TAKAKI ASANO
Last Updated :2024/10/02
- Affiliations, Positions
- Research Institute for Radiation Biology and Medicine, Associate Professor
- E-mail
- tasano02hiroshima-u.ac.jp
Basic Information
Major Professional Backgrounds
- 2023/04/01, Hiroshima university, Associate professor
- 2022/04/01, 2023/03/31, Hiroshima University, Hospital, Assistant professor
- 2019/10/01, 2022/03/31, The Rockefeller University, St. Giles Laboratory of Human Genetics of Infectious Diseases, Postdoctral Associate
- 2019/01/04, 2019/09/30, Funairi Citizens Hospital, Assistant director
- 2018/11/01, 2018/12, Onomichi general hospital, Assistant director
- 2018/06/01, 2018/10/31, Hiroshima University, Hospital, Clinical fellow
- 2015/04/01, 2018/05/31, Hiroshima University, Hospital, Clinical staff
- 2014/04/01, 2015/03/31, Hiroshima Nishi Medical Center, Clinical fellow
- 2011/04/01, 2013/03/31, Hiroshima University, Hospital, Clinical fellow
- 2009/04/01, 2011/03/31, Funairi Hospital, Clinical fellow
- 2008/04/01, 2009/03/31, TOYOTA memorial hospital, Clinical fellow
- 2006/04/01, 2008/03/31, TOYOTA memorial hospital, Clinical Resident
Educational Backgrounds
- Hiroshima University, 2013/04, 2018/05
- Hiroshima university, 2000/04, 2006/03
Academic Degrees
Research Fields
- Medicine,dentistry, and pharmacy;Clinical internal medicine;Pediatrics
Research Keywords
- Inborn errors of immunity
- COVID-19
- Hyper IgE syndrome
- Mendelian susceptibility to mycobacterial disease
- Chronic mucocutaneous candidiasis
- Combined immunodeficiencies
- Isolated congenital asplenia
Affiliated Academic Societies
- European Society for Immunodeficiencies (ESID)
- Asia Pacific Society for Immunodeficiencies
- Japan Pediatric Society
- Japanese Society for Immunodeficiency and Autoinflammatory Diseases
- The Japan Society of Human Genetics
- The japanese Society of Clinical Immunology
- Japanese College of Rheumatology
- Japanese Society of Pediatric Infectious Diseases
- Japanese Society of hematology
- Japanese Society for Immunology
- The Japan Society of Pediatric Genetics
Educational Activity
Course in Charge
- 2024, Undergraduate Education, 2Term, Pediatrics
- 2024, Undergraduate Education, 2Term, Pediatrics
Research Activities
Academic Papers
- Higher COVID-19 pneumonia risk associated with anti-IFN-alpha than with anti-IFN-omega auto-Abs in children, J. Exp. Med, 221(2), 202402
- Isolated Chronic Mucocutaneous Candidiasis due to a Novel Duplication Variant of IL17RC, J. Clin. Immunol, 44(18), 2024
- ★, Human STAT1 gain of function with chronic mucocutaneous candidiasis: A comprehensive review for strengthening the connection between bedside observations and laboratory research, Immunological reviews, 1-17, 202311
- Fatal COVID-19 infection in two children with STAT1 gain-of-function, J. Clin. Immunol, 44(20), 2024
- A complementary approach for genetic diagnosis of inborn errors of immunity using proteogenomic analysis, PNAS NEXUS, 2(4), 20230403
- Human RELA dominant-negative mutations underlie type I interferonopathy with autoinflammation and autoimmunity, JOURNAL OF EXPERIMENTAL MEDICINE, 220(9), 20230605
- Human PIK3R1 mutations disrupt lymphocyte differentiation to cause activated PI3K delta syndrome 2, JOURNAL OF EXPERIMENTAL MEDICINE, 220(6), 20230321
- Human genetic and immunological determinants of critical COVID-19 pneumonia, NATURE, 603(7902), 587-598, 20220324
- Human RELA dominant-negative mutations underlie type I interferonopathy with autoinflammation and autoimmunity, J Exp Med, 220(9), e20212276, 20230605
- ★, Inborn errors of immunity with loss- and gain-of-function germline mutations in STAT1, CLINICAL AND EXPERIMENTAL IMMUNOLOGY, 212(2), 96-106, 20230425
- ★, Inborn errors of immunity with loss- and gain-of-function germline mutations in STAT1, Clinical and Experimental Immunology,, 222(2), 96-106, 202304
- Rare predicted loss-of-function variants of type I IFN immunity genes are associated with life-threatening COVID-19, Genome Med, 15(22), 202304
- Proteomic analysis is complementary to targeted RNA sequencing and improves diagnostic yield in Inborn Errors of Immunity, PNAS Nexus, 2(4), 202303
- Novel NF-kappa B Inhibitor Alpha Gain of Function Variant in an Infant with Lymphocytosis and Recurrent Serratia Bacteremia., J Clin Immunol, 202304
- Human PIK3R1 mutations disrupt lymphocyte differentiation to cause activated PI3K- delta syndrome 2, J Exp Med, 220(6), e20221020, 202303
- Recessive inborn errors of type I IFN immunity in children with COVID-19 pneumonia, J Exp Med, 219(8), e20220131, 20220616
- Isolated congenital asplenia: An overlooked cause of thrombocytosis. American Journal of Hematology, Am J Hematol, 20220309
- Human genetic and immunological determinants of critical COVID-19 pneumonia., Nature, 603(7902), 587-598, 20220128
- X-linked TLR7 deficiency underlies critical COVID-19 pneumonia in a male patient with ataxia-telangiectasia, J. Clin. Immunol, 42(1), 1-9, 20211023
- ★, X-linked recessive TLR7 deficiency in ~1% of men under 60 years old with life-threatening COVID-19, Sci. Immunol, 6(11), eabl14348, 20210820
- Biochemically deleterious human NFKB1 variants underlie an autosomal dominant form of common variable immunodeficiency, J Exp Med, 218(11), e20210566, 20210816
- Association of rare predicted loss-of-function variants of influenza-related type I IFN genes with critical COVID-19 pneumonia, J Clin Invest, 131(15), e152474, 20210802
- ★, Human STAT3 variants underlie autosomal dominant hyper-IgE syndrome by negative dominance, J Exp Med, 218(8), e20202592, 20210518
- Inherited CARD9 deficiency in a child with invasive disease due to Exophiala dermatitidis and two older but asymptomatic siblings, J. Clin. Immunol, 41, 975-986, 20210208
- ★, Human STAT1 Gain-of-function heterozygous mutations: Chronic Mucocutaneous Candidiasis and type I interferonopathy, J. Clin. Immunol, 40, 1065-1080, 20200827
- Human gain-of-function STAT1 mutation disturbs IL-17 immunity in mice, Int. Immunol, 32(4), 259-272, 20191223
- Gain–of-function IKBKB mutation causes human combined immune deficiency, J Exp Med., 215(11), 2715-2724, 20180924
- ★, Enhanced AKT phosphorylation of circulating B cells in patients with activated PI3K delta syndrome, Front Immunol., 9(568), 20180405
- Genetic, immunological, and clinical features of patients with bacterial and fungal infections due to inherited IL-17RA deficiency, Proc Natl Acad Sci U S A., 113(15), E8277-E8285, 20161207
- Phosphatase and tensin homolog (PTEN) mutation can cause activated phosphatidylinositol 3-kinase delta syndrome-like immunodeficiency, J Allergy Clin Immunol., 138(6), 1672-1680, 20160714
- Clinical and immune phenotype associated with activated phosphorinositide 3 kinase delta syndrome 2: A cohort study, J Allergy Clin Immunol., 138(1), 210-218, 20160421
- Effective treatment of childhood blastic plasmacytoid dendritic cell neoplasm with a cutaneous tumor alone by stem cell transplantation with reduced intensity, Indian J Hematol Blood Transfus., 26-31, 20150421
Publications such as books
- 2022/05/25, Clinical Immunology & Allergology, 2022, 05, Single work, 日本語, Takaki Asano, 560-567
Invited Lecture, Oral Presentation, Poster Presentation
- How to find PIDs (Primary Immunodeficiencies), Takaki Asano, 4th ASIA-PACIFIC SOCIETY FOR IMMUNODEFICIENCIES CONGRESS, 2022/04/01, With Invitation, English, Malaysia
- Human STAT3 variants underlie autosomal dominant hyper IgE syndrome by negative dominance., Takaki Asano, Bertrand Boisson, Jean-Laurent Casanova, 2021 NYC Primary Immunodeficiency – Inborn Errors of Immunity Symposium, 2021/01/13, Without Invitation, English, NYC PID meeting, New York
- Anti-N-methyl-D-aspartate receptor encephalitis associated with IRAK-4 deficiency, Takaki Asano, IAPIDS Advanced PID school 2020, 2020/01/30, Without Invitation, English, International Alliance of Primary Immunodeficiency Societies, Portugal
- Anti-N-methyl-D-aspartate receptor encephalitis associated with IRAK-4 deficiency, Takaki Asano, Shiho Nishimura, Yoshiyuki Kobayashi, Miyuki Tsumura, Nobutsune Ishikawa, Hidenori Ohnishi, Hidetoshi Takada, Vanessa Snacho-Shimizu, Kunihiko Moriya, Anne Puel, Capucine Picard, Sarosh R Irani, Jean-Laurent Casanova, Satoshi Okada, Masao Kobayashi, 18th Biennial Meeting of the European Society for immunodeficiencies (ESID 2018), 2018/10/24, Without Invitation, English, Portugal
- Hematopoietic stem cell transplantation for patients with gain of function in STAT1 mutation, Takaki Asano, Satoshi Okada, Jennifer W. Leiding, Troy R. Thorgerson, Tomohiro Morio, Masao Kobayashi, 2017/10/20, Without Invitation, Japanese, Tokyo
- Flow cytometry based simple diagnosis of activated PI3Kdelta syndrome by evaluating pAKT in circulating B cells., Takaki Asano, Miyuki Tsumura, Satoshi Okada, Masao Kobayashi, 17th Biennial Meeting of the European Society for immunodeficiencies (ESID 2016), 2016/09/21, Without Invitation, English, Spain
- Excessive phosphorylation of AKT in CD19-positive B cells in patients with Activated PI3Kdelta syndrome, 2016/05/13, Without Invitation, Japanese
- Gastric cancer in a patient with primary immune deficiency, Takaki Asano, Asia Pacific Society for Immunodeficiencies (APSID 2016), 2016/05/01, Without Invitation, English, Hong Kong
- The detection of excess AKT phosphorylation by flow cytometry in patients with activated PI3Kdelta syndrome, Takaki Asano, Miyuki Tsumura, Satoshi Okada, Masao Kobayashi, 2015/11/18, Without Invitation, Japanese, Sapporo
- Successful HSCT with non-irradiation conditioning regimen with 3 infant cases of FHL, Takaki Asano, Yasuhiko Sera, Maiko Shimomura, Aya Furue, Ikue Chijimatsu, Mizuka Miki, Hiroshi Kawaguchi, Kazuhiro Nakamura, Masao Kobayashi, 2012/10/19, Without Invitation, Japanese, Kyoto
Awards
- 2016/09/23, ESID2016 Best E-poster award, The European Society for Immunodeficiencies (ESID), Flow cytometry based simple diagnosis of activated PI3Kdelta syndrome by evaluating pAKT in circulating B cells