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003 | OSt | ||
005 | 20240305193721.0 | ||
008 | 221103b |||||||| |||| 00| 0 eng d | ||
022 | _a 2049-9957 | ||
028 | _b Phone: +255 28 298 3384 | ||
028 | _b Fax: +255 28 298 3386 | ||
028 | _b Email: vc@bugando.ac.tz | ||
035 | _a Website: www.bugando.ac.tz | ||
040 | _cDLC | ||
100 |
_aHumphrey D Mazigo _922835 |
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222 | _a HIV-1 S. mansoni Co-infection Praziquantel Efficacy Tanzania | ||
245 | _aPraziquantel efficacy against Schistosoma mansoni among HIV-1 infected and uninfected adults living in fishing villages along Lake Victoria, Northwest Tanzania | ||
260 |
_aMwanza: _bBioMed Central & _bTanzania Catholic University of Health and Allied Sciences [CUHAS – Bugando] _c15 December 2014 |
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300 | _a Pages 1-10 | ||
490 | _v Infectious Diseases of Poverty Volume 3 Issue 1 | ||
520 | _aAbstract Background: Animal studies have demonstrated that functional immune responses, as determined by the levels of CD4+ cell counts and anti-schistosome antibodies responses, determine the efficacy of praziquantel. Based on this evidence, it has been hypothesised that the immunodeficiency effects of the human immunodeficiency virus (HIV)-1 infection may affect the efficacy of praziquantel in co-infected human hosts. Thus, the present study assessed the efficacy of praziquantel by comparing parasitological cure rates and the reduction in infection intensity in HIV-1 seronegative individuals infected with S. mansoni and HIV-1 seropositive individuals co-infected with S. mansoni, following treatment with a single oral dose of praziquantel. Methods: This was a prospective longitudinal study which included, at baseline, 555 S. mansoni infected adults aged 21–55 years, who were either co-infected or not with HIV-1 and who lived in fishing villages along Lake Victoria in Northwest Tanzania. These individuals were treated with a single oral dose of praziquantel (40 mg/kg) and, at 12 weeks, single stool samples were obtained and examined for S. mansoni eggs using the Kato-Katz technique. Finger prick and venous blood samples were collected for HIV-1 screening and CD4+ cell quantification. Results: The parasitological cure rate did not differ significantly from the HIV-1 serostatus (P = 0.12): among the co-infected individuals, the cure rate was 48.3% (14/29), and among the individuals infected only with S. mansoni, the cure rate was 62.6% (329/526). The egg reduction rate did not vary with the HIV-1 serostatus (P = 0.22): 77.22% for HIV-1 seronegative and 75% for HIV-1 seropositive individuals. The level of CD4+ cell counts (median 228 cells/μL: range 202–380 cells) did not influence the cure rate (P = 0.23) or the reduction in the intensity of the infection (P = 0.37). Conclusion: The HIV-1 infection per se or its moderate immunodeficiency effects, demonstrated by the range of CD4+ cell counts observed in co-infected individuals, did not affect praziquantel efficacy, as measured by the parasitological cure rate and the reduction in intensity of infection in the present study cohort. | ||
700 |
_a David W Dunne _922988 |
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700 |
_aSafari M Kinung’hi _922991 |
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700 |
_a Fred Nuwaha _922993 |
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856 | _uhttps://doi.org/10.1186/2049-9957-3-47 | ||
942 |
_2ddc _cVM |
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_c19276 _d19276 |