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Immunoregulatory and lipid presentation pathways are upregulated in human face transplant rejection
TS. Win, WJ. Crisler, B. Dyring-Andersen, R. Lopdrup, JE. Teague, Q. Zhan, V. Barrera, S. Ho Sui, S. Tasigiorgos, N. Murakami, A. Chandraker, SG. Tullius, B. Pomahac, LV. Riella, RA. Clark
Language English Country United States
Document type Clinical Trial, Journal Article, Multicenter Study, Research Support, N.I.H., Extramural, Research Support, Non-U.S. Gov't, Research Support, U.S. Gov't, Non-P.H.S.
Grant support
K08 DK120868
NIDDK NIH HHS - United States
P30 AR069625
NIAMS NIH HHS - United States
UL1 RR025758
NCRR NIH HHS - United States
NLK
Free Medical Journals
from 1924 to 1 year ago
Freely Accessible Science Journals
from 1924 to 1 year ago
PubMed Central
from 1924 to 1 year ago
Europe PubMed Central
from 1924 to 1 year ago
ProQuest Central
from 2002-07-01
Open Access Digital Library
from 1924-10-01
Open Access Digital Library
from 1925-08-01
Medline Complete (EBSCOhost)
from 2002-01-01 to 2021-08-16
Nursing & Allied Health Database (ProQuest)
from 2002-07-01
Health & Medicine (ProQuest)
from 2002-07-01
ROAD: Directory of Open Access Scholarly Resources
from 1924
PubMed
33667197
DOI
10.1172/jci135166
Knihovny.cz E-resources
- MeSH
- Skin immunology pathology MeSH
- Humans MeSH
- Lipids immunology MeSH
- Follow-Up Studies MeSH
- Antigen Presentation * MeSH
- Prospective Studies MeSH
- Receptors, Antigen, T-Cell * genetics immunology MeSH
- Graft Rejection genetics immunology pathology MeSH
- Gene Expression Profiling * MeSH
- T-Lymphocytes immunology MeSH
- Facial Transplantation * MeSH
- Check Tag
- Humans MeSH
- Male MeSH
- Female MeSH
- Publication type
- Journal Article MeSH
- Clinical Trial MeSH
- Multicenter Study MeSH
- Research Support, Non-U.S. Gov't MeSH
- Research Support, N.I.H., Extramural MeSH
- Research Support, U.S. Gov't, Non-P.H.S. MeSH
BACKGROUNDRejection is the primary barrier to broader implementation of vascularized composite allografts (VCAs), including face and limb transplants. The immunologic pathways activated in face transplant rejection have not been fully characterized.METHODSUsing skin biopsies prospectively collected over 9 years from 7 face transplant patients, we studied rejection by gene expression profiling, histology, immunostaining, and T cell receptor sequencing.RESULTSGrade 1 rejection did not differ significantly from nonrejection, suggesting that it does not represent a pathologic state. In grade 2, there was a balanced upregulation of both proinflammatory T cell activation pathways and antiinflammatory checkpoint and immunomodulatory pathways, with a net result of no tissue injury. In grade 3, IFN-γ-driven inflammation, antigen-presenting cell activation, and infiltration of the skin by proliferative T cells bearing markers of antigen-specific activation and cytotoxicity tipped the balance toward tissue injury. Rejection of VCAs and solid organ transplants had both distinct and common features. VCA rejection was uniquely associated with upregulation of immunoregulatory genes, including SOCS1; induction of lipid antigen-presenting CD1 proteins; and infiltration by T cells predicted to recognize CD1b and CD1c.CONCLUSIONOur findings suggest that the distinct features of VCA rejection reflect the unique immunobiology of skin and that enhancing cutaneous immunoregulatory networks may be a useful strategy in combatting rejection.Trial registrationClinicalTrials.gov NCT01281267.FUNDINGAssistant Secretary of Defense and Health Affairs, through Reconstructive Transplant Research (W81XWH-17-1-0278, W81XWH-16-1-0647, W81XWH-16-1-0689, W81XWH-18-1-0784, W81XWH-1-810798); American Society of Transplantation's Transplantation and Immunology Research Network Fellowship Research Grant; Plastic Surgery Foundation Fellowship from the American Society of Plastic Surgeons; Novo Nordisk Foundation (NNF15OC0014092); Lundbeck Foundation; Aage Bangs Foundation; A.P. Moller Foundation for the Advancement of Medical Science; NIH UL1 RR025758.
References provided by Crossref.org
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