Human TMEFF1 is a restriction factor for herpes simplex virus in the brain

Nature. 2024 Aug;632(8024):390-400. doi: 10.1038/s41586-024-07745-x. Epub 2024 Jul 24.

Abstract

Most cases of herpes simplex virus 1 (HSV-1) encephalitis (HSE) remain unexplained1,2. Here, we report on two unrelated people who had HSE as children and are homozygous for rare deleterious variants of TMEFF1, which encodes a cell membrane protein that is preferentially expressed by brain cortical neurons. TMEFF1 interacts with the cell-surface HSV-1 receptor NECTIN-1, impairing HSV-1 glycoprotein D- and NECTIN-1-mediated fusion of the virus and the cell membrane, blocking viral entry. Genetic TMEFF1 deficiency allows HSV-1 to rapidly enter cortical neurons that are either patient specific or derived from CRISPR-Cas9-engineered human pluripotent stem cells, thereby enhancing HSV-1 translocation to the nucleus and subsequent replication. This cellular phenotype can be rescued by pretreatment with type I interferon (IFN) or the expression of exogenous wild-type TMEFF1. Moreover, ectopic expression of full-length TMEFF1 or its amino-terminal extracellular domain, but not its carboxy-terminal intracellular domain, impairs HSV-1 entry into NECTIN-1-expressing cells other than neurons, increasing their resistance to HSV-1 infection. Human TMEFF1 is therefore a host restriction factor for HSV-1 entry into cortical neurons. Its constitutively high abundance in cortical neurons protects these cells from HSV-1 infection, whereas inherited TMEFF1 deficiency renders them susceptible to this virus and can therefore underlie HSE.

Publication types

  • Case Reports

MeSH terms

  • Animals
  • Brain* / cytology
  • Brain* / metabolism
  • Brain* / virology
  • Child, Preschool
  • Encephalitis, Herpes Simplex* / metabolism
  • Encephalitis, Herpes Simplex* / virology
  • Female
  • Herpesvirus 1, Human* / pathogenicity
  • Herpesvirus 1, Human* / physiology
  • Homozygote
  • Humans
  • Interferon Type I / immunology
  • Interferon Type I / metabolism
  • Male
  • Membrane Proteins* / deficiency
  • Membrane Proteins* / genetics
  • Membrane Proteins* / metabolism
  • Nectins / genetics
  • Nectins / metabolism
  • Neurons / cytology
  • Neurons / metabolism
  • Neurons / virology
  • Pedigree
  • Pluripotent Stem Cells / cytology
  • Virus Internalization*
  • Virus Replication
  • Young Adult

Substances

  • Interferon Type I
  • Membrane Proteins
  • NECTIN1 protein, human
  • Nectins
  • TMEFF1 protein, human