Transcriptomic immune profiles of human flavivirus-specific T-cell responses

Immunology. 2020 May;160(1):3-9. doi: 10.1111/imm.13161. Epub 2020 Jan 7.

Abstract

The Flavivirus genus of viruses includes dengue (DENV), Zika (ZIKV), yellow fever (YFV), Japanese encephalitis (JEV), and West Nile (WNV) viruses. Infections with these species combined are prevalent in tropical and sub-tropical areas, affecting millions of people and ranging from asymptomatic to severe forms of the disease. They therefore pose a serious threat to global public health. Several studies imply a role for T cells in the protection but also pathogenesis against the different flavivirus species. Identifying flavivirus-specific T-cell immune profiles and determining how pre-exposure of one species might affect the immune response against subsequent infections from other species is important to further define the role of T cells in the immune response against infection. Understanding the immune profiles of the flavivirus-specific T-cell response in natural infection is important to understand the T-cell response in the context of vaccination. In this review, we summarize the current knowledge on human immune profiles of flavivirus-specific T-cell reactivity, comparing natural infection with the acute form of the disease and vaccination in different flavivirus infections.

Keywords: Dengue virus; T cells; Zika virus; transcriptomic; yellow fever virus.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Cross Reactions / immunology
  • Flavivirus / immunology*
  • Flavivirus / pathogenicity
  • Flavivirus Infections / diagnosis
  • Flavivirus Infections / immunology*
  • Flavivirus Infections / prevention & control
  • Flavivirus Infections / virology
  • Gene Expression Profiling
  • Host Microbial Interactions / genetics
  • Host Microbial Interactions / immunology
  • Humans
  • Immunity, Cellular
  • Immunogenicity, Vaccine
  • Severity of Illness Index
  • T-Lymphocytes / immunology*
  • T-Lymphocytes / metabolism
  • Transcriptome / immunology*
  • Viral Vaccines / immunology*

Substances

  • Viral Vaccines