Araki T, Nakata H, Kusunoki S, Arai Y, Katayama Y
Department of Neurology, Kawaguchi Municipal Medical Center.
Rinsho Shinkeigaku. 2000 Oct;40(10):979-85.
Immunoadsorption therapy (IAT) using TR-350 was performed for 14 patients with Guillain-Barré syndrome (GBS). Presence of serum antiganglioside antibodies (AGA) was investigated in all the patients in the acute phase. In 14 patients studied, 6 men and 8 women, ages from 24 to 74 years(mean, 42.5 years), 7 patients had suffered from common cold and 3 from diarrhea before neurological onset. Ophthalmoplegia was seen in 6 patients, facial palsy in 6, bulbar palsy in 3 and cerebellar sign in 2. Functional grade scores (FGS) by Hughes et al. of the patients were from 5 to 1 (mean, 3.3). In 4 patients, whose FGS were 1 or 2, IAT were performed, because of worsting of bulbar palsy, bilateral facial palsy and limb weakness. Relapse occurred in one patient. IAT was started from 2 to 18 days (mean, 8.4) after neurological onset and performed 3 to 14 times (mean, 7.5) for each patient. Mean FGS improved from 3.3 to 2.1 after IAT. The mean time to improve 1 grade was 10.3 days and mean time to improve 2 grades was 39.0 days. The mean FGS after 1 month was 1.4 and that after 3 months was 0.4. Some of 14 patients had elevated titers of AGA in sera in the acute phase. Four patients had anti-GQ1b IgG antibody and showed external ophthalmoplegia. One patient with anti-GD1b IgG antibody had cerebellar signs as well as peripheral neuropathy. Those AGAs decreased after IAT in parallel with improvement. IAT is an effective treatment in acute phase of GBS.
对14例吉兰-巴雷综合征(GBS)患者采用TR-350进行免疫吸附治疗(IAT)。对所有急性期患者检测血清抗神经节苷脂抗体(AGA)。在研究的14例患者中,男性6例,女性8例,年龄24至74岁(平均42.5岁),7例患者在神经症状出现前患过感冒,3例患过腹泻。6例患者出现眼肌麻痹,6例出现面瘫,3例出现延髓麻痹,2例出现小脑体征。患者的Hughes等人的功能分级评分(FGS)为5至1(平均3.3)。4例FGS为1或2的患者,因延髓麻痹、双侧面瘫和肢体无力加重而接受IAT治疗。1例患者复发。IAT在神经症状出现后2至18天(平均8.4天)开始,每位患者进行3至14次(平均7.5次)。IAT后平均FGS从3.3提高到2.1。提高1级的平均时间为10.3天,提高2级的平均时间为39.0天。1个月后的平均FGS为1.4,3个月后的平均FGS为0.4。14例患者中的一些在急性期血清中AGA滴度升高。4例患者有抗GQ1b IgG抗体并表现为外展神经麻痹。1例抗GD1b IgG抗体患者有小脑体征以及周围神经病变。IAT后这些AGA与病情改善同时下降。IAT是GBS急性期的一种有效治疗方法。