Linn M. Eggesbø

ORCID: 0000-0002-5271-7703
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About
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Research Areas
  • Celiac Disease Research and Management
  • Microscopic Colitis
  • Acute Lymphoblastic Leukemia research
  • Galectins and Cancer Biology
  • Childhood Cancer Survivors' Quality of Life
  • Chronic Myeloid Leukemia Treatments
  • COVID-19 and Mental Health
  • Chronic Lymphocytic Leukemia Research
  • T-cell and B-cell Immunology
  • Infection Control and Ventilation
  • COVID-19 epidemiological studies
  • Helicobacter pylori-related gastroenterology studies
  • SARS-CoV-2 and COVID-19 Research
  • Renal and related cancers
  • Single-cell and spatial transcriptomics

Norwegian Institute of Public Health
2024

Oslo University Hospital
2020-2022

University of Oslo
2016-2021

University of California, San Francisco
2016-2017

657 Oslo
2016

University of San Francisco
2015

Inactivation of the tumor suppressor gene encoding transcriptional regulator Ikaros (IKZF1) is a hallmark BCR-ABL1+ precursor B cell acute lymphoblastic leukemia (pre-B ALL). However, mechanisms by which functions as in pre-B ALL remain poorly understood. Here, we analyzed mouse model together with new inducible expression wild-type IKZF1 mutant human ALL. We performed integrated genome-wide chromatin and analyses identified target genes ALL, revealing novel conserved pathways associated...

10.1084/jem.20160049 article EN cc-by-nc-sa The Journal of Experimental Medicine 2017-02-11

Disease-specific plasma cells (PCs) reactive with transglutaminase 2 (TG2) or deamidated gluten peptides (DGPs) are abundant in celiac disease (CeD) gut lesions. Their contribution toward CeD pathogenesis is unclear. We assessed expression of markers associated PC longevity 15 untreated and 26 treated patients addition to 13 non-CeD controls performed RNA sequencing clonal inference transcriptomic analysis 3,251 single PCs. observed antigen-dependent V-gene selection stereotypic antibodies....

10.1084/jem.20200852 article EN cc-by-nc-sa The Journal of Experimental Medicine 2020-10-23

Gut intraepithelial γδ and CD8+ αβ T lymphocytes have been connected to celiac disease (CeD) pathogenesis. Based on the previous observation that activated (CD38+), gut-homing (CD103+) cells increase in blood upon oral gluten challenge, we wanted shed light pathogenic involvement of these by examining clonal relationship between gut during exposure. Of 20 gluten-challenged CeD patients, 8 10 had (CD38+CD103+) cells, respectively, while 16 gluten-specific CD4+ cells. We obtained TCR sequences...

10.1038/s41385-021-00385-8 article EN publisher-specific-oa Mucosal Immunology 2021-03-02

A hallmark of celiac disease (CeD), a chronic condition driven by cereal gluten exposure, is increase gut intraepithelial γδ T cells. This may indicate pathogenic involvement cells and existence disease-specific T-cell receptors (TCRs) recognizing defined antigen(s). We performed high-throughput paired TCR sequencing single untreated CeD patients (n = 8; 1821 cells), treated with gluten-free diet 5; 436 cells) controls 7; 1068 cells). found that patients, both treated, had larger more...

10.1038/s41385-019-0222-9 article EN publisher-specific-oa Mucosal Immunology 2019-11-14

For many people public transport is the only mode of travel, and it can be challenging to keep necessary distances in such a restricted space. The exact role transportation risk SARS-CoV-2 transmission not known.Participants (n = 121,374) were untested adult Norwegian residents recruited through social media who spring 2020 completed baseline questionnaire on demographics use transport. Incident cases 1069) had positive polymerase chain reaction test registered at Messaging System for...

10.1186/s12879-022-07233-5 article EN cc-by BMC Infectious Diseases 2022-03-14

Chronic inflammation of the small intestine in celiac disease is driven by activation CD4+ T cells that recognize gluten peptides presented disease-associated HLA-DQ molecules. We have performed direct cell cloning duodenal biopsies from five untreated and one refractory patients, three non-celiac control subjects order to assess, an unbiased fashion, frequency gluten-reactive disease-affected tissue as well antigen fine specificity responding cells. From active lesions 19 T-cell clones were...

10.3389/fimmu.2021.646163 article EN cc-by Frontiers in Immunology 2021-03-16

Abstract Heterogeneity in vaccine response, particularly vulnerable populations like the elderly, represents a significant public health challenge. We conducted an in-depth examination of immune cell profiles before and after SARS-CoV-2 vaccination utilizing mass cytometry cohort healthy Norwegian seniors (65–80 years). have demonstrated that higher pre-vaccination frequencies CD27 + IgD - class-switched memory B cells subsets CD24 CD38 transitional were associated with robust response....

10.1038/s41541-024-01028-2 article EN cc-by npj Vaccines 2024-11-29

ABSTRACT Disease-specific plasma cells (PCs) reactive with transglutaminase 2 (TG2) or deamidated gluten peptides (DGP) are abundant in celiac disease (CeD) gut lesions. Their contribution toward CeD pathogenesis is unclear. We assessed expression of markers associated PC longevity 15 untreated and 26 treated patients addition to 13 non-CeD controls, performed RNA-sequencing clonal inference transcriptomic analysis 3251 single PCs. observed antigen-dependent V-gene selection stereotypic...

10.1101/2020.04.30.058560 preprint EN bioRxiv (Cold Spring Harbor Laboratory) 2020-05-02

Abstract Ikaros is a zinc finger transcription factor required for B-cell development and proper hematopoiesis, an important tumor suppressor in developing lymphocytes. To understand the mechanism of function potentially develop new improved targeted therapies, it to elucidate downstream target genes involved. With this aim, we combine mouse models pre-B ALL vitro culture human patient-derived cells. A model with deletion fourth DNA-binding resulted loss function, limited set deregulated...

10.4049/jimmunol.194.supp.131.19 article EN The Journal of Immunology 2015-05-01

Abstract Inactivation of the transcriptional factor Ikaros (IKZF1) correlates with poor prognosis in progenitor B-cell acute lymphoblastic leukemia (pre-B ALL), and is a hallmark BCR-ABL1+ subgroup pre-B ALL. critical regulator hematopoietic development required for development, however mechanisms by which functions as tumor suppressor ALL remain poorly understood. We analyzed recently developed mouse models containing targeted deletions DNA-binding zinc finger domains together new model...

10.4049/jimmunol.196.supp.122.6 article EN The Journal of Immunology 2016-05-01

Abstract Background: For many people public transport is the only mode of travel, and it can be challenging to keep necessary distances in such a restricted space. The exact role transportation risk SARS-CoV-2 transmission not known. Methods: Participants (n=121 374) were untested adult Norwegian residents recruited through social media who spring 2020 completed baseline questionnaire on demographics use transport. Incident cases (n=1069) had positive polymerase chain reaction test...

10.21203/rs.3.rs-1031652/v1 preprint EN cc-by Research Square (Research Square) 2021-11-10
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