Evaluation of vascular repair by tissue-engineered human acellular vessels or expanded polytetrafluoroethylene grafts in a porcine model of limb ischemia and reperfusion.

J Trauma Acute Care Surg

From the Humacyte, Inc. (R.D.K., H.L.P., L.E.N.), Durham, North Carolina; Department of Surgery (J.D.B.W.), Keesler Medical Center, Biloxi, Massachusetts; Department of Surgery (R.H.), William Beaumont Army Medical Center, El Paso, Texas; Department of Surgery (T.E.R.), Division of Vascular and Endovascular Surgery, Mayo Clinic, Rochester, Minnesota.

Published: August 2023

AI Article Synopsis

  • The study assessed a tissue-engineered human acellular vessel (HAV) in pigs after inducing acute vascular injury and ischemia, comparing its performance to synthetic ePTFE grafts.
  • Thirty-six pigs were implanted with either HAV or ePTFE grafts after ischemia periods of 0 or 6 hours, with postoperative evaluations including limb function and graft patency over 28 days.
  • Results showed improved limb function and patency for HAV over ePTFE, with more host integration and cell infiltration observed in HAV grafts, suggesting potential for future research on HAV's long-term efficacy.

Article Abstract

Background: This study evaluated performance of a tissue-engineered human acellular vessel (HAV) in a porcine model of acute vascular injury and ischemia. The HAV is an engineered blood vessel consisted of human vascular extracellular matrix proteins. Limb reperfusion and vascular outcomes of the HAV were compared with those from synthetic expanded polytetrafluoroethylene (ePTFE) grafts.

Methods: Thirty-six pigs were randomly assigned to four treatment groups, receiving either the HAV or a PTFE graft following a hind limb ischemia period of either 0 or 6 hours. All grafts were 3-cm-long interposition 6-mm diameter grafts implanted within the right iliac artery. Animals were not immunosuppressed and followed for up to 28 days after surgery. Assessments performed preoperatively and postoperatively included evaluation of graft patency, hind limb function, and biochemical markers of tissue ischemia or reperfusion injury. Histological analysis was performed on explants to assess host cell responses.

Results: Postoperative gait assessment and biochemical analysis confirmed that ischemia and reperfusion injury were caused by 6-hour ischemia, regardless of vascular graft type. Hind limb function and tissue damage biomarkers improved in all groups postoperatively. Final patency rates at postoperative day 28 were higher for HAV than for ePTFE graft in both the 0-hour (HAV, 85.7%; ePTFE, 66.7%) and 6-hour (HAV, 100%; ePTFE, 75%) ischemia groups, but these differences were not statistically significant. Histological analyses identified some intimal hyperplasia and host reactivity to the xenogeneic HAV and also to the synthetic ePTFE graft. Positive host integration and vascular cell infiltration were identified in HAV but not ePTFE explants.

Conclusion: Based on the functional performance and the histologic profile of explanted HAVs, this study supports further investigation to evaluate long-term performance of the HAV when used to repair traumatic vascular injuries.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10389495PMC
http://dx.doi.org/10.1097/TA.0000000000003974DOI Listing

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