Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Maribel Aranda-Guillén"'
Autor:
Ahmet Yalcinkaya, Marco Cavalli, Maribel Aranda-Guillén, Axel Cederholm, Almira Güner, Isabel Rietrae, Hedvig Mildner, Anish Behere, Oskar Eriksson, Laura Gonzalez, Constantin Habimana Mugabo, Anette Johnsson, Tadepally Lakshmikanth, Petter Brodin, Mia Wadelius, Pär Hallberg, Nils Landegren
Publikováno v:
Scientific Reports, Vol 14, Iss 1, Pp 1-13 (2024)
Abstract While Coronavirus disease 2019 (COVID-19) vaccines have proven to be both effective and generally safe, rare but severe adverse events following immunization (AEFIs) are described. Autoantibodies to platelet factor-4 are associated with cata
Externí odkaz:
https://doaj.org/article/b3f0daac9c2541ba8d790503c67ed99b
No link between type I interferon autoantibody positivity and adverse reactions to COVID-19 vaccines
Autor:
Ahmet Yalcinkaya, Marco Cavalli, Axel Cederholm, Maribel Aranda-Guillén, Anish Behere, Hedvig Mildner, Tadepally Lakshmikanth, Laura Gonzalez, Constantin Habimana Mugabo, Anette Johnsson, Olov Ekwall, Olle Kämpe, Sophie Bensing, Petter Brodin, Pär Hallberg, Mia Wadelius, Nils Landegren
Publikováno v:
npj Vaccines, Vol 9, Iss 1, Pp 1-6 (2024)
Abstract Type I interferons act as gatekeepers against viral infection, and autoantibodies that neutralize these signaling molecules have been associated with COVID-19 severity and adverse reactions to the live-attenuated yellow fever vaccine. On thi
Externí odkaz:
https://doaj.org/article/ec0a193a12544f03967d6f45840767f0
Autor:
Haydee Artaza, Daniel Eriksson, Ksenia Lavrichenko, Maribel Aranda-Guillén, Eirik Bratland, Marc Vaudel, Per Knappskog, Eystein S. Husebye, Sophie Bensing, Anette S. B. Wolff, Olle Kämpe, Ellen C. Røyrvik, Stefan Johansson
Publikováno v:
Frontiers in Immunology, Vol 15 (2024)
Autoimmune Addison’s disease (AAD) is a rare but life-threatening endocrine disorder caused by an autoimmune destruction of the adrenal cortex. A previous genome-wide association study (GWAS) has shown that common variants near immune-related genes
Externí odkaz:
https://doaj.org/article/376fa9347c4d468b88cff95fd54a54b8
Autor:
Daniel Eriksson, Ellen Christine Røyrvik, Maribel Aranda-Guillén, Amund Holte Berger, Nils Landegren, Haydee Artaza, Åsa Hallgren, Marianne Aardal Grytaas, Sara Ström, Eirik Bratland, Ileana Ruxandra Botusan, Bergithe Eikeland Oftedal, Lars Breivik, Marc Vaudel, Øyvind Helgeland, Alberto Falorni, Anders Palmstrøm Jørgensen, Anna-Lena Hulting, Johan Svartberg, Olov Ekwall, Kristian Johan Fougner, Jeanette Wahlberg, Bjørn Gunnar Nedrebø, Per Dahlqvist, The Norwegian Addison Registry Study Group, The Swedish Addison Registry Study Group, Per Morten Knappskog, Anette Susanne Bøe Wolff, Sophie Bensing, Stefan Johansson, Olle Kämpe, Eystein Sverre Husebye
Publikováno v:
Nature Communications, Vol 12, Iss 1, Pp 1-14 (2021)
Autoimmune Addison’s disease is a rare complex disease, which has not yet been characterized by non-biased genetic studies. Here, the authors perform the first GWAS for the disease, identifying nine loci including two coding variants in the gene Au
Externí odkaz:
https://doaj.org/article/0be85e9204274eff9b1cb72be80b2205
Autor:
Sara Öster, Daniela Esposito, Maribel Aranda-Guillén, Anna-Karin Åkerman, Jeanette Wahlberg, Eystein Sverre Husebye, Olle Kämpe, Ileana Ruxandra Botusan, Per Dahlqvist, Ragnhildur Bergthorsdottir, Sophie Bensing
ObjectiveAutoimmune Addison's disease (AAD) entails a chronic adrenal insufficiency and is associated with an increased risk of severe infections. It is, however, unknown how patients with AAD were affected by the coronavirus disease 2019 (COVID-19)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0397788f6c6f550714d9cdf41a8970fd
http://urn.kb.se/resolve?urn=urn:nbn:se:umu:diva-208080
http://urn.kb.se/resolve?urn=urn:nbn:se:umu:diva-208080
Autor:
Hassan Abolhassani, Nils Landegren, Paul Bastard, Marie Materna, Mohammadreza Modaresi, Likun Du, Maribel Aranda-Guillén, Fabian Sardh, Fanglei Zuo, Peng Zhang, Harold Marcotte, Nico Marr, Taushif Khan, Manar Ata, Fatima Al-Ali, Remi Pescarmona, Alexandre Belot, Vivien Béziat, Qian Zhang, Jean-Laurent Casanova, Olle Kämpe, Shen-Ying Zhang, Lennart Hammarström, Qiang Pan-Hammarström
Publikováno v:
Journal of Clinical Immunology
Journal of Clinical Immunology, 2022, 42 (3), pp.471-483. ⟨10.1007/s10875-022-01215-7⟩
Journal of Clinical Immunology, 2022, 42 (3), pp.471-483. ⟨10.1007/s10875-022-01215-7⟩
Background Inborn errors of immunity (IEI) and autoantibodies to type I interferons (IFNs) underlie critical COVID-19 pneumonia in at least 15% of the patients, while the causes of multisystem inflammatory syndrome in children (MIS-C) remain elusive.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fa08b5b99ab34063cdafbf79e5804d50
https://u-paris.hal.science/hal-03691612
https://u-paris.hal.science/hal-03691612
Autor:
Hassan Abolhassani, Samaneh Delavari, Nils Landegren, Sima Shokri, Paul Bastard, Likun Du, Fanglei Zuo, Reza Hajebi, Farhad Abolnezhadian, Sara Iranparast, Mohammadreza Modaresi, Ahmad Vosughimotlagh, Fereshte Salami, Maribel Aranda-Guillén, Aurélie Cobat, Harold Marcotte, Shen-Ying Zhang, Qian Zhang, Nima Rezaei, Jean-Laurent Casanova, Olle Kämpe, Lennart Hammarström, Qiang Pan-Hammarström
Publikováno v:
The Journal of Allergy and Clinical Immunology
Background: Most severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2)-infected individuals are asymptomatic or only exhibit mild disease. In about 10% of cases, the infection leads to hypoxemic pneumonia, although it is much more rare in chil
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5469fbdd4140fae65284bf82a345032d
http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-493407
http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-493407
Autor:
Nils, Landegren, Norito, Ishii, Maribel, Aranda-Guillén, Hörður Ingi, Gunnarsson, Fabian, Sardh, Åsa, Hallgren, Mona, Ståhle, Eva, Hagforsen, Maria, Bradley, Per-Henrik D, Edqvist, Fredrik, Pontén, Outi, Mäkitie, Liv, Eidsmo, Lars, Norlén, Adnane, Achour, Ingrid, Dahlbom, Ilma, Korponay-Szabó, Daniel, Agardh, Mohammad, Alimohammadi, Daniel, Eriksson, Takashi, Hashimoto, Olle, Kämpe
Publikováno v:
Proceedings of the National Academy of Sciences of the United States of America
Significance The nine-member transglutaminase protein family includes five known autoantigens. Because of the frequent roles of transglutaminases in autoimmunity, we decided to explore whether the remaining members might also constitute autoantigens,