The Four Most Common Pediatric Immunodeficiencies

REFERENCES

• Al-Attas R. A., Rahi A. H. Primary antibody deficiency in Arabs: First report from eastern Saudi Arabia. J. Clin. Immunol. 1998; 18: 368–371
   PubMed Web of Science ®Google Scholar
• Ambrosino D. M., Siber G. R., Chilmonczyk B. A., Jernberg J. B., Finberg R. W. An immunodeficiency characterized by impaired antibody responses to polysaccharides. New Engl. J. Med. 1987; 316: 790–792
   PubMed Web of Science ®Google Scholar
• Blecher T. E., Soothill J. F., Voyce M. A., Walker W. H. Antibody deficiency syndrome: A case with normal immunoglobulin levels. Clin. Exp. Immunol. 1968; 3: 47–56
   PubMedGoogle Scholar
• Blum P. M., Stiehm E. R., Hong R. Spontaneous recovery of selective IgA deficiency: Additional case report and review. Clin. Pediatr. 1982; 21: 77–80
   PubMed Web of Science ®Google Scholar
• Buckley R. H. Immunoglobulin G subclass deficiency: Fact or fancy?. Curr. Allergy Asthma Rep. 2002; 2: 356–360
   PubMedGoogle Scholar
• Castigli E., Wilson S. A., Garibyan L., Rachid R., Bonilla F., Schneider L., Geha R. S. TACI is mutant in common variable immunodeficiency and IgA deficiency. Nat. Genet. 2005; 37: 829–834
   PubMed Web of Science ®Google Scholar
• Cunningham-Rundles C. Selective IgA deficiency. Immunologic Disorders in Infants and Children, Edition 5, E. R. Stiehm, H. D. Ochs, J. A. Winkelstein. Elsevier, Philadelphia 2004; 427–446
   Google Scholar
• Dalal I., Roifman C. H. Transient hypogammaglobulinemia of infancy. 2006; 1–10, www.uptodate.com UpToDate
   Google Scholar
• Dalal I., Reid B., Nisbet-Brown E., Roifman C. M. The outcome of patients with hypogammaglobulinemia in infancy and early childhood. J. Pediatr. 1998; 133: 144–146
   PubMedGoogle Scholar
• Fudenberg H. H., Fudenberg B. R. Antibody to hereditary human gammaglobulin (Gm) factor resulting from maternal-fetal incompatibility. Science 1964; 145: 170–171
   PubMed Web of Science ®Google Scholar
• Gitlin D., Janeway C. A. Agammaglobulinemia: Congenital, acquired, and transient forms. Prog. Hematol. 1956; 1: 318–329
   PubMedGoogle Scholar
• Goldblum R. M., Garofalo R. P. The mucosal defense system. Immunologic Disorders in Infants and Children, Edition 5, E. R. Stiehm, H. D. Ochs, J. A. Winkelstein. Elsevier, Philadelphia 2004; 205–244
   Google Scholar
• Granoff D. M., Shackelford P. G., Pandey J. P., Boies E. G. Antibody responses to Haemophilus influenzae type b polysaccharide vaccine in relation to Km(1) and G2m(23) immunoglobulin alloytpes. J. Infect. Dis. 1986a; 154: 257–264
   PubMedGoogle Scholar
• Granoff D. M., Shackelford P. G., Suarez B. K., Nahm M. H., Cates K. L., Murphy T. V., Karasic R., Osterholm M. T., Paudey J. P., Daum M. D., The Collaborative Group. Hemophilus influenzae type B disease in children vaccinated with type B polysaccharide vaccine. New Engl. J. Med. 1986b; 315: 1584–1590
   PubMed Web of Science ®Google Scholar
• Herrod H. G. Management of the patient with IgG subclass deficiency and/or selective antibody deficiency. Ann. Allergy 1993; 70: 3–7
   PubMedGoogle Scholar
• Hostoffer R. IgA deficiency. 2006; 1–14, www.uptodate.com UpToDate 2006
   Google Scholar
• Immune Deficiency Foundation. Primary immune deficiency diseases in America: The first national survey of patients and specialists. Immune Deficiency Newsletter. Towson, MD 1999
   Google Scholar
• Jeffrey Modell Foundation. Survey results for primary immunodeficiency Global Reports. Jeffrey Modell Foundation, New York 2005
   Google Scholar
• Kalfa V., Roberts R. L., Stiehm E. R. The syndrome of chronic mucocutaneous candidiasis with selective antibody deficiency. Ann. Allergy Asthma Immunol. 2003; 90: 259–264
   PubMed Web of Science ®Google Scholar
• Kanoh T., Mizumoto T., Yasuda N., Koya M., Ohno Y., Uchino H., Yoshimura K., Ohkubo Y., Yamaguchi H. Selective IgA deficiency in Japanese blood donors: Frequency and statistical analysis. Vox Sang. 1986; 50: 81–86
   PubMed Web of Science ®Google Scholar
• Kavanaugh A. F., Huston D. P. Immunoglobulin G subclass deficiency. Insights in Allergy 1989; 4: 1–7
   Google Scholar
• Koistinen J. Familial clustering of selective IgA deficiency. Vox Sang. 1976; 30: 181–190
   PubMed Web of Science ®Google Scholar
• Kowalczyk D., Mytar B., Zembala M. Cytokine production in transient hypo-gammaglobulinemia and isolated IgA deficiency. J. Allergy Clin. Immunol. 1997; 100: 556–562
   PubMedGoogle Scholar
• Lakhanpal S., O'Duffy J. D., Homburg H. A., Moore S. B. Evidence for linkage of IgA deficiency with the major histocompatibility complex. Mayo Clin. Proc. 1988; 63: 461–465
   PubMedGoogle Scholar
• Lefranc G., Chaabani H., Loghem E. V., Lefranc M. P., De Lange G., Helal A. N. Simultaneous absence of the human IgG1, IgG2, IgG4, and IgA1 subclasses: Immunological and immunogenetical considerations. Eur. J. Immunol. 1983; 13: 240–244
   PubMed Web of Science ®Google Scholar
• Lemmon J. K., Knutsen A. P. Clinical manifestations, diagnosis and treatment of IgG subclass deficiency. 2006; 1–14, www.uptodate.com UpToDate
   Google Scholar
• Migone N., Oliviero S., Lange G. E., Delacroix D. L., Boschis D., Altruda F., Silengo L., DeMarchi M., Carbonara A. O. Multiple gene deletions within the human immunoglobulin heavy-chain cluster. Proc. Natl. Acad. Sci. USA 1984; 81: 5811–5815
   PubMed Web of Science ®Google Scholar
• Nathenson G., Schorr J. B., Litwin S. D. Gm factor feto-maternal gamma globulin incompatibility. Pediatr. Res. 1971; 5: 2–9
   Google Scholar
• Oxelius V. A., Laurell A. B., Linquist B., Golebiowska H., Axelsson U., Bjorkander J., Hanson L. A. IgA subclasses in selective IgA deficiency. New Engl. J. Med. 1981; 304: 1476–1477
   PubMed Web of Science ®Google Scholar
• Rockey J. H., Hanson L. A., Heremans J. F., Kunkel H. G. β 2A-Agamma-globulinemia in two healthy men. J. Lab. Clin. Med. 1964; 63: 205–212
   PubMed Web of Science ®Google Scholar
• Roifman C. M. Immunodeficiency Disorders: General Considerations. Immunologic Disorders in Infants and Children, Edition 5, E. R. Stiehm, H. D. Ochs, J. A. Winkelstein. Elsevier, Philadelphia 2004; 391–393
   Google Scholar
• Saxon A., Kobayashi R. H., Stevens R. H., Singer A. D., Stiehm E. R., Siegel S. C. In vitro analysis of humoral immunity in antibody deficiency with normal immunoglobulins. Clin. Immunol. Immunopath. 1980; 17: 235–244
   PubMedGoogle Scholar
• Schur P. H., Borel H., Gelfand E. W., Alper C. A., Rosen F. S. Selective gamma-G globulin deficiencies in patients with recurrent pyogenic infections. New Engl. J. Med. 1970; 283: 631–634
   PubMed Web of Science ®Google Scholar
• Siegel R. L., Issekutz T., Schwaber J., Rosen F. S., Geha R. S. Deficiency of T-helper cells in transient hypogammaglobulinemia of infancy. New Engl. J. Med. 1981; 3005: 1307–1313
   Google Scholar
• Soothill J. F. Immunoglobulins in first-degree relatives of patients with hypogamma-globulinaemia. Transient hypogammaglobulinaemia: A possible manifestation of heterozygocity. Lancet 1968; 1: 1001–1003
   PubMedGoogle Scholar
• Sorensen R. U., Paris K. Selective antibody deficiency with normal immunoglobulins (polysaccharide non-responses). 2006; 1–10, www.uptodate.com UpToDate
   Google Scholar
• Stiehm E. R. The B-Lymphocyte System: Clinical Immunology. Immunologic Disorders in Infants and Children, Edition 5, E. R. Stiehm, H. D. Ochs, J. A. Winkelstein. Elsevier, Philadelphia 2004; 85–108
   Google Scholar
• Stiehm E. R., Ochs H. D., Winkelstein J. A. Immunodeficiency Disorders: General Considerations. Immunologic Disorders in Infants and Children, Edition 5, E. R. Stiehm, H. D. Ochs, J. A. Winkelstein. Elsevier, Philadelphia 2004a; 289–355
   Google Scholar
• Stiehm E. R., Ochs H. D., Winkelstein J. A. Impaired polysacchride responsiveness (selective antibody deficiency). Immunologic Disorders in Infants and Children, Edition 5, E. R. Stiehm, H. D. Ochs, J. A. Winkelstein. Elsevier, Philadelphia 2004b; 398–401
   Google Scholar
• Stiehm E. R., Ochs H. D., Winkelstein J. A. IgG subclass deficiencies. Immunologic Disorders in Infants and Children, Edition 5, E. R. Stiehm, H. D. Ochs, J. A. Winkelstein. Elsevier, Philadelphia 2004c; 393–398
   Google Scholar
• Thieffrey S., Arthuis M., Aicardi J., Lyon G. L'ataxie-telangiectasie (7 observations personnelles). Rev Neurol (Paris) 1961; 105: 390–405
   PubMedGoogle Scholar
• Timens W., Poppema S. Impaired immune response to polysaccharides. New Engl. J. Med. 1987; 317: 837–838
   PubMedGoogle Scholar
• West C. D., Hong R., Holland N. H. Immunoglobulin levels from the newborn period to adulthood and in immunoglobulin deficiency states. J. Clin. Invest. 1962; 41: 2054–2064
   PubMed Web of Science ®Google Scholar
• Whelan M. A., Hwan W. H., Beausoleil J., Hauck W. W., McGeady S. J. Infants presenting with recurrent infections and low immunoglobulins: Characteristics and analysis of normalization. J. Clin. Immunol. 2006; 26: 7–11
   PubMedGoogle Scholar
• Wood P., Mayne A., Joyce H., Smith C. L., Granoff D. M., Kumararatne D. S. A mutation in Bruton's tyrosine kinase as a cause of selective anti-polysaccharide antibody deficiency. J. Pediatr. 2001; 139: 148–151
   PubMedGoogle Scholar