Title | Pediatric human nose organoids demonstrate greater susceptibility, epithelial responses, and cytotoxicity than adults during RSV infection. |
Publication Type | Journal Article |
Year of Publication | 2024 |
Authors | Aloisio, GM, Nagaraj, D, Murray, AM, Schultz, EM, McBride, T, Aideyan, L, Nicholson, EG, Henke, D, Ferlic-Stark, L, Rajan, A, Kambal, A, Johnson, HL, Mosa, E, Stossi, F, Blutt, SE, Piedra, PA, Avadhanula, V |
Journal | bioRxiv |
Date Published | 2024 Feb 01 |
ISSN | 2692-8205 |
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. |
DOI | 10.1101/2024.02.01.578466 |
Alternate Journal | bioRxiv |
PubMed ID | 38352333 |
PubMed Central ID | PMC10862794 |
Grant List | U19 AI144297 / AI / NIAID NIH HHS / United States U19 AI116497 / AI / NIAID NIH HHS / United States P30 DK056338 / DK / NIDDK NIH HHS / United States S10 OD030414 / OD / NIH HHS / United States P30 ES030285 / ES / NIEHS NIH HHS / United States P30 CA125123 / CA / NCI NIH HHS / United States |