Immune characterization of a xenogeneic human lung cross-circulation support system

Author:

Wu Wei K.12ORCID,Stier Matthew T.3ORCID,Stokes John W.1ORCID,Ukita Rei1ORCID,Patel Yatrik J.1ORCID,Cortelli Michael1ORCID,Landstreet Stuart R.3ORCID,Talackine Jennifer R.1,Cardwell Nancy L.1ORCID,Simonds Elizabeth M.1ORCID,Mentz Meredith1,Lowe Cindy4,Benson Clayne5,Demarest Caitlin T.1,Alexopoulos Sophoclis P.2,Shaver Ciara M.3ORCID,Bacchetta Matthew16ORCID

Affiliation:

1. Department of Cardiac Surgery, Vanderbilt University Medical Center, Nashville, TN, USA.

2. Department of Surgery, Division of Hepatobiliary Surgery and Liver Transplantation, Vanderbilt University Medical Center, Nashville, TN, USA.

3. Department of Medicine, Division of Allergy, Pulmonary, and Critical Care Medicine, Vanderbilt University Medical Center, Nashville, TN, USA.

4. Department of Pathology, Microbiology and Immunology, Vanderbilt University Medical Center, Nashville, TN, USA.

5. Department of Anesthesiology, Vanderbilt University Medical Center, Nashville, TN, USA.

6. Department of Biomedical Engineering, Vanderbilt University, Nashville, TN, USA.

Abstract

Improved approaches to expanding the pool of donor lungs suitable for transplantation are critically needed for the growing population with end-stage lung disease. Cross-circulation (XC) of whole blood between swine and explanted human lungs has previously been reported to enable the extracorporeal recovery of donor lungs that declined for transplantation due to acute, reversible injuries. However, immunologic interactions of this xenogeneic platform have not been characterized, thus limiting potential translational applications. Using flow cytometry and immunohistochemistry, we demonstrate that porcine immune cell and immunoglobulin infiltration occurs in this xenogeneic XC system, in the context of calcineurin-based immunosuppression and complement depletion. Despite this, xenogeneic XC supported the viability, tissue integrity, and physiologic improvement of human donor lungs over 24 hours of xeno-support. These findings provide targets for future immunomodulatory strategies to minimize immunologic interactions on this organ support biotechnology.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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