Sankhla C, Jankovic J, Duane D
Movement Disorders Clinic, Department of Neurology, Baylor College of Medicine, Houston, Texas 77030, USA.
Mov Disord. 1998 Jan;13(1):150-4. doi: 10.1002/mds.870130128.
Immunoresistance (Ab+) to botulinum toxin type A (BTX-A) has been a serious concern since the introduction of BTX-A in the treatment of dystonia and other disorders associated with abnormal muscle contractions. We studied seven patients who developed Ab+ and later reverted to antibody-negative (Ab-) status. These seven patients, six women (mean age, 56 years; range, 41-80 years), with an average duration of dystonia for all patients of 197 months (range, 84-360 months), received a total mean cumulative dose of 1659 units (U) (range, 810-1975 U), with an average dose of 207 U per visit. All of these patients became unresponsive to BTX-A treatment and became Ab+ as determined by mouse bioassay. Their response to BTX-A after they reverted to Ab- was analyzed. The average latency between the initial BTX-A treatment and development of Ab+ was 27 months (range, 1543 months). The average duration between the detection of Ab+ status and subsequent reversal to Ab- status was 30 months (range, 10-78 months). Six of these Ab- patients were reinjected with BTX-A, and all six benefited from repeat injections comparable with their earlier response. Three patients lost their clinical response to subsequent injections and were found to be again Ab+. Two of the five patients who became immunoresistant to BTX-A received botulinum toxin type F (BTX-F) injections and one patient received a single session of BTX-B with improvement in their symptoms. In conclusion, this unique group of patients who were Ab+ and became Ab- responded favorably to repeat BTX-A injections, but some lost the benefit with subsequent injections. These observations suggest that the anamnestic immunologic response to BTX-A can wane, but can be reactivated by repeat BTX-A treatments. The presence of antibodies did not interfere with the response to BTX-F or BTX-B injections, thus confirming the antigenic specificity of various BTX serotypes.
自A型肉毒杆菌毒素(BTX-A)被用于治疗肌张力障碍及其他与异常肌肉收缩相关的疾病以来,对其产生免疫抵抗(Ab+)一直是一个严重问题。我们研究了7例出现Ab+但随后又恢复为抗体阴性(Ab-)状态的患者。这7例患者中,6例为女性(平均年龄56岁;范围41 - 80岁),所有患者肌张力障碍的平均病程为197个月(范围84 - 360个月),平均累积总剂量为1659单位(U)(范围810 - 1975 U),每次就诊的平均剂量为207 U。所有这些患者对BTX-A治疗均无反应,并经小鼠生物测定确定为Ab+。分析了他们恢复为Ab-后对BTX-A的反应。首次BTX-A治疗至出现Ab+的平均潜伏期为27个月(范围15 - 43个月)。检测到Ab+状态至随后恢复为Ab-状态的平均持续时间为30个月(范围10 - 78个月)。其中6例Ab-患者再次注射BTX-A,所有6例患者从重复注射中获益,与早期反应相当。3例患者对后续注射失去临床反应,被发现再次变为Ab+。5例对BTX-A产生免疫抵抗的患者中有2例接受了F型肉毒杆菌毒素(BTX-F)注射,1例患者接受了单次BTX-B注射,症状均有改善。总之,这组独特的先为Ab+后变为Ab-的患者对重复BTX-A注射反应良好,但部分患者后续注射失去益处。这些观察结果表明,对BTX-A的回忆性免疫反应可能减弱,但可通过重复BTX-A治疗重新激活。抗体的存在并不干扰对BTX-F或BTX-B注射的反应,从而证实了各种BTX血清型的抗原特异性。