ISG15 protects human Tregs from interferon alpha-induced contraction in a cell-intrinsic fashion.
ISG15 protects human Tregs from interferon alpha-induced contraction in a cell-intrinsic fashion.
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DOI：
10.1002/cti2.1221
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发表时间：
2020
影响因子：
5.8
通讯作者：
Piconese S
中科院分区：
文献类型：
--
作者：
Pacella I;Spinelli FR;Severa M;Timperi E;Tucci G;Zagaglioni M;Ceccarelli F;Rizzo F;Coccia EM;Patel RS;Martin-Fernandez M;Bogunovic D;Conti F;Barnaba V;Piconese S
Type I interferons (IFNs) inhibit regulatory T‐cell (Treg) expansion and activation, making them beneficial in antiviral responses, but detrimental in autoimmune diseases. Herein, we investigate the role of ISG15 in human Tregs in the context of refractoriness to type I IFN stimulation. ISG15 expression and Treg dynamics were analysed in vitro and ex vivo from patients with chronic hepatitis C, with lupus and ISG15 deficiency. ISG15 is expressed at high levels in human Tregs, renders them refractory to the IFN‐STAT1 signal, and protects them from IFN‐driven contraction. In vitro, Tregs from healthy controls upregulate ISG15 upon activation to higher levels than conventional CD4 T cells, and ISG15‐silenced Tregs are more susceptible to IFNα‐induced contraction. In human ISG15 deficiency, patient Tregs display an elevated IFN signature relative to Tregs from healthy control. In vivo, in patients with chronic hepatitis C, 2 days after starting pegIFN/ribavirin therapy, a stronger ISG15 inducibility correlates with a milder Treg depletion. Ex vivo, in systemic lupus erythematosus patients, higher levels of ISG15 are associated to reduced STAT1 phosphorylation in response to IFNα, and also to increased frequencies of Tregs, characterising active disease. Our results reveal a Treg‐intrinsic role of ISG15 in dictating their refractoriness to the IFN signal, thus preserving the Treg population under inflammatory conditions. Tregs are particularly sensitive to the detrimental effects of type I IFNs. Here, we show that an IFN‐stimulated gene, ISG15, mediates Treg refractoriness to IFN‐induced contraction in vitro. In lupus patients, high ISG15 expression sustains high Treg frequencies in active disease. In human ISG15 deficiency, Tregs show an elevated IFN signature.
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影响因子：
--
作者：
Golding, Amit;Hasni, Sarfaraz;Illei, Gabor;Shevach, Ethan M.
通讯作者：
Shevach, Ethan M.
DOI：
10.1084/jem.20021553
发表时间：
2003-03-17
期刊：
The Journal of experimental medicine
影响因子：
--
作者：
Bennett L;Palucka AK;Arce E;Cantrell V;Borvak J;Banchereau J;Pascual V
通讯作者：
Pascual V
DOI：
10.1038/s41579-018-0020-5
发表时间：
2018-07
期刊：
Nature reviews. Microbiology
影响因子：
--
作者：
Perng YC;Lenschow DJ
通讯作者：
Lenschow DJ
影响因子：
13.5
作者：
Piconese, Silvia;Timperi, Eleonora;Barnaba, Vincenzo
通讯作者：
Barnaba, Vincenzo
影响因子：
7.7
作者：
Regev, Aviv;Teichmann, Sarah A;Yosef, Nir
通讯作者：
Yosef, Nir