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Mesenchymal stromal cell conditioned media for lung disease: a systematic review and meta-analysis of preclinical studies.
Emukah, Chimobi; Dittmar, Evan; Naqvi, Rija; Martinez, John; Corral, Alexis; Moreira, Axel; Moreira, Alvaro.
Afiliação
  • Emukah C; Department of Pediatrics, Division of Neonatology, University of Texas Health-San Antonio, San Antonio, Texas, 78229-3900, USA.
  • Dittmar E; Department of Pediatrics, Division of Neonatology, University of Texas Health-San Antonio, San Antonio, Texas, 78229-3900, USA.
  • Naqvi R; Department of Pediatrics, Division of Neonatology, University of Texas Health-San Antonio, San Antonio, Texas, 78229-3900, USA.
  • Martinez J; Department of Pediatrics, Division of Neonatology, University of Texas Health-San Antonio, San Antonio, Texas, 78229-3900, USA.
  • Corral A; Department of Pediatrics, Division of Neonatology, University of Texas Health-San Antonio, San Antonio, Texas, 78229-3900, USA.
  • Moreira A; Department of Pediatrics, Texas Children's Hospital, Houston, Texas, USA.
  • Moreira A; Department of Pediatrics, Division of Neonatology, University of Texas Health-San Antonio, San Antonio, Texas, 78229-3900, USA. MoreiraA@uthscsa.edu.
Respir Res ; 20(1): 239, 2019 Oct 30.
Article em En | MEDLINE | ID: mdl-31666086
BACKGROUND: Inflammation plays an important role in the pathogenesis of many lung diseases. Preclinical studies suggest that mesenchymal stromal cell (MSC) conditioned media (CdM) can attenuate inflammation. Our aim was threefold: (1) summarize the existing animal literature evaluating CdM as a therapeutic agent for pediatric/adult lung disease, (2) quantify the effects of CdM on inflammation, and (3) compare inflammatory effects of CdM to MSCs. METHODS: Adhering to the Systematic Review Protocol for Animal Intervention Studies, a systematic search of English articles was performed in five databases. Meta-analysis and meta-regression were performed to generate random effect size using standardized mean difference (SMD). RESULTS: A total of 10 studies met inclusion. Lung diseases included bronchopulmonary dysplasia, asthma, pulmonary hypertension, and acute respiratory distress syndrome. CdM decreased inflammatory cells (1.02 SMD, 95% CI 0.86, 1.18) and cytokines (0.71 SMD, 95% CI 0.59, 0.84). The strongest effect for inflammatory cells was in bronchopulmonary dysplasia (3.74 SMD, 95% CI 3.13, 4.36) while pulmonary hypertension had the greatest reduction in inflammatory cytokine expression (1.44 SMD, 95% CI 1.18, 1.71). Overall, CdM and MSCs had similar anti-inflammatory effects. CONCLUSIONS: In this meta-analysis of animal models recapitulating lung disease, CdM improved inflammation and had an effect size comparable to MSCs. While these findings are encouraging, the risk of bias and heterogeneity limited the strength of our findings.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Meios de Cultivo Condicionados / Transplante de Células-Tronco Mesenquimais / Modelos Animais de Doenças / Células-Tronco Mesenquimais / Pneumopatias Tipo de estudo: Guideline / Prognostic_studies / Systematic_reviews Limite: Animals / Humans Idioma: En Revista: Respir Res Ano de publicação: 2019 Tipo de documento: Article País de afiliação: Estados Unidos País de publicação: Reino Unido

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Meios de Cultivo Condicionados / Transplante de Células-Tronco Mesenquimais / Modelos Animais de Doenças / Células-Tronco Mesenquimais / Pneumopatias Tipo de estudo: Guideline / Prognostic_studies / Systematic_reviews Limite: Animals / Humans Idioma: En Revista: Respir Res Ano de publicação: 2019 Tipo de documento: Article País de afiliação: Estados Unidos País de publicação: Reino Unido