The innate immune response to allotransplants: mechanisms and therapeutic potentials

Jordi Ochando, Farideh Ordikhani, Peter Boros, Stefan Jordan

Research output: Contribution to journalReview articlepeer-review

60 Scopus citations

Abstract

Surgical trauma and ischemia reperfusion injury (IRI) are unavoidable aspects of any solid organ transplant procedure. They trigger a multifactorial antigen-independent inflammatory process that profoundly affects both the early and long-term outcomes of the transplanted organ. The injury associated with donor organ procurement, storage, and engraftment triggers innate immune activation that inevitably results in cell death, which may occur in many different forms. Dying cells in donor grafts release damage-associated molecular patterns (DAMPs), which alert recipient innate cells, including macrophages and dendritic cells (DCs), through the activation of the complement cascade and toll-like receptors (TLRs). The long-term effect of inflammation on innate immune cells is associated with changes in cellular metabolism that skew the cells towards aerobic glycolysis, resulting in innate immune cell activation and inflammatory cytokine production. The different roles of proinflammatory cytokines in innate immune activation have been described, and these cytokines also stimulate optimal T-cell expansion during allograft rejection. Therefore, early innate immune events after organ transplantation determine the fate of the adaptive immune response. In this review, we summarize the contributions of innate immunity to allograft rejection and discuss recent studies and emerging concepts in the targeted delivery of therapeutics to modulate the innate immune system to enhance allograft survival.

Original languageEnglish
Pages (from-to)350-356
Number of pages7
JournalCellular and Molecular Immunology
Volume16
Issue number4
DOIs
StatePublished - 1 Apr 2019

Fingerprint

Dive into the research topics of 'The innate immune response to allotransplants: mechanisms and therapeutic potentials'. Together they form a unique fingerprint.

Cite this