A new model of Hantaan virus persistence in mice: the balance between HTNV infection and CD8(+) T-cell responses

Virology. 2004 May 1;322(2):318-27. doi: 10.1016/j.virol.2004.01.030.

Abstract

We established a viral persistence model that involves the adoptive transfer of spleen cells from immunocompetent mice (H-2(d)) into Hantaan virus (HTNV)-infected severe combined immunodeficient (SCID, H-2(d)) mice. The infection is maintained despite the presence of neutralizing antibodies, without apparent signs of disease, and there is a correlation between HTNV persistence and the lack of HTNV-specific CD8(+) T cells. In addition, disseminated HTNV infection before the initiation of immune responses appears to be important for virus persistence. The suppression of HTNV-specific CD8(+) T cells in the present model appears to occur at the periphery. The present study also demonstrates that CD8(+) T cells contribute to the clearance of HTNV. Thus, it seems that HTNV-specific CD8(+) T cells play a key role in HTNV persistence in mice. This model of viral persistence is useful for studies of immune responses and immunocytotherapy against viral infection.

Publication types

  • Evaluation Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adoptive Transfer
  • Animals
  • CD8-Positive T-Lymphocytes / immunology*
  • Capsid Proteins / metabolism
  • Chronic Disease
  • Cytotoxicity, Immunologic
  • Disease Models, Animal*
  • Hantaan virus / immunology
  • Hantaan virus / pathogenicity*
  • Hemorrhagic Fever with Renal Syndrome / immunology*
  • Hemorrhagic Fever with Renal Syndrome / physiopathology*
  • Humans
  • Mice
  • Mice, Inbred BALB C
  • Mice, Nude
  • Viral Core Proteins / metabolism

Substances

  • Capsid Proteins
  • Viral Core Proteins
  • nucleocapsid protein, Hantaan virus