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Results of an international transferability study of the BINACLE (binding and cleavage) assay for in vitro detection of tetanus toxicity
Institution:1. Public Health Institution of Turkey, Microbiology Reference Laboratories, Ankara, Turkey;2. Diskapi Yildirim Beyazit Training and Research Hospital, Medical Microbiology Department, Ankara, Turkey;3. Ataturk Training and Research Hospital, Medical Microbiology Department, Ankara, Turkey;4. Ankara Training and Research Hospital, Medical Microbiology Department, Ankara, Turkey
Abstract:Tetanus vaccines contain detoxified tetanus neurotoxin. In order to check for residual toxicity, the detoxified material (toxoid) has to be tested in guinea pigs. These tests are time-consuming and raise animal welfare issues. In line with the “3R” principles of replacing, reducing and refining animal tests, the “binding and cleavage” (BINACLE) assay for detection of active tetanus neurotoxin has been developed as a potential alternative to toxicity testing in animals. This in vitro test system can discriminate well between toxic and detoxified toxin molecules based on their receptor-binding and proteolytic characteristics.Here we describe an international study to assess the transferability of the BINACLE assay. We show that all participating laboratories were able to successfully perform the assay. Generally, assay variability was within an acceptable range. A toxin concentration-dependent increase of assay signals was observed in all tests. Furthermore, participants were able to detect low tetanus neurotoxin concentrations close to the estimated in vivo detection limit.In conclusion, the data from this study indicate that the methodology of the BINACLE assay seems to be robust, reproducible and easily transferable between laboratories. These findings substantiate our notion that the method can be suitable for the routine testing of tetanus toxoids.
Keywords:Tetanus neurotoxin  Toxoid vaccines  Transferability study  BINACLE"}  {"#name":"keyword"  "$":{"id":"kwrd0035"}  "$$":[{"#name":"text"  "_":"binding and cleavage  BSA"}  {"#name":"keyword"  "$":{"id":"kwrd0045"}  "$$":[{"#name":"text"  "_":"bovine serum albumin  ELISA"}  {"#name":"keyword"  "$":{"id":"kwrd0055"}  "$$":[{"#name":"text"  "_":"enzyme-linked immunosorbent assay  IVI"}  {"#name":"keyword"  "$":{"id":"kwrd0065"}  "$$":[{"#name":"text"  "_":"Institute of Virology and Immunology  NIBSC"}  {"#name":"keyword"  "$":{"id":"kwrd0075"}  "$$":[{"#name":"text"  "_":"National Institute for Biological Standards and Control  PBS"}  {"#name":"keyword"  "$":{"id":"kwrd0085"}  "$$":[{"#name":"text"  "_":"phosphate buffered saline  PEI"}  {"#name":"keyword"  "$":{"id":"kwrd0095"}  "$$":[{"#name":"text"  "_":"Paul-Ehrlich-Institut  PIPES"}  {"#name":"keyword"  "$":{"id":"kwrd0105"}  "$$":[{"#name":"text"  "_":"piperazine-N  N′-bis(ethanesulfonic acid)  TCEP"}  {"#name":"keyword"  "$":{"id":"kwrd0115"}  "$$":[{"#name":"text"  "_":"tris(2-carboxyethyl)phosphine hydrochloride  TeNT"}  {"#name":"keyword"  "$":{"id":"kwrd0125"}  "$$":[{"#name":"text"  "_":"tetanus neurotoxin  TMAO"}  {"#name":"keyword"  "$":{"id":"kwrd0135"}  "$$":[{"#name":"text"  "_":"trimethylamine N-oxide  TMB"}  {"#name":"keyword"  "$":{"id":"kwrd0145"}  "$$":[{"#name":"text"  "_":"3  3′  5  5′-tetramethylbenzidine
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