Primary Immunodeficiency Diseases Worldwide: More Common than Generally Thought

被引:211
作者
Bousfiha, Ahmed Aziz [1 ]
Jeddane, Leila [1 ,2 ]
Ailal, Fatima [1 ]
Benhsaien, Ibtihal [1 ]
Mahlaoui, Nizar [3 ]
Casanova, Jean-Laurent [3 ,4 ,5 ,6 ]
Abel, Laurent [4 ,5 ,6 ]
机构
[1] King Hassan II Univ, Averroes Hosp, Clin Immunol Unit, Casablanca, Morocco
[2] King Mohamed V Agdal Univ, Lab Biochem Immunol, Rabat, Morocco
[3] Univ Paris 05, Necker Enfants Malad Hosp, AP HP, Pediat Immunol Hematol Unit, Paris, France
[4] Rockefeller Univ, St Giles Lab Human Genet Infect Dis, Rockefeller Branch, New York, NY 10065 USA
[5] Univ Paris 05, Necker Branch, Lab Human Genet Infect Dis, Paris, France
[6] Necker Med Sch, INSERM, U980, Paris, France
关键词
Primary immunodeficiency; prevalence; incidence; mortality; INBORN-ERRORS; DEFICIENCY; CHILDREN; IMMUNITY; HUMANS; UPDATE;
D O I
10.1007/s10875-012-9751-7
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Purpose Primary immunodeficiency diseases (PIDs) comprise at least 176 hereditary disorders that are thought to be individually and collectively rare. The actual prevalence and incidence of PIDs remains unclear, but recent epidemiologic studies have suggested that PIDs are more common than generally thought. Based on these studies, we attempted to estimate the worldwide prevalence and incidence of PIDs. Methods Using data from registries and two recent epidemiologic surveys estimating the frequencies of PIDs, we extrapolated the frequencies reported for certain countries to the populations of continents and of the world. Results Our upper estimates suggest that six million people may be living with a PID worldwide, whereas only 27,000-60,000 have been identified to date (all national registries and the Jeffrey Modell Centers Network, respectively). For Europe, our upper estimate was 638,000 cases, and 15,052 cases are currently registered (2.27 %). In Africa, up to 902,631 people may have a PID, whereas only 1,016 cases are currently registered. We also found that PIDs were prevalent not only in children, but also in adults, who were strongly underrepresented in registries. Conclusion Specific, dedicated epidemiologic studies are required, to obtain more realistic statistics for PIDs and to increase the awareness of physicians and public health systems about these diseases. Furthermore, the field of PIDs is continually growing, and this is likely to lead to a revision of the definition of these conditions, potentially increasing estimates of their impact on both adults and children, at the population level.
引用
收藏
页码:1 / 7
页数:7
相关论文
共 41 条
[1]   Primary immunodefciency diseases: an update on the classification from the International Union of Immunological Societies Expert Committee for Priary Immunodeficiency [J].
Al-Herz, Waleed ;
Bousfiha, Aziz ;
Casanova, Jean-Laurent ;
Chapel, Helen ;
Conley, Mary Ellen ;
Cunningham-Rundles, Charlotte ;
Etzioni, Amos ;
Fischer, Alain ;
Luis Franco, Jose ;
Geha, Raif S. ;
Hammarstrom, Lennart ;
Nonoyama, Shigeaki ;
Notarangelo, Luigi Daniele ;
Ochs, Hans Dieter ;
Puck, Jennifer M. ;
Roifman, Chaim M. ;
Seger, Reinhard ;
Tang, Mimi L. K. .
FRONTIERS IN IMMUNOLOGY, 2011, 2
[2]   Tuberculosis in children and adults:: two distinct genetic diseases [J].
Alcaïs, A ;
Fieschi, C ;
Abel, L ;
Casanova, JL .
JOURNAL OF EXPERIMENTAL MEDICINE, 2005, 202 (12) :1617-1621
[3]   Life-threatening infectious diseases of childhood: single-gene inborn errors of immunity? [J].
Alcais, Alexandre ;
Quintana-Murci, Lluis ;
Thaler, David S. ;
Schurr, Erwin ;
Abel, Laurent ;
Casanova, Jean-Laurent .
YEAR IN HUMAN AND MEDICAL GENETICS: NEW TRENDS IN MENDELIAN GENETICS, 2010, 1214 :18-33
[4]   Impairment of mycobacterial immunity in human interleukin-12 receptor deficiency [J].
Altare, F ;
Durandy, A ;
Lammas, D ;
Emile, JF ;
Lamhamedi, S ;
Le Deist, F ;
Drysdale, P ;
Jouanguy, E ;
Döffinger, R ;
Bernaudin, F ;
Jeppsson, O ;
Gollob, JA ;
Meinl, E ;
Segal, AW ;
Fischer, A ;
Kumararatne, D ;
Casanova, JL .
SCIENCE, 1998, 280 (5368) :1432-1435
[5]  
[Anonymous], 2011, RAR DIS
[6]  
[Anonymous], 2004, TOT NUMB PAT USIDNET
[7]   Ten warning signs of primary immunodeficiency: a new paradigm is needed for the 21st century [J].
Arkwright, Peter D. ;
Gennery, Andrew R. .
YEAR IN HUMAN AND MEDICAL GENETICS: INBORN ERRORS OF IMMUNITY I, 2011, 1238 :7-14
[8]   Primary immunodeficiencies in highly consanguineous North African populations [J].
Barbouche, Mohamed-Ridha ;
Galal, Nermeen ;
Ben-Mustapha, Imen ;
Jeddane, Leila ;
Mellouli, Fethi ;
Ailal, Fatima ;
Bejaoui, Mohamed ;
Boutros, Jeanette ;
Marsafy, Aisha ;
Bousfiha, Ahmed Aziz .
YEAR IN HUMAN AND MEDICAL GENETICS: INBORN ERRORS OF IMMUNITY I, 2011, 1238 :42-52
[9]   X-linked lymphoproliferative disease (XLP): a model of impaired anti-viral, anti-tumor and humoral immune responses [J].
Bassiri, Hamid ;
Yeo, W. C. Janice ;
Rothman, Jennifer ;
Koretzky, Gary A. ;
Nichols, Kim E. .
IMMUNOLOGIC RESEARCH, 2008, 42 (1-3) :145-159
[10]   The French national registry of primary immunodeficiency diseases [J].
Beaute, Julien ;
Mahlaoui, Nizar ;
Dudoit, Yasmine ;
Micot, Romain ;
Le Mignot, Loic ;
Hilpert, Sophie ;
de Vergnes, Nathalie ;
Obenga, Gaelle ;
Ben Slama, Lilia ;
Gathmann, Benjamin ;
Kindle, Gerhard ;
Boileau, Julien ;
Heinz, Nathatie ;
Korganow, Anne-Sophie ;
Lutz, Patrick ;
Pasquali, Jean-Louis ;
Aladjidi, Nathalie ;
Micheau, Marguerite ;
Perel, Yves ;
Viallard, Jean-Francois ;
Bonnotte, Bernard ;
Briandet, Claire ;
Couillault, Gerard ;
Legrand, Faezeh ;
Rohrlich, Pierre-Simon ;
Decaux, Olivier ;
Gandemer, Virginie ;
Grosbois, Bernard ;
Le Gall, Edouard ;
Lemoine, Philippe ;
Aaron, Laurent ;
Hoarau, Cyrille ;
Lebranchu, Yvon ;
Jaussaud, Rolland ;
Munzer, Martine ;
Marie-Cardine, Aude ;
Vannier, Jean-Pierre ;
Jacquot, Serge ;
Tron, Francois ;
Fieschi, Claire ;
Galicier, Lionel ;
Malphettes, Marion ;
Leverger, Guy ;
Catherinot, Emilie ;
Coignard-Biehler, Helene ;
Lanternier, Fanny ;
Chandesris, Olivia ;
Blanche, Stephane ;
Casanova, Jean-Laurent ;
Debre, Marianne .
CLINICAL IMMUNOLOGY, 2010, 135 (02) :264-272