Published in

American Association of Immunologists, The Journal of Immunology, 4(159), p. 1876-1884, 1997

DOI: 10.4049/jimmunol.159.4.1876

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Virus dissemination through the brain parenchyma without immunologic control

Journal article published in 1997 by Pg G. Stevenson, S. Freeman, Crm R. Bangham ORCID, S. Hawke
This paper is made freely available by the publisher.
This paper is made freely available by the publisher.

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Abstract

Abstract After inoculation into the cerebrospinal fluid, the neurovirulent influenza virus A/WSN caused a rapidly progressive encephalitis that was uniformly fatal within 8 days. After inoculation into the brain parenchyma, the same virus replicated for 7 to 20 days without causing clinical illness, but when infection reached the cerebrospinal fluid, encephalitis was lethal within a further 6 days. As the virus spread through the brain parenchyma, there was intense intracerebral inflammation, with up-regulation of MHC class I and MHC class II expression and recruitment of CD44(high) CD49d(high) T cells. However, this was not associated with antiviral Ab production, and the infiltrating cells, unlike primed A/WSN-specific T cells, did not eliminate the virus in vivo or show evidence of virus recognition in vitro. Thus, a neurovirulent virus was able to disseminate widely through the brain parenchyma and induce considerable intracerebral inflammation without eliciting protective immunity.