PMID- 21521503 OWN - NLM STAT- MEDLINE DCOM- 20110909 LR - 20211020 IS - 1465-993X (Electronic) IS - 1465-9921 (Print) IS - 1465-9921 (Linking) VI - 12 IP - 1 DP - 2011 Apr 26 TI - Ingraft chimerism in lung transplantation--a study in a porcine model of obliterative bronchiolitis. PG - 56 LID - 10.1186/1465-9921-12-56 [doi] AB - BACKGROUND: Bronchial epithelium is a target of the alloimmune response in lung transplantation, and intact epithelium may protect allografts from rejection and obliterative bronchiolitis (OB). Herein we study the influence of chimerism on bronchial epithelium and OB development in pigs. METHODS: A total of 54 immunosuppressed and unimmunosuppressed bronchial allografts were serially obtained 2-90 days after transplantation. Histology (H&E) was assessed and the fluorescence in situ hybridization (FISH) method for Y chromosomes using pig-specific DNA-label was used to detect recipient derived cells in graft epithelium and bronchial wall, and donor cell migration to recipient organs. Ingraft chimerism was studied by using male recipients with female donors, whereas donor cell migration to recipient organs was studied using female recipients with male donors. RESULTS: Early appearance of recipient-derived cells in the airway epithelium appeared predictive of epithelial destruction (R=0.610-0.671 and p<0.05) and of obliteration of the bronchial lumen (R=0.698 and p<0.01). All allografts with preserved epithelium showed epithelial chimerism throughout the follow-up. Antirejection medication did not prevent, but delayed the appearance of Y chromosome positive cells in the epithelium (p<0.05), or bronchial wall (p<0.05). CONCLUSIONS: In this study we demonstrate that early appearance of Y chromosomes in the airway epithelium predicts features characteristic of OB. Chimerism occurred in all allografts, including those without features of OB. Therefore we suggest that ingraft chimerism may be a mechanism involved in the repair of alloimmune-mediated tissue injury after transplantation. FAU - Paivaniemi, Outi E AU - Paivaniemi OE AD - Department of Cardiothoracic Surgery, Helsinki University Hospital, University of Helsinki, P.O. Box 340, 00029 HUS, Helsinki, Finland. outi.paivaniemi@fimnet.fi FAU - Musilova, Petra AU - Musilova P FAU - Raivio, Peter M AU - Raivio PM FAU - Maasilta, Paula K AU - Maasilta PK FAU - Alho, Hanni S AU - Alho HS FAU - Rubes, Jiri AU - Rubes J FAU - Aittomaki, Kristiina AU - Aittomaki K FAU - Salminen, Ulla-Stina AU - Salminen US LA - eng PT - Journal Article PT - Research Support, Non-U.S. Gov't DEP - 20110426 PL - England TA - Respir Res JT - Respiratory research JID - 101090633 RN - 0 (Genetic Markers) RN - 0 (Immunosuppressive Agents) SB - IM MH - Animals MH - Bronchi/drug effects/immunology/pathology/*transplantation MH - Bronchiolitis Obliterans/genetics/*immunology/pathology/prevention & control MH - *Cell Movement MH - Disease Models, Animal MH - Female MH - Genetic Markers MH - Graft Rejection/genetics/*immunology/pathology/prevention & control MH - Immunosuppressive Agents/pharmacology MH - In Situ Hybridization, Fluorescence MH - Lung Transplantation/*immunology MH - Male MH - Respiratory Mucosa/drug effects/immunology/pathology/*transplantation MH - Staining and Labeling MH - Sus scrofa MH - Time Factors MH - *Transplantation Chimera MH - Transplantation Tolerance MH - Transplantation, Homologous MH - Y Chromosome PMC - PMC3111361 EDAT- 2011/04/28 06:00 MHDA- 2011/09/10 06:00 PMCR- 2011/04/26 CRDT- 2011/04/28 06:00 PHST- 2010/12/06 00:00 [received] PHST- 2011/04/26 00:00 [accepted] PHST- 2011/04/28 06:00 [entrez] PHST- 2011/04/28 06:00 [pubmed] PHST- 2011/09/10 06:00 [medline] PHST- 2011/04/26 00:00 [pmc-release] AID - 1465-9921-12-56 [pii] AID - 10.1186/1465-9921-12-56 [doi] PST - epublish SO - Respir Res. 2011 Apr 26;12(1):56. doi: 10.1186/1465-9921-12-56.