This revision application entitled ?Regeneration of acutely injured lungs using adult human stem cells? is to expand the scope of the parent grant ?Modeling, pathogenesis and treatment of idiopathic pulmonary fibrosis? into studies that will further regenerative medicine and accelerate its use by developing an adult stem cell therapy for acute lung injury. The treatment modality we propose is to regenerate acutely injured lungs by targeted removal of damaged pulmonary epithelium (while preserving lung vasculature and surrounding parenchymal tissue), followed by delivery of iPSC-derived pulmonary cells. Both the parent grant and this application are based on three highly innovative translational technologies recently developed in our labs: (i) derivation of large numbers of pulmonary progenitors from adult human iPSCs, (ii) prolongation of ex vivo lung support from 6 hours to 3?5 days by normothermic cross-circulation, and (iii) a non- invasive theranostic system for real-time monitoring of cell delivery and lung regeneration. For maximal significance, we focus on one of the most common causes of acute lung injury - gastric aspiration - that frequently leads to acute respiratory distress syndrome (ARDS). For maximal translational potential, we chose to develop an in-situ approach to lung regeneration, where an interventional procedure will be performed in the patient, by replacing defective cells in the region(s) of injury with therapeutic human iPSC-derived pulmonary cells using a very thin, flexible, imaging-guided bronchoscope. We will study lung regeneration ex vivo under cross-circulation and ventilation (over 3?5 days) and in situ (over 1 month) in a clinically relevant porcine model, using protocols established in our previous and preliminary studies. The project is designed to collect data for preparing the IRB/FDA applications for Phase I human trials to treat acute lung injury with therapeutic human iPSC-derived pulmonary cells by the end of the 1-year grant.

Public Health Relevance

Lung disease is a leading cause of morbidity and mortality worldwide. Acute lung injury, which affects over 200,000 patients per year and can lead to severe lung dysfunction, has no viable treatment options. We propose to develop an adult human stem cell treatment based on the use of highly innovative bioengineering technologies established in our previous and preliminary studies. Over one year, we will collect data necessary to file the required applications for ?first-in-human? clinical studies.

Agency
National Institute of Health (NIH)
Institute
National Heart, Lung, and Blood Institute (NHLBI)
Type
Research Project--Cooperative Agreements (U01)
Project #
3U01HL134760-02S1
Application #
9516638
Study Section
Special Emphasis Panel (ZHL1)
Program Officer
Lin, Sara
Project Start
2016-09-20
Project End
2018-05-31
Budget Start
2017-09-26
Budget End
2018-05-31
Support Year
2
Fiscal Year
2017
Total Cost
Indirect Cost
Name
Columbia University (N.Y.)
Department
Internal Medicine/Medicine
Type
Schools of Medicine
DUNS #
621889815
City
New York
State
NY
Country
United States
Zip Code
10032
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Kim, Jinho; Guenthart, Brandon; O'Neill, John D et al. (2017) Controlled delivery and minimally invasive imaging of stem cells in the lung. Sci Rep 7:13082
Chen, Ya-Wen; Huang, Sarah Xuelian; de Carvalho, Ana Luisa Rodrigues Toste et al. (2017) A three-dimensional model of human lung development and disease from pluripotent stem cells. Nat Cell Biol 19:542-549
Dorrello, N Valerio; Guenthart, Brandon A; O'Neill, John D et al. (2017) Functional vascularized lung grafts for lung bioengineering. Sci Adv 3:e1700521