Navrazhina Kristina, Garcet Sandra, Gonzalez Juana, Grand David, Frew John W, Krueger James G
Laboratory of Investigative Dermatology, The Rockefeller University, New York, New York, USA; Weill Cornell/Rockefeller/Sloan Kettering Tri-Institutional MD-PhD Program, New York, New York, USA.
Laboratory of Investigative Dermatology, The Rockefeller University, New York, New York, USA.
J Invest Dermatol. 2021 Sep;141(9):2197-2207. doi: 10.1016/j.jid.2021.02.742. Epub 2021 Mar 22.
Hidradenitis suppurativa is a chronic inflammatory dermatosis with presentations ranging from painful nodules and abscesses to draining tunnels. Using an unbiased proteomics approach, we assessed cardiovascular-, cardiometabolic-, and inflammation-related biomarkers in the serum of patients with moderate-to-severe hidradenitis suppurativa. The serum of patients with hidradenitis suppurativa clustered separately from that of healthy controls and had an upregulation of neutrophil-related markers (Cathepsin D, IL-17A, CXCL1). Patients with histologically diagnosed dermal tunnels had higher serum lipocalin-2 levels compared with those without tunnels. Consistent with this, patients with tunnels had a more neutrophilic-rich serum signature, marked by Cathepsin D, IL-17A, and IL-17D alterations. There was a significant serum‒skin correlation between proteins in the serum and the corresponding mRNA expression in skin biopsies, with healthy-appearing perilesional skin demonstrating a significant correlation with neutrophil-related proteins in the serum. CSF3 mRNA levels in lesional skin significantly correlated with neutrophil-related proteins in the serum, suggesting that CFS3 in the skin may be a driver of neutrophilic inflammation. Clinical significantly correlated with the levels of lipocalin-2 and IL-17A in the serum. Using an unbiased, large-scale proteomic approach, we demonstrate that hidradenitis suppurativa is a systemic neutrophilic dermatosis, with a specific molecular signature associated with the presence of dermal tunnels.
化脓性汗腺炎是一种慢性炎症性皮肤病,表现范围从疼痛性结节和脓肿到引流窦道。我们采用无偏倚蛋白质组学方法,评估了中度至重度化脓性汗腺炎患者血清中的心血管、心脏代谢和炎症相关生物标志物。化脓性汗腺炎患者的血清与健康对照者的血清聚类分离,且中性粒细胞相关标志物(组织蛋白酶D、白细胞介素-17A、CXC趋化因子配体1)上调。组织学诊断为真皮窦道的患者血清中的lipocalin-2水平高于无窦道的患者。与此一致的是,有窦道的患者血清中嗜中性粒细胞更为丰富,以组织蛋白酶D、白细胞介素-17A和白细胞介素-17D的改变为特征。血清中的蛋白质与皮肤活检中相应的mRNA表达之间存在显著的血清-皮肤相关性,外观正常的病灶周围皮肤与血清中的中性粒细胞相关蛋白存在显著相关性。病灶皮肤中的CSF3 mRNA水平与血清中的中性粒细胞相关蛋白显著相关,提示皮肤中的CFS3可能是嗜中性粒细胞炎症的驱动因素。临床情况与血清中lipocalin-2和白细胞介素-17A的水平显著相关。我们采用无偏倚的大规模蛋白质组学方法证明,化脓性汗腺炎是一种全身性嗜中性粒细胞性皮肤病,具有与真皮窦道存在相关的特定分子特征。