Acute Immune Response in Venoarterial and Venovenous Extracorporeal Membrane Oxygenation Models of Rats.
Hwa-Jin ChoMukhammad KayumovDo Wan KimKyo Seon LeeFrancis Obiweluozor OnyekachiKyung-Woon JeungYong Sook KimJacky Y SuenJohn F FraserIn Seok JeongPublished in: ASAIO journal (American Society for Artificial Internal Organs : 1992) (2021)
Although experimental extracorporeal membrane oxygenation (ECMO) animal models have been reported, there are few studies on the immune response to ECMO. We developed the venoarterial (VA) and venovenous (VV) model in rats and serially investigated the changes in the distribution of immune cells. Forty rats underwent both VA and VV modes of ECMO, and blood samples were collected at 1 day before ECMO (D-1), at the end of ECMO run (D+0), and 3 days after the ECMO (D+3). Flow cytometry was used to characterize surface marker expression (CD3, CD4, CD8, CD43, CD45, CD45R, CD161, and His48) on immune cells. Granulocytes were initially activated in both ECMO types and were further reduced but not normalized until 3 days of decannulation. Monocyte and natural killer cells were decreased initially in VA mode. B lymphocytes, helper T lymphocytes, and cytotoxic T lymphocytes also significantly decreased in VA modes after ECMO, but this phenomenon was not prominent in the VV modes. Overall immune cells proportion changed after ECMO run in both modes, and the immunologic balance altered significantly in the VA than in VV mode. Our ECMO model is feasible for the hemodynamic and immunologic research, and further long-term evaluation is needed.
Keyphrases
- extracorporeal membrane oxygenation
- acute respiratory distress syndrome
- respiratory failure
- immune response
- mechanical ventilation
- flow cytometry
- dendritic cells
- poor prognosis
- liver failure
- mass spectrometry
- hepatitis b virus
- toll like receptor
- endothelial cells
- intensive care unit
- inflammatory response
- high resolution
- binding protein
- single molecule
- anti inflammatory