Forskergrupper
Kort info
I lead several biobanks: Immune deficiency Western Norway, Enamel and celiac disease in the young at Helse Bergen and TK Vestland and the 21OHautoantibody-project biobank at Helse Bergen.
Undervisning
From 2026: MEDDOD1, MEDDOD2, BMED330 (cell communication and intracel. sign.), TPBAKBP (lab for oral hygenists)
Previously: ODPATIM2; immunology for dentists.
Publikasjoner
Vitenskapelig artikkel
- Thea Sjøgren; Jan-Inge Bjune; Eystein Sverre Husebye et al. (2024). Regulatory T cells in autoimmune primary adrenal insufficiency. (ekstern lenke)
- Marissa Penna-Martinez; Gesine Meyer; Anette Susanne Bøe Wolff et al. (2021). Vitamin D status and pathway genes in five European autoimmune Addison's disease cohorts. (ekstern lenke)
- Ingeborg Brønstad; Lars Ertesvåg Breivik; Paal Methlie et al. (2014). Functional studies of novel CYP21A2 mutations detected in Norwegian patients with congenital adrenal hyperplasia. (ekstern lenke)
- Beate Skinningsrud; Eystein Sverre Husebye; Simon H. Pearce et al. (2008). Polymorphisms in CLEC16A and CIITA at 16p13 are associated with primary adrenal insufficiency. (ekstern lenke)
- Marianne Astor; Kristian Løvås; Anette Susanne Bøe Wolff et al. (2015). Hypomagnesemia and functional hypoparathyroidism due to novel mutations in the Mg-channel TRPM6. (ekstern lenke)
- Anette Susanne Bøe; Anders Mølster (1992). Albueartroskopi. (ekstern lenke)
- Bergithe Eikeland Oftedal; Amund Holte Berger; Øyvind Bruserud et al. (2023). A partial form of AIRE deficiency underlies a mild form of autoimmune polyendocrine syndrome type 1. (ekstern lenke)
- Haydee Artaza; Daniel Eriksson; Ksenia Lavrichenko et al. (2024). Rare copy number variation in autoimmune Addison’s disease. (ekstern lenke)
- Hans Olav Ueland; Arve Ulvik; Kristian Løvås et al. (2023). Systemic Activation of the Kynurenine Pathway in Graves Disease With and Without Ophthalmopathy. (ekstern lenke)
- O Furnes; Anette Susanne Bøe; E Sudmann (1996). Lumbale skiveprolapser hos ungdom. (ekstern lenke)
- Antonella Meloni; Maria Furcas; Filomena Cetani et al. (2008). Autoantibodies against Type I Interferons as an Additional Diagnostic Criterion for Autoimmune Polyendocrine Syndrome Type I. (ekstern lenke)
- Bergithe Eikeland Oftedal; Nicolas Delaleu; David William Peter Dolan et al. (2023). Systemic interferon type I and B cell responses are impaired in autoimmune polyendocrine syndrome type 1. (ekstern lenke)
- Anette Susanne Bøe Wolff; Jaanika Kärner; Jone Furulund Owe et al. (2014). Clinical and serologic parallels to APS-I in patients with thymomas and autoantigen transcripts in their tumors. (ekstern lenke)
- Martina Moter Erichsen; Martina M Erichsen; Kristian Løvås et al. (2009). Clinical, Immunological, and Genetic Features of Autoimmune Primary Adrenal Insufficiency: Observations from a Norwegian Registry. (ekstern lenke)
- Eirik Bratland; Ng'weina Francis Magitta; Anette Susanne Bøe Wolff et al. (2013). Autoantibodies against aromatic amino acid hydroxylases in patients with autoimmune polyendocrine syndrome type 1 target multiple antigenic determinants and reveal regulatory regions crucial for enzymatic activity. (ekstern lenke)
- Mikael Thomassen Neset; Roy Miodini Nilsen; Kristian Løvås et al. (2025). Exploring tear fluid biomarkers and the ocular surface in thyroid eye disease. (ekstern lenke)
- Dmytro Fishman; Kai Kisand; Christina Hertel et al. (2017). Autoantibody Repertoire in APECED Patients Targets Two Distinct Subgroups of Proteins. (ekstern lenke)
- Kai Kisand; Maire Link; Anette Susanne Bøe Wolff et al. (2008). Interferon autoantibodies associated with AIRE deficiency decrease the expression of IFN-stimulated genes. (ekstern lenke)
- Sigrid Aslaksen; Anette Susanne Bøe Wolff; Magnus Dehli Vigeland et al. (2019). Identification and characterization of rare Toll-like receptor 3 variants in patients with autoimmune Addison’s disease. (ekstern lenke)
- Ingeborg Brønstad; Beate Skinningsrud; Eirik Bratland et al. (2014). CYP21A2 polymorphisms in patients with autoimmune Addison's disease, and linkage disequilibrium to HLA risk alleles. (ekstern lenke)
- Steffen Meyer; Martin Woodward; Christina Hertel et al. (2016). AIRE-Deficient Patients Harbor Unique High-Affinity Disease-Ameliorating Autoantibodies. (ekstern lenke)
- Bergithe Eikeland Oftedal; Ileana Mihaela Cuida Marthinussen; Martina Moter Erichsen et al. (2017). Impaired salivary gland activity in patients with autoimmune polyendocrine syndrome type I. (ekstern lenke)
- Anette Susanne Bøe Wolff; Anna L. Mitchell; Heather J. Cordell et al. (2015). CTLA-4 as a genetic determinant in autoimmune Addison's disease. (ekstern lenke)
- P Helland; Anette Susanne Bøe; Anders Mølster et al. (1996). Open tibial fractures treated with the Ex-fi-re external system. (ekstern lenke)
- Maribel Aranda-Guillén; Ellen Christine Røyrvik; Sara Fletcher-Sandersjöö et al. (2023). A polygenic risk score to help discriminate primary adrenal insufficiency of different etiologies. (ekstern lenke)
- Daniel Eriksson; Ellen Christine Røyrvik; Maribel Aranda-Guillen et al. (2021). GWAS for autoimmune Addison's disease identifies multiple risk loci and highlights AIRE in disease susceptibility. (ekstern lenke)
- Anette Susanne Bøe Wolff; Adrien Katalin Sarkadi; László Maródi et al. (2013). Anti-cytokine autoantibodies preceding onset of autoimmune polyendocrine syndrome type I features in early childhood. (ekstern lenke)
- Ng'weina Francis Magitta; Mikulás Pura; Anette Susanne Bøe Wolff et al. (2008). Autoimmune polyendocrine syndrome type I in Slovakia: relevance of screening patients with autoimmune Addison's disease. (ekstern lenke)
- Beate Skinningsrud; Benedicte Alexandra Lie; Ewa Lavant et al. (2011). Multiple loci in the HLA complex are associated with Addison's Disease. (ekstern lenke)
- Anette Susanne Bøe Wolff; Lena Hansen; Marianne Aardal Grytaas et al. (2023). Vaccination prevents severe COVID-19 outcome in patients with neutralizing type 1 interferon autoantibodies. (ekstern lenke)
- Yael Gruper; Anette Susanne Bøe Wolff; Liad Glanz et al. (2023). Autoimmune amelogenesis imperfecta in patients with APS-1 and coeliac disease. (ekstern lenke)
- Anette Susanne Bøe Wolff; Kjell-Morten Myhr; Christian A. Vedeler et al. (2007). Fc gamma receptor polymorphisms are not associated with autoimmune Addison's disease. (ekstern lenke)
- Bergithe Eikeland Oftedal; Anette Susanne Bøe Wolff; Eirik Bratland et al. (2008). Radioimmunoassay for autoantibodies against interferon omega; its use in the diagnosis of autoimmune polyendocrine syndrome type I. (ekstern lenke)
- Dorsa Iraji; Bergithe Eikeland Oftedal; Anette Susanne Bøe Wolff (2023). Th17 Cells: Orchestrators of Mucosal Inflammation and Potential Therapeutic Targets. (ekstern lenke)
- Sigrid Aslaksen; Paal Methlie; Magnus Dehli Vigeland et al. (2019). Coexistence of congenital adrenal hyperplasia and autoimmune Addison's disease. (ekstern lenke)
- Eystein S.Junior Husebye; Anette Susanne Bøe; F Rorsman et al. (2000). Inhibition of aromatic 1-amino acid decarboxylase by human autoantibodies. (ekstern lenke)
- Isil Kucuka; Dorsa Iraji; Sarah Braun et al. (2025). Longitudinal Immune Profiling in Autoimmune Polyendocrine Syndrome Type 1. (ekstern lenke)
- Anette Susanne Bøe Wolff; Bergithe Eikeland Oftedal; Kai Kisand et al. (2010). Flow cytometry study of blood cell subtypes reflects autoimmune and inflammatory processes in autoimmune polyendocrine syndrome type I. (ekstern lenke)
- Kristian Løvås; Clara G Gjesdal; Monica Christensen et al. (2009). Glucocorticoid replacement therapy and pharmacogenetics in Addison's disease: effects on bone. (ekstern lenke)
- Antonella Meloni; Nick Willcox; Anthony Meager et al. (2012). Autoimmune polyendocrine syndrome Type 1: an Eetensive longitudinal study in Sardinian patients. (ekstern lenke)
- Muhammad Rahman; André Sulen; Lars Ertesvåg Breivik et al. (2025). Anti-perilipin-1 autoantibodies in autoimmune Addison’s disease and related endocrine disorders. (ekstern lenke)
- Alexander Hellesen; Sigrid Aslaksen; Lars Ertesvåg Breivik et al. (2021). 21-Hydroxylase-Specific CD8+ T Cells in Autoimmune Addison’s Disease Are Restricted by HLA-A2 and HLA-C7 Molecules. (ekstern lenke)
- shahinul islam; Bergithe Eikeland Oftedal; Miriam Gjerdevik et al. (2025). Immune cell subsets in autoimmune polyendocrine syndrome type I. (ekstern lenke)
- Anette Susanne Bøe Wolff; Martina Moter Erichsen; Anthony Meager et al. (2007). Autoimmune polyendocrine syndrome type 1 in Norway: Phenotypic variation, autoantibodies, and novel mutations in the autoimmune regulator gene. (ekstern lenke)
- Bergithe Eikeland Oftedal; Olle Kämpe; Anthony Meager et al. (2011). Measuring autoantibodies against IL-17F and IL-22 in Autoimmune Polyendocrine Syndrome Type I by radioligand binding assay using fusion proteins. (ekstern lenke)
- Anna L. Mitchell; Katie D.R. Macarthur; Earn H. Gan et al. (2014). Association of autoimmune Addison's disease with alleles of STAT4 and GATA3 in European Cohorts. (ekstern lenke)
- Liv Hapnes; Nick Willcox; Bergithe Eikeland Oftedal et al. (2012). Radioligand-binding assay reveals distinct autoantibody preferences for type I interferons in APS I and myasthenia gravis subgroups. (ekstern lenke)
- Beata Toth; Anette Susanne Bøe Wolff; Zita Halász et al. (2010). Novel sequence variation of AIRE and detection of interferon-ω antibodies in early infancy. (ekstern lenke)
- Anette Susanne Bøe; Geir Bredholt; Per Knappskog et al. (2004). Autoantibodies against 21-hydroxylase and side-chain cleavage enzyme in autoimmune Addison's disease are mainly immunoglobulin G1. (ekstern lenke)
- Beate Skinningsrud; Eystein Sverre Husebye; Kristina Gervin et al. (2008). Mutation screening of PTPN22: association of the 1858T-allele with Addison's disease. (ekstern lenke)
- Bergithe Eikeland Oftedal; Alexander Hellesen; Martina Moter Erichsen et al. (2015). Dominant mutations in the autoimmune regulator AIRE are associated with common organ-specific autoimmune diseases. (ekstern lenke)
- Elizaveta M. Orlova; Leila S. Sozaeva; Maria A. Kareva et al. (2017). Expanding the Phenotypic and Genotypic Landscape of Autoimmune Polyendocrine Syndrome Type 1.. (ekstern lenke)
- Haydee Artaza Alvarez; Ksenia Lavrichenko; Anette Susanne Bøe Wolff et al. (2024). Rare copy number variant analysis in case–control studies using snp array data: a scalable and automated data analysis pipeline. (ekstern lenke)
- Dmytro Fishman; Kai Kisand; Christina Hertel et al. (2017). Autoantibody repertoire in APECED patients targets two distinct subgroups of proteins. (ekstern lenke)
- Thea Sjøgren; shahinul islam; Igor Filippov et al. (2024). Single cell characterization of blood and expanded regulatory T cells in autoimmune polyendocrine syndrome type 1. (ekstern lenke)
- Anette Susanne Bøe Wolff; Bergithe Eikeland Oftedal; Stefan Johansson et al. (2008). AIRE variations in Addison's disease and autoimmune polyendocrine syndromes (APS): partial gene deletions contribute to APS I. (ekstern lenke)
- Amund Holte Berger; Bergithe Eikeland Oftedal; Anette Susanne Bøe Wolff et al. (2025). High-resolution transcriptional impact of AIRE: effects of pathogenic variants p.Arg257Ter, p.Cys311Tyr, and polygenic risk variant p.Arg471Cys. (ekstern lenke)
- Øyvind Bruserud; Bergithe Eikeland Oftedal; Nils Landegren et al. (2016). A longitudinal follow-up of autoimmune polyendocrine syndrome type 1. (ekstern lenke)
- Ingeborg Brønstad; Anette Susanne Bøe Wolff; Kristian Løvås et al. (2011). Genome-wide copy number variation (CNV) in patients with autoimmune Addison's disease. (ekstern lenke)
- Thea Sjøgren; Eirik Bratland; Ellen Christine Røyrvik et al. (2022). Screening patients with autoimmune endocrine disorders for cytokine autoantibodies reveals monogenic immune deficiencies. (ekstern lenke)
- Kari Lima; Tore G Abrahamsen; Anette Susanne Bøe Wolff et al. (2011). Hypoparathyroidism and autoimmunity in the 22q11.2 deletion syndrome. (ekstern lenke)
- Øyvind Bruserud; Huma Siddiqui; Ileana Mihaela Cuida Marthinussen et al. (2018). Oral microbiota in autoimmune polyendocrine syndrome type 1. (ekstern lenke)
- Jaanika Kärner; Anthony Meager; Maris Laan et al. (2013). Anti-cytokine autoantibodies suggest pathogenetic links with autoimmune regulator deficiency in humans and mice. (ekstern lenke)
- Morten Andreas Horn; Martina Moter Erichsen; Anette Susanne Bøe Wolff et al. (2013). Screening for X-linked adrenoleukodystrophy among adult men with Addison's disease. (ekstern lenke)
- Anna L. Mitchell; Heather J. Cordell; Rachel Soemedi et al. (2009). Programmed Death Ligand 1 (PD-L1) Gene Variants Contribute to Autoimmune Addison’s Disease and Graves’ Disease Susceptibility. (ekstern lenke)
- Iivo Hetemäki; Nelli Heikkilä; Pärt Peterson et al. (2024). Decreased T-cell response against latent cytomegalovirus infection does not correlate with anti-IFN autoantibodies in patients with APECED. (ekstern lenke)
- Anette Susanne Bøe; G. Bredholt; Per Knappskog et al. (2004). Pyridoxal phosphatase is a novel cancer autoantigen in the central nervous system. (ekstern lenke)
Doktorgradsavhandling
Vitenskapelig litteraturgjennomgang
- Bergithe Eikeland Oftedal; Anette Susanne Bøe Wolff (2020). New ERA of therapy for endocrine autoimmune disorders. (ekstern lenke)
- Anette Susanne Bøe Wolff; Sarah Braun; Eystein Sverre Husebye et al. (2021). B cells and autoantibodies in aire deficiency. (ekstern lenke)
- Bergithe Eikeland Oftedal; Thea Sjøgren; Anette Susanne Bøe Wolff (2024). Interferon autoantibodies as signals of a sick thymus. (ekstern lenke)
- Anette Susanne Bøe Wolff; Isil Kucuka; Bergithe Eikeland Oftedal (2023). Autoimmune primary adrenal insufficiency -current diagnostic approaches and future perspectives. (ekstern lenke)
- Øyvind Bruserud; Bergithe Eikeland Oftedal; Anette Susanne Bøe Wolff et al. (2016). AIRE-mutations and autoimmune disease. (ekstern lenke)
- Andre Sulen; Shahinul Islam; Anette Susanne Bøe Wolff et al. (2020). The prospects of single-cell analysis in autoimmunity. (ekstern lenke)
Vitenskapelig bokkapittel
Konferanseabstrakt
- Bergithe Eikeland Oftedal; Martina Moter Erichsen; Alexander Hellesen et al. (2013). Dominant Inheritance in Autoimmune Endocrine Syndrome Type 1. (ekstern lenke)
- Eirik Bratland; Anette Susanne Bøe Wolff; Jan Haavik et al. (2007). Epitope mapping of human aromatic L-amino acid decarboxylase. (ekstern lenke)
- Marissa Penna-Martinez; Julia M. Schwartz; Faroquhi Shoghi et al. (2013). Human leukocyte antigen (DQ2/DQ8) and 21-hydroxylase antibodies determine the thyroid peroxidase antibody status of patients in autoimmune Addison's disease. (ekstern lenke)
- Anette Susanne Bøe Wolff; Kai Kisand; Anthony Meager et al. (2011). Cytokine Antibodies in Autoimmune Polyendocrine Syndrome Type I Correlates to Chronic candidiasis. (ekstern lenke)
- Bergithe Eikeland Oftedal; Anette Susanne Bøe Wolff; Olle Kämpe et al. (2010). Nucleoporin 62, a Novel Autoantigen in Patients with Autoimmune Polyendocrine Syndrome Type I (APS I). (ekstern lenke)
- Adrien Sarkadi; Szilvia Taskó; Anette Susanne Bøe Wolff et al. (2012). Increased anti-cytokine autoantibodies without disease manifestion in a 4 year-old boy with autoimmune polyendocrine syndrome )APS)-1. (ekstern lenke)
- B.E.V. Oftedal; A Meager; Eystein Sverre Husebye et al. (2012). Measuring autoantibodies against IL-17F and IL-22 in autoimmune polyedocrine sydnrome type I. (ekstern lenke)
- Ingeborg Brønstad; Beate Skinningsrud; Anette Susanne Bøe Wolff et al. (2013). Characterisation of the CYP21A2 Gene in Patients with Autoimmune Addison's Disease. (ekstern lenke)
Se en full oversikt over publikasjoner i Cristin
12 chosen publications 10 last years (In total 87 publications)
2025 Single cell characterization of blood and expanded regulatory T cells in autoimmune polyendocrine syndrome type 1. Thea Sjøgren, Shahinul Islam#, Igor Filippov#, Adrianna Jebrzycka, André Sulen, Lars E. Breivik, Alexander Hellesen, Anders P. Jørgensen, Kari Lima, Liina Tserel, Kai Kisand, Pärt Peterson, Annamari Ranki, Eystein S. Husebye, Bergithe E. Oftedal, Anette S. B. Wolff (corr.author). Accepted iScience 25.03.24. DOI: 10.1016/j.isci.2024.109610
Here we describe the function and phenotype of regulatory T cells in patients with mutations in the Autoimmune Regulator gene using single cell sequencing, and mass and flow cytometry.
2024 Interferon autoantibodies as signals of a sick thymus. Bergithe E. Oftedal, Thea Sjøgren and Anette S. B. Wolff (corr.author). Review. Front Immunol. 2024 Feb 22;15:1327784. doi: 10.3389/fimmu.2024.1327784. IF 5.9.
A review describing different deficiencies of the thymus which co-occur with presence of cytokine autoantibodies. We further propose underlying mechanisms.
2024 Immune cell subsets in Autoimmune Polyendocrine Syndrome Type 1 Shahinul Islam, Bergithe E. Oftedal, Miriam Gjerdevik, Lars Breivik, Ellen C. Røyrvik, Kari Lima, Anders P. Jørgensen, Ifunanya Nwakwuo, Jørn Skavland, Eystein S. Husebye, Anette S. B. Wolff (corr.author). Sci Rep. 2025 Aug 4;15(1):28398. doi: 10.1038/s41598-025-12634-y.
In this work we characterised immune cell subsets in patients with mutations in the AIRE gene (N=19 patients).
2023 Breakdown of tolerance to ameloblast-specific proteins results in tooth autoimmunity in APS1 and celiac patients. Yael Gruper, Anette S. B. Wolff*, Liad Glanz, František Špoutil, Yonatan Herzig, Yael Goldfarb, Goretti A. Novaliches, Adriana Osičková, Jan Dobeš, Noam Kadouri, Osher Ben-Nun, Amit Binyamin, Bar Lavi, Tal Givony, Razi Khalaila, Tom Gome, Tomáš Wald, Blanka Mrázková, Carmel Shochen, Mihaela Cuida Marthinussen, Marine Besnard, Shifra Ben-Dor, Ester Feldmesser, Elisaveta M. Orlova, Carole Guillonneau, Csaba Hegedűs, István Lampé, Tamás Papp, Szabolcs Felszeghy, Dror Shouval, Noa Tal, Esti Davidovich, Raanan Shamir, Zsuzsa Szondy, Knut E.A. Lundin, Radim Osička, Jan Procházka, Eystein S. Husebye and Jakub Abramson* (Wolff joint corresponding author). Nature 23.10.23. DOI 10.1038/s41586-023-06776-0.
Open access: https://www.nature.com/articles/s41586-023-06776-0
Here, we describe a new disease syndrome, autoimmune amelogenesis imperfecta, affecting tooth enamel. We describe the same outcome for two autoimmune disorders and how tolerance may fail to cause autoimmunity against ameloblasts. I coordinated the patient-part on this study, both regarding APS-1 patients and celiac patients. I was involved in forming hypotheses, analyse samples and the whole writing process. I am corresponding author together with Abramson.
2023 Vaccination prevents severe outcome of COVID-19 in patients with high levels of neutralizing type 1 interferon autoantibodies Anette S. B. Wolff (*), Lena Hansen, Marianne Aa. Grytaas, Bergithe E. Oftedal, Lars Breivik, Fan Zhou, Karl Ove Hufthammer, Thea Sjøgren, Jan Stefan Olofsson, Mai Chi Trieu, Anthony Meager, Anders P. Jørgensen, Kari Lima, Kristin G-I Mohn, Nina Langeland#, Rebecca Jane Cox# and Eystein S. Husebye#.(*). iScience 06.06.23.
Here we have teamed up with the Cox/Langeland team at Haukeland and performed a study on SARS-CoV vaccination in patients with pre-existing autoantibodies against interferons, namely APS-1 patients. We also found that vaccination prevents severe COVID-19 course in these individuals. I came up with the idea, coordinated patient sampling and performed several of the analyses in the study.
2023 A polygenic risk score for autoimmune Addison’s disease estimates individual risk and identifies patients with monogenic adrenal insufficiency. Maribel Aranda-Guillén, Ellen Christine Røyrvik, Sara Ström, Haydee Artaza Alvarez, Ileana Botusan, Marianne Grytaas, Åsa Hallgren, Lars Breivik, Maria Pettersson, Anders P. Jørgensen, Anna Lindstrand, Elinor Vogt, The Norwegian Addison Registry Study Group, The Swedish Addison Registry Study Group, Eystein S. Husebye, Olle Kämpe, Anette S. Bøe Wolff, Sophie Bensing, Stefan Johansson, Daniel Eriksson. J Intern Med. 2023 May 8. doi: 10.1111/joim.13649.
Open access
In this multisenter study we performed a polygenic risk score to predict autoimmune Addison’s disease in risk individuals. I coordinated the Norwegian part of this study.
2023 Systemic interferon type I and B cell regulation responses are impaired in autoimmune polyendocrine syndrome type 1. Bergithe E. Oftedal, Nicolas Delaleu, David Dolan, Anthony Meager, Eystein S. Husebye, Anette S. B. Wolff. (corr.author). FEBS Lett. 2023 Apr 13. doi: 10.1002/1873-3468.14625.
Here we used several approaches to map molecular signal profiles in blood of patients with APS-1. We found impaired B cell and interferon responses. I came up with the hypotheses, performed several of the wet lab tasks and also analyses in the study.
Open access
2022. Screening patients with autoimmune endocrine disorders for cytokine autoantibodies reveals monogenic immune deficiencies
Thea Sjøgren, Eirik Bratland, Ellen C. Røyrvik, Marianne Grytaas, Andreas Benneche, Per M. Knappskog, Bergithe E. Oftedal, Eystein S. Husebye and Anette S. B. Wolff(corr.author). J Autoimm. 2022 Dec;133:102917.
Open access
https://www.sciencedirect.com/science/article/abs/pii/S0896841122001251?via%3Dihub
Here, my PhD student Thea (now Post.doc.) screened a large cohort of patients with adrenal failure and other autoimmune endocrine conditions and found several cases with autoantibodies against interferons who had mutations in genes encoding immune regulatory genes. This study is the initial part of a larger effort to describe cytokine autoantibodies as early risk markers of genetic impairments implicating failure of immune regulation culminating in autoimmunity.
2021. Genome-wide association study links autoimmune Addison’s disease to break of central tolerance. Daniel Eriksson*, Ellen Christine Røyrvik*, Maribel Aranda-Guillén*, …, Anette Susanne Bøe Wolff, Sophie Bensing, Stefan Johansson§, Olle Kämpe§, Eystein S. Husebye§. Nat Commun.. 2021 Feb 11;12(1):959. doi: 10.1038/s41467-021-21015-8.
The first ever GWAS on Addison’s disease. I coordinated this study from A to Z and was one of the senior authors. The study shows 9 genetic loci convincingly giving risk to Addison’s disease. All risk loci encode factors of adaptive immunity and the T cell pathway in specific. The results can be used to make polygenic risk scores to be able to predict risk for Addison’s disease in screening efforts. This again can lead to earlier diagnosis of patients, which in turn can save lives.
2021. The natural history of 21-hydroxylase autoantibodies in autoimmune Addison’s disease. Anette S. B. Wolff, Lars Breivik, Karl Ove Hufthammer, Marianne Grytaas, Eirik Bratland, Eystein S. Husebye, Bergithe E. Oftedal. EJE 2021. Volume 184: Issue 4. Page 607-15. https://doi.org/10.1530/EJE-20-1268 .
We have here studied samples spanning 25 years from the largest registry and biobank of autoimmune Addison’s disease worldwide. I participated in the whole process.
2016 AIRE-Deficient Patients Harbor Unique High-Affinity Disease-Ameliorating Autoantibodies: Steffen Meyer, Martin Woodward, Christina Hertel, Philip Vlaicu, Yasmin Haque, Dimitri Fishman, Hedi Peterson, Jaanika Kärner, Kaja Metsküla, Raivo Uibo, Anette S. B. Wolff, APECED patient collaborative, Kai Krohn, Annamari Ranki, Pärt Peterson, Kai Kisand & Adrian Hayday. Cell Volume 166, Issue 3, p582–595, 28 July 2016. IF 41.5 (Citations 123).
Here we describe patients with APS-I having unique autoantibodies against a battery of proteins of the body, and that presence of these markers for autoimmunity may indeed be beneficial for not acquiring some components of APS-I, like type I diabetes, i.e. cytokine-autoantibodies may have protective roles.
2015. Dominant Autoimmune Regulator mutations associated with common organ-specific autoimmune diseases: PhD Bergithe E. Oftedal, MSc Alexander Hellesen, MD PhD Martina Moter Erichsen, PhD Eirik Bratland, MSc Ayelet Vardi, MD PhD Jaakko Perheentupa, PhD E. Helen Kemp, MD PhD Torunn Fiskerstrand, PhD Marte K. Viken, MD PhD Anthony P. Weetman, PhD Sarel J. Fleishman, MD PhD Siddharth Banka, MD PhD William G. Newman, MD PhD W.A.C Sewell, MD Leila S. Sozaeva, MD PhD Tetyana Zayats,, MD PHD Kristoffer Haugarvoll,PhD MD Elizaveta M. Orlova, PhD MD Jan Haavik, PhD Stefan Johansson, PhD Per M. Knappskog, MD PhD Kristian Løvås, PhD Anette S. B. Wolff, PhD Jakub Abramson, MD PhD Eystein S. Husebye. Immunity.2015 Jun 16;42(6):1185-96. (Citations 108).
In this paper, where I am one of the senior researchers, we describe and characterize novel dominant mutations in the autoimmune regulator (AIRE) gene, which could be a common susceptibility factor for autoimmune susceptibility.
Prosjekter
Cytokine autoantibodies in patients with autoimmune diseases and immunodeficiencies. Including genomics and functional genetics on germline and somatic immune gene variants.
Funding; Norwegian Research council, Novo Nordisk Fonden, Western Norway Health Authorities.
People: Thea Sjøgren (post.doc), Ivan Abbedissen (PhD student), Kristin Watnedal Olsen (PhD student), Julie Sølversen (Researcher), Alexander Hellesen (post.doc.), Mona Bjune (post.doc), Cecilie Gjerde (oral tissue), Kathrine Skarstein (biopsies, pathology), Ingvild Olerud (master student 2025-26), Victoria Olsvold (master student 2026-27), Elisabet Ognedal (genetic expert). Collaboration with Bergithe Oftedal, Harald Carlsen and Preben Boysen on mice studies.
Biobanks/registries, ROAS (Registry and biobank for organ specific autoimmune disorders), Western Norway immune deficiency biobank, Norsk systemisk bindevevssykdom og vaskulittregister (NOSVAR), Norsk diabetesregister
Autoimmune amelogenesis imperfecta and celiac disease
People: Eystein Husebye, Nancy Bletsa, Mihaela C. Marthinussen, Erling Tjora (barn Haukeland), Rene Fjellander (voksne Haukeland), Birgitte Emken (voksne Haukeland), Ingvild Brusevold (UiO), Tove Wigen (UiO).
Biobanks/registries, ROAS (Registry and biobank for organ specific autoimmune disorders), Biobank for enamel failure and celiac disease children at Haukeland.
Genetics in autoimmune Addison's disease
Funding; Norwegian Research council, Western Norway Health Authorities
People: Eystein S. Husebye, Marianne Grytaas, Ellen Røyrvik, Tetyana Zayats, Bergithe Oftedal, Julie Sølversen (researcher). Collaboration with Olle Kampe at KI, Sweden.
Biobank: Norway and Sweden Addison registry (Norway: ROAS)
Natural course of Addison's disease
People: Eystein Husebye, Marianne Øksnes, ROAS network, Grethe Ueland, Ann Elin Stokland, Eivind Ness-Jensen++
Funding: Norwegian Research council, Western Norway Health Authorities
Biobanks/registries, ROAS (Registry and biobank for organ specific autoimmune disorders), Norsk diabetesregister, HUNT Norway, DIPP Finland
Collaboration with the flow cytometry and genomic facility at UiB for all projects