Clinical efficacy of tacrolimus for treating myasthenia gravis and its influence on lymphocyte subsets

他克莫司 重症肌无力 医学 强的松 胃肠病学 白细胞介素2受体 内科学 硫唑嘌呤 免疫学 免疫系统 T细胞 移植 疾病
作者
Jianhong Bao,Shengqiang Gao,Yiyun Weng,Jun Zhu,H. Ye,X. Zhang
出处
期刊:Revue Neurologique [Elsevier BV]
卷期号:175 (1-2): 65-72 被引量:7
标识
DOI:10.1016/j.neurol.2018.01.377
摘要

This study aimed to determine the clinical efficacy and effects of tacrolimus in treating myasthenia gravis (MG).A total of 45 outpatients and inpatients were divided into a tacrolimus group (n=15) and non-tacrolimus group (n=30): those in the former group were treated with 3mg/day of tacrolimus for 24 weeks, while those in the latter (control) group took other immunosuppressants (prednisone, azathioprine combined with prednisone). Each group was evaluated at weeks 4, 8, 12, 16, 20 and 24 by Myasthenia Gravis Foundation of America Quantitative Myasthenia Gravis (MGFA-QMG) Test, activities of daily living (ADL) profiles, and manual muscle (MMT) and fatigue tests. Dynamic changes in CD4+CD25+high cells were tested by flow cytometry. Inflammatory cytokines were also evaluated in the tacrolimus group.Efficacy index scores decreased significantly compared with baseline at every test week in both groups (P<0.01), although improvements were more evident with than without tacrolimus treatment (F=9.312, P<0.01 vs. F=24.551, P<0.01 and F=10.710, P<0.01). At week 24, peripheral blood CD4+CD25+high T cells with tacrolimus decreased significantly (P<0.01), but increased significantly without tacrolimus (P<0.01). During treatment, CD19+BAFF-R B cells in peripheral blood decreased in both groups (P<0.05). Interferon (IFN)-γ concentrations in peripheral blood also diminished significantly with tacrolimus (P<0.01).A relatively low dose of tacrolimus can affect multiple immune-system targets and, thus, can treat MG effectively in terms of both clinical symptoms and immunological responses.
最长约 10秒,即可获得该文献文件

科研通智能强力驱动
Strongly Powered by AbleSci AI
更新
PDF的下载单位、IP信息已删除 (2025-6-4)

科研通是完全免费的文献互助平台,具备全网最快的应助速度,最高的求助完成率。 对每一个文献求助,科研通都将尽心尽力,给求助人一个满意的交代。
实时播报
简单的师发布了新的文献求助10
1秒前
宁阿霜完成签到,获得积分10
1秒前
执着的若灵完成签到,获得积分10
1秒前
Eric发布了新的文献求助10
2秒前
guohh发布了新的文献求助10
2秒前
TT完成签到,获得积分10
2秒前
潇大王完成签到,获得积分10
3秒前
开朗的访彤完成签到,获得积分10
3秒前
不想起名字完成签到,获得积分10
3秒前
舒心谷雪完成签到 ,获得积分10
4秒前
HHHHHH发布了新的文献求助10
4秒前
柒咩咩发布了新的文献求助30
4秒前
现代的东蒽完成签到,获得积分10
4秒前
tutu完成签到,获得积分10
5秒前
充电宝应助Naive采纳,获得10
5秒前
王木木完成签到,获得积分10
5秒前
orixero应助hkh采纳,获得10
5秒前
6秒前
popo完成签到,获得积分10
6秒前
6秒前
6秒前
7秒前
摆哥完成签到,获得积分10
7秒前
无限的小懒虫完成签到,获得积分10
7秒前
keke完成签到,获得积分10
7秒前
cici发布了新的文献求助10
7秒前
111完成签到,获得积分10
7秒前
笑点低草莓关注了科研通微信公众号
7秒前
小二郎应助文静的白羊采纳,获得10
8秒前
However完成签到,获得积分10
8秒前
xixi完成签到,获得积分10
9秒前
永不言弃的鱼完成签到,获得积分10
9秒前
joybee完成签到,获得积分0
10秒前
SciGPT应助dddd采纳,获得10
11秒前
赘婿应助不想起名字采纳,获得10
11秒前
12秒前
徐进完成签到,获得积分10
12秒前
羞涩的孙发布了新的文献求助10
12秒前
cherry完成签到,获得积分10
12秒前
DA发布了新的文献求助10
13秒前
高分求助中
(应助此贴封号)【重要!!请各用户(尤其是新用户)详细阅读】【科研通的精品贴汇总】 10000
Acute Mountain Sickness 2000
A novel angiographic index for predicting the efficacy of drug-coated balloons in small vessels 500
Textbook of Neonatal Resuscitation ® 500
Thomas Hobbes' Mechanical Conception of Nature 500
The Affinity Designer Manual - Version 2: A Step-by-Step Beginner's Guide 500
Affinity Designer Essentials: A Complete Guide to Vector Art: Your Ultimate Handbook for High-Quality Vector Graphics 500
热门求助领域 (近24小时)
化学 医学 生物 材料科学 工程类 有机化学 内科学 生物化学 物理 计算机科学 纳米技术 遗传学 基因 复合材料 化学工程 物理化学 病理 催化作用 免疫学 量子力学
热门帖子
关注 科研通微信公众号,转发送积分 5093986
求助须知:如何正确求助?哪些是违规求助? 4307375
关于积分的说明 13419555
捐赠科研通 4133722
什么是DOI,文献DOI怎么找? 2264715
邀请新用户注册赠送积分活动 1268237
关于科研通互助平台的介绍 1204202