Psoriasis, Cardiovascular Events, and Biologics: Lights and Shadows.
Psoriasis, Cardiovascular Events, and Biologics: Lights and Shadows.
复制标题
DOI:
10.3389/fimmu.2018.01668
复制
发表时间:
2018
影响因子:
7.3
通讯作者:
Balato A
中科院分区:
文献类型:
--
作者:
Caiazzo G;Fabbrocini G;Di Caprio R;Raimondo A;Scala E;Balato N;Balato A
Nowadays, it is well established a link between psoriasis and cardiovascular (CV) diseases. A series of different overlapping mechanisms including inflammation, homeostasis dysregulation, and genetic susceptibility are thought to underlie this association. Advances in understanding the molecular patterns involved in the complex scenario of psoriasis have highlighted a tight correlation with atherosclerosis. Indeed, common profiles are shared in term of inflammatory cytokines and cell types. In the last decade, the management of psoriasis patients has been revolutionized with the introduction of biological therapies, such as tumor necrosis factor-alpha (TNF-α), interleukin (IL)-12/23, and IL-17 inhibitors. In clinical setting, the effectiveness of these therapies as well as the incidence of CV events is related to the type of biologics. In particular, anti-TNF-α agents seem to reduce these events in psoriasis patients whereas anti-IL-12/23 agents related CV events reduction still remain to clarify. It has to be taken into account that IL-12/23 inhibitors have a shorter post-marketing surveillance period. An even more restricted observational time is available for anti-IL-17 agents. IL-17 is associated with psoriasis, vascular disease, and inflammation. However, IL-17 role in atherosclerosis is still debated, exerting both pro-atherogenic and anti-atherogenic effects depending on the specific context. In this review, we will discuss the differences between the onset of CV events in psoriasis patients, referred to specific biological therapy and the underlying immunological mechanism. Given the development of new therapeutic strategies, the investigation of these inhibitors impact on heart failure outcome is extremely important.
登录
查看更多内容
影响因子:
8.6
作者:
Cheng, Xiang;Yu, Xian;Liao, Yu-hua
通讯作者:
Liao, Yu-hua
影响因子:
2
作者:
Bradburn, Michael J.;Deeks, Jonathan J.;Localio, A. Russell
通讯作者:
Localio, A. Russell
DOI:
10.1177/039463200902200411
发表时间:
2009-10-01
影响因子:
3.5
作者:
Caldarola, G.;De Simone, C.;Feliciani, C.
通讯作者:
Feliciani, C.
DOI:
10.1084/jem.20060244
发表时间:
2006-11-27
期刊:
The Journal of experimental medicine
影响因子:
--
作者:
Chan JR;Blumenschein W;Murphy E;Diveu C;Wiekowski M;Abbondanzo S;Lucian L;Geissler R;Brodie S;Kimball AB;Gorman DM;Smith K;de Waal Malefyt R;Kastelein RA;McClanahan TK;Bowman EP
通讯作者:
Bowman EP
DOI:
10.1186/1740-2557-3-5
发表时间:
2006-10-05
期刊:
Journal of autoimmune diseases
影响因子:
--
作者:
Cordiali-Fei P;Trento E;D'Agosto G;Bordignon V;Mussi A;Ardigò M;Mastroianni A;Vento A;Solivetti F;Berardesca E;Ensoli F
通讯作者:
Ensoli F