Molecular characterization of human plasmacytoid dendritic cells

Wei Cao

Research output: Contribution to journalReview articlepeer-review

31 Scopus citations

Abstract

Introduction: Plasmacytoid dendritic cells (pDCs) represent a unique and important immune cell population capable of producing large quantifies of type I interferon (IFN) in response to viruses as well as nucleic acid-containing complexes from the host. These rare and mysterious cells have been revealed by in-depth molecular characterization. Several innate sensors and signaling molecules enriched in pDCs allow their specialized innate immune functions. In addition, human pDCs use a group of surface receptors that, through activation of a B-cell receptor (BCR)-like signaling pathway, modulate type I IFN responses. It is clear now that pDC development is influenced by distinctive transcription factors that specify a unique lineage. CD4+CD56 + hematodermic neoplasm of human pDC origin has been revealed in explicit molecular terms. Conclusion: A detailed molecular description of pDCs helps us better define, understand, and track human pDCs in relation to their functions and physiological involvement.

Original languageEnglish (US)
Pages (from-to)257-264
Number of pages8
JournalJournal of Clinical Immunology
Volume29
Issue number3
DOIs
StatePublished - May 2009

Keywords

  • CD4CD56 hematodermic neoplasm
  • PDC development
  • Plasmacytoid dendritic cells
  • Regulation of interferon responses
  • Type I interferon production

ASJC Scopus subject areas

  • Immunology and Allergy
  • Immunology

MD Anderson CCSG core facilities

  • Monoclonal Antibody Facility
  • Flow Cytometry and Cellular Imaging Facility

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