A dominant EV71-specific CD4+ T cell epitope is highly conserved among human enteroviruses

PLoS One. 2012;7(12):e51957. doi: 10.1371/journal.pone.0051957. Epub 2012 Dec 14.

Abstract

CD4+ T cell-mediated immunity plays a central role in determining the immunopathogenesis of viral infections. However, the role of CD4+ T cells in EV71 infection, which causes hand, foot and mouth disease (HFMD), has yet to be elucidated. We applied a sophisticated method to identify promiscuous CD4+ T cell epitopes contained within the sequence of the EV71 polyprotein. Fifteen epitopes were identified, and three of them are dominant ones. The most dominant epitope is highly conserved among enterovirus species, including HFMD-related coxsackieviruses, HFMD-unrelated echoviruses and polioviruses. Furthermore, the CD4+ T cells specific to the epitope indeed cross-reacted with the homolog of poliovirus 3 Sabin. Our findings imply that CD4+ T cell responses to poliovirus following vaccination, or to other enteroviruses to which individuals may be exposed in early childhood, may have a modulating effect on subsequent CD4+ T cell response to EV71 infection or vaccine.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Antibodies, Viral / immunology
  • Antigens, Viral / immunology
  • CD4-Positive T-Lymphocytes / immunology*
  • Cross Reactions / immunology
  • Enterovirus A, Human / immunology*
  • Enterovirus Infections / immunology*
  • Enterovirus Infections / virology
  • Epitopes, T-Lymphocyte / immunology*
  • Hand, Foot and Mouth Disease / immunology
  • Hand, Foot and Mouth Disease / virology
  • Humans
  • Immunity / immunology
  • Leukocytes, Mononuclear / immunology
  • Leukocytes, Mononuclear / virology
  • Poliovirus / immunology
  • Polyproteins / immunology
  • Viral Vaccines / immunology

Substances

  • Antibodies, Viral
  • Antigens, Viral
  • Epitopes, T-Lymphocyte
  • Polyproteins
  • Viral Vaccines

Grants and funding

This work was supported by the National Basic Research Program of China [973 Program, grant number 2011CB504903], the National Natural Science Foundation of China [grant numbers 81172807, 31270951 and 30972726], the Li Ka Shing Foundation and the 100-Talent Program of CAS. QL is supported by the SA-SIBS Scholarship Program. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.