Activities

Stress represents the single most important cause of disease, causing costs as high as 3-4 % of the European GNP, and up to 60% of all work-days lost to disease. Many of these diseases are related to infections and aberrant immune reactions. Our interest is in elucidating genetic, epigenetic, transcriptional, translation and post-translational mechanisms underlying environmental control of the stress reaction, particularly within the negative feedback loop of the HPA axis.

The main goal of our research is to understand the molecular mechanisms underlying the environmental control of phenotype development, in the HPA axis and in the immune system

Collaborations:

  • “Forschungsinstitut für Psychobiologie des Stresses” University Trier,
  • Research Unit INSIDE, University of Luxembourg
  • Leiden-Amsterdam Centre for Drug Research (LACDR)
  • Department of Periodontology University of Oslo & Department of Medical Psychology, Bergen, Norway
  • Luxembourg Centre for Systems Biology (LCSB)
  • Luxembourg Immune Mediated Inflammatory Disease Research Association (LIMIDRA)
  • ZithaKlinik, Luxembourg
  • Proteome and Genome Research Unit, LIH

Research projects

  • EpiPath – Severe childhood adversity is thought to be one of the strongest risk factors for three major public health problems: cardiovascular disease, upper respiratory tract infections (URTI) and mental health problems. The principal interface between the environment and the genome is epigenetic methylation of genomic DNA. Our working hypothesis is that early life adversity induces high risk epigenetic modifications, and a cohort of young adults that experienced poor early life conditions are currently being recruited.

  • MetCOEPs -Environmentally induced epigenetic modifications are set in place many years before the associated type 2 diabetes, major depression, schizophrenia, hypertension and cardiovascular diseases becomes detectable. MetCOEPs looks at how these entirely natural modifications to our genome influence the activity of the associated genes, and the proteins they produce. Understanding this cascade of events will allow us to better understand how our environment influences our wellbeing, and to understand how these epigenetic markers can be used to identify people at risk of many diseases, allowing for suitable early interventions that reduce the eventual disease risk.

  • ESPoiRe - Although rheumatoid arthritis treatment options have improved significantly over recent years, we cannot currently predict which therapeutic option would suit individual patients leading to the current “trial and error” treatment approach “testing” patients for clinical efficacy drug by drug. Preliminary evidence suggests a large role for DNA methylation in RA. Together with Luxembourg rheumatologists we will generate epigenomes from clear clinical phenotypes, and further develop the LUXIMID register together with LIMIDRA and the LCSB to improve patient stratification and treatment choice.

Featured Publications

The COVID-19 pandemic: Does our early life environment, life trajectory and socioeconomic status determine disease susceptibility and severity?

  • Immune Endocrine and Epigenetics
July 19, 2020
2020 Jul. Int J Mol Sci.21(14):E5094.
By:
  • Holuka C
  • Merz MP
  • Fernandes SB
  • Charalambous EG
  • Seal SV
  • Grova N
  • Turner JD.

The atypical chemokine receptor ACKR3/CXCR7 is a broad-spectrum scavenger for opioid peptides.

  • Immuno-Pharmacology and Interactomics
  • Immune Endocrine and Epigenetics
  • Transversal Translational Medicine
  • Allergy and Clinical Immunology
June 19, 2020
2020 Jun. Nat Commun.11(1):3033.
By:
  • Meyrath M
  • Szpakowska M
  • Zeiner J
  • Massotte L
  • Merz MP
  • Benkel T
  • Simon K
  • Ohnmacht J
  • Turner JD
  • Kruger R
  • Seutin V
  • Ollert M
  • Kostenis E
  • Chevigne A.
See all publications

Contacts

Jonathan Turner

Ph.D.

29, rue Henri Koch
L-4354Esch-sur-Alzette
Luxembourg
Tel. : +352 26970-629