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Pediatric human nose organoids demonstrate greater susceptibility, epithelial responses, and cytotoxicity than adults during RSV infection.
Aloisio, Gina M; Nagaraj, Divya; Murray, Ashley M; Schultz, Emily M; McBride, Trevor; Aideyan, Letisha; Nicholson, Erin G; Henke, David; Ferlic-Stark, Laura; Rajan, Anubama; Kambal, Amal; Johnson, Hannah L; Mosa, Elina; Stossi, Fabio; Blutt, Sarah E; Piedra, Pedro A; Avadhanula, Vasanthi.
Afiliação
  • Aloisio GM; Department of Molecular Virology and Microbiology, Baylor College of Medicine, Houston, Texas, USA.
  • Nagaraj D; Department of Pediatrics, Baylor College of Medicine, Houston, Texas, USA.
  • Murray AM; Department of Molecular Virology and Microbiology, Baylor College of Medicine, Houston, Texas, USA.
  • Schultz EM; Department of Molecular Virology and Microbiology, Baylor College of Medicine, Houston, Texas, USA.
  • McBride T; Department of Molecular Virology and Microbiology, Baylor College of Medicine, Houston, Texas, USA.
  • Aideyan L; Department of Molecular Virology and Microbiology, Baylor College of Medicine, Houston, Texas, USA.
  • Nicholson EG; Department of Molecular Virology and Microbiology, Baylor College of Medicine, Houston, Texas, USA.
  • Henke D; Department of Molecular Virology and Microbiology, Baylor College of Medicine, Houston, Texas, USA.
  • Ferlic-Stark L; Department of Pediatrics, Baylor College of Medicine, Houston, Texas, USA.
  • Rajan A; Department of Molecular Virology and Microbiology, Baylor College of Medicine, Houston, Texas, USA.
  • Kambal A; Department of Molecular Virology and Microbiology, Baylor College of Medicine, Houston, Texas, USA.
  • Johnson HL; Department of Molecular Virology and Microbiology, Baylor College of Medicine, Houston, Texas, USA.
  • Mosa E; Department of Molecular Virology and Microbiology, Baylor College of Medicine, Houston, Texas, USA.
  • Stossi F; Advanced Technology Cores, Baylor College of Medicine, Houston, Texas, USA.
  • Blutt SE; Advanced Technology Cores, Baylor College of Medicine, Houston, Texas, USA.
  • Piedra PA; Advanced Technology Cores, Baylor College of Medicine, Houston, Texas, USA.
  • Avadhanula V; Department of Molecular and Cellular Biology, Baylor College of Medicine, Houston, Texas, USA.
bioRxiv ; 2024 Feb 01.
Article em En | MEDLINE | ID: mdl-38352333
ABSTRACT
Respiratory syncytial virus (RSV) is a common cause of respiratory infections, causing significant morbidity and mortality, especially in young children. Why RSV infection in children is more severe as compared to healthy adults is not fully understood. In the present study, we infect both pediatric and adult human nose organoid-air liquid interface (HNO-ALIs) cell lines with two contemporary RSV isolates and demonstrate how they differ in virus replication, induction of the epithelial cytokine response, cell injury, and remodeling. Pediatric HNO-ALIs were more susceptible to early RSV replication, elicited a greater overall cytokine response, demonstrated enhanced mucous production, and manifested greater cellular damage compared to their adult counterparts. Adult HNO-ALIs displayed enhanced mucus production and robust cytokine response that was well controlled by superior regulatory cytokine response and possibly resulted in lower cellular damage than in pediatric lines. Taken together, our data suggest substantial differences in how pediatric and adult upper respiratory tract epithelium responds to RSV infection. These differences in epithelial cellular response can lead to poor mucociliary clearance and predispose infants to a worse respiratory outcome of RSV infection.

Texto completo: 1 Base de dados: MEDLINE Idioma: En Revista: BioRxiv Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Estados Unidos

Texto completo: 1 Base de dados: MEDLINE Idioma: En Revista: BioRxiv Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Estados Unidos