The many shades of macrophages in regulating transplant outcome

Cell Immunol. 2020 Mar:349:104064. doi: 10.1016/j.cellimm.2020.104064. Epub 2020 Feb 8.

Abstract

The shift of emphasis from short-term to long-term graft outcomes has led to renewed interests in how the innate immune cells regulate transplant survival, an area that is traditionally dominated by T cells in the adaptive system. This shift is driven largely by the limited efficacy of current immunosuppression protocols which primarily target T cells in preventing chronic graft loss, as well as by the rapid advance of basic sciences in the realm of innate immunity. In fact, the innate immune cells have emerged as key players in the allograft response in various models, contributing to both graft rejection and graft acceptance. Here, we focus on the macrophages, highlighting their diversity, plasticity and emerging features in transplant models, as well as recent developments in our studies of diverse subsets of macrophages. We also discuss challenges, unsolved questions, and emerging approaches in therapeutically modulating macrophages in further improvement of transplant outcomes.

Keywords: Chronic rejection; Inflammation; Innate immunity; Macrophages; Transplantation.

Publication types

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

MeSH terms

  • Allografts / immunology*
  • Animals
  • Antigens, CD / analysis
  • Carrageenan / pharmacology
  • Cell Differentiation
  • Cell Lineage
  • Cytokines / immunology
  • Graft Rejection / immunology*
  • Graft Survival / immunology*
  • Humans
  • Immunity, Innate
  • Immunologic Memory
  • Macrophages / classification
  • Macrophages / drug effects
  • Macrophages / immunology*
  • Mice
  • Models, Immunological
  • Myeloid-Derived Suppressor Cells / immunology
  • Purinergic P2X Receptor Antagonists / pharmacology
  • TOR Serine-Threonine Kinases / antagonists & inhibitors

Substances

  • Antigens, CD
  • Cytokines
  • Purinergic P2X Receptor Antagonists
  • Carrageenan
  • TOR Serine-Threonine Kinases