Antibodies targeting the shared cytokine receptor IL-1 receptor accessory protein invoke distinct mechanisms to block all cytokine signaling.
Antibodies targeting the shared cytokine receptor IL-1 receptor accessory protein invoke distinct mechanisms to block all cytokine signaling.
复制标题
靶向共享细胞因子受体 IL-1 受体辅助蛋白的抗体会调用不同的机制来阻断所有细胞因子信号传导。
DOI:
10.1016/j.celrep.2024.114099
复制
发表时间:
2024
期刊:
影响因子:
8.8
通讯作者:
Huyhn,Chau
中科院分区:
文献类型:
--
作者:
Fields,JamesK;Gyllenbäck,ElinJaensson;Bogacz,Marek;Obi,Juliet;Birkedal,GabrielSvensson;Sjöström,Kjell;Maravillas,Kino;Grönberg,Caitríona;Rattik,Sara;Kihn,Kyle;Flowers,Maria;Smith,AllyK;Hansen,Nils;Fioretos,Thoas;Huyhn,Chau
Interleukin-1 (IL-1)-family cytokines are potent modulators of inflammation, coordinating a vast array of immunological responses across innate and adaptive immune systems. Dysregulated IL-1-family cytokine signaling, however, is involved in a multitude of adverse health effects, such as chronic inflammatory conditions, autoimmune diseases, and cancer. Within the IL-1 family of cytokines, six—IL-1, IL-1, IL-33, IL-36, IL-36, and IL-36—require the IL-1 receptor accessory protein (IL-1RAcP) as their shared co-receptor. Common features of cytokine signaling include redundancy of signaling pathways, sharing of cytokines and receptors, pleiotropy of the cytokines themselves, and multifaceted immune responses. Accordingly, targeting multiple cytokines simultaneously is an emerging therapeutic strategy and can provide advantages over targeting a single cytokine pathway. Here, we show that two monoclonal antibodies, CAN10 and 3G5, which target IL-1RAcP for broad blockade of all associated cytokines, do so through distinct mechanisms and provide therapeutic opportunities for the treatment of inflammatory diseases.
登录
查看更多内容
影响因子:
32.4
作者:
Garlanda C;Dinarello CA;Mantovani A
通讯作者:
Mantovani A
DOI:
10.1016/j.jid.2018.07.025
发表时间:
2019-01
期刊:
The Journal of investigative dermatology
影响因子:
--
作者:
Cai Y;Xue F;Quan C;Qu M;Liu N;Zhang Y;Fleming C;Hu X;Zhang HG;Weichselbaum R;Fu YX;Tieri D;Rouchka EC;Zheng J;Yan J
通讯作者:
Yan J
影响因子:
158.5
作者:
Klein, Allan L.;Imazio, Massimo;Paolini, John F.
通讯作者:
Paolini, John F.
DOI:
--
发表时间:
2022
期刊:
Cancer Immunology and Immunotherapy
影响因子:
--
作者:
Camilla Rydberg Millrud;Adnan Deronic;C. Grönberg;Elin Jaensson Gyllenbäck;K. Wachenfeldt;G. Forsberg;D. Liberg
通讯作者:
D. Liberg
影响因子:
32.4
作者:
Günther S;Deredge D;Bowers AL;Luchini A;Bonsor DA;Beadenkopf R;Liotta L;Wintrode PL;Sundberg EJ
通讯作者:
Sundberg EJ