Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Evaluation of CD4+ CD25+/- CD39+ T-cell populations in peripheral blood of patients following kidney transplantation and during acute allograft rejection.

Nephrology (Carlton, Vic.) - 1 Jul 2017

McRae Jennifer L, Chia Joanne Sj, Pommey Sandra A, Dwyer Karen M

Abstract excerpt

AIM: Regulatory T cells (Treg) are important in mediating immune tolerance and outcomes of allotransplantation. CD4+ CD25+ CD39+ co-expression identifies memory Treg; CD4+ CD25- CD39+ memory T effectors. We sought to determine CD4+ CD25+/- CD39+ expression from the peripheral blood of patients with end stage renal failure, following transplantation and during episodes of acute cellular rejection. METHODS: CD4+ T...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Allografts
Share to Apyrase

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Graft Rejection

Share to Graft Survival

Share to Interleukin-2 Receptor alpha Subunit

Share to Kidney Failure, Chronic

Share to T-Lymphocytes, Regulatory

Share to Transplantation Tolerance

Source

Identifiers

PMID: 27517975
DOI: 10.1111/nep.12894

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Evaluation of CD4+ CD25+/- CD39+ T-cell populations in peripheral blood of patients following kidney transplantation and during acute allograft rejection.PMID 27517975Read ↗

Expression of CD39 by human peripheral blood CD4+ CD25+ T cells denotes a regulatory memory phenotype.Semantic proximity Read ↗

An investigation to assess the potential of CD25highCD4+ T cells to regulate responses to donor alloantigens in clinically stable renal transplant recipients.Semantic proximity Read ↗

TCR usage, gene expression and function of two distinct FOXP3(+)Treg subsets within CD4(+)CD25(hi) T cells identified by expression of CD39 and CD45RO.Semantic proximity Read ↗

Clinical and immunological follow-up of very long-term kidney transplant recipients treated with calcineurin inhibitors indicates dual phenotypes.Semantic proximity Read ↗

Regulatory T cells in solid organ transplantationSemantic proximity Read ↗

Longitudinal analysis of T and B cell phenotype and function in renal transplant recipients with or without rituximab induction therapy.Semantic proximity Read ↗

Single-cell and multi-omic characterization of ex vivo expanded ASTRLs from stable kidney transplant recipients reveals a regulatory T cell phenotype.Semantic proximity Read ↗

Blockade of chronic graft-versus-host disease by alloantigen-induced CD4+CD25+Foxp3+ regulatory T cells in nonlymphopenic hosts.Semantic proximity Read ↗

CD25 expression on donor CD4+ or CD8+ T cells is associated with an increased risk for graft-versus-host disease after HLA-identical stem cell transplantation in humansSemantic proximity Read ↗

Clinical adoptive regulatory T Cell therapy: State of the art, challenges, and prospectiveSemantic proximity Read ↗

Monitoring of molecular profiling of regulatory T cell biomarkers by using non- invasive strategies to predict outcome in renal transplantationSemantic proximity Read ↗

Separation of human CD4+CD39+ T cells by magnetic beads reveals two phenotypically and functionally different subsets.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.