Zobrazeno 1 - 10
of 48
pro vyhledávání: '"Sophie Ohlsson"'
Autor:
Iva Gunnarsson, Lars Rönnblom, Annette Bruchfeld, Mårten Segelmark, Solbritt Rantapää-Dahlqvist, Aladdin J Mohammad, Ewa Berglin, Roland Jonsson, Roald Omdal, Per Eriksson, Kerstin Lindblad-Toh, Hilde Haukeland, Ann Knight, Øyvind Palm, Peter Söderkvist, Johanna Dahlqvist, Christian Lundtoft, Jennifer R S Meadows, Åsa Karlsson, Sophie Ohlsson
Publikováno v:
RMD Open, Vol 10, Iss 2 (2024)
Objective The antineutrophil cytoplasmic antibody (ANCA)-associated vasculitides (AAV) are inflammatory disorders with ANCA autoantibodies recognising either proteinase 3 (PR3-AAV) or myeloperoxidase (MPO-AAV). PR3-AAV and MPO-AAV have been associate
Externí odkaz:
https://doaj.org/article/0e24bc5d016444e398feb4940ea67dd2
Autor:
Martina Frodlund, Per Nived, Katerina Chatzidionysiou, Anna Södergren, Eva Klingberg, Monica Hansson, Sophie Ohlsson, Elisa Pin, Anders Bengtsson, Lars Klareskog, Meliha Kapetanovic
Publikováno v:
Microbiology Spectrum, Vol 12, Iss 4 (2024)
ABSTRACTStudies investigating the immunogenicity of additional COVID-19 vaccine doses in immunosuppressed patients with inflammatory rheumatic diseases (IRD) are still limited. The objective was to explore the antibody response including response to
Externí odkaz:
https://doaj.org/article/a78c269abba540efa24f1311c7f723e0
Autor:
Sofia Smargianaki, Evelina Elmér, Sandra Lilliebladh, Sophie Ohlsson, Åsa Pettersson, Thomas Hellmark, Åsa CM Johansson
Publikováno v:
Journal of Immunology Research, Vol 2024 (2024)
Antineutrophil cytoplasmic antibody (ANCA)-associated vasculitis (AAV) is a group of autoimmune diseases with inflammation affecting small blood vessels and includes granulomatosis with polyangiitis (GPA) and microscopic polyangiitis (MPA). In this s
Externí odkaz:
https://doaj.org/article/bbee54f7bf7f4c97bfc82bfb37c0c826
Autor:
Paul A Lyons, James E Peters, Federico Alberici, James Liley, Richard M. R. Coulson, William Astle, Chiara Baldini, Francesco Bonatti, Maria C Cid, Heather Elding, Giacomo Emmi, Jörg Epplen, Loïc Guillevin, David R. W. Jayne, Tao Jiang, Iva Gunnarsson, Peter Lamprecht, Stephen Leslie, Mark A. Little, Davide Martorana, Frank Moosig, Thomas Neumann, Sophie Ohlsson, Stefanie Quickert, Giuseppe A. Ramirez, Barbara Rewerska, Georg Schett, Renato A. Sinico, Wojciech Szczeklik, Vladimir Tesar, Damjan Vukcevic, The European Vasculitis Genetics Consortium, Benjamin Terrier, Richard A Watts, Augusto Vaglio, Julia U Holle, Chris Wallace, Kenneth G. C. Smith
Publikováno v:
Nature Communications, Vol 10, Iss 1, Pp 1-13 (2019)
Eosinophilic granulomatosis with polyangiitis (EGPA) is a rare inflammatory disorder characterised by asthma, eosinophilia and vasculitis. Here, the authors describe a genome-wide association study of EGPA that reveals clinical and genetic difference
Externí odkaz:
https://doaj.org/article/ff891c79b773423a95539793d707bc9a
Publikováno v:
BMC Rheumatology, Vol 3, Iss 1, Pp 1-12 (2019)
Abstract Background Anti-neutrophil cytoplasmic antibodies associated vasculitides (AAV) are characterized by autoimmune small vessel inflammation. Eosinophils are multifunctional cells with both pro-inflammatory and immunoregulatory properties. Tiss
Externí odkaz:
https://doaj.org/article/8a895880e7aa4619891e23dd3aa225a1
Autor:
Evelina Elmér, Sofia Smargianaki, Åsa Pettersson, Lillemor Skattum, Sophie Ohlsson, Thomas Hellmark, Åsa C. M. Johansson
Publikováno v:
Journal of Immunology Research, Vol 2020 (2020)
B cells are thought to play a central role in the pathogenesis of antineutrophil cytoplasmic antibody- (ANCA-) associated vasculitis (AAV). ANCAs have been proposed to cause vasculitis by activating primed neutrophils to damage small blood vessels. W
Externí odkaz:
https://doaj.org/article/dbab7619cb3949da94d64ae32baa1600
Autor:
Sophie Ohlsson, Lisa Holm, Christina Hansson, Susanne M Ohlsson, Lena Gunnarsson, Åsa Pettersson, Lillemor Skattum
Publikováno v:
PLoS ONE, Vol 14, Iss 6, p e0218272 (2019)
Anti-neutrophil cytoplasmic antibody (ANCA)-associated vasculitides (AAV), including granulomatosis with polyangiitis (GPA) and microscopic polyangiitis (MPA), are autoimmune conditions associated with small vessel inflammation. Earlier studies indic
Externí odkaz:
https://doaj.org/article/c375ccc960fb4f2db60a6b8f82fffbb6
Publikováno v:
Mediators of Inflammation, Vol 2018 (2018)
Antineutrophil cytoplasmic autoantibody- (ANCA-) associated vasculitis (AAV) are relapsing-remitting disorders with unpredictable prognosis. There is a need of biomarkers for distinguishing which patients will have a more severe outcome and also for
Externí odkaz:
https://doaj.org/article/697966dee6b7407799d90e23b95c69da
Publikováno v:
Journal of Immunology Research, Vol 2018 (2018)
T cell-mediated immune responses are thought to play an important role in the pathogenesis of anti-neutrophil cytoplasmic antibody- (ANCA-) associated vasculitides (AAV). CD4+ T cells can be divided into subsets depending on their expression of chemo
Externí odkaz:
https://doaj.org/article/0b1b3122fd3d4bc2bedcfb389d9368f4
Publikováno v:
Mediators of Inflammation, Vol 13, Iss 4, Pp 275-283 (2004)
AIMS: The anti-neutrophilic cytoplasmatic autoantibody-associated vasculitides (AASV) are diseases of relapsing-remitting inflammation. Here we explore the cytokine profile in different phases of disease, looking for pathogenic clues of possible prog
Externí odkaz:
https://doaj.org/article/cba3f8f0e3ae464baabf2e49239a5f46