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Spatial transcriptomics reveals organized and distinct immune activation in cutaneous granulomatous disorders.
Daccache, Joseph; Park, Eunsuh; Junejo, Muhammad; Abdelghaffar, Mariam; Hwang, Erica; Mohanty, Chitrasen; Singh, Chandra K; Wang, Guilin; Wheeler, John O; Shields, Bridget E; Nelson, Caroline A; Wang, Yiwei; Damsky, William.
Afiliação
  • Daccache J; Department of Pathology, NYU Langone Health, New York, NY; Department of Dermatology, Yale School of Medicine, New Haven, Conn. Electronic address: joseph.daccache@nyulangone.org.
  • Park E; Department of Dermatology, Yale School of Medicine, New Haven, Conn.
  • Junejo M; Department of Dermatology, Yale School of Medicine, New Haven, Conn.
  • Abdelghaffar M; School of Medicine, Royal College of Surgeons in Ireland, Adliya, Bahrain.
  • Hwang E; Department of Dermatology, Yale School of Medicine, New Haven, Conn.
  • Mohanty C; Department of Biostatistics and Medical Informatics, University of Wisconsin, Madison, Wis.
  • Singh CK; Department of Dermatology, University of Wisconsin School of Medicine and Public Health, Madison, Wis.
  • Wang G; Keck Microarray Shared Resource, Yale School of Medicine, New Haven, Conn.
  • Wheeler JO; Keck Microarray Shared Resource, Yale School of Medicine, New Haven, Conn.
  • Shields BE; Department of Dermatology, University of Wisconsin School of Medicine and Public Health, Madison, Wis.
  • Nelson CA; Department of Dermatology, Yale School of Medicine, New Haven, Conn.
  • Wang Y; Department of Dermatology, Yale School of Medicine, New Haven, Conn.
  • Damsky W; Department of Dermatology, Yale School of Medicine, New Haven, Conn; Department of Pathology, Yale School of Medicine, New Haven, Conn. Electronic address: william.damsky@yale.edu.
Article em En | MEDLINE | ID: mdl-39098508
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.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: J Allergy Clin Immunol Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: J Allergy Clin Immunol Ano de publicação: 2024 Tipo de documento: Article