Neointimal hyperplasia in allogeneic and autologous venous grafts is not different in nature

Publikation: Beitrag in FachzeitschriftForschungsartikelBeigetragenBegutachtung

Beitragende

  • Albert Busch - , Universitätsklinikum Würzburg (Autor:in)
  • Elena Hartmann - (Autor:in)
  • Nicole Wagner - (Autor:in)
  • Süleyman Ergün - (Autor:in)
  • Ralph Kickuth - (Autor:in)
  • Richard Kellersmann - (Autor:in)
  • Udo Lorenz - (Autor:in)

Abstract

Neointimal hyperplasia, transplant rejection and thus immunogenicity of allografts are possible reasons for poorer patency rates in cryopreserved venous allografts for peripheral bypass surgery in comparison with autologous venous grafts. To expand the limited knowledge from human allografts, we histologically investigated allogeneic and autologous venous grafts in arterial location. Specimens of allogeneic and autologous venous graft stenosis, harvested 6 months after bypass implantation, were immunohistochemically characterized. Examination of the lesions showed a uniform morphological pattern. A continuous endothelial layer, tissue fibrosis and a thickened neointima with monocytes and dedifferentiated vascular smooth muscle cells were seen in both conduits with very low cell turnover and the absence of acute and chronic inflammation. Neoangiogenesis with CD34-positive endothelium was abundant in the vessel media. The morphological patterns of allogeneic and autologous neointima formation are similar. Consequently, neointimal hyperplasia in venous grafts may reflect a uniform physiological host response of non-immunological factors with the reasons for poorer clinical outcome of cryopreserved allografts yet to be elucidated.

Details

OriginalspracheEnglisch
Seiten (von - bis)59-66
Seitenumfang8
FachzeitschriftHistochemistry and cell biology
Jahrgang144
Ausgabenummer1
PublikationsstatusVeröffentlicht - Juli 2015
Peer-Review-StatusJa
Extern publiziertJa

Externe IDs

Scopus 84931566973

Schlagworte

Schlagwörter

  • Allografts, Autografts, Cryopreservation, Endothelium, Vascular/pathology, Humans, Hyperplasia, Muscle, Smooth, Vascular/pathology, Neointima/immunology, Neovascularization, Pathologic, Saphenous Vein/transplantation