Publication:
Induction of long-lasting regulatory B lymphocytes by modified immune cells in kidney transplant recipients

dc.contributor.coauthorMorath, Christian
dc.contributor.coauthorSchaier, Matthias
dc.contributor.coauthorIbrahim, Eman
dc.contributor.coauthorWang, Lei
dc.contributor.coauthorKleist, Christian
dc.contributor.coauthorOpelz, Gerhard
dc.contributor.coauthorPonath, Gerald
dc.contributor.coauthorAly, Mostafa
dc.contributor.coauthorAlvarez, Cristiam M.
dc.contributor.coauthorKälble, Florian
dc.contributor.coauthorSpeer, Claudius
dc.contributor.coauthorBenning, Louise
dc.contributor.coauthorNusshag, Christian
dc.contributor.coauthorPego Da Silva, Luiza
dc.contributor.coauthorSommerer, Claudia
dc.contributor.coauthorHückelhoven-Krauss, Angela
dc.contributor.coauthorCzock, David
dc.contributor.coauthorMehrabi, Arianeb
dc.contributor.coauthorSchwab, Constantin
dc.contributor.coauthorWaldherr, Rüdiger
dc.contributor.coauthorSchnitzler, Paul
dc.contributor.coauthorMerle, Uta
dc.contributor.coauthorTran, Thuong Hien
dc.contributor.coauthorScherer, Sabine
dc.contributor.coauthorBöhmig, Georg A.
dc.contributor.coauthorMüller-Tidow, Carsten
dc.contributor.coauthorReiser, Jochen
dc.contributor.coauthorZeier, Martin
dc.contributor.coauthorSchmitt, Michael
dc.contributor.coauthorTerness, Peter
dc.contributor.coauthorSchmitt, Anita
dc.contributor.coauthorDaniel, Volker
dc.contributor.departmentKUTTAM (Koç University Research Center for Translational Medicine)
dc.contributor.facultymemberYes
dc.contributor.kuauthorSüsal, Caner
dc.contributor.schoolcollegeinstituteResearch Center
dc.date.accessioned2024-11-09T23:58:44Z
dc.date.issued2023
dc.description.abstractBackground: We recently demonstrated that donor-derived modified immune cells (MICs)-PBMCs that acquire immunosuppressive properties after a brief treatment-induced specific immunosuppression against the allogeneic donor when administered before kidney transplantation. We found up to a 68-fold increase in CD19 + CD24 hi CD38 hi transitional B lymphocytes compared with transplanted controls. Methods: Ten patients from a phase 1 clinical trial who had received MIC infusions before kidney transplantation were followed to post-transplant day 1080. Results: Patients treated with MICs had a favorable clinical course, showing no donor-specific human leukocyte antigen antibodies or acute rejections. The four patients who had received the highest dose of MICs 7 days before surgery and were on reduced immunosuppressive therapy showed an absence of in vitro lymphocyte reactivity against stimulatory donor blood cells, whereas reactivity against third party cells was preserved. In these patients, numbers of transitional B lymphocytes were 75-fold and seven-fold higher than in 12 long-term survivors on minimal immunosuppression and four operationally tolerant patients, respectively ( P <0.001 for both). In addition, we found significantly higher numbers of other regulatory B lymphocyte subsets and a gene expression signature suggestive of operational tolerance in three of four patients. In MIC-treated patients, in vitro lymphocyte reactivity against donor blood cells was restored after B lymphocyte depletion, suggesting a direct pathophysiologic role of regulatory B lymphocytes in donor-specific unresponsiveness. Conclusions: These results indicate that donor-specific immunosuppression after MIC infusion is long-lasting and associated with a striking increase in regulatory B lymphocytes. Donor-derived MICs appear to be an immunoregulatory cell population that when administered to recipients before transplantation, may exert a beneficial effect on kidney transplants.
dc.description.fulltextNo
dc.description.harvestedfromManual
dc.description.indexedbyWOS
dc.description.indexedbyScopus
dc.description.indexedbyPubMed
dc.description.openaccessYES
dc.description.peerreviewstatusN/A
dc.description.publisherscopeInternational
dc.description.readpublishN/A
dc.description.sponsoredbyTubitakEuN/A
dc.description.sponsorshipFederal Ministry for Economic Affairs and Technology, Berlin, Germany [FKZ 03EFBBW056]
dc.description.sponsorshipFederal Ministry of Education & Research (BMBF) [FKZ 161B0560A, 161B0560B, 031B0560A, 031B0560B]
dc.description.sponsorshipTolerogenixX GmbH, Heidelberg, Germany
dc.description.studentonlypublicationNo
dc.description.studentpublicationNo
dc.description.versionN/A
dc.identifier.doi10.1681/ASN.2022020210
dc.identifier.eissn1533-3450
dc.identifier.embargoN/A
dc.identifier.endpage174
dc.identifier.grantnoFKZ 03EFBBW056
dc.identifier.grantnoFKZ 161B0560A
dc.identifier.grantno161B0560B
dc.identifier.grantno031B0560A
dc.identifier.grantno031B0560B
dc.identifier.issn1046-6673
dc.identifier.issue1
dc.identifier.pubmed36137752
dc.identifier.quartileQ1
dc.identifier.scopus2-s2.0-85142532651
dc.identifier.startpage160
dc.identifier.urihttps://doi.org/10.1681/ASN.2022020210
dc.identifier.urihttps://hdl.handle.net/20.500.14288/15519
dc.identifier.volume34
dc.identifier.wos000917990700018
dc.keywordsClinical trial
dc.keywordsImmunosuppression
dc.keywordsKidney transplantation
dc.keywordsRegulatory B lymphocyte
dc.keywordsTolerance
dc.language.isoeng
dc.publisherWolters Kluwer Health
dc.relation.affiliationKoç University
dc.relation.collectionKoç University Institutional Repository
dc.relation.ispartofJournal of the American Society of Nephrology
dc.relation.openaccessN/A
dc.rightsN/A
dc.subjectUrology
dc.subjectNephrology
dc.titleInduction of long-lasting regulatory B lymphocytes by modified immune cells in kidney transplant recipients
dc.typeJournal Article
dspace.entity.typePublication
local.contributor.kuauthorSüsal, Caner
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relation.isGoalOfPublication.latestForDiscoverya9786601-9431-4553-9a46-013bb366fb87
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