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治疗肉毒杆菌毒素后出现类似流感的症状及相关免疫反应。

Flu-like symptoms and associated immunological response following therapy with botulinum toxins.

机构信息

Parkinson's Disease Center and Movement Disorders Clinic, Department of Neurology, Baylor College of Medicine, The Smith Tower, Suite 1801, 6550 Fannin, Houston, TX 77030, USA.

出版信息

Neurotox Res. 2013 Aug;24(2):298-306. doi: 10.1007/s12640-013-9400-9. Epub 2013 May 16.

Abstract

We aimed to define the frequency and risk factors associated with flu-like symptoms (FLS) and other systemic symptoms following treatment with botulinum toxins (BoNT) and correlate them with the immunological response as determined by blood cytokines. The study involved prospective clinical and serological evaluation for cytokine analysis in patients receiving BoNT for movement disorders. We interviewed 218 patients about FLS following BoNT injections and prospectively studied 117 patients (females 67.5 %; mean age 59.74 ± 12.39 years) treated with BoNT in a total of 143 treatment cycles. While no patient reported any FLS at baseline, the symptom complex was subsequently reported in 19 patients (16.3 %) and in 20 (14 %) treatment cycles, with at least one systemic symptom reported in 49 (42 %) patients in 59 (41.3 %) treatment cycles. FLS and at least one symptom were reported more frequently by women (P = 0.006 and P = 0.049, respectively) and by younger patients: 55.6 versus 61.7 years (P = 0.022). Although the symptoms were usually considered mild, they were rated as moderate to serious after 18 (12 %) cycles. The following interleukins showed increased levels at 7-10 days after the BoNT injections: IL-1β, IL-8, GROα, eotaxin, MCP-1 and 2, RANTES, TARC, and inducible protein 10 (IP10), but only the latter showed significantly increased levels in patients with FLS: 69 versus 3 pg/ml (P = 0.007). FLS and other systemic symptoms occur after about 14 % of treatment visits in patients receiving BoNT. IP10 levels correlate with the presence and severity of FLS.

摘要

我们旨在定义在接受肉毒毒素 (BoNT) 治疗后出现流感样症状 (FLS) 和其他全身症状的频率和相关风险因素,并将其与通过血液细胞因子确定的免疫反应相关联。这项研究涉及对接受 BoNT 治疗运动障碍的患者进行前瞻性临床和血清学评估以进行细胞因子分析。我们采访了 218 名接受 BoNT 注射后的 FLS 患者,并前瞻性研究了 117 名(女性 67.5%;平均年龄 59.74 ± 12.39 岁)在总共 143 个治疗周期中接受 BoNT 治疗的患者。虽然没有患者在基线时报告任何 FLS,但随后有 19 名(16.3%)患者和 20 名(14%)治疗周期报告了该症状综合征,在 59 个(41.3%)治疗周期中,有 49 名(42%)患者报告至少有一个全身症状。女性(P=0.006 和 P=0.049)和年轻患者(55.6 岁 vs 61.7 岁,P=0.022)更频繁地报告 FLS 和至少一种症状。尽管这些症状通常被认为是轻度的,但在 18 次(12%)循环后被评定为中度至严重。在 BoNT 注射后 7-10 天,以下白细胞介素的水平升高:IL-1β、IL-8、GROα、嗜酸性粒细胞趋化因子、MCP-1 和 2、RANTES、TARC 和诱导蛋白 10(IP10),但只有后者在有 FLS 的患者中显示出明显增加:69 与 3 pg/ml(P=0.007)。在接受 BoNT 治疗的患者中,约有 14%的治疗就诊后会出现 FLS 和其他全身症状。IP10 水平与 FLS 的存在和严重程度相关。

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