The hyper-IgE syndromes.

The hyper IgE syndromes (HIES) are rare primary immune deficiencies characterized by elevated serum IgE, rash, and recurrent bacterial infections of the skin and lung. Autosomal dominant HIES, the most common disease in this group, results from STAT3 mutations and has a variety of connective tissue and skeletal abnormalities. The genetic etiologies of the more rare autosomal recessive forms still need delineation. Treatment of these syndromes has relied on prophylactic and therapeutic antimicrobial agents and aggressive skin care. The new and evolving genetic and immunologic understandings of this previously elusive set of diseases should lead to more effective disease-specific therapies.

[1]  M. Alakavuklar,et al.  The Development of Pulmonary Adenocarcinoma in a Patient with Job's Syndrome, A Rare Immunodeficiency Condition , 2004, Tumori.

[2]  S. Holland,et al.  Delayed eruption of permanent teeth in hyperimmunoglobulinemia E recurrent infection syndrome. , 2000, Oral surgery, oral medicine, oral pathology, oral radiology, and endodontics.

[3]  R. Thompson,et al.  HYPER-IgE SYNDROME AND H2-RECEPTOR BLOCKADE , 1989, The Lancet.

[4]  R. Buckley,et al.  Extreme hyperimmunoglobulinemia E and undue susceptibility to infection. , 1972, Pediatrics.

[5]  H. Kimata High-dose intravenous gamma-globulin treatment for hyperimmunoglobulinemia E syndrome. , 1995, The Journal of allergy and clinical immunology.

[6]  C. Griscelli,et al.  Cytokine-mediated bone resorption in patients with the hyperimmunoglobulin E syndrome. , 1995, Clinical immunology and immunopathology.

[7]  E. Fikrig,et al.  STAT3 deletion during hematopoiesis causes Crohn's disease-like pathogenesis and lethality: A critical role of STAT3 in innate immunity , 2003, Proceedings of the National Academy of Sciences of the United States of America.

[8]  A. Sher,et al.  A Critical Role for IL-21 in Regulating Immunoglobulin Production , 2002, Science.

[9]  S. Abramson,et al.  Regulation of immunoglobulin production in hyperimmunoglobulin E recurrent-infection syndrome by interferon gamma. , 1989, Proceedings of the National Academy of Sciences of the United States of America.

[10]  S. Holland,et al.  Dermatitis and the newborn rash of hyper-IgE syndrome. , 2004, Archives of dermatology.

[11]  Xin-Yuan Fu,et al.  Osteoporosis with increased osteoclastogenesis in hematopoietic cell-specific STAT3-deficient mice. , 2005, Biochemical and biophysical research communications.

[12]  Hideyuki Okano,et al.  Conditional ablation of Stat3 or Socs3 discloses a dual role for reactive astrocytes after spinal cord injury , 2006, Nature Medicine.

[13]  S. Holland,et al.  Autosomal recessive hyperimmunoglobulin E syndrome: a distinct disease entity. , 2004, The Journal of pediatrics.

[14]  A. Schäffer,et al.  The hyper IgE syndrome and mutations in TYK2. , 2007, Immunity.

[15]  C. Naspitz,et al.  CRANIAL SYNOSTOSIS IN JOB'S SYNDROME , 1978, The Lancet.

[16]  F. Greene,et al.  Cryptococcosis of the colon resembling Crohn's disease in a patient with the hyperimmunoglobulinemia E-recurrent infection (Job's) syndrome. , 1988, Gastroenterology.

[17]  A. Arai,et al.  Coronary artery aneurysms in patients with hyper IgE recurrent infection syndrome. , 2007, Clinical immunology.

[18]  S. Akira,et al.  Stat-3 is required for pulmonary homeostasis during hyperoxia. , 2004, The Journal of clinical investigation.

[19]  M. Abinun,et al.  Bone marrow transplantation does not correct the hyper IgE syndrome , 2000, Bone Marrow Transplantation.

[20]  W. Shearer,et al.  Burkitt's lymphoma developing in a 7-year-old boy with hyper-IgE syndrome. , 1989, The Journal of allergy and clinical immunology.

[21]  A. Schäffer,et al.  Genetic linkage of hyper-IgE syndrome to chromosome 4. , 1999, American journal of human genetics.

[22]  J. Carey,et al.  The face of Job. , 1998, The Journal of pediatrics.

[23]  H. Hill,et al.  Defective interleukin-12/interferon-gamma pathway in patients with hyperimmunoglobulinemia E syndrome. , 2000, The Journal of pediatrics.

[24]  H. Hill,et al.  Effects of allogeneic peripheral stem cell transplantation in a patient with job syndrome of hyperimmunoglobulinemia E and recurrent infections. , 1998, The American journal of medicine.

[25]  S. Holland,et al.  Hyper-IgE syndrome with recurrent infections--an autosomal dominant multisystem disorder. , 1999, The New England journal of medicine.

[26]  S. Holland,et al.  Pneumocystis jiroveci Infection in Patients With Hyper–Immunoglobulin E Syndrome , 2005, Pediatrics.

[27]  J. Gallin The Hyperimmunoglobulin E Recurrent‐Infection (Job's) Syndrome: A REVIEW OF THE NIH EXPERIENCE AND THE LITERATURE , 1983, Medicine.

[28]  B. Musiatowicz,et al.  STAT1 and STAT3 as intracellular regulators of vascular remodeling. , 2007, European journal of internal medicine.

[29]  M. de Carli,et al.  Defective in vitro production of gamma-interferon and tumor necrosis factor-alpha by circulating T cells from patients with the hyper-immunoglobulin E syndrome. , 1989, The Journal of clinical investigation.

[30]  C. Montoya,et al.  Interleukin 4 and interferon-gamma secretion by antigen and mitogen-stimulated mononuclear cells in the hyper-IgE syndrome: no TH-2 cytokine pattern. , 1998, Annals of allergy, asthma & immunology : official publication of the American College of Allergy, Asthma, & Immunology.

[31]  T. Yanagi Hyper-IgE syndrome , 1987, Indian journal of pediatrics.

[32]  S. Holland,et al.  Novel intraoral phenotypes in hyperimmunoglobulin-E syndrome. , 2007, Oral diseases.

[33]  D. Evans,et al.  NEW PATHOLOGICAL INSTITUTE AT THE LONDON. , 1965, Lancet.

[34]  E. Boltshauser,et al.  Craniosynostosis in hyper-IgE-syndrome , 1985, European Journal of Pediatrics.

[35]  P. Murray The JAK-STAT Signaling Pathway: Input and Output Integration1 , 2007, The Journal of Immunology.

[36]  Bodo Grimbacher,et al.  STAT3 mutations in the hyper-IgE syndrome. , 2007, The New England journal of medicine.

[37]  N. Shehadeh,et al.  Cyclosporin A in hyperimmunoglobulin E syndrome. , 1997, Annals of allergy, asthma & immunology : official publication of the American College of Allergy, Asthma, & Immunology.

[38]  H. Kimata High-dose intravenous γ-globulin treatment for hyperimmunoglobulinemia E syndrome , 1995 .

[39]  K. Sullivan,et al.  Cytokine and chemokine dysregulation in hyper-IgE syndrome. , 2001, Clinical immunology.

[40]  Vannier Jp,et al.  Hyperimmunoglobulin E recurrent infection (Job's) syndrome. , 1991 .

[41]  I. Frieden,et al.  Cutaneous manifestations of hyper-IgE syndrome in infants and children. , 2002, The Journal of pediatrics.

[42]  T. Morio,et al.  Human tyrosine kinase 2 deficiency reveals its requisite roles in multiple cytokine signals involved in innate and acquired immunity. , 2006, Immunity.

[43]  K. Asadullah,et al.  IL-22 increases the innate immunity of tissues. , 2004, Immunity.

[44]  S. Holland,et al.  Causes of death in hyper-IgE syndrome. , 2007, The Journal of allergy and clinical immunology.

[45]  W. Wilson,et al.  Non-Hodgkin's Lymphoma in Job's Syndrome: A Case Report and Literature Review , 2004, Leukemia & lymphoma.

[46]  H. Ochs,et al.  Defect in neutrophil granulocyte chemotaxis in Job's syndrome of recurrent "cold" staphylococcal abscesses. , 1974, Lancet.

[47]  V. Beral,et al.  INCIDENCE OF PITUITARY ADENOMA IN WOMEN , 1979, The Lancet.

[48]  J. Schaller,et al.  Job's Syndrome. Recurrent, "cold", staphylococcal abscesses. , 1966 .

[49]  S. Holland,et al.  Brain Abnormalities in Patients With Hyperimmunoglobulin E Syndrome , 2007, Pediatrics.

[50]  H. Takada,et al.  Dominant-negative mutations in the DNA-binding domain of STAT3 cause hyper-IgE syndrome , 2007, Nature.

[51]  R. Craig Interactions between chronic renal disease and periodontal disease. , 2007, Oral diseases.

[52]  D. Alling,et al.  Levamisole is inferior to placebo in the hyperimmunoglobulin E recurrent-infection (Job's) syndrome. , 1982, The New England journal of medicine.

[53]  R. Geha,et al.  Increased in vitro bone resorption by monocytes in the hyper-immunoglobulin E syndrome. , 1988, Journal of immunology.