Systems Vaccinology Identifies an Early Innate Immune Signature as a Correlate of Antibody Responses to the Ebola Vaccine rVSV-ZEBOV

Cell Rep. 2017 Aug 29;20(9):2251-2261. doi: 10.1016/j.celrep.2017.08.023.

Abstract

Predicting vaccine efficacy remains a challenge. We used a systems vaccinology approach to identify early innate immune correlates of antibody induction in humans receiving the Ebola vaccine rVSV-ZEBOV. Blood samples from days 0, 1, 3, 7, and 14 were analyzed for changes in cytokine levels, innate immune cell subsets, and gene expression. Integrative statistical analyses with cross-validation identified a signature of 5 early innate markers correlating with antibody titers on day 28 and beyond. Among those, IP-10 on day 3 and MFI of CXCR6 on NK cells on day 1 were independent correlates. Consistently, we found an early gene expression signature linked to IP-10. This comprehensive characterization of early innate immune responses to the rVSV-ZEBOV vaccine in humans revealed immune signatures linked to IP-10. These results suggest correlates of vaccine-induced antibody induction and provide a rationale to explore strategies for augmenting the effectiveness of vaccines through manipulation of IP-10.

Keywords: Ebola vaccine; IP-10; RNA sequencing; emerging infections; innate immunity; rVSV-ZEBOV; systems vaccinology; viral immunity.

Publication types

  • Clinical Trial

MeSH terms

  • Antibody Formation / immunology*
  • Biomarkers / metabolism
  • Chemokine CXCL10 / metabolism
  • Cytokines / blood
  • Ebola Vaccines / immunology*
  • Gene Expression Profiling
  • Gene Expression Regulation
  • Glycoproteins / immunology
  • Hemorrhagic Fever, Ebola / blood
  • Hemorrhagic Fever, Ebola / immunology
  • Hemorrhagic Fever, Ebola / virology
  • Humans
  • Immunity, Innate*
  • Linear Models
  • Multivariate Analysis
  • Sequence Analysis, RNA
  • Vaccination*

Substances

  • Biomarkers
  • Chemokine CXCL10
  • Cytokines
  • Ebola Vaccines
  • Glycoproteins