The Study of Mesenchymal Stem Cells Treat Autoimmune Pulmonary Alveolar in Vitro
试验速览
- 阶段
- 不适用
- 状态
- 进行中（未招募）
- 发起方
- 入组人数
- 26
- 试验地点
- 1
- 主要终点
- Genomics
研究概览
简要总结
Autoimmune pulmonary alveolar proteinosis (aPAP) is a respiratory disease characterized by massive deposition of pulmonary surfactant in the alveoli, involving a variety of immune cells and factor disorders. However, there are certain limits in treatment at present. MSCs can improve the microenvironment in the alveoli by regulating immunity, thereby achieving a good therapeutic effect. The purpose of this study is to use the lavage fluid obtained after whole lung lavage with aPAP to isolate alveolar macrophages, and to use MSC to complete the verification of the efficacy of aPAP primary alveolar macrophages in vitro. A series of protocols including multi-factor detection, cell phenotype analysis and phagocytosis assay were used to evaluate the efficacy of MSCs on alveolar macrophages.
研究设计
- 研究类型
- Observational
- 观察模型
- Cohort
- 时间视角
- Prospective
入排标准
- 年龄范围
- 18 Years 至 75 Years（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Sign an informed consent form before any research-related activities;
- •No gender restrictions, age ≥18 years old, and ≤75 years old;
- •Patients who need to receive whole lung lavage due to the needs of the disease, and the patient agrees to perform whole lung lavage. The standards are as follows:
- •The diagnosis of aPAP is clear, and the anti-GM-CSF antibody in serum is greater than 5 μg/ml;
- •PaO2 <65 mmHg;
- •P(A-a)O2>40 mmHg;
- •Intrapulmonary shunt >10%-12%.
排除标准
- •Suffering from multiple chronic respiratory diseases at the same time, including but not limited to chronic obstructive pulmonary disease, pulmonary fibrosis, and asthma;
- •Various malignant tumors or a history of malignant tumors;
- •Uncontrolled pulmonary or systemic infection;
- •Severe other systemic diseases: acute myocardial infarction, unstable angina pectoris, liver cirrhosis, acute glomerulonephritis, etc.;
- •Syphilis, HIV, HCV antibody positive;
- •Patients with coagulation disorders who cannot perform bronchoscopy, such as hemophilia, giant platelet syndrome, thrombocytopenia, etc.;
- •Severe renal impairment, serum creatinine > 1.5 times the upper limit of normal;
- •Liver disease or liver function damage: ALT, AST, total bilirubin > 2 times the upper limit of normal;
- •Have any coexisting medical conditions or diseases that the investigators judge may impair the development of this trial;
- •Social and mental disability, no legal capacity/limited capacity;
- •Refuse to sign the informed consent.
结局指标
主要结局
Genomics
时间窗: 2022.12.31-2023.03.01
次要结局
未报告次要终点
研究者
ShiYue Li
Professor
Guangzhou Institute of Respiratory Disease