Literature DB >> 7570930

Prevention of transfusion-associated Chagas' disease: efficacy of white cell-reduction filters in removing Trypanosoma cruzi from infected blood.

H Moraes-Souza1, J O Bordin, L Bardossy, D W MacPherson, M A Blajchman.   

Abstract

BACKGROUND: Transfusion-associated Chagas' disease (TA-CD) is a worldwide problem. Measures adopted to prevent TA-CD include the clinical and serologic screening of blood donors and/or the inactivation of Trypanosoma cruzi present in collected blood, using gentian violet as the trypanocidal agent. This study investigated the efficacy of white cell-reduction filters in removing T. cruzi from infected blood. STUDY DESIGN AND METHODS: Human blood was contaminated with 2 or 150 T. cruzi parasites per mL and then left unfiltered or filtered with white cell-reduction filters that provided either 2, 3, or 6 log10 white cell removal. The efficacy of the parasite removal of these filters was evaluated by microscopic enumeration of active forms of T. cruzi both in vivo and in vitro. The in vivo experiments were done in Swiss mice that had been intraperitoneally inoculated with T. cruzi-infected human blood. The in vitro experiments were performed with fresh human blood that had been deliberately contaminated with T. cruzi.
RESULTS: The number of parasites seen in mice inoculated with unfiltered blood containing 2 or 150 parasites per mL was significantly higher than the number of parasites seen in mice inoculated with blood from the same sample, but filtered with white cell-reduction filters providing 3 or 6 log10 white cell removal. Fifty to 70 percent of the mice given T. cruzi-infected (2 parasites/mL) filtered blood did not develop T. cruzi infection. In vitro, the use of white cell-reduction filters, providing 2, 3, or 6 log10 white cell removal, significantly reduced the number of parasites seen in culture.
CONCLUSION: The present experimental data provide evidence that white cell-reduction filters are effective in reducing the number of parasites in T. cruzi-infected blood and that this efficacy depends, in part, on the concentration of parasites in the artificially infected blood. Properly designed clinical studies of known carriers of T. cruzi must be conducted to determine whether the use of white cell-reduction filters may be an alternative method of reducing the incidence of TA-CD.

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Year:  1995        PMID: 7570930     DOI: 10.1046/j.1537-2995.1995.35996029154.x

Source DB:  PubMed          Journal:  Transfusion        ISSN: 0041-1132            Impact factor:   3.157


  5 in total

Review 1.  Chagas disease and transfusion medicine: a perspective from non-endemic countries.

Authors:  Andrea Angheben; Lucia Boix; Dora Buonfrate; Federico Gobbi; Zeno Bisoffi; Simonetta Pupella; Giorgio Gandini; Giuseppe Aprili
Journal:  Blood Transfus       Date:  2015-10       Impact factor: 3.443

Review 2.  Trypanosoma cruzi infection in transfusion medicine.

Authors:  Lina Andrea Gómez; Fredy R S Gutierrez; Oscar Andres Peñuela
Journal:  Hematol Transfus Cell Ther       Date:  2019-03-21

Review 3.  To filter blood or universal leukoreduction: what is the answer?

Authors:  Marc J Shapiro
Journal:  Crit Care       Date:  2004-06-14       Impact factor: 9.097

4.  Risk Factors and Screening for Trypanosoma cruzi Infection of Dutch Blood Donors.

Authors:  Ed Slot; Boris M Hogema; Michel Molier; Aldert Bart; Hans L Zaaijer
Journal:  PLoS One       Date:  2016-03-07       Impact factor: 3.240

Review 5.  Threats to blood safety posed by emerging protozoan pathogens.

Authors:  D A Leiby
Journal:  Vox Sang       Date:  2004-07       Impact factor: 2.144

  5 in total

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