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An In vitro Co-infection Model to Study Plasmodium falciparum-HIV-1 Interactions in Human Primary Monocyte-derived Immune Cells
Published on: August 15, 2012
[Post-transfusion malaria: is the risk irreconciliable with biological silence?]
1EFS Auvergne-Loire, 25, boulevard Pasteur, 42000 Saint-Etienne cedex 2, France. olivier.garraud@univ-st-etienne.fr
Abstract:
Despite the relatively high frequency of imported malaria in metropolitan France, the transmission of malaria by transfusion is exceptional. The screening of donations to determine those at risk is performed by an interview, and by the testing of serology for defined groups of donors. However, the exclusion of a candidate 'at risk' as a blood donor, by a pre-donation interview, is not completely mastered and the discrimination by biological examination lacks sensitivity, as much for methodological reasons as for reasons linked to the complex parasitic pathogenic agent (Plasmodium ssp.), as for the specific host defence system. The risk of introducing an unsafe-potentially dangerous (transfusion-transmitted malaria is often lethal)-element into the transfusional circuit is not completely covered. Is serology testing the most adequate test to avoid the risk of infected donations, in particular by Plasmodium falciparum; what are the alternatives and what will be the eventual added-costs of the biological qualification of such donations? The transfusional risk linked to Plasmodium seems, however, to be reduced to a minimum, concerning the circulation of plasma, which could represent an alternative for donors at real risk (rare) and those with a supposed risk (relatively numerous).
Insights
Transfusion-transmitted malaria is rare in France, but current screening methods, including interviews and serology, have limitations. Plasma donation may offer a safer alternative for at-risk individuals.
Area of Science:
- Transfusion Medicine
- Infectious Diseases
- Parasitology
Background:
- Imported malaria is frequent in metropolitan France, posing a potential risk for transfusion transmission.
- Current screening of blood donors relies on interviews and serology, but these methods have limitations in accurately identifying individuals at risk for malaria.
- Transfusion-transmitted malaria can be lethal, highlighting the need for robust screening protocols.
Purpose of the Study:
- To evaluate the adequacy of current serology testing for detecting Plasmodium-infected donations, particularly by Plasmodium falciparum.
- To explore alternative screening methods and their associated costs.
- To assess the overall risk of transfusion-transmitted malaria and potential mitigation strategies.
Main Methods:
- Review of existing screening protocols for blood donations in metropolitan France.
- Analysis of the sensitivity and limitations of serological tests for Plasmodium detection.
- Consideration of alternative biological qualification methods and plasma donation as a risk-reduction strategy.
Main Results:
- Current pre-donation interviews are not fully effective in excluding at-risk donors.
- Biological screening methods, including serology, lack sufficient sensitivity due to methodological challenges and the complexity of Plasmodium and host immune responses.
- The risk of transfusion-transmitted malaria is not entirely eliminated by existing measures.
Conclusions:
- Serology testing may not be the most adequate method to prevent Plasmodium-infected donations, especially from Plasmodium falciparum.
- Plasma donation circulation could minimize transfusion risks for both donors with actual and presumed risk.
- Further investigation into alternative screening methods and cost-effectiveness is warranted to enhance blood safety.
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