Non-Coding RNA Mediated Regulation of Allogeneic T Cell Responses After Hematopoietic Transplantation

Front Immunol. 2018 Jun 15:9:1110. doi: 10.3389/fimmu.2018.01110. eCollection 2018.

Abstract

Allogeneic bone marrow transplantation (BMT) is an effective therapy for several malignant and non-malignant disorders. The precise control of allogeneic T cells is critical for successful outcomes after BMT. The mechanisms governing desirable (graft-versus-leukemia) versus undesirable (graft-versus-host disease) allogeneic responses remain incompletely understood. Non-coding RNAs (ncRNA) are controllers of gene expression that fine-tune cellular responses. Multiple microRNAs (miRNAs), a type of ncRNA, have recently been shown to influence allogeneic T cell responses in both murine models and clinically. Here, we review the role of various miRNAs that regulate T cell responses, either positively or negatively, to allo-stimulation and highlight their potential relevance as biomarkers and as therapeutic targets for improving outcomes after allogeneic BMT.

Keywords: T cell; alloimmunity; bone marrow transplantation; graft-versus-host disease; microRNA.

Publication types

  • Research Support, N.I.H., Extramural
  • Review

MeSH terms

  • Animals
  • Biomarkers
  • Gene Expression Regulation
  • Graft vs Host Disease / etiology
  • Graft vs Leukemia Effect / genetics
  • Graft vs Leukemia Effect / immunology
  • Hematopoietic Stem Cell Transplantation* / adverse effects
  • Hematopoietic Stem Cell Transplantation* / methods
  • Humans
  • Lymphocyte Activation / genetics
  • Lymphocyte Activation / immunology
  • MicroRNAs / genetics
  • Models, Biological
  • RNA Interference
  • RNA, Long Noncoding / genetics
  • RNA, Untranslated / genetics*
  • T-Lymphocytes / immunology*
  • T-Lymphocytes / metabolism*
  • Transplantation, Homologous

Substances

  • Biomarkers
  • MicroRNAs
  • RNA, Long Noncoding
  • RNA, Untranslated