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Sökning: WFRF:(Tufveson G.) > (2020) > Targeting CXCR1/2 D...

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FältnamnIndikatorerMetadata
00006197naa a2200781 4500
001oai:gup.ub.gu.se/292433
003SwePub
008240528s2020 | |||||||||||000 ||eng|
009oai:DiVA.org:uu-409674
009oai:prod.swepub.kib.ki.se:143241199
024a https://gup.ub.gu.se/publication/2924332 URI
024a https://doi.org/10.2337/dc19-14802 DOI
024a https://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-4096742 URI
024a http://kipublications.ki.se/Default.aspx?queryparsed=id:1432411992 URI
040 a (SwePub)gud (SwePub)uud (SwePub)ki
041 a eng
042 9 SwePub
072 7a ref2 swepub-contenttype
072 7a art2 swepub-publicationtype
100a Maffi, P.u IRCCS Osped San Raffaele, San Raffaele Diabet Res Inst, Milan, Italy4 aut
2451 0a Targeting CXCR1/2 Does Not Improve Insulin Secretion After Pancreatic Islet Transplantation: A Phase 3, Double-Blind, Randomized, Placebo-Controlled Trial in Type 1 Diabetes
264 c 2020-02-04
264 1b American Diabetes Association,c 2020
520 a OBJECTIVE Reparixin is an inhibitor of CXCR1/2 chemokine receptor shown to be an effective anti-inflammatory adjuvant in a pilot clinical trial in allotransplant recipients. RESEARCH DESIGN AND METHODS A phase 3, multicenter, randomized, double-blind, parallel-assignment study () was conducted in recipients of islet allotransplants randomized (2:1) to reparixin or placebo in addition to immunosuppression. Primary outcome was the area under the curve (AUC) for C-peptide during the mixed-meal tolerance test at day 75 +/- 5 after the first and day 365 +/- 14 after the last transplant. Secondary end points included insulin independence and standard measures of glycemic control. RESULTS The intention-to-treat analysis did not show a significant difference in C-peptide AUC at both day 75 (27 on reparixin vs. 18 on placebo, P = 0.99) and day 365 (24 on reparixin vs. 15 on placebo, P = 0.71). There was no statistically significant difference between treatment groups at any time point for any secondary variable. Analysis of patient subsets showed a trend for a higher percentage of subjects retaining insulin independence for 1 year after a single islet infusion in patients receiving reparixin as compared with patients receiving placebo (26.7% vs. 0%, P = 0.09) when antithymocyte globulin was used as induction immunosuppression. CONCLUSIONS In this first double-blind randomized trial, islet transplantation data obtained with reparixin do not support a role of CXCR1/2 inhibition in preventing islet inflammation-mediated damage.
650 7a MEDICIN OCH HÄLSOVETENSKAPx Klinisk medicinx Endokrinologi och diabetes0 (SwePub)302052 hsv//swe
650 7a MEDICAL AND HEALTH SCIENCESx Clinical Medicinex Endocrinology and Diabetes0 (SwePub)302052 hsv//eng
653 a beta-cell function
653 a antiinflammatory strategies
653 a inhibition
653 a induction
653 a immunosuppression
653 a engraftment
653 a survival
653 a regimen
653 a Endocrinology & Metabolism
700a Lundgren, T.u Karolinska Institutet4 aut
700a Tufveson, Gunnaru Uppsala universitet,Transplantationskirurgi4 aut0 (Swepub:uu)gutuf839
700a Rafael, E.u Skane Univ Hosp, Malmo, Sweden4 aut
700a Shaw, J. A. M.u Newcastle Univ, Inst Cellular Med, Newcastle Upon Tyne, Tyne & Wear, England;Newcastle Upon Tyne Hosp NHS Fdn Trust, Freeman Hosp, Newcastle Upon Tyne, Tyne & Wear, England,IRCCS Osped San Raffaele, Milan, Italy4 aut
700a Liew, A.u Newcastle Univ, Inst Cellular Med, Newcastle Upon Tyne, Tyne & Wear, England;Newcastle Upon Tyne Hosp NHS Fdn Trust, Freeman Hosp, Newcastle Upon Tyne, Tyne & Wear, England4 aut
700a Saudek, F.u Inst Clin & Expt Med, Prague, Czech Republic4 aut
700a Witkowski, P.u Univ Chicago Med, Transplantat Inst, Chicago, IL USA4 aut
700a Golab, K.u Univ Chicago Med, Transplantat Inst, Chicago, IL USA4 aut
700a Bertuzzi, F.u Osped Niguarda Ca Granda, Milan, Italy4 aut
700a Gustafsson, Bengt,d 1946u Gothenburg University,Göteborgs universitet,Institutionen för neurovetenskap och fysiologi, sektionen för fysiologi,Institute of Neuroscience and Physiology, Department of Physiology,Univ Gothenburg, Gothenburg, Sweden4 aut0 (Swepub:gu)xgbenk
700a Daffonchio, L.u Dompe Farmaceut SpA, Dept Res & Dev, Milan, Italy4 aut
700a Ruffini, P. A.u Dompe Farmaceut SpA, Dept Res & Dev, Milan, Italy4 aut
700a Piemonti, L.u IRCCS Osped San Raffaele, San Raffaele Diabet Res Inst, Milan, Italy4 aut
700a Nano, R.u IRCCS Osped San Raffaele, Milan, Italy4 aut
700a Mercalli, A.4 aut
700a Lampasona, V.u IRCCS Osped San Raffaele, Milan, Italy4 aut
700a Magistretti, P.u IRCCS Osped San Raffaele, Milan, Italy4 aut
700a Sordi, V.u IRCCS Osped San Raffaele, Milan, Italy4 aut
700a Antonio, S.u IRCCS Osped San Raffaele, Milan, Italy4 aut
700a Antonioli, B.u Osped Niguarda Ca Granda, Milan, Italy4 aut
700a Galuzzi, M.u Osped Niguarda Ca Granda, Milan, Italy4 aut
700a Tosca, M. C.u Osped Niguarda Ca Granda, Milan, Italy4 aut
700a De Carlis, L.u Osped Niguarda Ca Granda, Milan, Italy4 aut
700a Colussi, G.u Osped Niguarda Ca Granda, Milan, Italy4 aut
700a Korsgren, Olleu Uppsala universitet,Klinisk immunologi4 aut0 (Swepub:uu)ollekors
700a Pollard, H.u Skane Univ Hosp, Malmo, Sweden4 aut
710a Karolinska Institutetb IRCCS Osped San Raffaele, San Raffaele Diabet Res Inst, Milan, Italy4 org
773t Diabetes Cared : American Diabetes Associationg 43:4, s. 710-718q 43:4<710-718x 0149-5992x 1935-5548
856u https://care.diabetesjournals.org/content/diacare/43/4/710.full.pdf
8564 8u https://gup.ub.gu.se/publication/292433
8564 8u https://doi.org/10.2337/dc19-1480
8564 8u https://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-409674
8564 8u http://kipublications.ki.se/Default.aspx?queryparsed=id:143241199

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