Movement Disorders (revue)

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Ninhydrin sweat test: A simple method for detecting antibodies neutralizing botulinum toxin type A

Identifieur interne : 003C38 ( Main/Exploration ); précédent : 003C37; suivant : 003C39

Ninhydrin sweat test: A simple method for detecting antibodies neutralizing botulinum toxin type A

Auteurs : Bernhard Voller [Autriche] ; Ekaterina Moraru [Autriche] ; Eduard Auff [Autriche] ; Michael Benesch [Autriche] ; Werner Poewe [Autriche] ; Jörg Wissel [Autriche] ; Jörg Müller [Autriche] ; Tanja Entner [Autriche] ; Hans Bigalke [Allemagne] ; Peter Schnider [Autriche]

Source :

RBID : ISTEX:734A0D9FE2530C498DB424107884CDCF310FF559

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Abstract

Approximately 5% of patients with cervical dystonia receiving repeated botulinum neurotoxin A (BoNT/A) injections develop secondary loss of treatment benefit. Currently available tests to directly detect neutralizing BoNT/A antibodies (BoNT/A‐AB) are either expensive or time consuming. To establish a simple, clinically useful test for antibody detection, we adapted the ninhydrin sweat test (NST). Eighteen dystonic patients with secondary nonresponse and clinically suspected BoNT/A‐AB formation were tested for BoNT/A‐AB in the mouse diaphragm test (MDT). In addition, the size of the anhidrotic area was determined by the NST 21 days after an intradermal dose of 10 U Dysport into the hypothenar region of the left palm. In nine patients, positive BoNT‐AB titers were found in the MDT. There was a significant correlation between the BoNT/A‐AB titers and the anhidrotic area (Spearman's rho = −0.9, P < 0.0001). Both tests provided comparably good results with respect to qualitative antibody detection. In the clinical situation of secondary nonresponse to BoNT/A therapy, the economical NST may be a helpful tool to detect neutralizing BoNT/A‐AB. © 2004 Movement Disorder Society

Url:
DOI: 10.1002/mds.20073


Affiliations:


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<div type="abstract" xml:lang="en">Approximately 5% of patients with cervical dystonia receiving repeated botulinum neurotoxin A (BoNT/A) injections develop secondary loss of treatment benefit. Currently available tests to directly detect neutralizing BoNT/A antibodies (BoNT/A‐AB) are either expensive or time consuming. To establish a simple, clinically useful test for antibody detection, we adapted the ninhydrin sweat test (NST). Eighteen dystonic patients with secondary nonresponse and clinically suspected BoNT/A‐AB formation were tested for BoNT/A‐AB in the mouse diaphragm test (MDT). In addition, the size of the anhidrotic area was determined by the NST 21 days after an intradermal dose of 10 U Dysport into the hypothenar region of the left palm. In nine patients, positive BoNT‐AB titers were found in the MDT. There was a significant correlation between the BoNT/A‐AB titers and the anhidrotic area (Spearman's rho = −0.9, P < 0.0001). Both tests provided comparably good results with respect to qualitative antibody detection. In the clinical situation of secondary nonresponse to BoNT/A therapy, the economical NST may be a helpful tool to detect neutralizing BoNT/A‐AB. © 2004 Movement Disorder Society</div>
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