| Literature DB >> 10073725 |
A Z Momeni1, T Jalayer, M Emamjomeh, A Khamesipour, F Zicker, R L Ghassemi, Y Dowlati, I Sharifi, M Aminjavaheri, A Shafiei, M H Alimohammadian, R Hashemi-Fesharki, K Nasseri, T Godal, P G Smith, F Modabber.
Abstract
Safety and efficacy of killed (autoclaved) L. major promastigotes, ALM, mixed with BCG against zoonotic cutaneous leishmaniasis was tested in healthy volunteers (n = 2453) in a randomized double blind trial vs. BCG as control. Side-effects were similar in both groups but tended to be slightly more frequent and prolonged in the ALM + BCG group. Leishmanin skin test conversion (induration > or =5 mm) was significantly greater in the ALM + BCG than in the BCG group (36.2% vs. 7.9% on day-80 and 33% vs. 19%, after 1 year, respectively). Cumulative incidence rates for 2 years, were similar in both groups (18.0% vs. 18.5%). However, LST responders on day 80 (> or =5 mm) had a significantly lower incidence (35%) of CL during the first year than non-responders. A single dose of ALM + BCG is not sufficiently immunogenic to provide a measurable response when compared to BCG alone. A single dose of this vaccine has been shown to be safe with no evidence of an exacerbating response following natural infection; hence, multiple doses or other adjuvants should be considered to increase its immunogenicity.Entities:
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Year: 1999 PMID: 10073725 DOI: 10.1016/s0264-410x(98)00220-5
Source DB: PubMed Journal: Vaccine ISSN: 0264-410X Impact factor: 3.641