Blood transmission studies of prion infectivity in the squirrel monkey (Saimiri sciureus): the Baxter study

Diane L Ritchie1, Susan V Gibson2, Christian R Abee3

  • 1National CJD Research & Surveillance Unit, Centre for Clinical Brain Sciences, University of Edinburgh, Western General Hospital, Edinburgh, Scotland.

Transfusion
|November 24, 2015
PubMed
Abstract

Insights

Blood transfusion studies in squirrel monkeys found no transmission of variant Creutzfeldt-Jakob disease (vCJD) or sporadic CJD (sCJD) infectivity. However, Gerstmann-Sträussler-Scheinker (GSS) disease was transmitted via blood, highlighting differential risks.

Area of Science:

  • Neuroscience
  • Prion Diseases
  • Infectious Disease Transmission

Background:

  • Variant Creutzfeldt-Jakob disease (vCJD) has been transmitted via blood transfusion.
  • Asymptomatic vCJD infection prevalence is estimated at 1 in 2000 in the UK.
  • Developing models to assess vCJD transmission risk via blood is crucial.

Purpose of the Study:

  • To investigate the transmission of vCJD and sCJD infectivity through blood transfusion.
  • To utilize the squirrel monkey model, known for susceptibility to human prion diseases.

Main Methods:

  • Whole blood from vCJD- and sCJD-infected squirrel monkeys was transfused into recipients.
  • Recipients were monitored for approximately 7 years post-transfusion.
  • Intracerebral (IC) and intravenous (IV) inoculations with blood components were also performed.

Main Results:

  • No clinical or pathological evidence of sCJD or vCJD was found in transfused monkeys.
  • Prion detection (PrP(TSE)) was negative in central nervous system and lymphoreticular tissues.
  • White blood cells from a Gerstmann-Sträussler-Scheinker (GSS) disease strain transmitted disease to recipient monkeys.

Conclusions:

  • Blood transfusion does not transmit sCJD or vCJD infectivity in the squirrel monkey model within a 7-year period.
  • Blood transmits GSS infectivity to IC-inoculated squirrel monkeys.
  • This suggests differential transmission risks for various prion diseases via blood.

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