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Published on: July 17, 2014
Malaria antibody persistence correlates with duration of exposure
H M Faddy1, C R Seed, M J Faddy
1Research and Development, Australian Red Cross Blood Service, Brisbane, Qld, Australia. hfaddy@redcrossblood.org.au
Background And Objectives:
In Australia, the risk of transfusion-transmitted malaria is managed through the identification of 'at-risk' donors, antibody screening enzyme-linked immunoassay (EIA) and, if reactive, exclusion from fresh blood component manufacture. Donor management depends on the duration of exposure in malarious regions (>6 months: 'Resident', <6 months: 'Visitor') or a history of malaria diagnosis. We analysed antibody testing and demographic data to investigate antibody persistence dynamics. To assess the yield from retesting 3 years after an initial EIA reactive result, we estimated the proportion of donors who would become non-reactive over this period.
Materials And Methods:
Test results and demographic data from donors who were malaria EIA reactive were analysed. Time since possible exposure was estimated and antibody survival modelled.
Results:
Among seroreverters, the time since last possible exposure was significantly shorter in 'Visitors' than in 'Residents'. The antibody survival modelling predicted 20% of previously EIA reactive 'Visitors', but only 2% of 'Residents' would become non-reactive within 3 years of their first reactive EIA.
Conclusion:
Antibody persistence in donors correlates with exposure category, with semi-immune 'Residents' maintaining detectable antibodies significantly longer than non-immune 'Visitors'.
Insights
Malaria antibody persistence in blood donors varies by exposure. Semi-immune residents retain antibodies longer than non-immune visitors, impacting donor screening strategies.
Area of Science:
- Immunology
- Transfusion Medicine
- Epidemiology
Background:
- Transfusion-transmitted malaria risk in Australia is managed by screening blood donors for malaria antibodies using enzyme-linked immunoassay (EIA).
- Donor management categorizes individuals based on duration of exposure in malarious regions ('Resident' >6 months, 'Visitor' <6 months) or malaria diagnosis history.
- Current screening relies on identifying 'at-risk' donors and excluding those with reactive antibody tests from fresh blood component manufacture.
Purpose of the Study:
- To investigate antibody persistence dynamics in malaria-exposed blood donors.
- To estimate the proportion of donors who become non-reactive (serorevert) within three years of an initial EIA-reactive result.
- To correlate antibody persistence with donor exposure categories (Resident vs. Visitor).
Main Methods:
- Analysis of malaria enzyme-linked immunoassay (EIA) test results and donor demographic data.
- Estimation of time since last possible malaria exposure for each donor.
- Modeling of antibody survival to predict seroreversion rates over time.
Main Results:
- The time since last possible malaria exposure was significantly shorter in 'Visitors' who seroreverted compared to 'Residents'.
- Antibody survival modeling predicted that 20% of previously EIA-reactive 'Visitors' would become non-reactive within three years.
- Conversely, only 2% of 'Residents' were predicted to become non-reactive within the same three-year period.
Conclusions:
- Antibody persistence in blood donors is significantly influenced by their exposure category.
- Semi-immune 'Residents' maintain detectable malaria antibodies for longer periods than non-immune 'Visitors'.
- These findings have implications for optimizing donor screening and blood safety protocols regarding transfusion-transmitted malaria.
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