Iob's syndrome (Iper-IgE) and Ipo-IgA. A case of associated immunodeficiences;Sindrome di Giobbe (Iper-IgE) ed Ipo-IgA. Rara associazione di immunodeficienze

Recenti Progressi in Medicina

Volumn 87, Issue 2, 1996, Pages 71-74

  Mazzone, Antonino ^a   Girola, Stefano ^a   Fossati, Gianluca ^a   Mazzucchelli, Iolanda ^a   Ricevuti, Giovanni ^a  

^a FONDAZIONE IRCCS POLICLINICO SAN MATTEO   (Italy)

Author keywords

IgA deficiency; Job's syndrome

Indexed keywords

IMMUNOGLOBULIN A; IMMUNOGLOBULIN E;

ADULT; BLOOD; CASE REPORT; CD8+ T LYMPHOCYTE; CELLULAR IMMUNITY; CHRONIC GRANULOMATOUS DISEASE; FEMALE; HUMAN; IMMUNOGLOBULIN A DEFICIENCY; IMMUNOLOGY; REVIEW;

ADULT; CD8-POSITIVE T-LYMPHOCYTES; FEMALE; HUMANS; IGA DEFICIENCY; IMMUNITY, CELLULAR; IMMUNOGLOBULIN A; IMMUNOGLOBULIN E; JOB'S SYNDROME;

EID: 0030078566     PISSN: 00341193     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (20)

1. Leung DYM, Geha RS. Clinical and immunological aspects of hyperimmunoglobulin E syndrome. Hematol Oncol North Am 1988; 2: 81-101.
2. Hill HR, Quie PG. Raised serum IgE levels and defective neutrophil chemotaxis in three children with eczema and recurrent bacterial infections. Lancet 1974; 1: 183-97.
3. Schopfer K, Baerlocher K, Proce P, Krech U, Quie PG, Douglas SD. Staphylococcal IgE antibodies, hyperimmunoglobulinemia E and Staphylococcus Aureus infections. N Engl J Med 1979; 300: 835-8.
4. Hill HR, Estensen RD, Hogan NA, Quie PG. Severe staphylococcal disease associated with allergic manifestations, hyperimmunoglobulinemia E and defective neutrophil chemotaxis. J Lab Clin Med 1976; 88: 796-806.
5. Buckley RH, Wray BB, Belmaker EZ. Extreme hyperimmunoglobulinemia E and undue susceptibility to infections. Pedriatrics 1972; 49: 59-70.
6. Stella M, Bulengo-Ransby SM, Headington JT, Cantu-Gonzales G, Rasmussen JE. Staphylococcal botryomycosis and hyperimmunoglobulin E (Job's) syndrome in an infant. J Am Ace of Dermatology 1993; 28: 109-11.
7. Clark RA, Root RK, Kimball HR, and Kirkpatrick CH. Defective recurrent infections. Ann Intern Med 1973; 78: 515-9.
8. 2 receptor blochade. Clin Immunol Immunopathol 1980; 17: 483-91.
9. Gallin JI. Disorders of phagocyte chemotaxis. Ann Intern Med 1980; 92: 520-38.
10. Conley ME, Coope MD. Immature IgA B cells in IgA-deficiency patients. N Engl J Med 1981; 305: 495-7.
11. Bachmann R. Studies on the serum gamma A-globulin level III. The frequency of A agammaglobulinemia. Scand J Clin Lab Invest 1965; 17: 316-20.
12. Ashmann RF, Saxon A, Stevens RH. Profile of multiple lymphocyte functional defects in acquired hypogammaglobulinemia derived from in vitro cell recombination analysis. J Allergy Clin Immunol 1980; 65: 242-56.
13. Waldmann TA, Durm M, Broder S, Blackman M, Blaese RM, Strober W. Role of suppressor T cells in pathogenesis of common variable hypogammaglobulinemia. Lancet 1974; 2: 609-13.
14. Sneller MC, Strober W. Abnormalities of lymphokine gene expression in patients with common variable immunodeficiency. J Immunol 1990; 144: 3762-9.
15. Roth J, Parker LT, Esterly N. The hyperimmunoglobulin E syndrome. Pediatric Dermatology 1992; 9: 4-24.
16. Jeppson J, Jaffet Hill HR. Use of recombinant human interferon gamma to enhance neutrophil chemotactic response in Job syndrome of hyperimmunoglobulin E and recurrent infections. J Pediatric 1991; 118: 383-5.
17. Raif Geha S, Reinherz E, Leung D, et al. Deficiency of suppressor T cells in the hyperimmunoglobulin E syndrome. J Clin Invest 1981; 68: 783-91.
18. Romagnani S, Del Prete GF, Maggi E, et al. In vitro production of IgE by peripheral blood mononuclears. Clin Exp Immunol 1980; 42: 579-88.
19. Donabedian H, Gallin J. Mononuclear cells from patients with the hyperimmunoglobulin E-recurrent infection syndrome produce an inhibitor of leukocyte chemotaxis. J Clin Invest 1982; 69: 1155-63.
20. Delespesse G, Gausset P, Cauchie C, Goaverts A. Cellular aspects of selective IgA deficiency. Clin Exp Immunol 1976; 24: 273-8.