Deficiency of Th17 cells in hyper IgE syndrome due to mutations in STAT3

Journal of Experimental Medicine

Volumn 205, Issue 7, 2008, Pages 1551-1557

  Ma, Cindy S ^a   Chew, Gary Y J ^b,c   Simpson, Nicholas ^c   Priyadarshi, Archana ^d   Wong, Melanie ^e   Grimbacher, Bodo ^g   Fulcher, David A ^f   Tangye, Stuart G ^a   Cook, Matthew C ^b,c,d  

^a GARVAN INSTITUTE OF MEDICAL RESEARCH   (Australia)

^b The Australian National University   (Australia)

^c Biology and Environment   (Australia)

^d CANBERRA HOSPITAL   (Australia)

^e CHILDREN S HOSPITAL AT WESTMEAD   (Australia)

^f WESTMEAD HOSPITAL   (Australia)

^g UNIVERSITY COLLEGE LONDON   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

INTERLEUKIN 17; RETINOID RELATED ORPHAN RECEPTOR GAMMA; STAT3 PROTEIN; TRANSCRIPTION FACTOR;

ADOLESCENT; ADULT; ARTICLE; CD4+ T LYMPHOCYTE; CLINICAL ARTICLE; CONTROLLED STUDY; ENZYME LINKED IMMUNOSORBENT ASSAY; FEMALE; HELPER CELL; HETEROZYGOSITY; HUMAN; HUMAN CELL; HYPER IGE SYNDROME; INFECTION SENSITIVITY; MALE; MISSENSE MUTATION; PHENOTYPE; PRIORITY JOURNAL; PROTEIN EXPRESSION; SCHOOL CHILD; TH17 CELL;

ANTIGENS, FUNGAL; CANDIDA ALBICANS; CANDIDIASIS; CHILD; FEMALE; HUMANS; INTERLEUKIN-17; JOB'S SYNDROME; MALE; RECEPTORS, CYTOPLASMIC AND NUCLEAR; STAPHYLOCOCCAL INFECTIONS; STAPHYLOCOCCUS AUREUS; STAT3 TRANSCRIPTION FACTOR; T-LYMPHOCYTES, HELPER-INDUCER;

EID: 46949089128     PISSN: 00221007     EISSN: 00221007     Source Type: Journal    
DOI: 10.1084/jem.20080218     Document Type: Article

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