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空间转录组学揭示了皮肤肉芽肿性疾病中组织有序且独特的免疫激活。

Spatial transcriptomics reveals organized and distinct immune activation in cutaneous granulomatous disorders.

机构信息

Department of Pathology, NYU Langone Health, New York, NY; Department of Dermatology, Yale School of Medicine, New Haven, Conn.

Department of Dermatology, Yale School of Medicine, New Haven, Conn.

出版信息

J Allergy Clin Immunol. 2024 Nov;154(5):1216-1231. doi: 10.1016/j.jaci.2024.07.021. Epub 2024 Aug 3.

Abstract

BACKGROUND

Noninfectious (inflammatory) cutaneous granulomatous disorders include cutaneous sarcoidosis (CS), granuloma annulare (GA), necrobiosis lipoidica (NL), and necrobiotic xanthogranuloma (NXG). These disorders share macrophage-predominant inflammation histologically, but the inflammatory architecture and the pattern of extracellular matrix alteration varies. The underlying molecular explanations for these differences remain unclear.

OBJECTIVE

We sought to understand spatial gene expression characteristics in these disorders.

METHODS

We performed spatial transcriptomics in cases of CS, GA, NL, and NXG to compare patterns of immune activation and other molecular features in a spatially resolved fashion.

RESULTS

CS is characterized by a polarized, spatially organized type 1-predominant response with classical macrophage activation. GA is characterized by a mixed but spatially organized pattern of type 1 and type 2 polarization with both classical and alternative macrophage activation. NL showed concomitant activation of type 1, type 2, and type 3 immunity with a mixed pattern of macrophage activation. Activation of type 1 immunity was shared among, CS, GA, and NL and included upregulation of IL-32. NXG showed upregulation of CXCR4-CXCL12/14 chemokine signaling and exaggerated alternative macrophage polarization. Histologic alteration of extracellular matrix correlated with hypoxia and glycolysis programs and type 2 immune activation.

CONCLUSIONS

Inflammatory cutaneous granulomatous disorders show distinct and spatially organized immune activation that correlate with hallmark histologic changes.

摘要

背景

非传染性(炎症性)皮肤肉芽肿性疾病包括皮肤结节病(CS)、环状肉芽肿(GA)、类脂质渐进性坏死(NL)和坏死性黄色肉芽肿(NXG)。这些疾病在组织学上具有以巨噬细胞为主的炎症,但炎症结构和细胞外基质改变的模式不同。这些差异的潜在分子解释尚不清楚。

目的

我们试图了解这些疾病的空间基因表达特征。

方法

我们对 CS、GA、NL 和 NXG 病例进行了空间转录组学分析,以比较免疫激活和其他分子特征的空间分辨模式。

结果

CS 的特征是极化的、空间组织的 1 型优势反应,具有经典的巨噬细胞激活。GA 的特征是 1 型和 2 型极化的混合但空间组织的模式,具有经典和替代的巨噬细胞激活。NL 显示出 1 型、2 型和 3 型免疫的同时激活,具有混合的巨噬细胞激活模式。1 型免疫的激活在 CS、GA 和 NL 中共享,并包括 IL-32 的上调。NXG 显示出 CXCR4-CXCL12/14 趋化因子信号和过度的替代巨噬细胞极化的上调。细胞外基质的组织学改变与缺氧和糖酵解程序以及 2 型免疫激活相关。

结论

炎症性皮肤肉芽肿性疾病表现出独特的、空间组织的免疫激活,与标志性的组织学变化相关。

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