Devastating voice loss (dysphonia or aphonia) impacts thousands of individuals in the United States each year undergoing traumatic or oncologic partial laryngectomies, or suffering muscle volume loss due to vocal fold paralysis. Voice restoration options for these patients are suboptimal, and, as a result, most patients are left with permanent voice loss and communication impairment. This application introduces a novel approach for restoring vocal fold muscle volume and function after direct vocal fold injury and/or denervation. Results may lead to improved surgical options for voice restoration in patients who have vocal paralysis and/or have undergone hemilaryngectomies, cordectomies, or traumatic avulsions. The first goal of this application is to engineer an autologous muscle-cartilage implant progenitor cell-derived implant (MI) that, after implantation in an animal model, receives strong innervation and becomes functional when used to repair a large laryngeal defect. To do this, we will fabricate MIs within a customized collagen matrix and pre-treat MIs with factors in vitro that induce the MI muscle to express motor endplates. The MIs will be used to replace a partial laryngectomy defect in a porcine model, and post-implantation innervation status, based on laryngeal electromyography and quantification of motor endplates with nerve contact, will be determined. Using this animal implant model, outcomes with the study MIs will be compared to those of control MIs in environments with and without recurrent laryngeal nerve integrity. Findings from the proposed studies should overcome current major hurdles to developing a functional tissue engineered MCC for hemilaryngeal reconstruction?those hurdles being inadequate cartilaginous support, poor innervation of the muscle, suboptimal organization of myofibers, and asynchronous firing of the muscle with the native adductor muscle. Furthermore, because these studies are being done now in a large animal (porcine) model, with laryngeal size and function very similar to that of humans, findings will be highly translational. Results from these experiments should lead to landmark clinical innovations that will be relevant to both voice restoration applications, and muscle repair concepts globally.

Public Health Relevance

Thousands of people in the United States each year suffer permanent voice loss because their voice boxes (larynges) are damaged from cancer, trauma, or nerve injury, as, in these cases, we currently have no options for restoration of normal laryngeal function. In this application, we explore novel methods for restoring function of the voice box (larynx) using adult-derived muscle and fat stem cells in a large animal model. We believe our findings will completely transform current paradigms for voice restoration in patients who have suffered severe laryngeal injuries.

Agency
National Institute of Health (NIH)
Institute
National Institute on Deafness and Other Communication Disorders (NIDCD)
Type
Research Project (R01)
Project #
2R01DC014070-06
Application #
9886615
Study Section
Motor Function, Speech and Rehabilitation Study Section (MFSR)
Program Officer
Shekim, Lana O
Project Start
2015-07-15
Project End
2025-06-30
Budget Start
2020-08-14
Budget End
2021-06-30
Support Year
6
Fiscal Year
2020
Total Cost
Indirect Cost
Name
Indiana University-Purdue University at Indianapolis
Department
Otolaryngology
Type
Schools of Medicine
DUNS #
603007902
City
Indianapolis
State
IN
Country
United States
Zip Code
46202
Zhang, Hongji; Voytik-Harbin, Sherry; Brookes, Sarah et al. (2018) Use of autologous adipose-derived mesenchymal stem cells for creation of laryngeal cartilage. Laryngoscope 128:E123-E129
Brookes, Sarah; Voytik-Harbin, Sherry; Zhang, Hongji et al. (2018) Three-dimensional tissue-engineered skeletal muscle for laryngeal reconstruction. Laryngoscope 128:603-609
Paniello, Randal C; Brookes, Sarah; Bhatt, Neel K et al. (2018) Improved adductor function after canine recurrent laryngeal nerve injury and repair using muscle progenitor cells. Laryngoscope 128:E241-E246