Simian foamy virus infection in a blood donor

R S Boneva1, A J Grindon, S L Orton

  • 1Division of AIDS, STD, and TB Laboratory Research, National Center for Infectious Diseases, Centers for Disease Control and Prevention, Atlanta, GA 30333, USA. rboneva@cdc.gov

Transfusion
|October 12, 2002
PubMed
Abstract

Insights

Simian foamy virus (SFV) transmission via blood transfusion was not detected in recipients from an infected donor. Further analysis confirmed SFV was absent in plasma-derived products, indicating low transfusion risk.

Area of Science:

  • Virology
  • Infectious Diseases
  • Public Health

Background:

  • Simian foamy virus (SFV) infections are common in nonhuman primates.
  • An occupationally exposed primate worker was confirmed to have SFV infection.
  • The potential for SFV transmission through blood transfusion and its effects in humans remain unstudied.

Purpose of the Study:

  • To investigate the risk of simian foamy virus (SFV) transmission through blood transfusion.
  • To determine if SFV can be transmitted from an infected human donor to blood recipients.
  • To assess the presence of SFV in plasma-derived products from the infected donor.

Main Methods:

  • Identified recipients of blood components from an SFV-infected donor.
  • Tested blood samples from recipients using Western blot and PCR assays for SFV.
  • Analyzed plasma-derived products (albumin, plasma protein fraction) for SFV antibodies and viral RNA.

Main Results:

  • Four recipients of cellular blood components (RBCs, WBC-reduced RBCs, platelets) tested negative for SFV up to 7 years post-transfusion.
  • Plasma-derived products manufactured from the donor's plasma tested negative for SFV.
  • Two recipients had died from unrelated causes; one platelet recipient was unavailable for testing.

Conclusions:

  • No evidence of SFV transmission was found among recipients of cellular blood products from an infected donor.
  • Plasma derivatives from the infected donor did not transmit SFV.
  • The study suggests a low risk of SFV transmission via blood transfusion.