| Literature DB >> 19208500 |
Troels Lillebaek1, Winnie Bergstedt, Pernille N Tingskov, Birgit Thierry-Carstensen, Henrik Aggerbeck, Soeren T Hoff, Karin Weldingh, Peter Andersen, Bolette Soborg, Vibeke O Thomsen, Aase B Andersen.
Abstract
Limited specificity of the tuberculin skin test incited the development of the intradermal Mycobacterium tuberculosis-specific rdESAT-6 skin test. Animal studies have shown, however, that there is a possible risk of sensitization when repeated injections of rdESAT-6 are given. The aim of this phase 1 open clinical trial was to assess the sensitization risk and safety of repeated administration of rdESAT-6 reagent in 31 healthy adult volunteers. Three groups of volunteers received two fixed doses of 0.1 microg rdESAT-6 28, 56 or 112 days apart, respectively. After the second injection, the diameter of induration and/or redness at the injection site was measured and taken as a possible sensitization reaction if >5mm. In vitro interferon gamma (IFN-gamma) responses were measured as supportive evidence. Local adverse reactions at the injection site and adverse events were recorded. One out of 31 (3%) volunteers showed a positive skin reaction (sensitization) upon a second injection of rdESAT-6 after 28days and an increased IFN-gamma response to ESAT-6. For 7 (23%) of the volunteers, local adverse reactions related to the product were registered, but all reactions were mild and predictable. In conclusion, repeated injections of the rdESAT-6 skin test reagent are safe, and sensitization occurs at a low rate, especially if the time span between succeeding doses is wide.Entities:
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Year: 2009 PMID: 19208500 DOI: 10.1016/j.tube.2008.09.007
Source DB: PubMed Journal: Tuberculosis (Edinb) ISSN: 1472-9792 Impact factor: 3.131