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Immunogenicity induced by botulinum toxin injections for limb spasticity: A systematic review - 14/07/19

Doi : 10.1016/j.rehab.2019.03.004 
Laure Mathevon a, 1, , Arnaud Declemy b, 1, Isabelle Laffont c, 2, Dominic Perennou a, d, 2
a Department of Physical and Rehabilitation Medicine, Institute of Rehabilitation, South Hospital–University Hospital Grenoble-Alpes, 38130 Grenoble, France 
b Department of Physical and Rehabilitation Medicine, University Hospital Nice, 06000 Nice, France 
c Department of Physical and Rehabilitation Medicine, Euromov, IFRH, Montpellier University Hospital, Montpellier University, 34090 Montpellier, France 
d University Hospital Grenoble-Alpes, CNRS, LPNC, 38000 Grenoble, France 

Corresponding author.

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Highlights

We need criteria to define non-response to botulinum toxin (BoNT) treatment for limb spasticity.
Immunogenicity is not the most common cause of non-response to BoNT treatment.
Immunogenicity is rare in BoNT treatment for spasticity: 1% to 2% among 1234 serum samples tested.
Individuals showing immunogenicity do not show response to BoNT injections or show partial response.
Some biological arguments exist to try another BoNT formulation, but no clinical evidence supports this strategy.

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Abstract

Background

The imputability of neutralizing antibodies (NABs) in secondary non-response (SnR) to botulinum toxin (BoNT) injections for limb spasticity is still debated.

Objective

This systematic literature review aimed to determine the prevalence of NABs after BoNT injections for limb spasticity and analyze their determinants and their causal role in SnR.

Methods

We searched MEDLINE via PubMed, Cochrane and Embase databases for articles published during 1990–2018. Two independent reviewers extracted the data and assessed the quality of studies with a specific scale (according to PRISMA and STROBE guidelines). Because the techniques used to detect NABs did not influence the results, we calculated the global (all studies) sensitivity and specificity of NAB positivity to reveal SnR.

Results

We included 14 articles published from 2002 to 2018 (including an epublication) describing 5 randomized controlled trials and 5 interventional and 4 observational studies. The quality was satisfactory (mean score 18/28 arbitrary units). NAB detection was the primary criterion in 5 studies and a secondary criterion in 9. In total, 1234 serum samples for 1234 participants (91% with stroke) were tested after injection. NAB prevalence was about 1%, with no significant difference among formulations. NAB positivity seemed favoured by long-duration therapy with high doses and a short interval between injections. The identification of non-response by NAB positivity had poor global sensitivity (56%) but very high specificity (99.6%). No consensual criteria were used to diagnose non-response to BoNT injection.

Conclusions

NAB prevalence is much lower after BoNT treatment for limb spasticity than cervical dystonia. Consensual criteria must be defined to diagnose non-response to BoNT injection. Because immunogenicity is not the most common cause of non-response to BoNT injection, NABs should be sought in individuals with SnR with no other cause explaining the treatment inefficacy. A test with 100% specificity is recommended. In cases for which immunogenicity is the most likely cause of non-response to BoNT injections, some biological arguments suggest trying another BoNT, but no clinical evidence supports this strategy.

Il testo completo di questo articolo è disponibile in PDF.

Keywords : Limb spasticity, Botulinum toxin, Immunogenicity, Resistance to treatment, Neutralizing antibody


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Vol 62 - N° 4

P. 241-251 - Luglio 2019 Ritorno al numero
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