Ma, CS and Chew, GYJ and Simpson, N and Priyadarshi, A and Wong, M and Grimbacher, B and Fulcher, DA and Tangye, SG and Cook, MC (2008) Deficiency of Th17 cells in hyper IgE syndrome due to mutations in STAT3. J EXP MED , 205 (7) 1551 - 1557. 10.1084/jem.20080218.
Full text not available from this repository.
Hyper-immunoglobulin E syndrome (HIES) is a primary immune deficiency characterized by abnormal and devastating susceptibility to a narrow spectrum of infections, most commonly Staphylococcus aureus and Candida albicans. Recent investigations have identified mutations in STAT3 in the majority of HIES patients studied. Despite the identification of the genetic cause of HIES, the mechanisms underlying the pathological features of this disease remain to be elucidated. Here, we demonstrate a failure of CD4(+) T cells harboring heterozygous STAT3 mutations to generate interleukin 17-secreting (i.e., T helper [Th] 17) cells in vivo and in vitro due to a failure to express sufficient levels of the Th17-specific transcriptional regulator retinoid-related orphan receptor gamma t. Because Th17 cells are enriched for cells with specificities against fungal antigens, our results may explain the pattern of infection susceptibility characteristic of patients with HIES. Furthermore, they underscore the importance of Th17 responses in normal host defense against the common pathogens S. aureus and C. albicans.
|Title:||Deficiency of Th17 cells in hyper IgE syndrome due to mutations in STAT3|
|Keywords:||HELPER T-CELLS, SAETHRE-CHOTZEN-SYNDROME, DNA-BINDING DOMAIN, GROWTH-FACTOR-BETA, INNATE IMMUNITY, HOST-DEFENSE, DIFFERENTIATION, GENERATION, INTERLEUKIN-6, REQUIREMENT|
|UCL classification:||UCL > School of Life and Medical Sciences > Faculty of Medical Sciences > Infection and Immunity (Division of) > Research Department of Immunology|
Archive Staff Only: edit this record