Immunological Consequences of Antihelminthic Treatment in Preschool Children Exposed to Urogenital Schistosome Infection

Author:

Rujeni Nadine1,Nausch Norman1,Midzi Nicholas23,Cowan Graeme J.1,Burchmore Richard4,Cavanagh David R.1,Taylor David W.5,Mduluza Takafira6,Mutapi Francisca1

Affiliation:

1. Institute of Immunology and Infection Research, School of Biological Sciences, Ashworth Laboratories, University of Edinburgh, King's Buildings, West Mains Road, Edinburgh EH9 3JT, UK

2. National Institute of Health Research, Box CY 570, Causeway, Harare, Zimbabwe

3. Research Council of Zimbabwe, Block A, Delken Complex, Mount Pleasant Business Park, Harare, Zimbabwe

4. Institute of Infection, Immunity and Inflammation, University of Glasgow, Sir Graeme Davies Building, 120 University Place, Glasgow G12 8TA, UK

5. Division of Pathway Medicine, School of Biomedical Sciences and Edinburgh Infectious Diseases, Ashworth Laboratories, University of Edinburgh, King's Buildings, West Mains Road, Edinburgh EH9 3JT, UK

6. Department of Biochemistry, University of Zimbabwe, P.O. Box 167, Mount Pleasant, Harare, Zimbabwe

Abstract

Urogenital schistosomiasis, due toSchistosoma haematobium,is endemic in sub-Saharan Africa. Control is by targeted treatment with praziquantel but preschool age children are excluded from control programs. Immunological studies on the effect of treatment at this young age are scarce. In light of studies in older individuals showing that praziquantel alters antischistosome immune responses and responses to bystander antigens, this study aims to investigate how these responses would be affected by treatment at this young age. Antibody responses directed against schistosome antigens,Plasmodium falciparumcrude and recombinant antigens, and the allergen house dust mite were measured in children aged 3 to 5 years before and 6 weeks after treatment. The change in serological recognition of schistosome proteins was also investigated. Treatment augmented antischistosome IgM and IgE responses. The increase in IgE responses directed against adult worm antigens was accompanied by enhanced antigen recognition by sera from the children. Antibody responses directed againstPlasmodiumantigens were not significantly affected by praziquantel treatment nor were levels of allergen specific responses. Overall, praziquantel treatment enhanced, quantitatively and qualitatively, the antiworm responses associated with protective immunity but did not alterPlasmodium-specific responses or allergen-specific responses which mediate pathology in allergic disease.

Funder

World Health Organization

Publisher

Hindawi Limited

Subject

General Medicine,Microbiology,Parasitology

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