Efficiency of human monocyte-derived suppressor cell-based treatment in graft-versus-host disease prevention while preserving graft-versus-leukemia effect.

Human monocyte-derived suppressor cells graft-versus-host disease graft-versus-leukemia effect immunosuppressive drugs inflammation regulatory T cells

Journal

Oncoimmunology
ISSN: 2162-402X
Titre abrégé: Oncoimmunology
Pays: United States
ID NLM: 101570526

Informations de publication

Date de publication:
19 02 2021
Historique:
entrez: 4 3 2021
pubmed: 5 3 2021
medline: 29 7 2021
Statut: epublish

Résumé

Immunosuppressive cell-based therapy is a recent strategy for controlling Graft- The objective of this study was to explore the therapeutic relevance of the HuMoSC in clinical conditions. Immune regulatory functions of HuMoSC were assessed in inflammatory conditions and in the presence of immunosuppressants. The therapeutic efficiency of the association of HuMoSC with immunosuppressants was evaluated in an experimental model of GvHD induced by human PBMC in NOD/SCID/IL2-Rγ Interestingly, the inhibitory functions of HuMoSC against T lymphocytes and their ability to polarize Treg are preserved, HuMoSC-based therapy represents a promising approach for controlling GvHD and could be quickly implemented in clinical practice.

Sections du résumé

Background
Immunosuppressive cell-based therapy is a recent strategy for controlling Graft-
The objective of this study was to explore the therapeutic relevance of the HuMoSC in clinical conditions.
Methods
Immune regulatory functions of HuMoSC were assessed in inflammatory conditions and in the presence of immunosuppressants. The therapeutic efficiency of the association of HuMoSC with immunosuppressants was evaluated in an experimental model of GvHD induced by human PBMC in NOD/SCID/IL2-Rγ
Interestingly, the inhibitory functions of HuMoSC against T lymphocytes and their ability to polarize Treg are preserved,
HuMoSC-based therapy represents a promising approach for controlling GvHD and could be quickly implemented in clinical practice.

Identifiants

pubmed: 33659098
doi: 10.1080/2162402X.2021.1880046
pii: 1880046
pmc: PMC7899641
doi:

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

1880046

Informations de copyright

© 2021 The Author(s). Published with license by Taylor & Francis Group, LLC.

Déclaration de conflit d'intérêts

The authors declare that they have no conflict of interest.

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Auteurs

Nona Janikashvili (N)

Univ. Bourgogne Franche-Comté, INSERM, EFS BFC, UMR1098, RIGHT Interactions Greffon-Hôte-Tumeur/Ingénierie Cellulaire Et Génique, Dijon, France.
Department of Immunology, Faculty of Medicine, Tbilisi State Medical University (TSMU), Tbilisi, Georgia.

Claire Gérard (C)

Univ. Bourgogne Franche-Comté, INSERM, EFS BFC, UMR1098, RIGHT Interactions Greffon-Hôte-Tumeur/Ingénierie Cellulaire Et Génique, Dijon, France.
Department of Internal Medicine, University Hospital, Dijon, France.

Marine Thébault (M)

Univ. Bourgogne Franche-Comté, INSERM, EFS BFC, UMR1098, RIGHT Interactions Greffon-Hôte-Tumeur/Ingénierie Cellulaire Et Génique, Dijon, France.

Andrea Brazdova (A)

Univ. Bourgogne Franche-Comté, INSERM, EFS BFC, UMR1098, RIGHT Interactions Greffon-Hôte-Tumeur/Ingénierie Cellulaire Et Génique, Dijon, France.
Institute of Organic Chemistry and Biochemistry of the Czech Academy of Sciences, Prague, Czech Republic.

Clovis Boibessot (C)

Univ. Bourgogne Franche-Comté, INSERM, EFS BFC, UMR1098, RIGHT Interactions Greffon-Hôte-Tumeur/Ingénierie Cellulaire Et Génique, Dijon, France.

Claudie Cladière (C)

Univ. Bourgogne Franche-Comté, INSERM, EFS BFC, UMR1098, RIGHT Interactions Greffon-Hôte-Tumeur/Ingénierie Cellulaire Et Génique, Dijon, France.

Marion Ciudad (M)

Univ. Bourgogne Franche-Comté, INSERM, EFS BFC, UMR1098, RIGHT Interactions Greffon-Hôte-Tumeur/Ingénierie Cellulaire Et Génique, Dijon, France.

Hélène Greigert (H)

Univ. Bourgogne Franche-Comté, INSERM, EFS BFC, UMR1098, RIGHT Interactions Greffon-Hôte-Tumeur/Ingénierie Cellulaire Et Génique, Dijon, France.

Séthi Ouandji (S)

Univ. Bourgogne Franche-Comté, INSERM, EFS BFC, UMR1098, RIGHT Interactions Greffon-Hôte-Tumeur/Ingénierie Cellulaire Et Génique, Dijon, France.

Thibault Ghesquière (T)

Univ. Bourgogne Franche-Comté, INSERM, EFS BFC, UMR1098, RIGHT Interactions Greffon-Hôte-Tumeur/Ingénierie Cellulaire Et Génique, Dijon, France.
Department of Internal Medicine, University Hospital, Dijon, France.

Maxime Samson (M)

Univ. Bourgogne Franche-Comté, INSERM, EFS BFC, UMR1098, RIGHT Interactions Greffon-Hôte-Tumeur/Ingénierie Cellulaire Et Génique, Dijon, France.
Department of Internal Medicine, University Hospital, Dijon, France.

Sylvain Audia (S)

Univ. Bourgogne Franche-Comté, INSERM, EFS BFC, UMR1098, RIGHT Interactions Greffon-Hôte-Tumeur/Ingénierie Cellulaire Et Génique, Dijon, France.
Department of Internal Medicine, University Hospital, Dijon, France.

Philippe Saas (P)

Univ. Bourgogne Franche-Comté, INSERM, EFS BFC, UMR1098, RIGHT Interactions Greffon-Hôte-Tumeur/Ingénierie Cellulaire Et Génique, Besançon, France.

Bernard Bonnotte (B)

Univ. Bourgogne Franche-Comté, INSERM, EFS BFC, UMR1098, RIGHT Interactions Greffon-Hôte-Tumeur/Ingénierie Cellulaire Et Génique, Dijon, France.
Department of Internal Medicine, University Hospital, Dijon, France.

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Classifications MeSH