Autologous transplantation of P63 + lung progenitor cells for chronic obstructive pulmonary disease therapy

Author:

Wang Yujia1ORCID,Meng Zili2ORCID,Liu Ming3ORCID,Zhou Yueqing14ORCID,Chen Difei3ORCID,Zhao Yu1ORCID,Zhang Ting4ORCID,Zhong Nanshan3ORCID,Dai Xiaotian5ORCID,Li Shiyue3ORCID,Zuo Wei146ORCID

Affiliation:

1. Department of Organ Regeneration, Shanghai East Hospital, Tongji University School of Medicine, Shanghai 200120, China.

2. Department of Respiratory and Critical Care Medicine, Affiliated Huai'an No. 1 People’s Hospital of Nanjing Medical University, Huai'an 223300, China.

3. State Key Laboratory of Respiratory Diseases, National Clinical Research Center for Respiratory Disease, Guangzhou Institute of Respiratory Disease, Guangzhou Medical University, Guangzhou 510120, China.

4. Super Organ R&D Center, Regend Therapeutics, Shanghai 201318, China.

5. Southwest Hospital, Third Military Medical University of PLA, Chongqing 400038, China.

6. West China Hospital, Sichuan University, Chengdu 610041, China.

Abstract

Adult lung resident stem/progenitor cells, including P63 + progenitor cells, have demonstrated the capacity for regeneration of lung epithelium in preclinical models. Here, we report a clinical trial of intrapulmonary P63 + progenitor cell transplantation in 28 participants with stage II to IV chronic obstructive pulmonary disease (COPD). Autologous P63 + progenitor cells were isolated from the airway basal layer of participants in the intervention group via bronchoscopic brushing, cultured for 3 to 5 weeks, and then transplanted back into the lungs via bronchoscopy at 0.7 × 10 6 to 5.2 × 10 6 cells per kilogram of body weight. Twenty patients were evaluable at the end of the study (intervention group, n = 17; control group, n = 3). No grade 3 to 5 adverse events (AEs) or serious AEs occurred. Although bronchoscopy-associated AEs were recorded in participants in the intervention group, other AEs were not substantial different between groups. Twenty-four weeks after transplantation, participants in the intervention group displayed improvement in gas transfer capacity [diffusing capacity of the lung for carbon monoxide (DLCO) change from baseline: +18.2%], whereas the control group experienced a decrease (DLCO change from baseline: −17.4%; P = 0.008). Furthermore, participants in the intervention group showed >30-meter increase in walking distance within 6 minutes. Transcriptomic analysis of progenitor cells isolated from responding and nonresponding individuals in the intervention group showed that higher expression of P63 was associated with treatment efficacy. In conclusion, transplantation of cultured P63 + lung progenitor cells was safe and might represent a potential therapeutic strategy for COPD.

Publisher

American Association for the Advancement of Science (AAAS)

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