奥萨尼莫德在患有中度至重度活跃克朗氏病的患者中对循环淋巴细胞子组产生不同影响
Sarah Harris1,2, Brian G Feagan3, Stephen Hanauer4
1Bristol Myers Squibb, Princeton, NJ, USA. sarah.harris@bms.com.
Digestive diseases and sciences
|April 3, 2024
概括
在克罗恩病中,用奥扎尼莫德治疗显著减少了循环中的B和T淋巴细胞,同时节省了免疫监测细胞. 未切换的B细胞与治疗疗效相关,表明潜在的反应标志物.
科学领域:
- 免疫学 免疫学 免疫学
- 胃肠病学 胃肠病学
- 药理学 药理学是指药理学的学科.
背景情况:
- 在2期STEPSTONE研究中,ozanimod在中度至重度克罗恩病中显示出有效性和安全性.
- 了解ozanimod对循环淋巴细胞的免疫调节作用对于克罗恩病的治疗至关重要.
研究的目的:
- 评估ozanimod对克罗恩病患者循环淋巴细胞群的影响.
- 为了确定淋巴细胞子集变化和治疗疗效之间的潜在关联.
主要方法:
- 克罗恩病患者在12周内接受了0.92毫克的ozanimod.
- 多色流细胞计分析了治疗前和12周血液样本中的淋巴细胞亚型.
- 统计分析包括威尔科克森的签名等级测试,斯皮尔曼的相关性和后勤回归.
主要成果:
- 奥扎尼莫德显著减少了总T细胞 (45.4%-76.8%) 和B细胞 (76.7%),大多数亚型减少了47.5%至91.3%.
- CD8+终端分化的效应体记忆细胞,单细胞和自然杀手细胞基本上没有受到影响.
- 基线和第12周未切换记忆B细胞水平的增加与临床,内镜和组织学疗效有显著关联.
结论:
- 奥扎尼莫德有效地减少了循环中的B和T细胞子集,显著地保留了免疫监视细胞.
- 观察到的淋巴细胞形状支持在慢性炎症疾病中使用ozanimod感染和恶性瘤的风险较低.
- 没有切换的B细胞水平可以作为克罗恩病中ozanimod反应的预测生物标志物.
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