Respiratory syncytial virus G and/or SH protein alters Th1 cytokines, natural killer cells, and neutrophils responding to pulmonary infection in BALB/c mice

J Virol. 1999 Sep;73(9):7099-107. doi: 10.1128/JVI.73.9.7099-7107.1999.

Abstract

BALB/c mice sensitized to vaccinia virus expressed G protein of respiratory syncytial virus (RSV) develop a Th2-type cytokine response and pulmonary eosinophilia when challenged with live RSV. In this study, BALB/c mice were immunized or challenged with an RSV mutant lacking the G and SH proteins or with DNA vaccines coding for RSV G or F protein. F or G protein DNA vaccines were capable of sensitizing for pulmonary eosinophilia. The absence of the G and/or SH protein in the infecting virus resulted in a consistent increase both in pulmonary natural killer cells and in gamma interferon and tumor necrosis factor expression, as well as, with primary infection, a variable increase in neutrophils and CD11b(+) cells. The development of pulmonary eosinophilia in formalin-inactivated RSV-vaccinated mice required the presence of the G and/or SH protein in the challenge virus. These data show that G and/or SH protein has a marked impact on the inflammatory and innate immune response to RSV infection.

Publication types

  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Animals
  • Chlorocebus aethiops
  • Cytokines / biosynthesis*
  • Disease Models, Animal
  • Female
  • HN Protein*
  • Histocompatibility Antigens Class I / immunology
  • Histocompatibility Antigens Class II / immunology
  • Humans
  • Killer Cells, Natural / immunology*
  • Lung Diseases / immunology
  • Mice
  • Mice, Inbred BALB C
  • Neutrophils / immunology*
  • Respiratory Syncytial Virus Infections / immunology*
  • Respiratory Syncytial Virus, Human / immunology*
  • T-Lymphocytes, Cytotoxic / immunology
  • Th1 Cells / immunology*
  • Vero Cells
  • Viral Envelope Proteins
  • Viral Proteins / immunology*

Substances

  • Cytokines
  • HN Protein
  • Histocompatibility Antigens Class I
  • Histocompatibility Antigens Class II
  • Viral Envelope Proteins
  • Viral Proteins
  • attachment protein G