Cited by 69T-cell and B-cell ImmunologyTransplantation: Methods and OutcomesRenal Transplantation Outcomes and Treatments

Harnessing FOXP3+ regulatory T cells for transplantation tolerance

Open access
Waldmann, Herman, Hilbrands, Robert, Howie, Duncan, Cobbold, Stephen·2014·Journal of Clinical Investigation

Abstract

Early demonstrations that mice could be tolerized to transplanted tissues with short courses of immunosuppressive therapy and that with regard to tolerance to self, CD4+FOXP3+ regulatory T cells (Tregs) appeared to play a critical role, have catalyzed strategies to harness FOXP3-dependent processes to control rejection in human transplantation. This review seeks to examine the scientific underpinning for this new approach to finesse immunosuppression.

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Crossref · 10.1172/jci67226

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References 110 · Cited by 69

Authors
Waldmann, H., Hilbrands, R., Howie, D., & Cobbold, S.
Affiliations
University of Oxford (GB)
Corresponding author
Waldmann, Herman
Venue
Journal of Clinical Investigation
Published
2014-04-01
Volume
124
Issue
4
Pages
1439-1445
ISSN
0021-9738 (ISSN-L)
OpenAlex
W2094284801
Cited by
69
References
110
Citations by year
2026: 4 · 2024: 5 · 2023: 5 · 2022: 3 · 2021: 3 · 2020: 5 · 2019: 8 · 2018: 5 · 2017: 6 · 2016: 10 · 2015: 10 · 2014: 5
FWCI
1.01
Type
journal article
Language
en
Open access
Locations
  • Journal of Clinical Investigation (publishedVersion)
  • PubMed Central (publishedVersion)
  • PubMed (publishedVersion)
  • VUBIR (Vrije Universiteit Brussel) (submittedVersion)
Funders
  • European Molecular Biology Organization
  • University of Oxford
Topics
  • Life Sciences › Immunology and Microbiology › Immunology › T-cell and B-cell Immunology
  • Health Sciences › Medicine › Surgery › Transplantation: Methods and Outcomes
  • Health Sciences › Medicine › Transplantation › Renal Transplantation Outcomes and Treatments
Keywords
Foxp3+ regulatory T cells, transplantation tolerance, immunosuppression, graft rejection, CD4+ T cells, self-tolerance, tolerance induction, transplantation immunology
MeSH terms
Animals, Humans, Immunosuppression Therapy, Receptors, Antigen, T-Cell, Signal Transduction, Transplantation Tolerance, Epigenesis, Genetic, T-Lymphocytes, Regulatory, Mice, Forkhead Transcription Factors

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