The hyper-IgE syndromes

被引:159
作者
Freeman, Alexandra F. [1 ]
Holland, Steven M. [1 ]
机构
[1] NIAID, Lab Clin Infect Dis, Bethesda, MD 20892 USA
关键词
D O I
10.1016/j.iac.2008.01.005
中图分类号
R392 [医学免疫学];
学科分类号
100102 ;
摘要
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.
引用
收藏
页码:277 / +
页数:16
相关论文
共 49 条
[11]   THE HYPERIMMUNOGLOBULIN-E RECURRENT-INFECTION (JOBS) SYNDROME - A REVIEW OF THE NIH EXPERIENCE AND THE LITERATURE [J].
DONABEDIAN, H ;
GALLIN, JI .
MEDICINE, 1983, 62 (04) :195-208
[12]   LEVAMISOLE IS INFERIOR TO PLACEBO IN THE HYPERIMMUNOGLOBULIN-E RECURRENT-INFECTION (JOBS) SYNDROME [J].
DONABEDIAN, H ;
ALLING, DW ;
GALLIN, JI .
NEW ENGLAND JOURNAL OF MEDICINE, 1982, 307 (05) :290-292
[13]   Dermatitis and the newborn rash of hyper-IgE syndrome [J].
Eberting, CLD ;
Davis, J ;
Puck, JM ;
Holland, SM ;
Turner, ML .
ARCHIVES OF DERMATOLOGY, 2004, 140 (09) :1119-1125
[14]   Cyclosporin A in hyperimmunoglobulin E syndrome [J].
Etzioni, A ;
Shehadeh, N ;
Brecher, A ;
Yorman, S ;
Pollack, S .
ANNALS OF ALLERGY ASTHMA & IMMUNOLOGY, 1997, 78 (04) :413-414
[15]   Causes of death in hyper-IgE syndrome [J].
Freeman, Alexandra F. ;
Kleiner, David E. ;
Nadiminti, Hari ;
Davis, Joie ;
Quezado, Martha ;
Anderson, Victoria ;
Puck, Jennifer M. ;
Holland, Steven M. .
JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY, 2007, 119 (05) :1234-1240
[16]   Brain abnormalities in patients with hyperimmunoglobulin E syndrome [J].
Freeman, Alexandra F. ;
Collura-Burke, Christina J. ;
Patronas, Nicholas J. ;
Ilcus, Lidia Stana ;
Darnell, Dirk ;
Davis, Joie ;
Puck, Jennifer M. ;
Holland, Steven M. .
PEDIATRICS, 2007, 119 (05) :E1121-E1125
[17]   Pneumocystis jiroveci infection in patients with hyper-immunoglobulin E syndrome [J].
Freeman, Alexandra F. ;
Davis, Joie ;
Anderson, Victoria L. ;
Barson, William ;
Darnell, Dirk N. ;
Puck, Jennifer M. ;
Holland, Steven M. .
PEDIATRICS, 2006, 118 (04) :E1271-E1275
[18]   Bone marrow transplantation does not correct the hyper IgE syndrome [J].
Gennery, AR ;
Flood, TJ ;
Abinun, M ;
Cant, AJ .
BONE MARROW TRANSPLANTATION, 2000, 25 (12) :1303-1305
[19]   BURKITTS-LYMPHOMA DEVELOPING IN A 7-YEAR-OLD BOY WITH HYPER-IGE SYNDROME [J].
GORIN, LJ ;
JEHA, SC ;
SULLIVAN, MP ;
ROSENBLATT, HM ;
SHEARER, WT .
JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY, 1989, 83 (01) :5-10
[20]   Genetic linkage of hyper-IgE syndrome to chromosome 4 [J].
Grimbacher, B ;
Schäffer, AA ;
Holland, SM ;
Davis, J ;
Gallin, JI ;
Malech, HL ;
Atkinson, TP ;
Belohradsky, BH ;
Buckley, RH ;
Cossu, F ;
Español, T ;
Garty, BZ ;
Matamoros, N ;
Myers, LA ;
Nelson, RP ;
Ochs, HD ;
Renner, ED ;
Wellinghausen, N ;
Puck, JM .
AMERICAN JOURNAL OF HUMAN GENETICS, 1999, 65 (03) :735-744