Neutrophil extracellular trap fragments stimulate innate immune responses that prevent lung transplant tolerance. Issue 4 (13th December 2018)

• Record Type: Journal Article
• Authors: Scozzi, Davide; Wang, Xingan; Liao, Fuyi; Liu, Zhiyi; Zhu, Jihong; Pugh, Katy; Ibrahim, Mohsen; Hsiao, Hsi‐Min; Miller, Mark J.; Yizhan, Guo; Mohanakumar, Thalachallour; Krupnick, Alexander S.; Kreisel, Daniel; Gelman, Andrew E.
• Is Part Of: American journal of transplantation. Volume 19:Issue 4(2019)
• Page Start: 1011
• Page End: 1023
• Publication Date: 2018-12-13
• Subjects: animal models: murine -- basic (laboratory) research/science -- cellular biology -- immunobiology -- innate immunity -- lung transplantation/pulmonology -- tolerance: mechanisms -- translational research/science; Transplantation of organs, tissues, etc -- Periodicals; 617.95
• DOI: 10.1111/ajt.15163
• Languages: English
• ISSNs: 1600-6135

Abstract

Abstract : Neutrophil extracellular traps (NETs) have been shown to worsen acute pulmonary injury including after lung transplantation. The breakdown of NETs by DNAse‐1 can help restore lung function, but whether there is an impact on allograft tolerance remains less clear. Using intravital 2‐photon microscopy, we analyzed the effects of DNAse‐1 on NETs in mouse orthotopic lung allografts damaged by ischemia‐reperfusion injury. Although DNAse‐1 treatment rapidly degrades intragraft NETs, the consequential release of NET fragments induces prolonged interactions between infiltrating CD4 + T cells and donor‐derived antigen presenting cells. DNAse‐1 generated NET fragments also promote human alveolar macrophage inflammatory cytokine production and prime dendritic cells for alloantigen‐specific CD4 + T cell proliferation through activating toll‐like receptor (TLR) — Myeloid Differentiation Primary Response 88 (MyD88) signaling pathways. Furthermore, and in contrast to allograft recipients with a deficiency in NET generation due to a neutrophil‐specific ablation of Protein Arginine Deiminase 4 (PAD4), DNAse‐1 administration to wild‐type recipients promotes the recognition of allo‐ and self‐antigens and prevents immunosuppression‐mediated lung allograft acceptance through a MyD88‐dependent pathway. Taken together, these data show that the rapid catalytic release of NET fragments promotes innate immune responses that prevent lung transplant tolerance. Abstract : Neutrophil extracellular trap fragments generated by DNAse treatment trigger toll‐like receptor signaling in antigen‐presenting cells that inhibit immunosuppression‐mediated lung transplant tolerance. See the videos online.