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Sustained low-dose interleukin-2 therapy alleviates pathogenic humoral immunity via elevating the Tfr/Tfh ratio in lupus
Clinical & Translational Immunology ( IF 5.8 ) Pub Date : 2021-06-01 , DOI: 10.1002/cti2.1293
Kaili Liang 1 , Jing He 2 , Yunbo Wei 3 , Qunxiong Zeng 1 , Dongcheng Gong 1 , Jiahuan Qin 1 , Huihua Ding 4, 5 , Zhian Chen 6 , Ping Zhou 4 , Peng Niu 4 , Qian Chen 7 , Chenguang Ding 8 , Liangjing Lu 5 , Xiao-Xiang Chen 5 , Zhanguo Li 2 , Nan Shen 1, 4, 5, 9 , Di Yu 1, 3, 6 , Jun Deng 1, 9
Affiliation  

Low-dose interleukin-2 (IL-2) has shown promising clinical benefits in the treatment of systemic lupus erythematosus (SLE), but how this therapy alleviates pathogenic humoral immunity remains not well understood. The dilemma is that IL-2 can suppress both follicular helper and regulatory T (Tfh and Tfr) cells, which counteract each other in regulating autoantibody production.

中文翻译:

持续的低剂量白细胞介素 2 疗法通过提高狼疮的 Tfr/Tfh 比率来减轻病原性体液免疫

低剂量白细胞介素 2 (IL-2) 在治疗系统性红斑狼疮 (SLE) 中显示出有希望的临床益处,但这种疗法如何减轻病原性体液免疫仍不清楚。困境在于 IL-2 可以抑制滤泡辅助细胞和调节性 T(Tfh 和 Tfr)细胞,它们在调节自身抗体产生时相互抵消。
更新日期:2021-06-02
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