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Evaluation of a gene expression biomarker to identify operationally tolerant liver transplant recipients: the LITMUS trial

LITMUS was a single-centre, Phase 2a study designed to investigate whether the gene biomarker FGL2/IFNG previously reported for the identification of tolerance in murine models could identify operationally tolerant liver transplant recipients. Multiplex RT-PCR was used to amplify eight immunoregulat...

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Autores principales: Chruscinski, Andrzej, Rojas-Luengas, Vanessa, Moshkelgosha, Sajad, Issachar, Assaf, Luo, Jane, Yowanto, Handy, Lilly, Leslie, Smith, Robert, Renner, Eberhard, Zhang, Jianhua, Epstein, Maor, Grant, David, McEvoy, Caitriona M, Konvalinka, Ana, Humar, Atul, Adeyi, Oyedele, Fischer, Sandra, Volmer, Felix H, Taubert, Richard, Jaeckel, Elmar, Juvet, Stephen, Selzner, Nazia, Levy, Gary A
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8802178/
https://www.ncbi.nlm.nih.gov/pubmed/35020854
http://dx.doi.org/10.1093/cei/uxab011
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author Chruscinski, Andrzej
Rojas-Luengas, Vanessa
Moshkelgosha, Sajad
Issachar, Assaf
Luo, Jane
Yowanto, Handy
Lilly, Leslie
Smith, Robert
Renner, Eberhard
Zhang, Jianhua
Epstein, Maor
Grant, David
McEvoy, Caitriona M
Konvalinka, Ana
Humar, Atul
Adeyi, Oyedele
Fischer, Sandra
Volmer, Felix H
Taubert, Richard
Jaeckel, Elmar
Juvet, Stephen
Selzner, Nazia
Levy, Gary A
author_facet Chruscinski, Andrzej
Rojas-Luengas, Vanessa
Moshkelgosha, Sajad
Issachar, Assaf
Luo, Jane
Yowanto, Handy
Lilly, Leslie
Smith, Robert
Renner, Eberhard
Zhang, Jianhua
Epstein, Maor
Grant, David
McEvoy, Caitriona M
Konvalinka, Ana
Humar, Atul
Adeyi, Oyedele
Fischer, Sandra
Volmer, Felix H
Taubert, Richard
Jaeckel, Elmar
Juvet, Stephen
Selzner, Nazia
Levy, Gary A
author_sort Chruscinski, Andrzej
collection PubMed
description LITMUS was a single-centre, Phase 2a study designed to investigate whether the gene biomarker FGL2/IFNG previously reported for the identification of tolerance in murine models could identify operationally tolerant liver transplant recipients. Multiplex RT-PCR was used to amplify eight immunoregulatory genes in peripheral blood mononuclear cells (PBMC) from 69 adult liver transplant recipients. Patients with PBMC FGL2/IFNG ≥ 1 and a normal liver biopsy underwent immunosuppression (IS) withdrawal. The primary end point was the development of operational tolerance. Secondary end points included correlation of tolerance with allograft gene expression and immune cell markers. Twenty-eight of 69 patients (38%) were positive for the PBMC tolerance biomarker and 23 proceeded to IS withdrawal. Nine of the 23 patients had abnormal baseline liver biopsies and were excluded. Of the 14 patients with normal biopsies, eight (57%) have achieved operational tolerance and are off IS (range 12–57 months). Additional studies revealed that all of the tolerant patients and only one non-tolerant patient had a liver gene ratio of FOXP3/IFNG ≥ 1 prior to IS withdrawal. Increased CD4(+) T regulatory T cells were detected both in PBMC and livers of tolerant patients following IS withdrawal. Higher expression of SELE (gene for E-selectin) and lower expression of genes associated with inflammatory responses (GZMB, CIITA, UBD, LSP1, and CXCL9) were observed in the pre-withdrawal liver biopsies of tolerant patients by RNA sequencing. These results suggest that measurement of PBMC FGL2/IFNG may enrich for the identification of operationally tolerant liver transplant patients, especially when combined with intragraft measurement of FOXP3/IFNG. Clinical Trial Registration: ClinicalTrials.gov (LITMUS: NCT02541916).
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spelling pubmed-88021782022-01-31 Evaluation of a gene expression biomarker to identify operationally tolerant liver transplant recipients: the LITMUS trial Chruscinski, Andrzej Rojas-Luengas, Vanessa Moshkelgosha, Sajad Issachar, Assaf Luo, Jane Yowanto, Handy Lilly, Leslie Smith, Robert Renner, Eberhard Zhang, Jianhua Epstein, Maor Grant, David McEvoy, Caitriona M Konvalinka, Ana Humar, Atul Adeyi, Oyedele Fischer, Sandra Volmer, Felix H Taubert, Richard Jaeckel, Elmar Juvet, Stephen Selzner, Nazia Levy, Gary A Clin Exp Immunol Research Articles LITMUS was a single-centre, Phase 2a study designed to investigate whether the gene biomarker FGL2/IFNG previously reported for the identification of tolerance in murine models could identify operationally tolerant liver transplant recipients. Multiplex RT-PCR was used to amplify eight immunoregulatory genes in peripheral blood mononuclear cells (PBMC) from 69 adult liver transplant recipients. Patients with PBMC FGL2/IFNG ≥ 1 and a normal liver biopsy underwent immunosuppression (IS) withdrawal. The primary end point was the development of operational tolerance. Secondary end points included correlation of tolerance with allograft gene expression and immune cell markers. Twenty-eight of 69 patients (38%) were positive for the PBMC tolerance biomarker and 23 proceeded to IS withdrawal. Nine of the 23 patients had abnormal baseline liver biopsies and were excluded. Of the 14 patients with normal biopsies, eight (57%) have achieved operational tolerance and are off IS (range 12–57 months). Additional studies revealed that all of the tolerant patients and only one non-tolerant patient had a liver gene ratio of FOXP3/IFNG ≥ 1 prior to IS withdrawal. Increased CD4(+) T regulatory T cells were detected both in PBMC and livers of tolerant patients following IS withdrawal. Higher expression of SELE (gene for E-selectin) and lower expression of genes associated with inflammatory responses (GZMB, CIITA, UBD, LSP1, and CXCL9) were observed in the pre-withdrawal liver biopsies of tolerant patients by RNA sequencing. These results suggest that measurement of PBMC FGL2/IFNG may enrich for the identification of operationally tolerant liver transplant patients, especially when combined with intragraft measurement of FOXP3/IFNG. Clinical Trial Registration: ClinicalTrials.gov (LITMUS: NCT02541916). Oxford University Press 2021-11-18 /pmc/articles/PMC8802178/ /pubmed/35020854 http://dx.doi.org/10.1093/cei/uxab011 Text en © The Author(s) 2021. Published by Oxford University Press on behalf of the British Society for Immunology. All rights reserved. For permissions, please e-mail: journals.permissions@oup.com https://academic.oup.com/journals/pages/open_access/funder_policies/chorus/standard_publication_modelThis article is published and distributed under the terms of the Oxford University Press, Standard Journals Publication Model (https://academic.oup.com/journals/pages/open_access/funder_policies/chorus/standard_publication_model)
spellingShingle Research Articles
Chruscinski, Andrzej
Rojas-Luengas, Vanessa
Moshkelgosha, Sajad
Issachar, Assaf
Luo, Jane
Yowanto, Handy
Lilly, Leslie
Smith, Robert
Renner, Eberhard
Zhang, Jianhua
Epstein, Maor
Grant, David
McEvoy, Caitriona M
Konvalinka, Ana
Humar, Atul
Adeyi, Oyedele
Fischer, Sandra
Volmer, Felix H
Taubert, Richard
Jaeckel, Elmar
Juvet, Stephen
Selzner, Nazia
Levy, Gary A
Evaluation of a gene expression biomarker to identify operationally tolerant liver transplant recipients: the LITMUS trial
title Evaluation of a gene expression biomarker to identify operationally tolerant liver transplant recipients: the LITMUS trial
title_full Evaluation of a gene expression biomarker to identify operationally tolerant liver transplant recipients: the LITMUS trial
title_fullStr Evaluation of a gene expression biomarker to identify operationally tolerant liver transplant recipients: the LITMUS trial
title_full_unstemmed Evaluation of a gene expression biomarker to identify operationally tolerant liver transplant recipients: the LITMUS trial
title_short Evaluation of a gene expression biomarker to identify operationally tolerant liver transplant recipients: the LITMUS trial
title_sort evaluation of a gene expression biomarker to identify operationally tolerant liver transplant recipients: the litmus trial
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8802178/
https://www.ncbi.nlm.nih.gov/pubmed/35020854
http://dx.doi.org/10.1093/cei/uxab011
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