Improved Overall Survival, Relapse-Free-Survival, and Less Graft-vs.-Host-Disease in Patients With High Immune Reconstitution of TCR Gamma Delta Cells 2 Months After Allogeneic Stem Cell Transplantation.


Journal

Frontiers in immunology
ISSN: 1664-3224
Titre abrégé: Front Immunol
Pays: Switzerland
ID NLM: 101560960

Informations de publication

Date de publication:
2019
Historique:
received: 21 12 2018
accepted: 07 08 2019
entrez: 12 9 2019
pubmed: 12 9 2019
medline: 2 10 2020
Statut: epublish

Résumé

T-cell receptor (TCR) γδ cells are perceived as innate-like effector cells with the possibility of mediating graft-vs. -tumor (GVT) without causing graft-vs.-host disease (GVHD) in the setting of hematopoietic allogeneic stem cell transplantation (HSCT). We conducted a prospective study to assess the clinical impact of TCR γδ cell immune reconstitution on overall survival, relapse-free-survival, relapse and GVHD. The impact of CD3, CD4, and CD8 T cells together with NK cells including subtypes were analyzed in parallel. A total of 108 patients with hematological malignancies transplanted with HLA-matched, T cell replete stem cell grafts were included for analyses of absolute concentrations of CD3, CD4, and CD8 positive T cells and NK cells together with a multi-color flow cytometry panel with staining for TCRαβ, TCRγδ, Vδ1, Vδ2, CD3, CD4, CD8, HLA-DR, CD196, CD45RO, CD45RA, CD16, CD56, CD337, and CD314 at 28, 56, 91, 180, and 365 days after transplantation. Immune reconstitution data including subsets and differentiation markers of T and NK cells during the first year after transplantation was provided. Patients with TCR γδ cell concentrations above the median value of 21 (0-416) × 10

Identifiants

pubmed: 31507601
doi: 10.3389/fimmu.2019.01997
pmc: PMC6714591
doi:

Substances chimiques

Receptors, Antigen, T-Cell, gamma-delta 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

1997

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Auteurs

Lia Minculescu (L)

Department of Clinical Immunology, Copenhagen University Hospital, Rigshospitalet, Copenhagen, Denmark.

Hanne Vibeke Marquart (HV)

Department of Clinical Immunology, Copenhagen University Hospital, Rigshospitalet, Copenhagen, Denmark.

Lars Peter Ryder (LP)

Department of Clinical Immunology, Copenhagen University Hospital, Rigshospitalet, Copenhagen, Denmark.

Niels Smedegaard Andersen (NS)

Department of Hematology, Copenhagen University Hospital, Rigshospitalet, Copenhagen, Denmark.

Ida Schjoedt (I)

Department of Hematology, Copenhagen University Hospital, Rigshospitalet, Copenhagen, Denmark.

Lone Smidstrup Friis (LS)

Department of Hematology, Copenhagen University Hospital, Rigshospitalet, Copenhagen, Denmark.

Brian Thomas Kornblit (BT)

Department of Hematology, Copenhagen University Hospital, Rigshospitalet, Copenhagen, Denmark.

Søren Lykke Petersen (SL)

Department of Hematology, Copenhagen University Hospital, Rigshospitalet, Copenhagen, Denmark.

Eva Haastrup (E)

Department of Clinical Immunology, Copenhagen University Hospital, Rigshospitalet, Copenhagen, Denmark.

Anne Fischer-Nielsen (A)

Department of Clinical Immunology, Copenhagen University Hospital, Rigshospitalet, Copenhagen, Denmark.

Joanne Reekie (J)

Department of Infectious Diseases, PERSIMUNE, Copenhagen University Hospital, Rigshospitalet, Copenhagen, Denmark.

Henrik Sengelov (H)

Department of Hematology, Copenhagen University Hospital, Rigshospitalet, Copenhagen, Denmark.

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Classifications MeSH