Boostani Reza, Vakili Rosita, Hosseiny Samane Sadat, Shoeibi Ali, Fazeli Bahare, Etemadi Mohammad Mehdi, Sabet Faeze, Valizade Narges, Rezaee Seyed Abdolrahim
Department of Neurology, Faculty of Medicine, Mashhad University of Medical Sciences, Mashhad, Iran.
Center of Pathological and Medical Diagnostic Services, Iranian Academic Center for Education, Culture & Research (ACECR), Mashhad Branch, Mashhad, Iran.
Neurotherapeutics. 2015 Oct;12(4):887-95. doi: 10.1007/s13311-015-0369-3.
Considering that there is no effective treatment for human T-cell leukemia virus type 1 (HTLV-1)-associated myelopathy/tropical spastic paraparesis, this study aimed to assess the impact of triple combination therapy-interferon-α, valproic acid, and prednisolone-on clinical outcomes, main HTLV-1 viral factors, and host anti-HTLV-1 antibody response. HTLV-1 proviral load (PVL), and HBZ and Tax mRNA expression levels were measured in peripheral blood mononuclear cells of 13 patients with HTLV-1-associated myelopathy/tropical spastic paraparesis before and after treatment with 180 μg pegylated interferon once a week, 10-20 mg/kg/day sodium valproate, and 5 mg/day prednisolone for 25 weeks using a TaqMan real-time polymerase chain reaction assay. Furthermore, anti-HTLV-1 titer, Osame Motor Disability Score, Ashworth spasticity scale, and urinary symptoms (through standard questionnaire and clinical monitoring) were assessed in patients before and after the treatment. HTLV-1 PVL and HBZ expression significantly decreased after the treatment [PVL from 1443 ± 282 to 660 ± 137 copies/10(4) peripheral blood mononuclear cells (p = 0.01); and HBZ from 8.0 ± 1.5 to 3.0 ± 0.66 (p < 0.01)]. Tax mRNA expression decreased after the treatment from 2.26 ± 0.45 to 1.44 ± 0.64, but this reduction was not statistically significant (p = 0.10). Furthermore, anti-HTLV-1 titer reduced dramatically after the treatment, from 3123 ± 395 to 815 ± 239 (p < 0.01). Clinical signs and symptoms, according to Osame Motor Disability Score and Ashworth score, improved significantly (both p < 0.01). Urinary symptoms and sensory disturbances with lower back pain were reduced, though not to a statistically significant degree. Although signs and symptoms of spasticity were improved, frequent urination and urinary incontinence were not significantly affected by the triple therapy. The results provide new insight into the complicated conditions underlying HTLV-1-associated diseases.
鉴于目前尚无针对1型人类T细胞白血病病毒(HTLV-1)相关脊髓病/热带痉挛性截瘫的有效治疗方法,本研究旨在评估三联联合疗法(干扰素-α、丙戊酸和泼尼松龙)对临床结局、主要HTLV-1病毒因子以及宿主抗HTLV-1抗体反应的影响。采用TaqMan实时聚合酶链反应分析法,对13例HTLV-1相关脊髓病/热带痉挛性截瘫患者在接受每周一次180μg聚乙二醇化干扰素、10 - 20mg/kg/天丙戊酸钠和5mg/天泼尼松龙治疗25周前后的外周血单个核细胞中的HTLV-1前病毒载量(PVL)、HBZ和Tax mRNA表达水平进行了检测。此外,还对患者治疗前后的抗HTLV-1滴度、小见运动障碍评分、Ashworth痉挛量表以及泌尿系统症状(通过标准问卷和临床监测)进行了评估。治疗后HTLV-1 PVL和HBZ表达显著降低[PVL从1443±282降至660±137拷贝/10(4)外周血单个核细胞(p = 0.01);HBZ从8.0±1.5降至3.0±0.66(p < 0.01)]。Tax mRNA表达在治疗后从2.26±0.45降至1.44±0.64,但这种降低无统计学意义(p = 0.10)。此外,治疗后抗HTLV-1滴度显著降低,从3123±395降至815±239(p < 0.01)。根据小见运动障碍评分和Ashworth评分,临床体征和症状有显著改善(均p < 0.01)。泌尿系统症状以及伴有下背部疼痛感觉障碍有所减轻,但未达到统计学显著程度。虽然痉挛体征和症状有所改善,但三联疗法对尿频和尿失禁无显著影响。这些结果为HTLV-1相关疾病的复杂发病机制提供了新的见解。