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Published on: September 12, 2016
The Interdependence between Schistosome Transmission and Protective Immunity.
Rebecca C Oettle1, Shona Wilson2
1Department of Pathology, University of Cambridge, Tennis Court Road, Cambridge CB2 1QP, UK. ro291@cam.ac.uk.
Mass drug administration (MDA) for schistosomiasis control impacts transmission via immunity and reduced intensity. Field studies are needed to validate immunity parameters in models, particularly IgE responses to tegument allergen-like (TAL) proteins.
Area of Science:
- Immunology
- Epidemiology
- Parasitology
Background:
- Mass drug administration (MDA) is a key strategy for schistosomiasis control.
- Current models suggest MDA affects transmission through immunity and reduced local intensity.
- Empirical validation of immunity parameters in these models is lacking.
Purpose of the Study:
- To highlight the need for field studies validating immunity parameters in MDA models.
- To investigate the role of IgE in acquired protective immunity against schistosomiasis reinfection.
- To bridge the gap between theoretical modeling and immuno-epidemiological data.
Main Methods:
- Review of existing phenomenological models of MDA and immunity.
- Analysis of empirical evidence for IgE-mediated protective immunity.
- Identification of research gaps in current field studies.
Main Results:
- Phenomenological models lack empirical validation for immunity parameters.
- IgE responses to tegument allergen-like (TAL) proteins are implicated in protective immunity.
- Existing field studies are not designed to address specific immunity questions.
Conclusions:
- There is a critical need for field studies designed to empirically define immunity parameters.
- Mechanistic models incorporating validated immunity parameters are essential for understanding schistosomiasis transmission dynamics.
- Understanding acquired immunity is increasingly important with long-term MDA implementation.
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