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LIBRIS Formathandbok  (Information om MARC21)
FältnamnIndikatorerMetadata
00003580naa a2200421 4500
001oai:DiVA.org:uu-357753
003SwePub
008180822s2018 | |||||||||||000 ||eng|
009oai:prod.swepub.kib.ki.se:138383208
024a https://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-3577532 URI
024a https://doi.org/10.1016/j.chest.2018.01.0202 DOI
024a http://kipublications.ki.se/Default.aspx?queryparsed=id:1383832082 URI
040 a (SwePub)uud (SwePub)ki
041 a engb eng
042 9 SwePub
072 7a ref2 swepub-contenttype
072 7a art2 swepub-publicationtype
100a Pincikova, Tereziau Uppsala universitet,Lung- allergi- och sömnforskning,Karolinska Univ Hosp Huddinge, Stockholm CF Ctr, Stockholm, Sweden;Karolinska Inst, Dept Clin Sci Intervent & Technol, Div Pediat, Stockholm, Sweden;Karolinska Univ Hosp Huddinge, Karolinska Inst, Ctr Infect Med, Dept Med, F59, S-14186 Stockholm, Sweden4 aut0 (Swepub:uu)terpi638
2451 0a Severely Impaired Control of Bacterial Infections in a Patient With Cystic Fibrosis Defective in Mucosal-Associated Invariant T Cells
264 1b ELSEVIER SCIENCE BV,c 2018
338 a print2 rdacarrier
520 a Here we report a unique case of a patient with cystic fibrosis characterized by severely impaired control of bacterial respiratory infections. This patient's susceptibility to such infections was much worse than expected from a cystic fibrosis clinical perspective, and he died at age 22 years despite extensive efforts and massive use of antibiotics. We found that this severe condition was associated with a near-complete deficiency in circulating mucosal-associated invariant T (MAIT) cells as measured at several time points. MAIT cells are a large, recently described subset of T cells that recognize microbial riboflavin metabolites presented by the highly evolutionarily conserved MR1 molecules. The MAIT cell deficiency was specific; other T-cell subsets were intact. Even though this is only one unique case, the findings lend significant support to the emerging role of MAIT cells in mucosal immune defense and suggest that MAIT cells may significantly modify the clinical phenotype of respiratory diseases.
650 7a MEDICIN OCH HÄLSOVETENSKAPx Klinisk medicinx Klinisk laboratoriemedicin0 (SwePub)302232 hsv//swe
650 7a MEDICAL AND HEALTH SCIENCESx Clinical Medicinex Clinical Laboratory Medicine0 (SwePub)302232 hsv//eng
653 a cystic fibrosis
653 a infection
653 a mucosal-associated invariant T cells
700a Paquin-Proulx, Dominicu Karolinska Univ Hosp Huddinge, Karolinska Inst, Ctr Infect Med, Dept Med, F59, S-14186 Stockholm, Sweden;George Washington Univ, Dept Microbiol Immunol & Trop Med, Washington, DC USA4 aut
700a Moll, Markusu Karolinska Institutet4 aut
700a Flodström-Tullberg, Malinu Karolinska Univ Hosp Huddinge, Karolinska Inst, Ctr Infect Med, Dept Med, F59, S-14186 Stockholm, Sweden4 aut
700a Hjelte, Lenau Karolinska Institutet4 aut
700a Sandberg, Johan K.u Karolinska Institutet4 aut
710a Uppsala universitetb Lung- allergi- och sömnforskning4 org
773t Chestd : ELSEVIER SCIENCE BVg 153:5, s. E93-E96q 153:5<E93-E96x 0012-3692x 1931-3543
856u http://journal.chestnet.org/article/S0012369218301491/pdf
8564 8u https://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-357753
8564 8u https://doi.org/10.1016/j.chest.2018.01.020
8564 8u http://kipublications.ki.se/Default.aspx?queryparsed=id:138383208

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