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Liver homing of clinical grade Tregs after therapeutic infusion in patients with autoimmune hepatitis
Autoimmune hepatitis (AIH) is an immune-mediated disease with no curative treatment. Regulatory T cell (Treg) therapy is potentially curative in AIH given the critical role of Tregs in preventing autoimmunity. To work effectively, adoptively transferred Tregs must migrate to and survive within the i...
Autores principales: | , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7001578/ https://www.ncbi.nlm.nih.gov/pubmed/32039380 http://dx.doi.org/10.1016/j.jhepr.2019.08.001 |
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author | Oo, Ye Htun Ackrill, Susan Cole, Richard Jenkins, Lee Anderson, Philip Jeffery, Hannah C. Jones, Nicholas Jeffery, Louisa E. Lutz, Philipp Wawman, Rebecca E. Athwal, Amrita Kaur Thompson, Jacqui Gray, Joanna Guo, Kathy Barton, Darren Hirschfield, Gideon M Wong, Timothy Guest, Peter Adams, David H. |
author_facet | Oo, Ye Htun Ackrill, Susan Cole, Richard Jenkins, Lee Anderson, Philip Jeffery, Hannah C. Jones, Nicholas Jeffery, Louisa E. Lutz, Philipp Wawman, Rebecca E. Athwal, Amrita Kaur Thompson, Jacqui Gray, Joanna Guo, Kathy Barton, Darren Hirschfield, Gideon M Wong, Timothy Guest, Peter Adams, David H. |
author_sort | Oo, Ye Htun |
collection | PubMed |
description | Autoimmune hepatitis (AIH) is an immune-mediated disease with no curative treatment. Regulatory T cell (Treg) therapy is potentially curative in AIH given the critical role of Tregs in preventing autoimmunity. To work effectively, adoptively transferred Tregs must migrate to and survive within the inflamed liver. We conducted a proof-of-concept study aiming to assess the safety and liver-homing properties of good manufacturing practice (GMP)-grade autologous Tregs in patients with AIH. METHODS: Autologous polyclonal GMP-grade Tregs were isolated using leukapheresis and CliniMACS, labelled with indium tropolonate and re-infused intravenously to 4 patients with AIH. GMP-Treg homing to the liver was investigated with longitudinal gamma camera and SPECT-CT scanning. GMP-Treg immunophenotype, function and immunometabolic state were assessed during the study. RESULTS: We observed that the isolated Tregs were suppressive and expressed CXCR3, a chemokine receptor involved in recruitment into the inflamed liver, as well as Treg functional markers CD39, CTLA-4 and the transcription factor Foxp3. Serial gamma camera and SPECT-CT imaging demonstrated that 22–44% of infused Tregs homed to and were retained in the livers of patients with autoimmune hepatitis for up to 72 h. The infused cells did not localise to any off-target organs other than the spleen and bone marrow. GMP-Tregs were metabolically competent and there were no infusion reactions or high-grade adverse effects after Treg infusion. CONCLUSION: Our novel findings suggest that the liver is a good target organ for Treg cellular therapy, supporting the development of clinical trials to test efficacy in autoimmune hepatitis and other autoimmune liver diseases. LAY SUMMARY: Autoimmune liver diseases occur when the body’s immune cells target their own liver cells. Regulatory T cells (Tregs) prevent autoimmunity, thus they are a potential therapy for autoimmune liver diseases. In patients with autoimmune hepatitis, Treg infusion is safe, with nearly a quarter of infused Tregs homing to the liver and suppressing tissue-damaging effector T cells. Thus, Tregs are a potentially curative immune cell therapy for early autoimmune liver diseases. |
format | Online Article Text |
id | pubmed-7001578 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-70015782020-02-07 Liver homing of clinical grade Tregs after therapeutic infusion in patients with autoimmune hepatitis Oo, Ye Htun Ackrill, Susan Cole, Richard Jenkins, Lee Anderson, Philip Jeffery, Hannah C. Jones, Nicholas Jeffery, Louisa E. Lutz, Philipp Wawman, Rebecca E. Athwal, Amrita Kaur Thompson, Jacqui Gray, Joanna Guo, Kathy Barton, Darren Hirschfield, Gideon M Wong, Timothy Guest, Peter Adams, David H. JHEP Rep Research Article Autoimmune hepatitis (AIH) is an immune-mediated disease with no curative treatment. Regulatory T cell (Treg) therapy is potentially curative in AIH given the critical role of Tregs in preventing autoimmunity. To work effectively, adoptively transferred Tregs must migrate to and survive within the inflamed liver. We conducted a proof-of-concept study aiming to assess the safety and liver-homing properties of good manufacturing practice (GMP)-grade autologous Tregs in patients with AIH. METHODS: Autologous polyclonal GMP-grade Tregs were isolated using leukapheresis and CliniMACS, labelled with indium tropolonate and re-infused intravenously to 4 patients with AIH. GMP-Treg homing to the liver was investigated with longitudinal gamma camera and SPECT-CT scanning. GMP-Treg immunophenotype, function and immunometabolic state were assessed during the study. RESULTS: We observed that the isolated Tregs were suppressive and expressed CXCR3, a chemokine receptor involved in recruitment into the inflamed liver, as well as Treg functional markers CD39, CTLA-4 and the transcription factor Foxp3. Serial gamma camera and SPECT-CT imaging demonstrated that 22–44% of infused Tregs homed to and were retained in the livers of patients with autoimmune hepatitis for up to 72 h. The infused cells did not localise to any off-target organs other than the spleen and bone marrow. GMP-Tregs were metabolically competent and there were no infusion reactions or high-grade adverse effects after Treg infusion. CONCLUSION: Our novel findings suggest that the liver is a good target organ for Treg cellular therapy, supporting the development of clinical trials to test efficacy in autoimmune hepatitis and other autoimmune liver diseases. LAY SUMMARY: Autoimmune liver diseases occur when the body’s immune cells target their own liver cells. Regulatory T cells (Tregs) prevent autoimmunity, thus they are a potential therapy for autoimmune liver diseases. In patients with autoimmune hepatitis, Treg infusion is safe, with nearly a quarter of infused Tregs homing to the liver and suppressing tissue-damaging effector T cells. Thus, Tregs are a potentially curative immune cell therapy for early autoimmune liver diseases. Elsevier 2019-08-21 /pmc/articles/PMC7001578/ /pubmed/32039380 http://dx.doi.org/10.1016/j.jhepr.2019.08.001 Text en © 2019 Published by Elsevier B.V. on behalf of European Association for the Study of the Liver (EASL). http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Research Article Oo, Ye Htun Ackrill, Susan Cole, Richard Jenkins, Lee Anderson, Philip Jeffery, Hannah C. Jones, Nicholas Jeffery, Louisa E. Lutz, Philipp Wawman, Rebecca E. Athwal, Amrita Kaur Thompson, Jacqui Gray, Joanna Guo, Kathy Barton, Darren Hirschfield, Gideon M Wong, Timothy Guest, Peter Adams, David H. Liver homing of clinical grade Tregs after therapeutic infusion in patients with autoimmune hepatitis |
title | Liver homing of clinical grade Tregs after therapeutic infusion in patients with autoimmune hepatitis |
title_full | Liver homing of clinical grade Tregs after therapeutic infusion in patients with autoimmune hepatitis |
title_fullStr | Liver homing of clinical grade Tregs after therapeutic infusion in patients with autoimmune hepatitis |
title_full_unstemmed | Liver homing of clinical grade Tregs after therapeutic infusion in patients with autoimmune hepatitis |
title_short | Liver homing of clinical grade Tregs after therapeutic infusion in patients with autoimmune hepatitis |
title_sort | liver homing of clinical grade tregs after therapeutic infusion in patients with autoimmune hepatitis |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7001578/ https://www.ncbi.nlm.nih.gov/pubmed/32039380 http://dx.doi.org/10.1016/j.jhepr.2019.08.001 |
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