Lupus flares when genetically predisposed people encounter certain environmental agents. How the environment alters the immune response to cause flares is unclear. The treatment of lupus is also imperfect, often requiring drugs with significant toxicities. Understanding how the environment causes lupus flares could indicate safer and more effective treatments. The lupus-inducing drugs procainamide and hydralazine, as well as oxidative stress such as that caused by UV light, silica and infections, inhibit T cell DNA methylation and increase expression of genes such as CDI l a , perforin, CD70, CD40L and KIR genes, converting normal

Public Health Relevance

Environmental agents associated with lupus alter the T cell epigenome, activating genes that convert normal T cells into autoreactive cells that cause lupus in mice. Similar changes characterize a T cell subset in patients with active lupus. This project characterizes the transcriptome and epigenome of this subset, with the goal of identifying targets for therapeutic approaches that eliminate or suppress the subset without affecting normal cells, improving the treatment of human lupus.

Agency
National Institute of Health (NIH)
Institute
National Institute of Allergy and Infectious Diseases (NIAID)
Type
Research Program--Cooperative Agreements (U19)
Project #
5U19AI110502-03
Application #
9059013
Study Section
Special Emphasis Panel (ZAI1)
Project Start
Project End
Budget Start
2016-05-01
Budget End
2017-04-30
Support Year
3
Fiscal Year
2016
Total Cost
Indirect Cost
Name
University of Michigan Ann Arbor
Department
Type
DUNS #
073133571
City
Ann Arbor
State
MI
Country
United States
Zip Code
48109
Gensterblum, Elizabeth; Renauer, Paul; Coit, Patrick et al. (2018) CD4+CD28+KIR+CD11ahi T cells correlate with disease activity and are characterized by a pro-inflammatory epigenetic and transcriptional profile in lupus patients. J Autoimmun 86:19-28
Ray, Donna; Strickland, Faith M; Richardson, Bruce C (2018) Oxidative stress and dietary micronutrient deficiencies contribute to overexpression of epigenetically regulated genes by lupus T cells. Clin Immunol 196:97-102
Richardson, Bruce (2018) The interaction between environmental triggers and epigenetics in autoimmunity. Clin Immunol 192:1-5
Weeding, Emma; Coit, Patrick; Yalavarthi, Srilakshmi et al. (2018) Genome-wide DNA methylation analysis in primary antiphospholipid syndrome neutrophils. Clin Immunol 196:110-116
Alperin, Jessie M; Ortiz-Fernández, Lourdes; Sawalha, Amr H (2018) Monogenic Lupus: A Developing Paradigm of Disease. Front Immunol 9:2496
Strickland, F M; Mau, T; O'Brien, M et al. (2017) Oxidative T Cell Modifications in Lupus and Sjogren's Syndrome. Lupus (Los Angel) 2:
Dozmorov, Mikhail G; Coit, Patrick; Maksimowicz-McKinnon, Kathleen et al. (2017) Age-associated DNA methylation changes in naive CD4+ T cells suggest an evolving autoimmune epigenotype in aging T cells. Epigenomics 9:429-445
Teruel, Maria; Sawalha, Amr H (2017) Epigenetic Variability in Systemic Lupus Erythematosus: What We Learned from Genome-Wide DNA Methylation Studies. Curr Rheumatol Rep 19:32
Tsou, Pei-Suen; Sawalha, Amr H (2017) Unfolding the pathogenesis of scleroderma through genomics and epigenomics. J Autoimmun 83:73-94
Figueroa-Romero, Claudia; Hur, Junguk; Lunn, J Simon et al. (2016) Expression of microRNAs in human post-mortem amyotrophic lateral sclerosis spinal cords provides insight into disease mechanisms. Mol Cell Neurosci 71:34-45

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