Successful Treatment of Patients With Refractory PLA2R-Associated Membranous Nephropathy With Obinutuzumab: A Report of 3 Cases

医学 美罗华 奥比努图库单抗 膜性肾病 CD20 肾病综合征 免疫学 内科学 抗体 胃肠病学 肾小球肾炎
作者
Nattawat Klomjit,Fernando C. Fervenza,Ladan Zand
出处
期刊:American Journal of Kidney Diseases [Elsevier]
卷期号:76 (6): 883-888 被引量:44
标识
DOI:10.1053/j.ajkd.2020.02.444
摘要

Membranous nephropathy (MN) is a common cause of nephrotic syndrome in adults. Rituximab, a type I anti-CD20 antibody, has been shown to be an effective therapy in treatment of patients with MN associated with M-type phospholipase A2 receptor (PLA2R) antibodies. Despite its effectiveness, up to 40% of patients may fail to respond to rituximab, which may be related to higher PLA2R antibody titers. Obinutuzumab, a type II anti-CD20 depleter, has been shown to produce a more profound CD20 depletion and be more efficacious in treating certain hematologic malignancies compared with rituximab. We report 3 patients with PLA2R-associated MN for whom rituximab failed to induce immunologic or clinical remisison, but who were successfully treated with obinutuzumab. Obinutuzumab resulted in complete immunologic remission in all 3 cases and was followed by partial remission in 2 of the cases. Obinutuzumab appears to be a promising treatment strategy for PLA2R-associated MN that fails to respond to rituximab. Membranous nephropathy (MN) is a common cause of nephrotic syndrome in adults. Rituximab, a type I anti-CD20 antibody, has been shown to be an effective therapy in treatment of patients with MN associated with M-type phospholipase A2 receptor (PLA2R) antibodies. Despite its effectiveness, up to 40% of patients may fail to respond to rituximab, which may be related to higher PLA2R antibody titers. Obinutuzumab, a type II anti-CD20 depleter, has been shown to produce a more profound CD20 depletion and be more efficacious in treating certain hematologic malignancies compared with rituximab. We report 3 patients with PLA2R-associated MN for whom rituximab failed to induce immunologic or clinical remisison, but who were successfully treated with obinutuzumab. Obinutuzumab resulted in complete immunologic remission in all 3 cases and was followed by partial remission in 2 of the cases. Obinutuzumab appears to be a promising treatment strategy for PLA2R-associated MN that fails to respond to rituximab.
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
大幅提高文件上传限制,最高150M (2024-4-1)

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
oracl完成签到 ,获得积分10
4秒前
游大达完成签到 ,获得积分10
16秒前
20秒前
祝您开心发布了新的文献求助10
25秒前
ZYQ完成签到 ,获得积分10
50秒前
51秒前
慧慧完成签到 ,获得积分10
54秒前
小燕子完成签到 ,获得积分10
55秒前
isedu完成签到,获得积分10
56秒前
zoele完成签到 ,获得积分10
56秒前
59秒前
哈哈哈哈发布了新的文献求助30
1分钟前
小鱼女侠完成签到 ,获得积分10
1分钟前
ww完成签到,获得积分10
1分钟前
忐忑的雪糕完成签到 ,获得积分10
1分钟前
lilylwy完成签到 ,获得积分10
1分钟前
钦影完成签到 ,获得积分10
1分钟前
永不止步完成签到 ,获得积分10
1分钟前
柒邪完成签到 ,获得积分10
1分钟前
蓝眸完成签到 ,获得积分10
1分钟前
哈哈哈哈完成签到,获得积分10
1分钟前
ttt完成签到 ,获得积分10
2分钟前
janer完成签到 ,获得积分10
2分钟前
华仔应助小林采纳,获得10
2分钟前
一个没自信的boy完成签到 ,获得积分10
2分钟前
loren313完成签到,获得积分10
2分钟前
sisea完成签到 ,获得积分10
2分钟前
奋斗的小张完成签到 ,获得积分10
2分钟前
wang完成签到,获得积分20
2分钟前
smy完成签到 ,获得积分10
2分钟前
ccc完成签到,获得积分10
2分钟前
山鸟与鱼不同路完成签到 ,获得积分10
3分钟前
3分钟前
小林发布了新的文献求助10
3分钟前
drtianyunhong完成签到,获得积分10
3分钟前
4分钟前
小林发布了新的文献求助10
4分钟前
nmm完成签到 ,获得积分10
4分钟前
饱满的绮烟完成签到,获得积分10
4分钟前
111完成签到,获得积分10
4分钟前
高分求助中
Thermodynamic data for steelmaking 3000
Manual of Clinical Microbiology, 4 Volume Set (ASM Books) 13th Edition 1000
Cross-Cultural Psychology: Critical Thinking and Contemporary Applications (8th edition) 800
Counseling With Immigrants, Refugees, and Their Families From Social Justice Perspectives pages 800
マンネンタケ科植物由来メロテルペノイド類の網羅的全合成/Collective Synthesis of Meroterpenoids Derived from Ganoderma Family 500
Electrochemistry 500
Broflanilide prolongs the development of fall armyworm Spodoptera frugiperda by regulating biosynthesis of juvenile hormone 400
热门求助领域 (近24小时)
化学 材料科学 医学 生物 有机化学 工程类 生物化学 纳米技术 物理 内科学 计算机科学 化学工程 复合材料 遗传学 基因 物理化学 催化作用 电极 光电子学 量子力学
热门帖子
关注 科研通微信公众号,转发送积分 2371818
求助须知:如何正确求助?哪些是违规求助? 2079799
关于积分的说明 5208412
捐赠科研通 1807177
什么是DOI,文献DOI怎么找? 902021
版权声明 558266
科研通“疑难数据库(出版商)”最低求助积分说明 481681