1203 STING/type i interferon pathway activation in patients with perniosis during the COVID–19 pandemic

J. An, A. Kalus, Sarah Chung, Brandon Seaton, Ata S. Moshiri, D. Lih, Ying Zheng, H. Krishnamurthy, Xizhang Sun, Lena Tanaka, K. Elkon
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Abstract

1203 Figure 1Clinical appearance of perniosis in study patients showing red and purple papules over several toes some with near blisters (A and B). MxA staining of skin from perniosis lesion (D) showing lymphocytic inflammation in the dermis with perivascular and periadenexal inflammation. There is prominent MxA staining in the epidermis, dermal inflammatory infiltrate and in the superficial endothelial cells indicating interferon activation in skin. This is compared to no MxA staining in normal skin (C).[Figure omitted. See PDF]ConclusionsThe frequency of perniosis during the COVID pandemic, suggests a relationship between these two conditions although direct evidence of COVID-19 infection has been limited. We observed a trend toward higher IFN-b gene expression in PBMC as well as higher phospho-STING protein expression in CD14 monocytes and, most significantly, strong expression of MxA in skin. While the small number of patients preclude a definitive explanation, our data suggest that COVID associated perniosis is an interferonopathy. We propose that acute, transient COVID infection led to monocyte activation, IFN-I production and damage to the small vessels, likely aggravated by cold exposure.
1203 STING/ i型干扰素途径在2019冠状病毒病大流行期间的激活
1203图1研究患者腹膜炎的临床表现为几个脚趾上的红色和紫色丘疹,一些伴有近水疱(A和B)。腹膜炎病变皮肤的MxA染色(D)显示真皮淋巴细胞炎症伴血管周围和腺性腺周围炎症。表皮、真皮炎症浸润和浅表内皮细胞中有明显的MxA染色,提示皮肤中有干扰素激活。与正常皮肤没有MxA染色相比(C)。[图略]结论尽管COVID-19感染的直接证据有限,但在COVID-19大流行期间,腐殖病的频率表明这两种情况之间存在关系。我们观察到PBMC中IFN-b基因的高表达趋势,CD14单核细胞中phospho-STING蛋白的高表达趋势,最显著的是皮肤中MxA的强表达。虽然患者数量少,无法给出明确的解释,但我们的数据表明,COVID相关的羊粪病是一种干扰素病。我们认为,急性、短暂的COVID感染导致单核细胞活化、IFN-I产生和小血管损伤,这可能因寒冷暴露而加剧。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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