Estimation of malaria transmission intensity in Sennar state, central Sudan

Understanding the behaviour of malaria vectors is crucial for planning mosquito control programmes. The aim of this study was to estimate the malaria transmission intensity in 2 different ecological zones in a highly endemic malaria area of Sennar state in central Sudan over the main transmission period. Species confirmation by PCR indicated that Anopheles arabiensis was the only malaria vector in the study area, with high anthropophilic behaviour [84.9% human-feeding]. ELISA studies showed Plasmodium falciparum sporozoite rates rose from 1.8% to 4.5% and the average entomological inoculation rates rose from 2.4 to 4.2 infectious bites per person per night in September [the beginning] to November [the end] of the 3-month transmission season. The proportion of malaria-positive slides ranged from 50.1% to 57.0%. The proportion of human-blood positive mosquitoes was significantly higher in the irrigated area [El Booster] compared with the non-irrigated area [Rahal]

Safety, immunogenicity and possible efficacy of immunochemotherapy of persistent post Kala-azaz dermal leishmaniasis

Post kala-azar dermal leishmaniasis [PKDL] is a common skin condition that follows successful treatment of visceral leishmaniasis [VL] in Sudanese patients. Lesions persist for years in 15% of patients and are viewed as reservoirs for the disease. Drug treatment is protracted, toxic and costly. Cure is strongly correlated with conversion in the leishmanin skin test. To determine safety, immunogenecity and possible efficacy of Alum-precipitated autoclaved L. major + BCG VL candidate vaccine combined with sodium stibogluconate [SSG] in patients with persistent PKDL. Following informed consent, the vaccine mixture was administered in a stepwise manner as follows: 5 patients received a single intradermal injection of 10 microg, 5 patients received a single dose of 100 microg and 2 patients received 4 doses of 100 microg at weekly intervals. Subsequently, the three groups of patients received means of 63.0 +/- 8.0, 53.0 +/- 5.0 and 40 days courses of SSG treatment respectively and were cured. Side effects were minimal and were confined to the vaccine injection site. Following completion of the safety study, eight patients were injected with 4-6 vaccine doses of 100 microg/dose at weekly intervals in combination with SSG. Patients were closely followed up in hospital, with minimal side effects and complete clearance of the skin rash in forty days. Alum/ALM + BCG vaccine mixture plus SSG was safe and was apparently effective in healing persistent PKDL lesions. SSG treatment duration could be shortened with the SSG/vaccine combination