Primary immunodeficiencies: Diagnosis approach in emergent countries;Déficits immunitaires primitifs: Approche diagnostique pour les pays émergents

Immuno-Analyse et Biologie Specialisee

Volumn 25, Issue 5-6, 2010, Pages 257-265

  Admou, B ^a   Haouach, K ^a   Ailal, F ^b   Benhsaine, I ^b   Barbouch, M R ^c   Bejaoui, M ^d   Bousfiha, A A ^b  

^a CADI AYYAD UNIVERSITY   (Morocco)

^b IBN ROCHD UNIVERSITY HOSPITAL   (Morocco)

^c PASTEUR INSTITUTE OF TUNIS   (Tunisia)

^d CENTRE NATIONAL DE GREFFE DE MOELLE OSSEUSE   (Tunisia)

Author keywords

Diagnostic approach; Emergent countries; Primary immunodeficiency

Indexed keywords

CD18 ANTIGEN; COMPLEMENT COMPONENT C3; COMPLEMENT COMPONENT C4; IMMUNOGLOBULIN A; IMMUNOGLOBULIN G; IMMUNOGLOBULIN M;

ACQUIRED IMMUNE DEFICIENCY SYNDROME; ANTIBODY DETECTION; ARTICLE; COMPLEMENT HEMOLYSIS TEST; GENOTYPE; HUMAN IMMUNODEFICIENCY VIRUS INFECTION; IMMUNE DEFICIENCY; LYMPHOCYTE SUBPOPULATION; NITROBLUE TETRAZOLIUM TEST; PHENOTYPE; PRIORITY JOURNAL; PROTEIN ELECTROPHORESIS;

EID: 78149465230     PISSN: 09232532     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.immbio.2010.09.003     Document Type: Article

References (34)

1. Notarangelo L.D., Fische A., Raif Geha S. Primary immunodeficiencies: 2009 update. International Union of Immunological Societies Expert Committee on Primary Immunodeficiencies. J Allergy Clin Immunol 2009, 124:1161-1178. Cochairs.
2. Samarghitean C., Vihinen M. Bioinformatics services related to diagnosis of primary immunodeficiencies [Primary immune deficiency disease: edited by Luigi D. Notarangelo and Thomas Fleisher]. Curr Opinion Allergy Clin Immunol 2009, 9(6):531-536.
3. Mouthon L., Berezné A., Guillevin L., Lassoued K. Diagnostic des déficits immunitaires primitifs à l'âge adulte. Presse Med 2006, 35:903-911.
4. Fieschi C., Malphettes M., Galicier L., Oksenhendler É. Hypogammaglobulinémies primitives découvertes à l'âge adulte. Presse Med 2006, 35:887-894.
5. Bousfiha A.A., Ailal F., Picard C., Fieschi C., Casanova J.L. Epidémiologie et classification des déficits immunitaires primitifs. Rev Mar Mal Enf 2008, 18:5-11.
6. Modell F., Puente D., Modell V. From genotype to phenotype. Further studies measuring the impact of a Physician Education and Public Awareness Campaign on early diagnosis and management of Primary Immunodeficiencies. Immunol Res 2009, 44:132-149.
7. Lee P.P., Lau Y.L. Primary immunodeficiencies: "new" disease in an old country. Cell Mol Immunol 2009, 6(6):397-406.
8. Schmidt R.E. Primary immunodeficiencies. Results of an European public health consensus conference. Bundesgesundheitsblatt Gesundheitsforschung Gesundheitss Chutz 2007, 50(12):1502-1506.
9. Fischer A. Physiopathologie et diagnostic des maladies héréditaires du système immunitaire. Med Ther Pediatr 1999, 2(2):117-124.
10. Le Deist F. Les déficits immunitaires héréditaires: de la physiopathologie au diagnostic. Rev Fr Lab 2000, 327.
11. Gathmann B., Grimbache B., Beauté J., Dudoit Y., Mahlaoui N., Fischer A., et al. The European internet-based patient and research database for primary immunodeficiencies: results 2006-2008. Clin Exp Immunol 2009, 157(Suppl. 1):3-11.
12. Bejaoui M., Barbouche M.R., Sassi A., Larguche B., Miladi N., Bouguerra A., et al. Les déficits immunitaires primitifs en Tunisie: étude de 152 cas. Arch Pediatr 1997, 4:827-831.
13. Bousfiha A.A., Ailal F., Fellah H., Maataoui O., Farouki B., Sekkat S., et al. Évoquer, explorer et diagnostiquer un déficit immunitaire primitif. Rev Mar Mal Enf 2005, 5:64-70.
14. Bussone G, Mouthon L. Déficits immunitaires primitifs de révélation tardive. Presse Med [corrected proof]. doi:10.1016/j.lpm.2009.04.006.
15. Mahlaoui N. Explorations immunitaires chez l'enfant suivi pour infections respiratoires récurrentes. Arch Pediatr 2007, 14:S203-S207.
16. Harry W, Schroeder J. Primary antibody deficiencies. In Clinical Immunology: Principles and Practice, 3rd Edition by Robert R and al. ISBN: 978-0-323-04404-2.
17. Aitouamar H., Chkirate B., Jabourik F., Rouichi A., Bentahila A., Belhadj A.M. Les déficits en protéines du complément en pathologie. Med Maghreb 1999, 78.
18. Dragon-Durey M.A., Fremeaux-Bacchi V. Déficits en protéines du complément en pathologie humaine. Presse Med 2006, 35:861-870.
19. Shearer W.T., Rosenblatt H.M., Gelman R.S., et al. Lymphocyte subsets in healthy children from birth through 18years of age: the Pediatric AIDS Clinical Trials Group P1009 study. J Allergy Clin Immunol 2003, 112:973-980.
20. Picard C. Comment explorer un déficit immunitaire héréditaire ?. Rev Prat 2007, 57:1671-1676.
21. Rebecca H., Buckley Primary immunodeficiency diseases due to defects in lymphocytes. N Engl J Med Adv Immunol 2000, 343(18):1313-1324.
22. Notarangelo L.D., Casanova J.L., Fischer A., Puck J., Rosen F., Seger R., et al. For the International Union of Immunological Societies Primary Immunodeficiency diseases classification committee. Primary immunodeficiency diseases: an update. J Allergy Clin Immunol 2004, 114:677-687.
23. Lefranc MP, Lefranc G. Déficits immunitaires primaires: les mécanismes moléculaires. http://imgt.cines.fr/textes/IMGTeducation/Tutorials/ISpathology/_FR/citer.html.
24. Durandy A., Honjo T. Human genetic defects in class-switch recombination (hyper-IgM syndromes). Curr Opin Immunol 2001, 13:543-548.
25. Erdos M., Durandy A., Marodi L. Genetically-acquired class-switch recombination defects: the multifaced hyper-IgM syndrome. Immunol Lett 2005, 97:1-6.
26. Chapel H., Geha R., Rosen F. Primary immunodeficiency diseases: an update. Clin Exp Immunol 2003, 132:9-15. The IUIS PID Classification Committee.
27. Lawrence T., Puel A., Reichenbach J., Ku C.L., Chapgier A., Renner E., et al. Autosomal-dominant primary immunodeficiencies. Curr Opin Hematol 2005, 12:22-30.
28. Minegishi Y. Hyper-IgE syndrome. Curr Opin Immunol 2009, 21(5):487-492.
29. Chaouki S., Benjelloun Dakhama B.S., Alaoui K., Arqam L., Atman S., Bouharrou A., et al. Ataxie télangiectasie: cas cliniques et revue de la littérature. J Pediatr Pueric 2008, 21:98-101.
30. Stéphan J.L. Le syndrome lymphoprolifératif lié à l'X (syndrome XLP): de la clinique au gène. Arch Pediatr 2000, 7:1205-1211.
31. Lakshman R., Finn A. Neutrophil disorders and their management. J Clin Pathol 2001, 54:7-19.
32. Cunningham-Rundles C., Ponda P.P. Molecular defects in T- and B-cell primary immunodeficiency diseases. Nature Rev Immunol 2005, 5:880-892.
33. Rosenzweig S.D., Holland S.M. Phagocyte immunodeficiencies and their infections. J Allergy Clin Immunol 2004, 113(4):620-626.
34. Drouet C., Ponard D., Monnier N., Lunard J., Bosson L. Classification et diagnostic biologique des angio-œdèmes. Rev Fr Allergol 2008, 48:441-446.