Human Inborn Errors of Immunity: 2019 Update on the Classification from the International Union of Immunological Societies Expert Committee

被引:273
作者
Tangye, Stuart G. [1 ,2 ]
Al-Herz, Waleed [3 ]
Bousfiha, Aziz [4 ]
Chatila, Talal [5 ]
Cunningham-Rundles, Charlotte [6 ,7 ]
Etzioni, Amos [8 ]
Franco, Jose Luis [9 ]
Holland, Steven M. [10 ]
Klein, Christoph [11 ]
Morio, Tomohiro [12 ]
Ochs, Hans D. [13 ,14 ]
Oksenhendler, Eric [15 ]
Picard, Capucine [16 ,17 ]
Puck, Jennifer [18 ,19 ]
Torgerson, Troy R. [13 ,14 ]
Casanova, Jean-Laurent [20 ,21 ,22 ,23 ]
Sullivan, Kathleen E. [24 ]
机构
[1] Garvan Inst Med Res, Sydney, NSW 2010, Australia
[2] UNSW, Fac Med, St Vincents Clin Sch, Sydney, NSW, Australia
[3] Kuwait Univ, Dept Pediat, Fac Med, Kuwait, Kuwait
[4] King Hassan II Univ, Lab Immunol Clin Inflammat & Allergy LICIA, Fac Med & Pharm,Ibn Rochd Univ Hosp, Clin Immunol Unit,Pediat Infectiouse Dis Dept,Chi, Casablanca, Morocco
[5] Childrens Hosp Boston, Div Immunol, Boston, MA USA
[6] Mt Sinai Sch Med, Dept Med, New York, NY USA
[7] Mt Sinai Sch Med, Dept Pediat, New York, NY USA
[8] Ruths Childrens Hosp Technion, Haifa, Israel
[9] Univ Antioquia UdeA, Fac Med, Grp Inmunodeficiencias Primarias, Medellin, Colombia
[10] NIAID, Lab Clin Immunol & Microbiol, NIH, 9000 Rockville Pike, Bethesda, MD 20892 USA
[11] Ludwig Maximilians Univ Munchen, Dr von Hauner Childrens Hosp, Munich, Germany
[12] TMDU, Dept Pediat & Dev Biol, Tokyo, Japan
[13] Univ Washington, Dept Pediat, Seattle, WA 98195 USA
[14] Seattle Childrens Res Inst, Seattle, WA USA
[15] Univ Paris Diderot, Sorbonne Paris Cite, Dept Clin Immunol, Hop St Louis,APHP, Paris, France
[16] Necker Hosp Sick Children, APHP, Study Ctr Primary Immunodeficiencies, Paris, France
[17] Paris Univ, Lab Lymphocyte Activat & Susceptibil EBV, INSERM UMR1163, Imagine Inst,Necker Hosp Sick Children, Paris, France
[18] Univ Calif San Francisco, Dept Pediat, San Francisco, CA USA
[19] UCSF, Benioff Childrens Hosp, San Francisco, CA USA
[20] Rockefeller Univ, St Giles Lab Human Genet Infect Dis, Rockefeller Branch, 1230 York Ave, New York, NY 10021 USA
[21] Howard Hughes Med Inst, New York, NY USA
[22] Paris Univ, Lab Human Genet Infect Dis, Necker Branch, Imagine Inst,Necker Hosp Sick Children,INSERM UMR, Paris, France
[23] Necker Hosp Sick Children, AP HP, Pediat Hematol Immunol Unit, Paris, France
[24] Univ Penn, Childrens Hosp Philadelphia, Div Allergy Immunol, Dept Pediat,Perelman Sch Med, Philadelphia, PA 19104 USA
关键词
IUIS; primary immune deficiency; inborn errors of immunity; immune dysregulation; autoinflammatory disorders; next-generation sequencing; PRIMARY IMMUNODEFICIENCY; HETEROZYGOUS MUTATIONS; DEFICIENCY; CELLS; SUSCEPTIBILITY; INFECTION; SPECTRUM; UNDERLIE; DEFECTS; DISEASE;
D O I
10.1007/s10875-019-00737-x
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
We report the updated classification of Inborn Errors of Immunity/Primary Immunodeficiencies, compiled by the International Union of Immunological Societies Expert Committee. This report documents the key clinical and laboratory features of 416 inborn errors of immunity, including 64 gene defects that have either been discovered in the past 2 years since the previous update (published January 2018) or were characterized earlier but have since been confirmed or expanded upon in subsequent studies. The application of next-generation sequencing continues to expedite the rapid identification of novel gene defects, rare or common; broaden the immunological and clinical phenotypes of conditions arising from known gene defects and even known variants; and implement gene-specific therapies. These advances are contributing to greater understanding of the molecular, cellular, and immunological mechanisms of disease, thereby enhancing immunological knowledge while improving the management of patients and their families. This report serves as a valuable resource for the molecular diagnosis of individuals with heritable immunological disorders and also for the scientific dissection of cellular and molecular mechanisms underlying inborn errors of immunity and related human diseases.
引用
收藏
页码:24 / 64
页数:41
相关论文
共 105 条
[1]   Loss-of-function variant in DNASE1L3 causes a familial form of systemic lupus erythematosus [J].
Al-Mayouf, Sulaiman M. ;
Sunker, Asma ;
Abdwani, Reem ;
Al Abrawi, Safiya ;
Almurshedi, Fathiya ;
Alhashmi, Nadia ;
Al Sonbul, Abdullah ;
Sewairi, Wafaa ;
Qari, Aliya ;
Abdallah, Eiman ;
Al-Owain, Mohammed ;
Al Motywee, Saleh ;
Al-Rayes, Hanan ;
Hashem, Mais ;
Khalak, Hanif ;
Al-Jebali, Latifa ;
Alkuraya, Fowzan S. .
NATURE GENETICS, 2011, 43 (12) :1186-1188
[2]   RAC2 loss-of-function mutation in 2 siblings with characteristics of common variable immunodeficiency [J].
Alkhairy, Omar K. ;
Rezaei, Nima ;
Graham, Robert R. ;
Abolhassani, Hassan ;
Borte, Stephan ;
Hultenby, Kjell ;
Wu, Chenglin ;
Aghamohammadi, Asghar ;
Williams, David A. ;
Behrens, Timothy W. ;
Hammarstrom, Lennart ;
Pan-Hammarstrom, Qiang .
JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY, 2015, 135 (05) :1380-+
[3]   Immunodeficiency and EBV-induced lymphoproliferation caused by 4-1BB deficiency [J].
Alosaimi, Mohammed F. ;
Hoenig, Manfred ;
Jaber, Faris ;
Platt, Craig D. ;
Jones, Jennifer ;
Wallace, Jacqueline ;
Debatin, Klaus-Michael ;
Schulz, Ansgar ;
Jacobsen, Eva ;
Moller, Peter ;
Shamseldin, Hanan E. ;
Abdulwahab, Ferdous ;
Ibrahim, Niema ;
Alardati, Hosam ;
Almuhizi, Faisal ;
Abosoudah, Ibraheem F. ;
Basha, Talal A. ;
Chou, Janet ;
Alkuraya, Fowzan S. ;
Geha, Raif S. .
JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY, 2019, 144 (02) :574-+
[4]   An essential role for the Zn2+ transporter ZIP7 in B cell development [J].
Anzilotti, Consuelo ;
Swan, David J. ;
Boisson, Bertrand ;
Deobagkar-Lele, Mukta ;
Oliveira, Catarina ;
Chabosseau, Pauline ;
Engelhardt, Karin R. ;
Xu, Xijin ;
Chen, Rui ;
Alvarez, Luis ;
Berlinguer-Palmini, Rolando ;
Bull, Katherine R. ;
Cawthorne, Eleanor ;
Cribbs, Adam P. ;
Crockford, Tanya L. ;
Dang, Tarana Singh ;
Fearn, Amy ;
Fenech, Emma J. ;
de Jong, Sarah J. ;
Lagerholm, B. Christoffer ;
Ma, Cindy S. ;
Sims, David ;
van den Berg, Bert ;
Xu, Yaobo ;
Cant, Andrew J. ;
Kleiner, Gary ;
Leahy, T. Ronan ;
de la Morena, M. Teresa ;
Puck, Jennifer M. ;
Shapiro, Ralph S. ;
van der Burg, Mirjam ;
Chapman, J. Ross ;
Christianson, John C. ;
Davies, Benjamin ;
McGrath, John A. ;
Przyborski, Stefan ;
Koref, Mauro Santibanez ;
Tangye, Stuart G. ;
Werner, Andreas ;
Rutter, Guy A. ;
Padilla-Parra, Sergi ;
Casanova, Jean-Laurent ;
Cornall, Richard J. ;
Conley, Mary Ellen ;
Hambleton, Sophie .
NATURE IMMUNOLOGY, 2019, 20 (03) :350-+
[5]   A homozygous loss-of-function mutation leading to CYBC1 deficiency causes chronic granulomatous disease [J].
Arnadottir, Gudny A. ;
Norddahl, Gudmundur L. ;
Gudmundsdottir, Steinunn ;
Agustsdottir, Arna B. ;
Sigurdsson, Snaevar ;
Jensson, Brynjar O. ;
Bjarnadottir, Kristbjorg ;
Theodors, Fannar ;
Benonisdottir, Stefania ;
Ivarsdottir, Erna V. ;
Oddsson, Asmundur ;
Kristjansson, Ragnar P. ;
Sulem, Gerald ;
Alexandersson, Kristjan F. ;
Juliusdottir, Thorhildur ;
Gudmundsson, Kjartan R. ;
Saemundsdottir, Jona ;
Jonasdottir, Adalbjorg ;
Jonasdottir, Aslaug ;
Sigurdsson, Asgeir ;
Manzanillo, Paolo ;
Gudjonsson, Sigurjon A. ;
Thorisson, Gudmundur A. ;
Magnusson, Olafur Th. ;
Masson, Gisli ;
Orvar, Kjartan B. ;
Holm, Hilma ;
Bjornsson, Sigurdur ;
Arngrimsson, Reynir ;
Gudbjartsson, Daniel F. ;
Thorsteinsdottir, Unnur ;
Jonsdottir, Ingileif ;
Haraldsson, Asgeir ;
Sulem, Patrick ;
Stefansson, Kari .
NATURE COMMUNICATIONS, 2018, 9
[6]   Human RELA haploinsufficiency results in autosomal-dominant chronic mucocutaneous ulceration [J].
Badran, Yousef R. ;
Dedeoglu, Fatma ;
Castillo, Juan Manuel Leyva ;
Bainter, Wayne ;
Ohsumi, Toshiro K. ;
Bousvaros, Athos ;
Goldsmith, Jeffrey D. ;
Geha, Raif S. ;
Chou, Janet .
JOURNAL OF EXPERIMENTAL MEDICINE, 2017, 214 (07) :1937-1947
[7]   Combined immunodeficiency in a patient with c-Rel deficiency [J].
Beaussant-Cohen, Sarah ;
Jaber, Faris ;
Massaad, Michel J. ;
Weeks, Sabrina ;
Jones, Jennifer ;
Alosaimi, Mohammed F. ;
Wallace, Jacqueline ;
Al-Herz, Waleed ;
Geha, Raif S. ;
Chou, Janet .
JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY, 2019, 144 (02) :606-+
[8]   Inherited IL-18BP deficiency in human fulminant viral hepatitis [J].
Belkaya, Serkan ;
Michailidis, Eleftherios ;
Korol, Cecilia B. ;
Kabbani, Mohammad ;
Cobat, Aurelie ;
Bastard, Paul ;
Lee, Yoon Seung ;
Hernandez, Nicholas ;
Drutman, Scott ;
de Jong, Ype P. ;
Vivier, Eric ;
Bruneau, Julie ;
Beziat, Vivien ;
Boisson, Bertrand ;
Lorenzo-Diaz, Lazaro ;
Boucherit, Soraya ;
Sebagh, Mylene ;
Jacquemin, Emmanuel ;
Emile, Jean-Francois ;
Abel, Laurent ;
Rice, Charles M. ;
Jouanguy, Emmanuelle ;
Casanova, Jean-Laurent .
JOURNAL OF EXPERIMENTAL MEDICINE, 2019, 216 (08) :1777-1790
[9]   Mutations in the SRP54 gene cause severe congenital neutropenia as well as Shwachman-Diamond-like syndrome [J].
Bellanne-Chantelot, Christine ;
Schmaltz-Panneau, Barbara ;
Marty, Caroline ;
Fenneteau, Odile ;
Callebaut, Isabelle ;
Clauin, Severine ;
Docet, Aurelie ;
Damaj, Gandhi-Laurent ;
Leblanc, Thierry ;
Pellier, Isabelle ;
Stoven, Cecile ;
Souquere, Sylvie ;
Antony-Debre, Ileana ;
Beaupain, Blandine ;
Aladjidi, Nathalie ;
Barlogis, Vincent ;
Bauduer, Frederic ;
Bensaid, Philippe ;
Boespflug-Tanguy, Odile ;
Berger, Claire ;
Bertrand, Yves ;
Carausu, Liana ;
Fieschi, Claire ;
Galambrun, Claire ;
Schmidt, Aline ;
Journel, Hubert ;
Mazingue, Francoise ;
Nelken, Brigitte ;
Thuan Chong Quah ;
Oksenhendler, Eric ;
Ouachee, Marie ;
Pasquet, Marlene ;
Saada, Veronique ;
Suarez, Felipe ;
Pierron, Gerard ;
Vainchenker, William ;
Plo, Isabelle ;
Donadieu, Jean .
BLOOD, 2018, 132 (12) :1318-1331
[10]   Homozygous transcription factor 3 gene (TCF3) mutation is associated with severe hypogammaglobulinemia and B-cell acute lympho blastic leukemia [J].
Ben-Ali, Meriem ;
Yang, Jing ;
Chan, Koon Wing ;
Ben-Mustapha, Imen ;
Mekki, Najla ;
Benabdesselem, Chaouki ;
Mellouli, Fethi ;
Bejaoui, Mohamed ;
Yang, Wanling ;
Aissaoui, Lamia ;
Lau, Yu Lung ;
Barbouche, Mohamed-Ridha .
JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY, 2017, 140 (04) :1191-+