Recent Advances in DOCK8 Immunodeficiency Syndrome

Qian Zhang, Huie Jing, Helen C. Su

Research output: Contribution to journalReview article

18 Citations (Scopus)

Abstract

Since the discovery of the genetic basis of DOCK8 immunodeficiency syndrome (DIDS) in 2009, several hundred patients worldwide have been reported, validating and extending the initial clinical descriptions. Importantly, the beneficial role of hematopoietic stem cell transplantation for this disease has emerged, providing impetus for improved diagnosis. Additionally, several groups have further elucidated the biological functions of DOCK8 in the immune system that help explain disease pathogenesis. Here, we summarize these recent developments.

Original languageEnglish
Pages (from-to)441-449
Number of pages9
JournalJournal of Clinical Immunology
Volume36
Issue number5
DOIs
Publication statusPublished - 1 Jul 2016

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Keywords

  • combined immunodeficiency
  • cutaneous virus infection
  • cytothripsis
  • DOCK8
  • eczema
  • food allergy
  • genetics
  • hematopoietic stem cell transplantation
  • hyperimmunoglobulinemia E syndrome
  • somatic reversion
  • tissue resident memory T cells (T)

ASJC Scopus subject areas

  • Immunology and Allergy
  • Immunology

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