Hefter Harald, Rosenthal Dietmar, Moll Marek
Department of Neurology University of Düsseldorf Düsseldorf Germany.
Mov Disord Clin Pract. 2016 May 19;3(5):500-506. doi: 10.1002/mdc3.12322. eCollection 2016 Sep-Oct.
The aim of this study was to determine the prevalence of neutralizing antibodies in a large cohort of long-term treated patients with cervical dystonia (CD) still responding to repetitive injections with botulinum toxin (BoNT).
Consecutively recruited CD patients (n = 221) under long-term BoNT treatment (≥2-21 years) underwent a clinical examination at the same time blood samples were taken for neutralizing antibody determination. Collected data included demographics, mean dose of the last 10 botulinum injections, treatment duration, Tsui score for CD severity, and patients' subjective impression of treatment effect. Blood samples were screened for antibody presence by ELISA; positive samples were further analyzed by mouse hemidiaphragm test. The two laboratories performing antibody testing were blinded to the coded samples.
Antibody status could be determined for 212 patients; 39 (18.4%) were ELISA positive and 31 (14.6%) additionally positive in the mouse hemidiaphragm test. Patients with positive neutralizing antibody titers had significantly higher Tsui scores and were treated for a significantly longer time with significantly higher doses. There were no differences between male and female patients and between onabotulinumtoxinA- and abobotulinumtoxinA-treated patients. When BoNT preparations had been switched during the last 10 injections, a significantly higher proportion of neutralizing antibody-positive patients was detected.
Neutralizing antibody prevalence in long-term treated, still responding CD patients is substantially higher than suggested by follow-up studies with a shorter time frame. It should therefore be emphasized that antigenicity of BoTN preparations is still a relevant problem and should be taken into account in long-term treatment decisions.
本研究的目的是确定一大群长期接受治疗且仍对肉毒杆菌毒素(BoNT)重复注射有反应的颈部肌张力障碍(CD)患者中中和抗体的流行情况。
连续招募长期接受BoNT治疗(≥2至21年)的CD患者(n = 221),在进行临床检查的同时采集血样以测定中和抗体。收集的数据包括人口统计学信息、过去10次肉毒杆菌注射的平均剂量、治疗持续时间、用于评估CD严重程度的徐氏评分以及患者对治疗效果的主观印象。通过酶联免疫吸附测定(ELISA)筛查血样中是否存在抗体;阳性样本进一步通过小鼠半膈肌试验进行分析。进行抗体检测的两个实验室对编码样本不知情。
可确定212例患者的抗体状态;39例(18.4%)ELISA呈阳性,31例(14.6%)在小鼠半膈肌试验中也呈阳性。中和抗体滴度呈阳性的患者徐氏评分显著更高,接受治疗的时间显著更长,剂量也显著更高。男性和女性患者之间以及接受A型肉毒毒素(onabotulinumtoxinA)和A型肉毒杆菌毒素(abobotulinumtoxinA)治疗的患者之间没有差异。当在过去10次注射期间更换了BoNT制剂时,检测到中和抗体阳性患者的比例显著更高。
长期接受治疗且仍有反应的CD患者中中和抗体的流行率显著高于时间框架较短的随访研究所表明的情况。因此,应该强调的是,BoTN制剂的抗原性仍然是一个相关问题,在长期治疗决策中应予以考虑。