Abstract

Background and Methods: Schistosomiasis is debilitating and reported to impair immune responsiveness of infected hosts. In Cameroon, mass drug administration (MDA) is used in schoolchildren to reduce transmission of S. haematobium and S. mansoni. The effects of MDA and the impact of schistosomiasis on the titers of antibodies in vaccinated children have been poorly studied. We therefore assessed the prevalence of schistosomiasis in schoolchildren, eight months after MDA, in two locations: Barombi Koto (BK), endemic for S. haematobium (N = 169) and Yoro (Y), endemic for S. mansoni (N = 356). Age, gender, residence time and frequency of contact with river water were assessed as risk factors for infection and morbidity in both localities. In 70 schoolchildren from BK and 83 from Y, ultrasound was used to assess morbidity according to the WHO guidelines. Evaluation of measles antibodies was performed in previously vaccinated schoolchildren (14 with S. haematobium and 12 egg-negative controls from BK and 47 with S. mansoni and12 egg-negative controls from Y).Principal Findings and conclusions: The prevalence of S. haematobium was 25. 4% in BK (43/169) and 34.8% for S. mansoni in Y (124/356), indicating the persistent transmission of schistosomiasis despite MDA. Older age (AOR 1.31; 95%CI 1.12–1.54) and higher frequencies of exposure to river water (AOR 1.99; 95%CI 1.03–3.86) were identified as risks for infection in BK whereas only older age (OR 1.15; 95%CI 1.04–1.27) was a risk for infection in Y. Bladder pathology (score 2 to 5) was observed in 29.2% (7/24) of egg-positive children in BK and liver pathology (pattern C) in 31.1% (19/61) of egg-positive children in Y. There was a positive correlation between S. haematobium egg burden and bladder pathology (AOR 1.01; 95% CI 0.99–1.02) and positive correlation between S. mansoni-driven liver pathology and female gender (AOR 3.01; 95% CI 0.88–10.26). Anti-measles antibodies in vaccinated children were significantly lower in S. mansoni-infected when compared to egg-negative controls (p = 0.001), which was not observed in the S. haematobium-infected group from BK. Our results demonstrate a questionable efficacy of MDA alone in halting schistosomiasis transmission and confirm a possible immunomodulatory effect of S. mansoni on response to vaccines.

Highlights

  • Previous mapping studies have defined that more than two million people have schistosomiasis infection in Cameroon and an additional five million live in high transmission areas within the country [1], a country with a population estimate of just over 20 million people [1]

  • We report on the strong tissue destructive nature of urogenital schistosomiasis; we present a positive correlation between the burdens of S. haematobium eggs and bladder morbidity on one of our study sites whereas S. mansoni egg burden did not appear to be associated with the development of liver pathology on another site

  • We report on the negative association of hepatointestinal schistosomiasis with anti-measles vaccine responses

Read more

Summary

Introduction

Previous mapping studies have defined that more than two million people have schistosomiasis infection in Cameroon and an additional five million live in high transmission areas within the country [1], a country with a population estimate of just over 20 million people [1]. Annual mass drug administration (MDA) of praziquantel to schoolchildren in endemic areas represents the country primary control strategy against the disease [2]. The prevalence of schistosomiasis in Cameroon in particular and Africa in general has been reduced over the last decades as a result of mapping of endemic areas and sustained MDA campaigns with praziquantel [9]. This has not been sufficient in interrupting the transmission cycle of the parasite and eliminate the disease. In Cameroon, mass drug administration (MDA) is used in schoolchildren to reduce transmission of S. haematobium and S. mansoni. Evaluation of measles antibodies was performed in previously vaccinated schoolchildren (14 with S. haematobium and 12 egg-negative controls from BK and 47 with S. mansoni and egg-negative controls from Y)

Methods
Results
Discussion
Conclusion
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call