Different Disease Endotypes in Phenotypically Similar Vasculitides Affecting Small-to-Medium Sized Blood Vessels

Front Immunol. 2021 Feb 22;12:638571. doi: 10.3389/fimmu.2021.638571. eCollection 2021.

Abstract

Objectives: Chronic primary vasculitis describes a group of complex and rare diseases that are characterized by blood vessel inflammation. Classification of vasculitis subtypes is based predominantly on the size of the involved vessels and clinical phenotype. There is a recognized need to improve classification, especially for small-to-medium sized vessel vasculitides, that, ideally, is based on the underlying biology with a view to informing treatment. Methods: We performed RNA-Seq on blood samples from children (n = 41) and from adults (n = 11) with small-to-medium sized vessel vasculitis, and used unsupervised hierarchical clustering of gene expression patterns in combination with clinical metadata to define disease subtypes. Results: Differential gene expression at the time of diagnosis separated patients into two primary endotypes that differed in the expression of ~3,800 genes in children, and ~1,600 genes in adults. These endotypes were also present during disease flares, and both adult and pediatric endotypes could be discriminated based on the expression of just 20 differentially expressed genes. Endotypes were associated with distinct biological processes, namely neutrophil degranulation and T cell receptor signaling. Conclusions: Phenotypically similar subsets of small-to-medium sized vessel vasculitis may have different mechanistic drivers involving innate vs. adaptive immune processes. Discovery of these differentiating immune features provides a mechanistic-based alternative for subclassification of vasculitis.

Keywords: ANCA; inflammation; neutrophils; transcriptome; vasculitis.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Blood Vessels / pathology*
  • Cell Degranulation / genetics
  • Child
  • Cohort Studies
  • Female
  • Humans
  • Inflammation / genetics*
  • Male
  • Neutrophils / immunology*
  • Organ Size
  • Phenotype
  • Receptors, Antigen, T-Cell / metabolism
  • Sequence Analysis, RNA
  • Signal Transduction
  • T-Lymphocytes / immunology*
  • Transcriptome
  • Vasculitis / genetics*

Substances

  • Receptors, Antigen, T-Cell

Grant support