Department of Ophthalmology, The Affiliated Huai'an Hospital of Xuzhou Medical University, Huai'an City, China.
Department of Rheumatology, The Affiliated Huai'an Hospital of Xuzhou Medical University, Huai'an City, China.
Sci Rep. 2023 Aug 19;13(1):13521. doi: 10.1038/s41598-023-40802-5.
The purpose of this trial was to clinically assess the effect and safety of Adipose Tissue-derived Stem Cells (ADSCs) treatment on primary Sjogren's Syndrome (pSS). In this 6-month randomized, triple-blind, placebo-controlled clinical trial, pSS patients were randomly assigned to two groups. After demographic characteristics and clinical examination were achieved, local injection of ADSCs into bilateral glands was performed with patients in ADSCs group (n = 35) and placebo solution was used for another group (n = 39) at three time points. Patients were followed up at 1-, 3- and 6-month. At each visit, studies of clinical and laboratory outcomes, as well as subjective symptoms, were conducted. A total of 74 subjects who met the including criteria were allocated in two groups and eventually 64 subjects (86.5%) completed the treatments and the follow-up assessments. Secretion of salivary and lachrymal glands were significantly improved in 3-month (P < 0.05). A great improvement of European League Against Rheumatism Sjögren's Syndrome Disease Activity Index (ESSDAI) was found after ADSCs treatment with intergroup comparison from baseline to follow-up (P < 0.05). There is also a significant difference of European Alliance of Associations for Rheumatology SS Patient Reported Index (ESSPRI) between the two groups in the follow-up (P < 0.05). A significant abatement of IgG, IgM, C3, C4 and ESR between two groups was observed in part of follow-up time points (P < 0.05). The ADSCs therapy can provide relief of oral and eye's dryness in our trial in a short time and has potential improvement of subjective and systemic syndromes of pSS.
本试验旨在临床评估脂肪组织源性干细胞(ADSCs)治疗原发性干燥综合征(pSS)的疗效和安全性。在这项为期 6 个月的随机、三盲、安慰剂对照临床试验中,pSS 患者被随机分为两组。在获得人口统计学特征和临床检查后,ADSCs 组患者(n=35)在三个时间点接受双侧腺体的 ADSCs 局部注射,另一组(n=39)给予安慰剂溶液。患者在 1、3 和 6 个月时进行随访。每次就诊时,均进行临床和实验室结局以及主观症状的研究。共有 74 名符合纳入标准的患者被分配到两组,最终 64 名患者(86.5%)完成了治疗和随访评估。3 个月时唾液腺和泪腺的分泌明显改善(P<0.05)。ADSCs 治疗后,欧洲抗风湿病联盟干燥综合征疾病活动指数(ESSDAI)显著改善,与基线至随访的组间比较(P<0.05)。在随访中,两组之间欧洲抗风湿病联盟干燥综合征患者报告指数(ESSPRI)也存在显著差异(P<0.05)。部分随访时间点观察到两组间 IgG、IgM、C3、C4 和 ESR 显著降低(P<0.05)。在本试验中,ADSCs 治疗可在短时间内缓解口干和眼干,并可能改善 pSS 的主观和全身症状。