Recipient Reaction and Composition of Autologous Sural Nerve Tissue Grafts into the Human Brain

Author:

Colvett Isaac1,Gilmore Anah1,Guzman Samuel2,Ledreux Aurélie1,Quintero Jorge E.345ORCID,Ginjupally Dhanunjaya Rao46,Gurwell Julie A.37,Slevin John T.37,Guduru Zain7,Gerhardt Greg A.3457,van Horne Craig G.345,Granholm Ann-Charlotte1ORCID

Affiliation:

1. Department of Neurosurgery, University of Colorado Anschutz Medical Campus, Aurora, CO 80045, USA

2. Department of Pathology, University of Colorado Anschutz Medical Campus, Aurora, CO 80045, USA

3. Brain Restoration Center, University of Kentucky, Lexington, KY 40536, USA

4. Department of Neurosurgery, University of Kentucky, Lexington, KY 40536, USA

5. Department of Neuroscience, University of Kentucky, Lexington, KY 40536, USA

6. Department of Neurosurgery, Krishna Institute of Medical Sciences, Secunderabad 500003, Telangana, India

7. Department of Neurology, University of Kentucky, Lexington, KY 40536, USA

Abstract

Parkinson’s disease (PD) is a severe neurological disease for which there is no effective treatment or cure, and therefore it remains an unmet need in medicine. We present data from four participants who received autologous transplantation of small pieces of sural nerve tissue into either the basal forebrain containing the nucleus basalis of Meynert (NBM) or the midbrain substantia nigra (SN). The grafts did not exhibit significant cell death or severe host-tissue reaction up to 55 months post-grafting and contained peripheral cells. Dopaminergic neurites showed active growth in the graft area and into the graft in the SN graft, and cholinergic neurites were abundant near the graft in the NBM. These results provide a histological basis for changes in clinical features after autologous peripheral nerve tissue grafting into the NBM or SN in PD.

Funder

the Ann Hanley Neuroscience Fund

the UK College of Medicine BRAIN Alliance

the National Center for Advancing Translational Sciences

Publisher

MDPI AG

Subject

General Medicine

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