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Updated: Jul 16, 2025

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Isolation and Th17 Differentiation of Naïve CD4 T Lymphocytes
Published on: September 26, 2013
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干白素17和干白素23抑制剂是否与恶性瘤有关? - - 来自国际人口研究的见解
Khalaf Kridin1,2,3, Mariam Abdelghaffar4, Noor Mruwat3
1Lűbeck Institute of Experimental Dermatology, University of Lübeck, Lübeck, Germany.
Journal of the European Academy of Dermatology and Venereology : JEADV
|September 21, 2023
概括
与瘤坏死因子抑制剂 (TNFi) 相比,黄素-17抑制剂 (IL-17i) 和黄素-23抑制剂 (IL-23i) 在牛皮患者中显示癌症风险降低. 这些发现对于生物处方决定至关重要.
科学领域:
- 免疫学 免疫学 免疫学
- 皮肤病学 皮肤病学
- 在瘤学瘤学.
背景情况:
- 与IL-23和IL-17抑制剂的长期癌症风险尚未完全理解.
- 牛皮患者需要安全有效的生物治疗.
研究的目的:
- 在接受IL-23抑制剂 (IL-23i) 和IL-17抑制剂 (IL-17i) 治疗的牛皮患者中评估恶性瘤风险.
- 为了比较这种风险与在治疗的前五年内接受瘤坏死因子抑制剂 (TNFi) 治疗的患者.
主要方法:
- 进行了一项基于人口的全球性队列研究.
- 两项分析比较了IL-17i与TNFi的新用户 (每个为15331名患者),以及IL-23i与TNFi的新用户 (每个为5832名患者).
主要成果:
- 使用IL-17i与降低非霍奇金淋巴瘤,结肠直肠癌,肝胆癌,卵巢癌,黑色素瘤和基底细胞癌的风险有关.
- 使用IL-23i与非霍奇金淋巴瘤,肝胆癌和基底细胞癌的风险降低有关.
- 敏感性分析证实IL-17i和IL-23i的恶性瘤风险降低,与以前没有生物药物治疗的患者相比.
结论:
- 互乐金-17 抑制剂和互乐金-23 抑制剂与几种恶性瘤的风险降低有关.
- 在为牛皮开处方生物药物之前,这些发现是重要的考虑因素.
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