai, Tomohiro Morio, Tetsushi Yoshikawa, Hirokazu Kanegane. Case Report: Rotavirus Vaccination and Severe Combined Immunodeficiency in Japan. Front Immunol. 2022.02; 13 786375. ( PubMed, DOI )

  15. Miyamoto S, Umeda K, Kurata M, Yanagimachi M, Iguchi A, Sasahara Y, Okada K, Koike T, Tanoshima R, Ishimura M, Yamada M, Sato M, Takahashi Y, Kajiwara M, Kawaguchi H, Inoue M, Hashii Y, Yabe H, Kato K, Atsuta Y, Imai K, Morio T.. Hematopoietic Cell Transplantation for Inborn Errors of Immunity Other than Severe Combined Immunodeficiency in Japan: Retrospective Analysis for 1985-2016. J Clin Immunol. 2022.01; ( PubMed, DOI )

  16. Tomomasa D, Isoda T, Mitsuiki N, Yamashita M, Morishita A, Tomoda T, Okano T, Endo A, Kamiya T, Yanagimachi M, Imai K, Kanegane H, Takagi M, Morio T . Successful ruxolitinib administration for a patient with steroid-refractory idiopathic pneumonia syndrome following hematopoietic stem cell transplantation: A case report and literature review. Clin Case Rep. 2021.12; 9 (12): e05242. ( PubMed, DOI )

  17. Isshiki K, Kamiya T, Endo A, Okamoto K, Osumi T, Kawai T, Arai K, Tomizawa D, Ohtsuka K, Nagahori M, Imai K, Kato M, Kanegane H. Vedolizumab therapy for pediatric steroid-refractory gastrointestinal acute graft-versus-host disease. Int J Hematol. 2021.11; ( PubMed, DOI )

  18. Toyohara M, Kajiho Y, Toyofuku E, Takahashi C, Owada K, Kanda S, Harita Y, Ohnishi H, Wada T, Imai K, Kanegane H, Morio T, Oka A. An infant with X-linked anhidrotic ectodermal dysplasia with immunodeficiency presenting with Pneumocystis pneumonia: A case report Clin Case Rep. 2021.11; 9 (11): e05093. ( PubMed, DOI )

  19. Ono S, Takeshita K, Kiridoshi Y, Kato M, Kamiya T, Hoshino A, Yanagimachi M, Arai K, Takeuchi I, Toita N, Imamura T, Sasahara Y, Sugita J, Hamamoto K, Takeuchi M, Saito S, Onuma M, Tsujimoto H, Yasui M, Taga T, Arakawa Y, Mitani Y, Yamamoto N, Imai K, Suda W, Hattori M, Ohara O, Morio T, Honda K, Kanegane H.. Hematopoietic Cell Transplantation Rescues Inflammatory Bowel Disease and Dysbiosis of Gut Microbiota in XIAP Deficiency. J Allergy Clin Immunol Pract. 2021.10; 9 (10): 3767-3780. ( PubMed, DOI )

  20. Okano T, Nishimura A, Inoue K, Naruto T, Tokoro S, Tomoda T, Kamiya T, Simbo A, Akutsu Y, Okamoto K, Yeh T, Isoda T, Yanagimachi M, Kajiwara M, Imai K, Kanegane H, Mori M, Morio,T, Takagi M. Somatic mutation in RUNX1 underlies mucocutaneus inflammatory manifestations. Rheumatology (Oxford). 2021.09; ( PubMed, DOI )

  21. Miyamoto S, Umeda K, Kurata M, Nishimura A, Yanagimachi M, Ishimura M, Sato M, Shigemura T, Kato M, Sasahara Y, Iguchi A, Koike T, Takahashi Y, Kajiwara M, Inoue M, Hashii Y, Yabe H, Kato K, Atsuta Y, Imai K, Morio T.. Hematopoietic Cell Transplantation for Severe Combined Immunodeficiency Patients: a Japanese Retrospective Study. J Clin Immunol. 2021.08; 41 (8): 1865-1877. ( PubMed, DOI )

  22. Takaki Asano, Bertrand Boisson, Fanny Onodi, Daniela Matuozzo, Marcela Moncada-Velez, Majistor Raj Luxman Maglorius Renkilaraj, Peng Zhang, Laurent Meertens, Alexandre Bolze, Marie Materna, Sarantis Korniotis, Adrian Gervais, Estelle Talouarn, Benedetta Bigio, Yoann Seeleuthner, Kaya Bilguvar, Yu Zhang, Anna-Lena Neehus, Masato Ogishi, Simon J Pelham, Tom Le Voyer, Jérémie Rosain, Quentin Philippot, Pere Soler-Palacín, Roger Colobran, Andrea Martin-Nalda, Jacques G Rivière, Yacine Tandjaoui-Lambiotte, Khalil Chaïbi, Mohammad Shahrooei, Ilad Alavi Darazam, Nasrin Alipour Olyaei, Davood Mansouri, Nevin Hatipoğlu, Figen Palabiyik, Tayfun Ozcelik, Giuseppe Novelli, Antonio Novelli, Giorgio Casari, Alessandro Aiuti, Paola Carrera, Simone Bondesan, Federica Barzaghi, Patrizia Rovere-Querini, Cristina Tresoldi, Jose Luis Franco, Julian Rojas, Luis Felipe Reyes, Ingrid G Bustos, Andres Augusto Arias, Guillaume Morelle, Kyheng Christèle, Jesús Troya, Laura Planas-Serra, Agatha Schlüter, Marta Gut, Aurora Pujol, Luis M Allende, Carlos Rodriguez-Gallego, Carlos Flores, Oscar Cabrera-Marante, Daniel E Pleguezuelo, Rebeca Pérez de Diego, Sevgi Keles, Gokhan Aytekin, Ozge Metin Akcan, Yenan T Bryceson, Peter Bergman, Petter Brodin, Daniel Smole, C I Edvard Smith, Anna-Carin Norlin, Tessa M Campbell, Laura E Covill, Lennart Hammarström, Qiang Pan-Hammarström, Hassan Abolhassani, Shrikant Mane, Nico Marr, Manar Ata, Fatima Al Ali, Taushif Khan, András N Spaan, Clifton L Dalgard, Paolo Bonfanti, Andrea Biondi, Sarah Tubiana, Charles Burdet, Robert Nussbaum, Amanda Kahn-Kirby, Andrew L Snow, , , , , , , , , , Jacinta Bustamante, Anne Puel, Stéphanie Boisson-Dupuis, Shen-Ying Zhang, Vivien Béziat, Richard P Lifton, Paul Bastard, Luigi D Notarangelo, Laurent Abel, Helen C Su, Emmanuelle Jouanguy, Ali Amara, Vassili Soumelis, Aurélie Cobat, Qian Zhang, Jean-Laurent Casanova. X-linked recessive TLR7 deficiency in ~1% of men under 60 years old with life-threatening COVID-19. Sci Immunol. 2021.08; 6 (62): ( PubMed, DOI )

  23. Imanaka Y, Taniguchi M, Doi T, Tsumura M, Nagaoka R, Shimomura M, Asano T, Kagawa R, Mizoguchi Y, Karakawa S, Arihiro K, Imai K, Morio T, Casanova JL, Puel A, Ohara O, Kamei K, Kobayashi M, Okada S. . Inherited CARD9 Deficiency in a Child with Invasive Disease Due to Exophiala dermatitidis and Two Older but Asymptomatic Siblings. J Clin Immunol. 2021.07; 41 (5): 975-986. ( PubMed, DOI )

  24. Yamashita M, Kuehn HS, Okuyama K, Okada S, Inoue Y, Mitsuiki N, Imai K, Takagi M, Kanegane H, Takeuchi M, Shimojo N, Tsumura M, Padhi AK, Zhang KYJ, Boisson B, Casanova JL, Ohara O, Rosenzweig SD, Taniuchi I, Morio T.. A variant in human AIOLOS impairs adaptive immunity by interfering with IKAROS. Nat Immunol. 2021.07; 22 (7): 893-903. ( PubMed, DOI )

  25. Mushino T, Hiroi T, Yamashita Y, Suzaki N, Mishima H, Ueno M, Kinoshita A, Minami K, Imai K, Yoshiura KI, Sonoki T, Tamura S.. Progressive Massive Splenomegaly in an Adult Patient with Kabuki Syndrome Complicated with Immune Thrombocytopenic Purpura. Intern Med. 2021.06; 60 (12): 1927-1933. ( PubMed, DOI )

  26. Kato T, Tamura Y, Matsumoto H, Kobayashi O, Ishiguro H, Ogawa M, Tsujikawa K, Hasegawa Y, Sakamoto M, Konagaya M, Houzen H, Takagi M, Imai K, Morio T, Yokoseki A, Onodera O, Nonoyama S.. Immunological abnormalities in patients with early-onset ataxia with ocular motor apraxia and hypoalbuminemia. Clin Immunol. 2021.06; 229 108776. ( PubMed, DOI )

  27. Sancho-Shimizu V, Brodin P, Cobat A, Biggs CM, Toubiana J, Lucas CL, Henrickson SE, Belot A, MIS-C@CHGE, Tangye SG, Milner JD, Levin M, Abel L, Bogunovic D, Casanova JL, Zhang SY.. SARS-CoV-2-related MIS-C: A key to the viral and genetic causes of Kawasaki disease? J Exp Med. 2021.06; 218 (6): ( PubMed, DOI )

  28. Dimitrova D, Nademi Z, Maccari ME, Ehl S, Uzel G, Tomoda T, Okano T, Imai K, Carpenter B, Ip W, Rao K, Worth AJJ, Laberko A, Mukhina A, Néven B, Moshous D, Speckmann C, Warnatz K, Wehr C, Abolhassani H, Aghamohammadi A, Bleesing JJ, Dara J, Dvorak CC, Ghosh S, Kang HJ, Markelj G, Modi A, Bayer DK, Notarangelo LD, Schulz A, Garcia-Prat M, Soler-Palacín P, Karakükcü M, Yilmaz E, Gambineri E, Menconi M, Masmas TN, Holm M, Bonfim C, Prando C, Hughes S, Jolles S, Morris EC, Kapoor N, Koltan S, Paneesha S, Steward C, Wynn R, Duffner U, Gennery AR, Lankester AC, Slatter M, Kanakry JA.. International retrospective study of allogeneic hematopoietic cell transplantation for activated PI3K-delta syndrome. J Allergy Clin Immunol. 2021.05; ( PubMed, DOI )

  29. Pilania RK, Rawat A, Vignesh P, Guleria S, Jindal AK, Das G, Suri D, Gupta A, Gupta K, Chan KW, Lau YL, Imai K, Singh S.. Liver Abscess in Chronic Granulomatous Disease-Two Decades of Experience from a Tertiary Care Centre in North-West India. J Clin Immunol. 2021.04; 41 (3): 552-564. ( PubMed, DOI )

  30. Totsune E, Nakano T, Moriya K, Sato D, Suzuki D, Miura A, Katayama S, Niizuma H, Kanno J, van Zelm MC, Imai K, Kanegane H, Sasahara Y, Kure S.. Case Report: Infantile-Onset Fulminant Type 1 Diabetes Mellitus Caused by Novel Compound Heterozygous LRBA Variants Front Immunol. 2021.04; 12 677572. ( PubMed, DOI )

  31. Vignesh P, Loganathan SK, Sudhakar M, Chaudhary H, Rawat A, Sharma M, Shekar A, Vaiphei K, Kumar N, Singh Sachdeva MU, Jindal AK, Suri D, Gupta A, Ray P, Imai K, Ohara O, Nonoyama S, Lau YL, Singh S.. Hemophagocytic Lymphohistiocytosis in Children with Chronic Granulomatous Disease-Single-Center Experience from North India. J Allergy Clin Immunol Pract. 2021.02; 9 (2): 771-782. ( PubMed, DOI )

  32. Kadowaki S, Hashimoto K, Nishimura T, Kashimada K, Kadowaki T, Kawamoto N, Imai K, Okada S, Kanegane H, Ohnishi H.. Functional analysis of novel A20 variants in patients with atypical inflammatory diseases. Arthritis Res Ther. 2021.02; 23 (1): 52. ( PubMed, DOI )

  33. Vignesh P, Rawat A, Kumrah R, Singh A, Gummadi A, Sharma M, Kaur A, Nameirakpam J, Jindal A, Suri D, Gupta A, Khadwal A, Saikia B, Minz RW, Sharma K, Desai M, Taur P, Gowri V, Pandrowala A, Dalvi A, Jodhawat N, Kambli P, Madkaikar MR, Bhattad S, Ramprakash S, Cp R, Jayaram A, Sivasankaran M, Munirathnam D, Balaji S, Rajendran A, Aggarwal A, Singh K, Na F, George B, Mehta A, Lashkari HP, Uppuluri R, Raj R, Bartakke S, Gupta K, Sreedharanunni S, Ogura Y, Kato T, Imai K, Chan KW, Leung D, Ohara O, Nonoyama S, Hershfield M, Lau YL, Singh S.. Clinical, Immunological, and Molecular Features of Severe Combined Immune Deficiency: A Multi-Institutional Experience From India. Front Immunol. 2021.02; 11 619146. ( PubMed, DOI )

  34. Rawat A, Vignesh P, Sudhakar M, Sharma M, Suri D, Jindal A, Gupta A, Shandilya JK, Loganathan SK, Kaur G, Chawla S, Patra PK, Khadwal A, Saikia B, Minz RW, Aggarwal V, Taur P, Pandrowala A, Gowri V, Desai M, Kulkarni M, Hule G, Bargir U, Kambli P, Madkaikar M, Bhattad S, Ginigeri C, Kumar H, Jayaram A, Munirathnam D, Sivasankaran M, Raj R, Uppuluri R, Na F, George B, Lashkari HP, Kalra M, Sachdeva A, Seth S, Sabui T, Gupta A, van Leeuwen K, de Boer M, Chan KW, Imai K, Ohara O, Nonoyama S, Lau YL, Singh S.. Clinical, Immunological, and Molecular Profile of Chronic Granulomatous Disease: A Multi-Centric Study of 236 Patients From India. Front Immunol. 2021.02; 12 625320. ( PubMed, DOI )

  35. Maiko Inoue, Takeshi Isoda, Motoi Yamashita, Takahiro Tomoda, Kento Inoue, Tsubasa Okano, Teppei Ohkawa, Akifumi Endo, Noriko Mitsuiki, Takahiro Kamiya, Masakatsu Yanagimachi, Kouhei Yamamoto, Yuichiro Inaba, Toru Sasaki, Masatoshi Takagi, Hirokazu Kanegane, Kohsuke Imai, Tomohiro Morio. Cytomegalovirus Laryngitis in Primary Combined Immunodeficiency Diseases. J Clin Immunol. 2021.01; 41 (1): 243-247. ( PubMed, DOI )

  36. Tanita K, Sakura F, Nambu R, Tsumura M, Imanaka Y, Ohnishi H, Kato Z, Pan J, Hoshino A, Suzuki K, Yasutomi M, Umetsu S, Okada C, Takagi M, Imai K, Ohara O, Muise AM, Okada S, Morio T, Kanegane H.. Clinical and Immunological Heterogeneity in Japanese Patients with Gain-of-Function Variants in STAT3 J Clin Immunol.. 2021.01; ( PubMed )

  37. Rawat A, Jindal AK, Suri D, Vignesh P, Gupta A, Saikia B, Minz RW, Banday AZ, Tyagi R, Arora K, Joshi V, Mondal S, Shandilya JK, Sharma M, Desai M, Taur P, Pandrowala A, Gowri V, Sawant-Desai S, Gupta M, Dalvi AD, Madkaikar M, Aggarwal A, Raj R, Uppuluri R, Bhattad S, Jayaram A, Lashkari HP, Rajasekhar L, Munirathnam D, Kalra M, Shukla A, Saka R, Sharma R, Garg R, Imai K, Nonoyama S, Ohara O, Lee PP, Chan KW, Lau YL, Singh S.. Clinical and Genetic Profile of X-Linked Agammaglobulinemia: A Multicenter Experience From India. Front Immunol. 2021.01; 11 612323. ( PubMed, DOI )

  38. Miyazaki H, Hoshi N, Kohashi M, Tokunaga E, Ku Y, Takenaka H, Ooi M, Yamamoto N, Uemura S, Nishimura N, Iijima K, Jimbo K, Okano T, Hoshino A, Imai K, Kanegane H, Kobayashi I, Kodama Y.. A case of autoimmune enteropathy with CTLA4 haploinsufficiency. Intest Res. 2021.01; ( PubMed, DOI )

  39. Suri D, Rikhi R, Jindal AK, Rawat A, Sudhakar M, Vignesh P, Gupta A, Kaur A, Sharma J, Ahluwalia J, Bhatia P, Khadwal A, Raj R, Uppuluri R, Desai M, Taur P, Pandrowala AA, Gowri V, Madkaikar MR, Lashkari HP, Bhattad S, Kumar H, Verma S, Imai K, Nonoyama S, Ohara O, Chan KW, Lee PP, Lau YL, Singh S.. Wiskott Aldrich Syndrome: A Multi-Institutional Experience From India. Front Immunol. 2021; 12 627651. ( PubMed, DOI )

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  152. Kanegane H, Imai K, Yamada M, Takada H, Ariga T, Bexon M, Rojavin M, Hu W, Kobayashi M, Lawo JP, Nonoyama S, Hara T, Miyawaki T. Efficacy and safety of IgPro20, a subcutaneous immunoglobulin, in Japanese patients with primary immunodeficiency diseases. J Clin Immunol. 2014.02; 34 204-211. ( PubMed )

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  163. Hiroyuki Ishida, Kosuke Imai, Kenichi Honma, Shin-Ichi Tamura, Toshihiko Imamura, Masafumi Ito, Shigeaki Nonoyama. GATA-2 anomaly and clinical phenotype of a sporadic case of lymphedema, dendritic cell, monocyte, B- and NK-cell (DCML) deficiency, and myelodysplasia. Eur J Pediatr. 2012.08; 171 (8): 1273-1276. ( PubMed, DOI )

  164. Oshima K, Nagase T, Imai K, Nonoyama S, Obara M, Mizukami T, Nunoi H, Kanegane H, Kuribayashi F, Amemiya S, Ohara O.. A Dual Reporter Splicing Assay Using HaloTag-containing Proteins. Curr Chem Genomics. 2012.07; 6 27-37. ( PubMed, DOI )

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  171. Göksel Leblebisatan, Ali Bay, Noriko Mitsuiki, Osamu Ohara, Kenichi Honma, Kohsuke İmai, Shigeaki Nonoyama. Wiskott-Aldrich syndrome mutation in two Turkish siblings with X-linked thrombocytopenia. Turk J Haematol. 2011.06; 28 (2): 139-141. ( PubMed, DOI )

  172. Asai E, Wada T, Sakakibara Y, Toga A, Toma T, Shimizu T, Nampoothiri S, Imai K, Nonoyama S, Morio T, Muramatsu H, Kamachi Y, Ohara O, Yachie A.. Analysis of mutations and recombination activity in RAG-deficient patients. Clin. Immunol.. 2011.02; 138 (2): 172-177. ( PubMed, DOI )

  173. Zhao M, Kanegane H, Kobayashi C, Nakazawa Y, Ishii E, Kasai M, Terui K, Gocho Y, Imai K, Kiyasu J, Nonoyama S, Miyawaki T.. Early and rapid detection of X-linked lymphoproliferative syndrome with SH2D1A mutations by flow cytometry. Cytometry B Clin Cytom. 2011.01; 80 (1): 8-13. ( PubMed, DOI )

  174. Yoshiko Hashii, Hisao Yoshida, Sato Kuroda, Shigenori Kusuki, Emiko Sato, Sadao Tokimasa, Hideaki Ohta, Yasutaka Matsubara, Seiji Kinoshita, Noriko Nakagawa, Kohsuke Imai, Shigeaki Nonoyama, Koichi Oshima, Osamu Ohara, Keiichi Ozono. Hemophagocytosis after bone marrow transplantation for JAK3-deficient severe combined immunodeficiency. Pediatr Transplant. 2010.12; 14 (8): E105-E109. ( PubMed, DOI )

  175. I Tsuge, Y Kondo, Y Nakajima, N Nakagawa, K Imai, S Nonoyama, K Oshima, O Ohara, M Hatanaka, E Kitano, H Kitamura, A Urisu. Hyper IgM syndrome and complement Clq deficiency in an individual with systemic lupus erythematosus-like disease. Clin Exp Rheumatol. 2010.07; 28 (4): 558-560. ( PubMed )

  176. A Aghamohammadi, K Imai, K Moazzami, H Abolhassani, M Tabatabaeiyan, N Parvaneh, R Nasiri Kalmarzi, N Nakagawa, K Oshima, O Ohara, S Nonoyama, N Rezaei. Ataxia-telangiectasia in a patient presenting with hyper-immunoglobulin M syndrome. J Investig Allergol Clin Immunol. 2010; 20 (5): 442-445. ( PubMed )

  177. Shivakumar Keerthikumar, Sahely Bhadra, Kumaran Kandasamy, Rajesh Raju, Y L Ramachandra, Chiranjib Bhattacharyya, Kohsuke Imai, Osamu Ohara, Sujatha Mohan, Akhilesh Pandey. Prediction of candidate primary immunodeficiency disease genes using a support vector machine learning approach. DNA Res. 2009.12; 16 (6): 345-351. ( PubMed, DOI )

  178. Naoki Uchisaka, Naomi Takahashi, Masaki Sato, Akira Kikuchi, Shinji Mochizuki, Kohsuke Imai, Shigeaki Nonoyama, Osamu Ohara, Fumiaki Watanabe, Shuki Mizutani, Ryoji Hanada, Tomohiro Morio. Two brothers with ataxia-telangiectasia-like disorder with lung adenocarcinoma. J Pediatr. 2009.09; 155 (3): 435-438. ( PubMed, DOI )

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  180. Yoichiro Tsuji, Issei Tokimatsu, Takashi Sugita, Masatoshi Nozaki, Daisuke Kobayashi, Kohsuke Imai, Kazuhiro Kogawa, Shigeaki Nonoyama. Quantitative PCR assay used to monitor serum Trichosporon asahii DNA concentrations in disseminated trichosporonosis. Pediatr Infect Dis J. 2008.11; 27 (11): 1035-1037. ( PubMed, DOI )

  181. Fujimoto M, Imai K, Hirata K, Kashiwagi R, Morinishi Y, Kitazawa K, Sasaki S, Arinami T, Nonoyama S, Noguchi E.. Immunological profile in a family with nephrogenic diabetes insipidus with a novel 11 kb deletion in AVPR2 and ARHGAP4 genes. 2008.05; ( PubMed )

  182. Yoichiro Tsuji, Kazuhiro Kogawa, Kohsuke Imai, Hirokazu Kanegane, Junichiro Fujimoto, Shigeaki Nonoyama. Evans syndrome in a patient with Langerhans cell histiocytosis: possible pathogenesis of autoimmunity in LCH. Int J Hematol. 2008.01; 87 (1): 75-77. ( PubMed, DOI )

  183. Yoichiro Tsuji, Kohsuke Imai, Yoichi Morinishi, Kazuhiro Kogawa, Masaaki Morino, Shigeaki Nonoyama. Successful unrelated cord blood transplantation for a patient with CD40 ligand deficiency. Haematologica. 2007.12; 92 (12): 1727-1728. ( PubMed, DOI )

  184. Tomoharu Tokutomi, Shin Hayashi, Kohsuke Imai, Ayako Chida, Takahiro Ishiwata, Yuh Asano, Johji Inazawa, Shigeaki Nonoyama. dup(8p)/del(8q) recombinant chromosome in a girl with hepatic focal nodular hyperplasia. Am J Med Genet A. 2007.06; 143A (12): 1334-1337. ( PubMed, DOI )

  185. Sophie Péron, Qiang Pan-Hammarström, Kohsuke Imai, Likun Du, Nadine Taubenheim, Ozden Sanal, Laszlo Marodi, Anne Bergelin-Besançon, Malika Benkerrou, Jean-Pierre de Villartay, Alain Fischer, Patrick Revy, Anne Durandy. A primary immunodeficiency characterized by defective immunoglobulin class switch recombination and impaired DNA repair. J Exp Med. 2007.05; 204 (5): 1207-1216. ( PubMed, DOI )

  186. Yoshiyuki Minegishi, Masako Saito, Tomohiro Morio, Ken Watanabe, Kazunaga Agematsu, Shigeru Tsuchiya, Hidetoshi Takada, Toshiro Hara, Nobuaki Kawamura, Tadashi Ariga, Hideo Kaneko, Naomi Kondo, Ikuya Tsuge, Akihiro Yachie, Yukio Sakiyama, Tsutomu Iwata, Fumio Bessho, Tsutomu Ohishi, Kosuke Joh, Kohsuke Imai, Kazuhiro Kogawa, Miwa Shinohara, Mikiya Fujieda, Hiroshi Wakiguchi, Srdjan Pasic, Mario Abinun, Hans D Ochs, Eleonore D Renner, Annette Jansson, Bernd H Belohradsky, Ayse Metin, Norio Shimizu, Shuki Mizutani, Toshio Miyawaki, Shigeaki Nonoyama, Hajime Karasuyama. Human tyrosine kinase 2 deficiency reveals its requisite roles in multiple cytokine signals involved in innate and acquired immunity. Immunity. 2006.11; 25 (5): 745-755. ( PubMed, DOI )

  187. Y Tsuji, K Imai, M Kajiwara, Y Aoki, T Isoda, D Tomizawa, M Imai, S Ito, H Maeda, Y Minegishi, H Ohkawa, J Yata, N Sasaki, K Kogawa, M Nagasawa, T Morio, S Nonoyama, S Mizutani. Hematopoietic stem cell transplantation for 30 patients with primary immunodeficiency diseases: 20 years experience of a single team. Bone Marrow Transplant. 2006.03; 37 (5): 469-477. ( PubMed, DOI )

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  190. Mansour Akbari, Marit Otterlei, Javier Peña-Diaz, Per Arne Aas, Bodil Kavli, Nina B Liabakk, Lars Hagen, Kohsuke Imai, Anne Durandy, Geir Slupphaug, Hans E Krokan. Repair of U/G and U/A in DNA by UNG2-associated repair complexes takes place predominantly by short-patch repair both in proliferating and growth-arrested cells. Nucleic Acids Res. 2004.10; 32 (18): 5486-5498. ( PubMed, DOI )

  191. Daisuke Tomizawa, Kohsuke Imai, Sukeyuki Ito, Michiko Kajiwara, Yoshiyuki Minegishi, Masayuki Nagasawa, Tomohiro Morio, Shigeaki Nonoyama, Shuki Mizutani. Allogeneic hematopoietic stem cell transplantation for seven children with X-linked hyper-IgM syndrome: a single center experience. Am J Hematol. 2004.05; 76 (1): 33-39. ( PubMed, DOI )

  192. Nadia Catalan, Françoise Selz, Kohsuke Imai, Patrick Revy, Alain Fischer, Anne Durandy. The block in immunoglobulin class switch recombination caused by activation-induced cytidine deaminase deficiency occurs prior to the generation of DNA double strand breaks in switch mu region. J Immunol. 2003.09; 171 (5): 2504-2509. ( PubMed, DOI )

  193. Van-Thanh Ta, Hitoshi Nagaoka, Nadia Catalan, Anne Durandy, Alain Fischer, Kohsuke Imai, Shigeaki Nonoyama, Junko Tashiro, Masaya Ikegawa, Satomi Ito, Kazuo Kinoshita, Masamichi Muramatsu, Tasuku Honjo. AID mutant analyses indicate requirement for class-switch-specific cofactors. Nat Immunol. 2003.09; 4 (9): 843-848. ( PubMed, DOI )

  194. Hirokazu Inoue, Hidemitsu Kurosawa, Shigeaki Nonoyama, Kohsuke Imai, Hisami Kumazaki, Takayuki Matsunaga, Yuya Sato, Kenichi Sugita, Mitsuoki Eguchi. X-linked thrombocytopenia in a girl. Br J Haematol. 2002.09; 118 (4): 1163-1165. ( PubMed, DOI )

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  196. Y Jin, S Nonoyama, T Morio, K Imai, H D Ochs, S Mizutani. Characterization of soluble CD40 ligand released from human activated platelets. J Med Dent Sci. 2001.03; 48 (1): 23-27. ( PubMed )

  197. S Kumaki, N Ishii, M Minegishi, Y Ohashi, I Hakozaki, S Nonoyama, K Imai, T Morio, I Tsuge, Y Sakiyama, A Miyanoshita, J Miura, M Mayumi, T Heike, K Katamura, H Takada, I Izumi, J Kamizono, S Hibi, H Sasaki, M Kimura, A Kikuta, Y Date, M Sako, H Tanaka, K Sano, K Sugamura, S Tsuchiya. Characterization of the gammac chain among 27 unrelated Japanese patients with X-linked severe combined immunodeficiency (X-SCID). Hum Genet. 2000.10; 107 (4): 406-408. ( PubMed, DOI )

  198. M Nagasawa, M Imai, K Imai, S Itoh, M Kajiwara, T Morio, S Nonoyama. In vivo class switch of B cells after cord blood stem cell transplantation in severe combined immune deficient (SCID) patient. Am J Hematol. 2000.10; 65 (2): 176-177. ( PubMed, DOI )

  199. S Itoh, S Nonoyama, T Morio, K Imai, H Okawa, H D Ochs, M Shimadzu, J Yata. Mutations of the WASP gene in 10 Japanese patients with Wiskott-Aldrich syndrome and X-linked thrombocytopenia. Int J Hematol. 2000.01; 71 (1): 79-83. ( PubMed )

  200. M Kajiwara, S Nonoyama, M Eguchi, T Morio, K Imai, H Okawa, M Kaneko, M Sako, S Ohga, M Maeda, S Hibi, H Hashimito, A Shibuya, H D Ochs, T Nakahata, J I Yata. WASP is involved in proliferation and differentiation of human haemopoietic progenitors in vitro. Br J Haematol. 1999.11; 107 (2): 254-262. ( PubMed, DOI )

  201. M Kato, H Miki, K Imai, S Nonoyama, T Suzuki, C Sasakawa, T Takenawa. Wiskott-Aldrich syndrome protein induces actin clustering without direct binding to Cdc42. J Biol Chem. 1999.09; 274 (38): 27225-27230. ( PubMed, DOI )

  202. Y Baba, S Nonoyama, M Matsushita, T Yamadori, S Hashimoto, K Imai, S Arai, T Kunikata, M Kurimoto, T Kurosaki, H D Ochs, J i Yata, T Kishimoto, S Tsukada. Involvement of wiskott-aldrich syndrome protein in B-cell cytoplasmic tyrosine kinase pathway. Blood. 1999.03; 93 (6): 2003-2012. ( PubMed )

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Conference Activities & Talks 【 display / non-display

  1. Imai K.. Newly reported primary antibody deficiencies (PADs). Chinese PID Summer School 2021.09.24 Shenzhen/Web

  2. Imai K.. Severe Combined Immunodeficiency (SCID). APSID Summer Webinar 2021 2021.06.16 web

  3. Takahiro Tomoda, Takahiro Kamiya, Tsubasa Okano, Miho Ashiarai, Hiroki Yoshihara, Kohsuke Imai, Hirokazu Kanegane, Masatoshi Takagi, Daisuke Hasegawa, Tomohiro Morio. 再発性MLL遺伝子再構成陽性乳児急性リンパ性白血病にCAR-T療法を施行した一例. 第62回日本小児血液・がん学会学術集会 2020.11.21 Web開催

  4. Imanaka Y, Taniguchi M, Doi T, Shimomura M, Tsumura M, Karakawa S, Imai K, Morio T, Puel A, Casanova-L, Ohara O, Kamei K, Kobayashi M, Okada S.. CARD9 DEFICIENCY IN A PATIENT WITH INVASIVE INFECTION DUE TO EXOPHIALA DERMATITIDIS AND THE ASYMPTOMATIC SIBLINGS. 19th Biennial Meeting of The European Society of immunodeficiencies (ESID 2020) 2020.10.14 web

  5. K. Tanita, F. Sakura, M. Tsumura, H. Ohnishi, A. Hoshino, K. Suzuki, S. Okada, R. Nambu, S. Umetsu, K. Imai, T. Morio, H. Kanegane. PATIENTS WITH THE GAIN-OF-FUNCTION MUTATIONS IN STAT3 PRESENT WITH A VARIETY OF AUTOIMMUNE DISEASES. 19th Biennial Meeting of The European Society of immunodeficiencies (ESID 2020) 2020.10.14 web

  6. P. Vignesh, A. Rawat, A. Singh, R. Kumrah, A. Gummadi, A. Kaur, S. Bhattad, A. Mehta, D. Suri, A. Jinda, D. Leung, S. Ramprakash, R. Cp, K.W. Chan, Y. Ogura, K. Imai, O. Ohara, S. Nonoyama, M. Hershfield, Y. Lau, S. Singh. CLINICAL, IMMUNOLOGICAL, AND MOLECULAR FEATURES OF SEVERE COMBINED IMMUNE DEFICIENCY: A REPORT OF 87 PATIENTS FROM 3 TERTIARY CARE CENTRES IN INDIA. 19th Biennial Meeting of The European Society of immunodeficiencies (ESID 2020) 2020.10.14 web

  7. Satoshi Miyamoto , Masakatsu Yanagimachi , Katsutsugu Umeda , Akihiro Iguchi , Yoji Sasahara , Hidetoshi Takada , Masafumi Yamada , Masataka Ishimura ,Takashi Koike , Masahiro Yasui , Yoshiyuki Takahashi , Hiroshi Kawaguchi , Michiko Kajiwara , Masami Inoue , Koji Kato, Yoshiko Hashii, Yoshiko Atsuta , Hiromasa Yabe , Kohsuke Imai , Tomohiro Morio. Hematopoietic stem cell transplantation for inborn errors of immunity in Japan: overview of a nationwide retrospective analysis. 46th Annual Meeting of the European Society for Blood and Marrow Transplantation (EBMT 2020 Virtual) 2020.08.29 WEB

  8. Satoshi Miyamoto, Masakatsu Yanagimachi, Katsutsugu Umeda, Akihiro Iguchi, Yoji Sasahara, Hidetoshi Takada, Yoshiyuki Takahashi, Michiko Kajiwara, Masami Inoue, Koji Kato, Yoshiko Hashii, Yoshiko Atsuta, Hiromasa Yabe, Kohsuke Imai, Tomohiro Morio. Hematopoietic stem cell transplantation for severe combined immunodeficiency in Japan: a nationwide retrospective analysis. 46th Annual Meeting of the European Society for Blood and Marrow Transplantation (EBMT 2020 Virtual) 2020.08.29 WEB

  9. Yoonsun Yoon, Ji-man Kang, Junsik Choi, Kangmo Ahn, Keon Hee Yoo, Eun-Suk Kang, Kyoung-Mee Kim, Jung Eun Lee, Geum-Youn gawk, Kihyun Kim, Kosuke Imai, Hirokazu Kanegane, Yae-jean Kim.. Cancer development in a Korean family with CTLA-4 haploinsufficiency. 第3回日本免疫不全・自己炎症学会総会・学術集会 2020.02.16 東京

  10. Miko Okamura, Kay Tanita, Hidetoshi Takada, Tetsuo Mitsui, Yoshiyuki Minegishi, Kohsuke Imai, Tomohiro Morio, Hirokazu Kanegane. Somatically reverted T cells in dedicator of cytokinesis 8 deficiency modify cellular immunity. 3rd Scientific Congress of Asia Pacific Society for Immunodeficiencies 2020.02.09 Chandigarh, India

  11. Takahiro Tomoda, Tsubasa Okano, Kento Inoue, Motoi Yamashita, Takahiro Kamiya, Takeshi Isoda Masakatsu Yanagimachi, Hirokazu Kanegane, Masatoshi Takagi, Tomohiro Morio, Kohsuke Imai. Second transplantation rescued the graft failure after hematopoietic stem cell transplantation. 3rd Scientific Congress of Asia Pacific Society for Immunodeficiencies 2020.02.09 Chandigarh, India.

  12. Imai K. Viral infections in patients with hypogammaglobulinemia - What is our current understanding. 3rd Scientific Congress of Asia Pacific Society for Immunodeficiencies 2020.02.09 Chandigarh, India.

  13. Imai K. How I Approach A Patient With Combined Immunodeficiency?. APSID2020 2020.02.06 India

  14. Takahiro Tomoda, Tsubasa Okano, Kento Inoue, Motoi Yamashita, Takahiro Kamiya, Takeshi Isoda, Masakatsu Yanagimachi, Hirokazu Kanegane, Masatoshi Takagi, Tomohiro Morio, Kohsuke Imai. An intractable case of hyper IgE syndrome. APSID (Asia Pacific Society for Immunodeficiencies) School cum Workshop 2020.02.06 Chandigarh, India.

  15. Imai K. Hematopoietic stem cell transplantation in PIDs. 3rd Scientific Congress of Asia Pacific Society for Immunodeficiencies 2020.02 India

  16. Okamura M, Terada N, Mitsuiki N, Ishii T, Morio T, Imai K. The first Cernunnos deficiency patient in Japan. 3rd Scientific Congress of Asia Pacific Society for Immunodeficiencies 2020.02 India

  17. Miyamoto T, Imai K. Japanese experience with UCBT in SCID. IEWP 2019.10.11 London

  18. Hoshino A, Okano T, Matsumoto K, Nishimura A, Shintaku H, Tokoro S, Okamoto H, Wada T, Mitsuiki N, Kajiwara M, Takagi M, Imai K, Kanegane H, Morio T. Plasmacytoma-Like Post-Transplant Lymphoproliferative Disorder with Multiple Autoantibodies in a XIAP Deficient Patient. 2019 Focused Meeting of the European Society of Immunodeficiencies (ESID 2019) 2019.09.20 Brussels

  19. Okano T, Imai K, Naruto T, Okada S, Okamoto K, Yamashita M, Yeh T. W, Takagi M, Kanegane H, Morio T. Diagnostic Approach by Whole Exome Sequencing for 141 Patients of Inborn Errors of Immunity. 2019 Focused Meeting of the European Society of Immunodeficiencies (ESID 2019) 2019.09.19 Brussels

  20. Sakata S, Okada S, Matsubayashi T, Tamaura M, Tsumura M, Okano T, Imai K, Bustamante J, Morio T, Casanova JL, Kobayashi M. . The First Intronic Mutations Which Caused Autosomal Recessive Complete STAT1 Deficiency. 2019 Focused Meeting of the European Society of Immunodeficiencies (ESID 2019) 2019.09.19 Brussels,Belgium

  21. Nishimura Akira, Aoki Yuki, Ishiwata Yasuyoshi, Inoue Maiko, Ichimura Takuya, Ueyama Junichi, Matsumoto Kazuaki, Inoue Kento, Hiroki Haruka, Ono Shintaro, Okano Tsubasa, Tanaka Mari, Miyamoto Satoshi, Ashiarai Miho, Miyawaki Reiji, Yamagishi Chika, Tezuka Mari, Okawa Teppei, Hoshino Akihiro, Endo Akifumi, Yasuhara Masato, Kamiya Takahiro, Mitsuiki Noriko, Ono Toshiaki, Yanagimachi Masakatsu, Isoda Takeshi, Tomizawa Daisuke, Nagasawa Masayuki, Kajiwara Michiko, Takagi Masatoshi, Mizutani Shuki, Kanegane Hirokazu, Imai Kohsuke, Morio Tomohiro. Hematopoietic cell transplantation with reduced intensity conditioning regimen using fludarabine/busulfan and fludarabine/melphalan for primary immunodeficiency diseases . The 45th Annual Meeting of the European Society for Blood and Marrow Transplantation 2019.03.24 Frankfurt

  22. Yeh T. W, Okano T, Okamoto K, Yamashita M, Takashima T, Mitsuki N, Okada S, Kanegane H, Imai K, Morio T.. April Deficiency as a Cause of Common Variable Immunodeficiency. . 18th Biennial Meeting of the European Society of Immunodeficiencies (ESID2018) 2018.10.25 Lisbon

  23. Imai K. Antibody deficiency: a diagnostic and management challenge. APSID Autumn School 2018.10.11 Bangkok

  24. Imai K. Newborn Screening for primary immunodeficiency (PID) in Japan and Asia. European Society for Blood and Marrow Transplantation 2018.09.27 Leiden

  25. Imai.k. PIDJ:primary immunodeficiency in japan project.. 2018samsung Medical Center Primary Immunodeficiency Symposium. 2018.07.14 seoul

  26. Imai K. Newborn Screening of PID in Japan. 7th Singapore Paediatric and Perinatal Annual Congress (SiPPAC) 2018.06.27 Singapore

  27. Imai K. Primary Antibody Deficiencies.. 7th Singapore Paediatric and Perinatal Annual Congress (SiPPAC). 2018.06.27 Singapore

  28. Imai K. PID research and clinical care in japan.. 2018samsung Medical Center Primary Immunodeficiency Symposium. 2018.05.08 Chongqing

  29. Imai K. Hematopoietic stem cell transplantation for radiosensible severe combined immunodeficiency. APSID 2018 Summer School 2018.05.08 Chongqing

  30. Yeh TW, Okano T, Okamoto K, Yamashta M, Takashima T, Mitusiki N, Okada S, Kaneganwe H, Imai K, Morio T. APRIL deficiency a as a cause of common variable immunodeficiency. The 2nd APSID Scientific Congress 2018.05.07 Chonquing, China

  31. Okamoto K, Shigemizu D, Okano T, Yeh TW, Takashima T, Yamashita M, Ono S, Mitsuiki N, Takagi M, Mori M, Kanegane H, Tsunoda T, Imai K, Morio T. whole exome sequence analysis using the known and candidate genes for primary immunodeficiency diseases. The 2nd APSID Scientific Congress 2018.05.07 Chonquing, China

  32. Imai K. HSCT for radiosensitive SCID. APSID2018 Summer School 2018.05.05 Chongqing

  33. 田村志宣、春谷勇平、小畑裕史、山下友佑、蒸野寿紀、細井裕樹、村田祥吾、西川彰則、吉浦孝一郎、今井耕輔、森尾友宏、園木孝志. Successful cord blood transplantation in a patient with adult-onset common variable immunodeficiency. 第1回日本免疫不全・自己炎症学会総会学術集会 2018.01.20 東京

  34. 山下基, 満生紀子, 岡田賢, 井上裕三朗, 中世古知昭, Aditya K. Padhi, Kam Y Zhang, 小原收, 今井耕輔, 高木正稔, 金兼弘和, 谷内一郎, 森尾友宏. IKZF3ヘテロ結合型ミスセンス変異によるB細胞欠損症. 第1回日本免疫不全・自己炎症学会総会・学術集会 2018.01.20 東京

  35. Imai K. Hematopoietic stem cell transplantation for primary immunodeficiency in Japan. KSPHO 2018 Seoul

  36. 今井耕輔. 原発性免疫不全症・自己炎症性疾患において考慮すべき遺伝医療の特性と課題. 第59回日本小児血液・がん学会学術集会 2017.11.09

  37. 井上健斗, 星野顕宏, 三浦浩樹, 朴明子, 今井耕輔, 吉川哲史, 金兼弘和, 森尾友宏. X連鎖リンパ増殖症候群2型におけるHHV-6 DNA高コピー数は再活性化か? . 第49回日本小児感染症学会学術集会 2017.10.21 石川

  38. Matsumoto K, Takagi M, Ishiwata Y, Aoki Y, Miyamoto S, Hoshino A, Nishimura A, Tanaka M, Yanagimachi M, Mitsuiki N, Imai K, Kanegnane H, Kajiwara M, Takikawa K, Mae T, Tomiota O, Fujimura J, Yasuhara M, Tomizawa D, Mizutani S, Morio T. HLA haploidentical HCT using clofarabine and busulfan for refractory pediatric leukemia. JSH 2017 2017.10.20 東京

  39. Imai.k. Newborn Screening of PID in japan. APSID 2017 Autumn School 2017.10.10 Hong Kong

  40. Kadawaki T, Ohnishi H, Kanegane H, Kawamoto N, Hori T, Nishimura K, Kobayashi C, Shigemura T, Ogata S, Inoue Y, Kawai T, Hiejima E, Takagi M, Imai K, Nishikomori R, Ito S, Heiki T, Ohara O, Morio T, Fukao T. A Nation-wide Survey of Haploinsufficiency of A20 Reveals the Frequent Coincidence of Autoimmunity in Japan. ESID 2017 2017.09.13 Edinburgh, UK

  41. Ono S, Yanagimachi M, Okano T, Hoshino A, Takagi M, Imai K, Morio T, Kanegane H. Inflammatory Bowel Disease Associated with XIAP Deficiency can be cured by Hematopoietic Stem Cell Transplantation. ESID 2017 2017.09.12 Edinburgh, UK

  42. Okano T, Imai K, Mitui-Sekinaka K, Yeh T.W, Takashima T, Kanegane H, Nonoyama S, Morio T. Combined Immunodeficiency and Progressive Lymphoproliferative Diseases of Activated P13Kδ Syndrome Rescued by Hematopoietic. ESID 2017 2017.09.12 Edinburgh, UK

  43. Okamoto K, Okano T, Kumaki E, Tanaka E, Ono S, Wada T, Ohnishi H, Kato Z, Nunoi N, Imai K, Kanegane H, Mori M, Morio T. A Case of Non-Pulmonary Sarcoidosis Due to Novel Hypomorphic Missense Mutation of NCF2. ESID 2017 2017.09.11 Edinburgh,UK

  44. Imai K. Hematpopoietic stem cell transplantation for P`rimary. The 21st Congress of the Asian Pacific Society of Respirology (APSR 2016) 2016.11.11 Thailand Bangkok

  45. Imai K. Primary antibody deficiency in Japan:overview and P13K related disorders. XLP-WAS 2016 Symposium-London 2016.09.27 London England

  46. Ono S, Okano T, Hoshino A, Yanagimachi M, Takagi M, Imai K, Morio T, Kanegane H. Hematopoietic stem cell transplantation for XIAP deficiency. XLP-WAS 2016 Symposium-London 2016.09.26 London

  47. Kanegane H, Hoshino A, Takashima T, Yeh T-W, Okano T, Yamashita M, Imai K, Morio T. . Selective dysregulation of Epstein Barr virus infection in hypomorphic ZAP70 mutation. . XLP-WAS 2016 Symposium-London 2016.09.26 London

  48. Schwab C, Gabrysch A, Hoshino M, Slatter M, Hayakawa S, Schubert D, Klemann C, Frede N, Salzer U, Speckmann C, Freiberger T, Lorenz H.M, Hauck F, Klobuch S, Zeissig S, Leichtner A, Van de Veerdonk F, Elemnto O, Giulino-Roth L, Duckers G, Niehues T, Alsina L, Deya-Martinez A, Kanderiva V, Fronkova E, Price C, Patino V, Blumberg R, Yesim Kucuk Z, Seneviratne S, Kanariou M, Lougaris V, Albert M, Giese T, Litzman J, Ehl S, Okada S, Imai K, Dybedai I, Tasken K, Wolff D, Warnatz K, Hambleton S, Arkwright P, Cant A, Kanegane H, Grimbacher B.. The Clinical Spectrum and Treatment Options of 82 Individuals with CTLA-4Deficiency. 17th Biennial Meeting of the European Society for Immunodeficiencies 2016.09.23 Barcelona, Spain

  49. Rojavin M, Kanegane H, Borte H, Imai K, Hubsch A, Jolles S.. Analysis of Patient Treatment Satisfaction from Five Studies of HIZENTRA 20% Subcutaneous Immunoglobulin. 17th Biennial Meeting of the European Society for Immunodeficiencies 2016.09.23 Barcelona, Spain

  50. Okano T, Watanabe E, Takashima T, Nishikawa T, Kawano Y, Tomoda T, Tanaka-Kubota M, Miyamoto S, Yeh T, Yamashita M, Tanaka K, Mitusiki N, Ohara O, Takagi M, Imai K, Kanegane H, Morio T.. IgG1 Gammopathy in X-SCID Caused by Maternal T and B cell Engraftment. 17th Biennial Meeting of the European Society for Immunodeficiencies 2016.09.23 Barcelona, Spain

  51. Moriya K, Tanita K, Ohnishi H, Niizuma H, Rikiishi T, Nishikomori R, Ishige T, Imai K, Kanegane H, Sasahara Y, Arakawa H, Kure S, Morio T.. I⃐B-α S32 Mutations Underly Ectodermal Dysplasia with Immunodeficiency Manifestations and Correlation with Immunological Parameters.. 17th Biennial Meeting of the European Society for Immunodeficiencies 2016.09.23 Brcelona, Spain

  52. T. Mizukami,M. Iwata-Okada, T. Nishimura, T. Kawai, M. Onodera, K. Imai, S. Nonoyama, O. Ohara, H. Nunoi. CLINICAL AND GENETIC PROFILES OF CHRONIC GRANULOMATOUS DISEASE IN JAPAN. 17th Biennial Meeting of the European Society for Immunodeficiencies 2016.09.23 Barucelona Spain

  53. Jolles S, Rojavin M, Nelson Jr. R, Wasserman R.L, Borte M, Kanegane H, Imai K.. Efficacy and Safety of HIZENTRA in Patients with Primary Immunodeficiency in Japan, Europe, and the US. 17th Biennial Meeting of17th Biennial Meeting of the European Society for Immunodeficiencies 2016.09.23 Barcelona, Spain

  54. Hoshino A, Okada S, Yoshida K, Nishida N, Yamashita M, Okano T, Tsumura M, Nishimura S, Sakata S, Takagi M, Imai K, Miyano S, Ogawa S, Kojima S, Nonoyama S, Morio T, Kanegane H. . Abnormal Hematopoiesis and Autoimmunity in Humans with Germline IKZF1 Mutations. 17th Biennial Meeting of the European Society for Immunodeficiencies 2016.09.22 Barcelona, Spain

  55. Sekinaka Y,Mitsuiki N,Imai K,Yabe M,Mitsui-Sekinaka K,Honma K,Arai A,Yoshida K,Miyano S,Seiji K,Hira A,Takata M,Ohara O,Ogawa S,Morio T,Nonoyama S. Common Variable Immunodeficiency Caused by Fanc Mutations. 17th Biennial Meeting of the European Society for Immunodeficiencies 2016.09.22 Brcelona, Spain

  56. L.A. Henderson, A.E. O'Connell, J.I. Chu, Y.N. Lee, S. Volpi, M. Armant, I.B. Barlan, A. Ozen, S. Baris, I.C. Hanson, J.M. Despotovic, A. Saitoh, T. Takachi, K. Imai, A. King, S. Arredondo, A. Galy, D.A. Williams,S.Y. Pai, L.D. Notarangelo. GENE THERAPY USING A SELF-INACTIVATING LENTIVIRAL VECTOR AMELIORATES T CELL RECEPTOR REPERTOIRE ABNORMALITIES IN PATIENTS WITH WISKOTT-ALDRICH SYNDROME. 17th Biennial Meeting of the European Society for Immunodeficiency 2016.09.22 Barcelona Spain

  57. S. Singh, A. Rawat, D. Suri, A. Gupta, R. Garg, B. Saikia, R. Minz, S. Sehga, K. Chan, Y. Lau, C. Kamae, K. Honma, N. Nakagawa, K. Imai, S. Nonoyama, K. Oshima, N. Mitsuiki, O. Ohara. SPECTRUM OF BTK GENE MUTATIONS IN A SINGLE-CENTRE COHORT OF X-LINKED AGAMMAGLOBULINEMIA FROM NORTH INDIA. 17th Biennial Meeting of the European Society for Immunodeficiency 2016.09.22 Barcelona Spain

  58. Leiding J,Okada S,Shcherbina A,Abinun M,Pulsipher M,Hagin D,Linemans C,Sullivan K,Bunin N,Kilic S,De La Calle-Martin O,Roiman C,Aldave J.C,Iguchi A,Imai K,Ohkawa T,Gennery A,Slatter M,Ochs H,MorioT,Torgerson T. Hematopoietic Stem cell Transplantation in Patients with Gain of Function STAT1 Mutation. 17th Biennial Meeting of the European Society for Immunodeficiencies 2016.09.22 Barcelona, Spain

  59. Mitsui-Sekinaka K, Imai K, Tsujita Y, Mitsuiki N, Asano T, Sekinaka Y, Kanegane H, Yoshida K, Miyano S, Kojima S, Ogawa S, Ohara O, Okada S, Kobayashi M, Takagi M, Morio T, Nonoyama S.. Activated P13 Kinase Delta Syndrome (APDS)-Like Immunodeficiency Caused by PTEN Mutation. 17th Biennial Meeting of the European Society for Immunodeficiencies 2016.09.22 Barcelona, Spain

  60. Okano T, Imai K, Tsujita Y, Mitsuiki , Mitsui-Sekinaka K, Takashima T, Kanegane H, Nonoyma S. Broad Spectrum of Clinical Manifestations and Outcome of Hematopoietic Stem Cell Transplantation in Japanese Patients with Activated P13KD Syndrome Type1. ASPID Spring School 2016.05.01 Hong Kong

  61. Imai K. HYPER-IGM SYNDROMES DUE TO CSR DEFECTS-HOW TO TREAT ACCORDING TO GENETIC SUBTYPES?. ASPID Spring School 2016.04.27 HongKong

  62. Imai K. PIDJ AND PIER-PID DATABASE IN JAPAN FOR DOCTORS AND PATIENTS-HOW IT FACILITATES CARE AND RESEARCH?. ASPID Spring School 2016.04.27 HongKong

  63. Mikhail Rojavin, Hirokazu Kanegane, Michael Borte, Imai k , Alphonse P. Hubsch, Helena Soop, Stephen R. Jolles. Pooled Analysis of Patient Treatment Satisfaction from Five Hizentra Studies. 2016 AAAAI ANNUAL MEETING 2016.03.04 Los Angeles

  64. 高木正稔,今井耕輔,朴今花,山下基,星野顕宏,岡野翼,金兼弘和,松村秀樹,奥野友介,吉田健一,上野浩生,白石友一,千葉健一,田中洋子,宮野悟,小川誠司,林泰秀,小島勢二,森尾友宏. 自己免疫性リンパ増殖症様疾患に対する全エクソーム解析の経験Whole-exome analysis of autoimmune lymphoproliferative syndrome-like diseases. 第57回日本小児血液・がん学会学術集会 2015.11.29 山梨

  65. 小野真太郎,金兼弘和,我有茉希,久保田真理,足洗美穂,宮本智史,小林千佳,満生紀子,今井耕輔,高木正稔,梶原道子,森尾友宏. 炎症性腸疾患を合併したXIAP 欠損症患者に対する骨髄移植成功例Successful bone marrow transplantation in an XIAP-deficient patient associated with inflammatory bowel disease. 第57回日本小児血液・がん学会学術集会 2015.11.29 山梨

  66. T. Wada, T. Toma, M. Yasui, M. Inoue, K. Kawa, K. Imai, T. Morio, A. Yachie. Different leaky phenotype in two siblings with x-linked severe combined immunodeficiency. 16th Biennial Meeting of the European society for immunodeficiencies 2014.10.31 Prague, Czech Republic

  67. K. Imai, Y. Tsujita, K. Mitsui-Sekinaka, N. Mitsuiki, T. Takashima, T. Okano, Y. Aoki, F. Kimoto, M. Inoue, F. Iwasaki, T. Kaneko, T. Waragai, H. Sano, A. Kikuta, T. Morio, S. Nonoyama. Hematopoietic stem cell transplantation for the patients with activated PI3K-delta syndrome. 16th Biennial Meeting of the European society for immunodeficiencies 2014.10.30 Prague, Czech Republic

  68. T.Takashima, Y. Tsujita, T.W.Yeh, N. Mitsuiki, H. Kanegane, S Kracker, A.Durandy, S. Nonoyama, T. Morio, K. Imai. Clinical and immunological features of patients with gain-of-function PIK3CD mutations in japan. 16th Biennial Meeting of the European society for immunodeficiencies 2014.10.30 Prague, Czech Republic

  69. N. Mitsuiki, X. Yang, S. Bartol, Y.Kosaka, H.Takada, K. Imai, H. Kanegane, S. Mizutani, M. Van der Burg, M. Van Zelm, O. Ohara, T. Morio. Mutations in bruton's tyrosine kinase impair IgA responses. 16th Biennial Meeting of the European society for immunodeficiencies 2014.10.30 Prague, Czech Republic

  70. 今井耕輔. ヒト免疫異常症における免疫担当細胞亜群解析の標準化. 第58回日本リウマチ学会総会・学術集会 2014.04.26

  71. Mari Tezuka, Kohsuke Imai, Teppei Okawa, Daisuke Tomizawa, Masatoshi Takagi, Michiko Kajiwara, Masayuki Nagasawa, Tomohiro Morio, and Shuki Mizutani. Fatal Outcome Due to Parainfluenza-3 Pneumonitis in a Patient with Atypical Complete DiGeorge Syndrome. The 4th JSH International Symposium 2013 in EHIME 2013.05 EHIME, Japan

  72. Takada H, Ishimura M, Imai K, Morio T, Kobayashi M, Nonoyama S, Hara O.. Endocrine complications in primary immunodeficiency diseases in Japan.. 第41回日本免疫学会総会・学術集会 2012.12 神戸

  73. 長澤正之、大川哲平、遠藤明史、満生紀子、青木由貴、小野敏明、磯田健志、富澤大輔、今井耕輔、高木正稔、梶原道子、森尾友宏、水谷修紀. . Thrombomodulin-alpha improves the coagulation disorder associated transplantation-related mortality after allogeneic SCT.. 第74回日本血液学会 2012.10.21 京都

  74. Takagi M, Imai K, Nakagawa M, Morio T, Mizutani S. . The Research Front Line of Immune Thrombocytopenia Chronic immune thrombocytopenia as a disease with or without association of defined diseases in children. . 第74回日本血液学会学術集会 2012.10 京都

  75. H. Takada, M. Ishimura, T. Doi, K. Imai, Y. Sasahara, H Kanegane, R. Nishikomori, T. Morio, T. Heike, M. Kobayashi, T. Ariga, S. Tsuchiya, S. Nonoyama, T. Miyawaki, T. Hara. Nation-wide survey of patients with primary immunodeficiency diseases in japan:2008. 15th Biennial Meeting of the European Society of Immunodeficiencies (ESID2012). 2012.10 Florence, Italy.

  76. Mitsuiki N, Oshim K, Imai K, Ohara O, Morio T, Mizutani S.. Genetic Analysis For 207 Cases With Primary Immunodeficiency (PID) Consulted to A Single Center Through PID Network in JAPAN (PIDJ) in 5 Years (2007-2011).. 15th Biennial Meeting of the European Society of Immunodeficiencies (ESID2012). 2012.10 Florence, Italy.

  77. Honma K, Imai K, Kamae C, Ishida H, Ito Y, Kojima S, Yokosuka T, Kanegane H, Morio T, Sasahara Y, Fujiwara T, Harigae H, Hashii Y, Ohara O, Nonoyama S.. Clinical features and immunological abnormalities of GATA2 deficiency in JAPAN. . 15th Biennial Meeting of the European Society of Immunodeficiencies (ESID2012). 2012.10 Florence, Italy.

  78. Kamae C, Nakagawa N, Sato H, Honma K, Mitsuiki N, Ohara O, Kanegane H, Pasic S, Pan-Hammarström Q, MC van Zelm, Morio T, Imai K, Nonoyama S.. Classification of common variable immunodeficiency by quantification of T cell receptor recombination excision circles (TREC) and Ig kappa-deleting recombination excision circles (KREC). . 15th Biennial Meeting of the European Society of Immunodeficiencies (ESID2012). 2012.10 Florence, Italy.

  79. Mitsuiki N, Oshima K, Imai K, Ohara O, Morio T, Mizutani S.. Genetic analysis for 207 cases with primary immunodeficiency (PID) consulted to a single center through PID network in Japan (PIDJ) in 5 years (2007-2011).. 15th Biennial Meeting of the European Society of Immunodeficiencies (ESID2012). 2012.10 Florence, Italy.

  80. Endou A, Ookawa T, Tomizawa D, Imai K, Takagi M, Nagasawa M, Morio T, Mizutani S. . Acute myeloid leukemia with EWSR1 split signal.. 第74回日本血液学会学術集会 2012.10 京都

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