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Schistosome vaccine testing: lessons from the baboon model.
Patricia S Coulson1, Thomas M Kariuki
1Department of Biology, University of York, York, United Kingdom. psc3@york.ac.uk
Memorias Do Instituto Oswaldo Cruz
|February 20, 2007
Summary
A schistosome vaccine shows promise for humans, even in infected individuals. However, current indirect measures of infection intensity may overestimate vaccine efficacy in human trials.
Area of Science:
- Immunology
- Vaccinology
- Parasitology
Background:
- Radiation-attenuated schistosome vaccines elicit high protection in animal models.
- Human vaccine administration will likely occur in individuals with prior or current schistosome infections.
- Investigating the impact of schistosome infection on vaccine-induced immunity is crucial for human trials.
Purpose of the Study:
- To determine if schistosome infection compromises vaccine-induced immunity in olive baboons.
- To evaluate the accuracy of indirect measures of infection intensity for assessing vaccine efficacy in human trials.
Main Methods:
- Olive baboons were vaccinated and exposed to schistosome infection, with some receiving chemotherapy.
- Immune responses (IgM, IgG) were monitored following vaccination and infection.
- Worm burden was assessed as a definitive measure of protection.
- Fecal eggs and circulating antigens were used as indirect measures of infection intensity.
Main Results:
- Neither prior nor ongoing schistosome infection diminished vaccine-induced protection.
- IgM responses were transient, while IgG responses increased with repeated vaccination.
- Indirect measures (fecal eggs, circulating antigens) consistently overestimated protection compared to worm burden.
- Assay sensitivity threshold was identified as the primary reason for overestimation.
Conclusions:
- Schistosomiasis vaccine-induced immunity is not compromised by infection in baboons.
- Current indirect measures of infection intensity require improvement for accurate assessment of vaccine efficacy in human schistosomiasis trials.
- More sensitive diagnostic tools are needed to reliably evaluate schistosome vaccine effectiveness in human populations.

