Harris group
The Harris group focuses on the disease juvenile idiopathic arthritis (JIA) and the protein HMGB1, a substance which the body uses as a chemical alarm signal. Our goal is to contribute to the development of new drugs that can help people with chronic or acute inflammation and give them better life quality.
About the research group
Helena Erlandsson Harris leads the Harris group. She did her undergraduate training at the University of Uppsala and PhD at the Karolinska Institutet, Sweden. She was appointed professor at Karolinska institutet in 2014. She was head of the Broegelmann Research Laboratory and Professor in Immunology at the University of Bergen in 2022 until 2026.
The group focuses in juvenile idiopathic arthritis (JIA), a disease that each year 15 per 100 000 children in the Nordic countries are diagnosed and is characterised by childhood onset of chronic joint inflammation. There is a great need for improved diagnostic and prognostics tools as well as new therapeutic options. In addition to joint inflammation, destruction of joint tissue and pain are hallmarks of the disease. An improved, in depth understanding of the molecular mechanisms driving these three hallmarks forms the basis for development of diagnostic/prognostic biomarker tests as well as development of new, subgroup specific therapy – precision medicine.
To that end the groups research focuses on the protein HMGB1, a prototypic alarmin, a nuclear protein during tissue homeostasis that when released can induce cell migration, cytokine production, cell differentiation and regeneration. All important features of the inflammatory response. Our research has clearly demonstrated HMGB1 as a mediator of inflammation. In arthritis, HMGB1 mediates inflammation, destruction and pain. The group utilises molecular and cellular functional studies, to investigate the the potential of treatments targeting HMGB1 improves these three arthritis hallmarks.
Projects
Our projects are focused on expanding the molecular knowledge of the immune mechanisms active in JIA as a basis for biomarker and therapy development. To achieve this we analyse biosamples collected from children with JIA, our Swedish sample collection JABBA, and compare generated data with information retrieved from the national quality register Svenska barnreumaregistret. In parallel, we are establishing a JIA sample collection in Bergen (region West). In a recently started project we are investigating the possible connection of JIA, neuroinflammation and its potential influence on quality of life.
How HMGB1 is contributing to inflammation, pain and destruction is studied with a translational approach using molecular and cellular functional studies, analyses of HMGB1 in patient samples and model systems.
Publications
Selected publications
Immunoprofiling of active and inactive systemic juvenile idiopathic arthritis reveals distinct biomarkers: a single-center study. Qu H, Sundberg E, Aulin C, Neog M, Palmblad K, Horne AC, Granath F, Ek A, Melén E, Olsson M, Harris HE.
Pediatr Rheumatol Online J. 2021 Dec 28;19(1):173
Disulfide and Fully Reduced HMGB1 Induce Different Macrophage Polarization and Migration Patterns.
Salo H, Qu H, Mitsiou D, Aucott H, Han J, Zhang XM, Aulin C, Erlandsson Harris H
Biomolecules 2021 05;11(6)
Juvenile idiopathic arthritis patients have a distinct cartilage and bone biomarker profile that differs from healthy and knee-injured children.
Struglics A, Saleh R, Sundberg E, Olsson M, Erlandsson Harris H, Aulin C
Clin Exp Rheumatol ;38(2):355-365
Cleavage of HMGB1 by Proteolytic Enzymes Associated with Inflammatory Conditions.
Sowinska A, Rensing M, Klevenvall L, Neog M, Lundbäck P, Harris HE
Front Immunol 2020 ;11():448262
A novel high mobility group box 1 neutralizing chimeric antibody attenuates drug-induced liver injury and postinjury inflammation in mice.
Lundbäck P, Lea JD, Sowinska A, Ottosson L, Fürst CM, Steen J, Aulin C, Clarke JI, Kipar A, Klevenvall L, Yang H, Palmblad K, Park BK, Tracey KJ, Blom AM, Andersson U, Antoine DJ, Erlandsson Harris H
Hepatology 2016 11;64(5):1699-1710
Therapeutic administration of etoposide coincides with reduced systemic HMGB1 levels in macrophage activation syndrome.
Palmblad K, Schierbeck H, Sundberg E, Horne AC, Erlandsson Harris H, Henter JI, Andersson U
Mol Med 2021 05;27(1):48
People
Group manager
Helena Harris Professor
Group members
Harini Pechiappan PhD Candidate
Andrea Papdine Morovicz Postdoctoral Fellow
Emilie Torkildsen Johansen Master student
Contact
For inquiries about our research, or inquiries about joining our group contact Helena Harris.
- Emails
- Helena.Harris@uib.no