eprintid: 1489732
rev_number: 29
eprint_status: archive
userid: 608
dir: disk0/01/48/97/32
datestamp: 2016-05-05 16:02:57
lastmod: 2021-10-04 00:57:31
status_changed: 2016-05-05 16:02:57
type: article
metadata_visibility: show
creators_name: Pike, R
creators_name: Thomas, N
creators_name: Workman, S
creators_name: Ambrose, L
creators_name: Guzman, D
creators_name: Sivakumaran, S
creators_name: Johnson, M
creators_name: Thorburn, D
creators_name: Harber, M
creators_name: Chain, B
creators_name: Stauss, HJ
title: PD1-Expressing T Cell Subsets Modify the Rejection Risk in Renal Transplant Patients
ispublished: pub
divisions: UCL
divisions: B02
divisions: C10
divisions: D15
divisions: D17
keywords: transplantation, rejection, T cells, protein death 1, risk factor
note: Copyright © 2016 Pike, Thomas, Workman, Ambrose, Guzman, Sivakumaran, Johnson, Thorburn, Harber, Chain and Stauss. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY) (http://creativecommons.org/licenses/by/4.0/). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
abstract: We tested whether multi-parameter immune phenotyping before or after renal ­transplantation can predict the risk of rejection episodes. Blood samples collected before and weekly for 3 months after transplantation were analyzed by multi-parameter flow cytometry to define 52 T cell and 13 innate lymphocyte subsets in each sample, producing more than 11,000 data points that defined the immune status of the 28 patients included in this study. Principle component analysis suggested that the patients with histologically confirmed rejection episodes segregated from those without rejection. Protein death 1 (PD-1)-expressing subpopulations of regulatory and conventional T cells had the greatest influence on the principal component segregation. We constructed a statistical tool to predict rejection using a support vector machine algorithm. The algorithm correctly identified 7 out of 9 patients with rejection, and 14 out of 17 patients without rejection. The immune profile before transplantation was most accurate in determining the risk of rejection, while changes of immune parameters after transplantation were less accurate in discriminating rejection from non-rejection. The data indicate that pretransplant immune subset analysis has the potential to identify patients at risk of developing rejection episodes, and suggests that the proportion of PD1-expressing T cell subsets may be a key indicator of rejection risk.
date: 2016-04-11
date_type: published
official_url: http://dx.doi.org/10.3389/fimmu.2016.00126
oa_status: green
full_text_type: pub
language: eng
primo: open
primo_central: open_green
verified: verified_manual
elements_id: 1127413
doi: 10.3389/fimmu.2016.00126
lyricists_name: Chain, Benjamin
lyricists_name: Harber, Mark
lyricists_name: Stauss, Hans
lyricists_name: Thorburn, Douglas
lyricists_id: BMCHA43
lyricists_id: MAHAR54
lyricists_id: HJSTA69
lyricists_id: DTHOR21
actors_name: Chain, Benjamin
actors_id: BMCHA43
actors_role: owner
full_text_status: public
publication: Frontiers in Immunology
volume: 7
article_number: 126
issn: 1664-3224
citation:        Pike, R;    Thomas, N;    Workman, S;    Ambrose, L;    Guzman, D;    Sivakumaran, S;    Johnson, M;                 ... Stauss, HJ; + view all <#>        Pike, R;  Thomas, N;  Workman, S;  Ambrose, L;  Guzman, D;  Sivakumaran, S;  Johnson, M;  Thorburn, D;  Harber, M;  Chain, B;  Stauss, HJ;   - view fewer <#>    (2016)    PD1-Expressing T Cell Subsets Modify the Rejection Risk in Renal Transplant Patients.                   Frontiers in Immunology , 7     , Article 126.  10.3389/fimmu.2016.00126 <https://doi.org/10.3389/fimmu.2016.00126>.       Green open access   
 
document_url: https://discovery.ucl.ac.uk/id/eprint/1489732/1/Chain_fimmu-07-00126.pdf