# Differences in the DNA Methylome of T cells in Adults With Asthma of Varying Severity

**Authors:** Yixuan Liao, Raymond Cavalcante, Jonathan Waller, Furong Deng, Anne Scruggs, Yvonne Huang, Ulus Atasoy, Yahong Chen, Steven Huang

PMC · DOI: 10.21203/rs.3.rs-4476948/v1 · 2024-06-10

## TL;DR

This study shows that DNA methylation in T cells differs among adults with asthma of varying severity, potentially influencing disease progression and characteristics.

## Contribution

The study identifies specific DNA methylation differences in T cells linked to asthma severity and airway inflammation in adults.

## Key findings

- DNA methylation patterns in T cells differ significantly among adults with varying asthma severity and airway inflammation.
- Differentially methylated genes are enriched in pathways related to asthma, T cell function, and drug metabolism.
- Key genes like RUNX3, HLA family members, and others in JAK2 and TNF pathways show methylation changes based on asthma severity.

## Abstract

DNA methylation plays a critical role in asthma development, but differences in DNA methylation among adults with varying asthma severity or asthma endotypes are less well-defined.

To examine how DNA methylomic patterns differ among adults with asthma based on asthma severity and airway inflammation.

Peripheral blood T cells from 35 adults with asthma in Beijing, China were serially collected over time (130 samples total) and analyzed for global DNA methylation using the Illumina MethylationEPIC Array. Differential methylation was compared among subjects with varying airway inflammation and severity, as measured by fraction of exhaled nitric oxide, forced expiratory volume in one second (FEV1), and Asthma Control Test (ACT) scores.

Significant differences in DNA methylation were noted among subjects with different degrees of airway inflammation and asthma severity. These differences in DNA methylation were annotated to genes that were enriched in pathways related to asthma or T cell function and included gene ontology categories related to MHC class II assembly, T cell activation, interleukin (IL)-1, and IL-12. Genes related to P450 drug metabolism, glutathione metabolism, and developmental pathways were also differentially methylated in comparisons between subjects with high vs low FEV1 and ACT. Notable genes that were differentially methylated based on asthma severity included RUNX3, several members of the HLA family, AGT, PTPRC, PTPRJ, and several genes downstream of the JAK2 and TNF signaling pathway.

These findings demonstrate how adults with asthma of varying severity possess differences in peripheral blood T cell DNA methylation that contribute to the phenotype and severity of their overall disease.

## Linked entities

- **Genes:** RUNX3 (RUNX family transcription factor 3) [NCBI Gene 864], AGT (angiotensinogen) [NCBI Gene 183], PTPRC (protein tyrosine phosphatase receptor type C) [NCBI Gene 5788], PTPRJ (protein tyrosine phosphatase receptor type J) [NCBI Gene 5795], JAK2 (Janus kinase 2) [NCBI Gene 3717], TNF (tumor necrosis factor) [NCBI Gene 7124]
- **Diseases:** asthma (MONDO:0004979)

## Full-text entities

- **Genes:** IL12B (interleukin 12B) [NCBI Gene 3593] {aka CLMF, CLMF2, IL-12B, IMD28, IMD29, NKSF}, JAK2 (Janus kinase 2) [NCBI Gene 3717] {aka JTK10}, PTPRJ (protein tyrosine phosphatase receptor type J) [NCBI Gene 5795] {aka CD148, DEP1, HPTP eta, HPTPeta, R-PTP-ETA, R-PTP-J}, HLA-A (major histocompatibility complex, class I, A) [NCBI Gene 3105] {aka HLAA}, RUNX3 (RUNX family transcription factor 3) [NCBI Gene 864] {aka AML2, CBFA3, PEBP2aC}, TNF (tumor necrosis factor) [NCBI Gene 7124] {aka DIF, IMD127, TNF-alpha, TNFA, TNFSF2, TNLG1F}, AGT (angiotensinogen) [NCBI Gene 183] {aka ANHU, SERPINA8, hFLT1}, PTPRC (protein tyrosine phosphatase receptor type C) [NCBI Gene 5788] {aka B220, CD45, CD45R, GP180, IMD105, L-CA}
- **Diseases:** airway inflammation (MESH:D007249), Asthma (MESH:D001249)

## Figures

7 figures with captions in the complete paper: https://tomesphere.com/paper/PMC11213176/full.md

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Source: https://tomesphere.com/paper/PMC11213176