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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.
Afiliação
  • Oo YH; Centre for Liver and Gastroenterology Research, Institute of Immunology and Immunotherapy, University of Birmingham.
  • Ackrill S; National Institute of Health Research Birmingham Biomedical Research Centre.
  • Cole R; Liver Transplant and Hepato-biliary Unit, Queen Elizabeth Hospital, University Hospital Birmingham National Health Service Foundation Trust, Birmingham, United Kingdom.
  • Jenkins L; Clinical Radiopharmacy, Imaging and Nuclear Medicine Department, University Hospital of Birmingham National Health Service Foundation Trust; Birmingham.
  • Anderson P; Clinical Radiopharmacy, Imaging and Nuclear Medicine Department, University Hospital of Birmingham National Health Service Foundation Trust; Birmingham.
  • Jeffery HC; Clinical Radiopharmacy, Imaging and Nuclear Medicine Department, University Hospital of Birmingham National Health Service Foundation Trust; Birmingham.
  • Jones N; Clinical Radiopharmacy, Imaging and Nuclear Medicine Department, University Hospital of Birmingham National Health Service Foundation Trust; Birmingham.
  • Jeffery LE; Centre for Liver and Gastroenterology Research, Institute of Immunology and Immunotherapy, University of Birmingham.
  • Lutz P; Institute of Life Science, Swansea University Medical School, Singleton Park, Swansea.
  • Wawman RE; Centre for Liver and Gastroenterology Research, Institute of Immunology and Immunotherapy, University of Birmingham.
  • Athwal AK; Centre for Liver and Gastroenterology Research, Institute of Immunology and Immunotherapy, University of Birmingham.
  • Thompson J; Centre for Liver and Gastroenterology Research, Institute of Immunology and Immunotherapy, University of Birmingham.
  • Gray J; Cancer Research Clinical Trial Unit, University of Birmingham.
  • Guo K; National Health Services Blood and Transplant, Birmingham.
  • Barton D; National Institute of Health Research Wellcome Trust Clinical Research Facility, Birmingham.
  • Hirschfield GM; National Institute of Health Research Birmingham Biomedical Research Centre.
  • Wong T; Department of Haematology, University Hospital Birmingham National Health Service Foundation Trust.
  • Guest P; Cancer Research Clinical Trial Unit, University of Birmingham.
  • Adams DH; Centre for Liver and Gastroenterology Research, Institute of Immunology and Immunotherapy, University of Birmingham.
JHEP Rep ; 1(4): 286-296, 2019 Oct.
Article em En | MEDLINE | ID: mdl-32039380
ABSTRACT
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.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2019 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2019 Tipo de documento: Article