Toll-like receptor induced pro-interleukin-1beta and interleukin-6 in monocytes are lower in healthy infants compared to adults
| dc.contributor.author | Libraty, Daniel H. | |
| dc.contributor.author | Zhang, Lei | |
| dc.contributor.author | Woda, Marcia | |
| dc.contributor.author | Acosta, Luz P. | |
| dc.contributor.author | Obcena, Anamae | |
| dc.contributor.author | Brion, Job D. | |
| dc.contributor.author | Capeding, Rosario Z. | |
| dc.date | 2022-08-11T08:09:41.000 | |
| dc.date.accessioned | 2022-08-23T16:40:05Z | |
| dc.date.available | 2022-08-23T16:40:05Z | |
| dc.date.issued | 2013-10-25 | |
| dc.date.submitted | 2014-02-07 | |
| dc.identifier.citation | Libraty DH, Zhang L, Woda M, Acosta LP, Obcena A, et al. (2013) Toll-Like Receptor Induced Pro-Interleukin-1β and Interleukin-6 in Monocytes Are Lower in Healthy Infants Compared to Adults. PLoS ONE 8(10): e78018. doi:10.1371/journal.pone.0078018 <a href="http://dx.doi.org/10.1371/journal.pone.0078018">Link to article on publisher's site</a> | |
| dc.identifier.issn | 1932-6203 (Linking) | |
| dc.identifier.doi | 10.1371/journal.pone.0078018 | |
| dc.identifier.pmid | 24205068 | |
| dc.identifier.uri | http://hdl.handle.net/20.500.14038/39611 | |
| dc.description.abstract | Infants have long been known to have higher infectious diseases morbidity and mortality and suboptimal vaccination responses compared to older children and adults. A variety of differences in innate and adaptive immune responses have been described between these two groups. We compared Toll-like receptor (TLR)-induced production of pro-interleukin (IL)-1beta, IL-6, and tumor necrosis factor (TNF)-alpha between 2-month-old infants and adults. TLR 7/8-induced production of pro-IL-1beta and IL-6 in monocytes was lower in 2-month-old infants compared to adults. There was no difference in TLR 7/8-induced production of TNF-alpha. Lower TLR-induced production of pro-IL-1beta and IL-6 in innate immune cells during early infancy likely contributes to suboptimal vaccine responses and infectious diseases susceptibility. | |
| dc.language.iso | en_US | |
| dc.relation | <a href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=pubmed&cmd=Retrieve&list_uids=24205068&dopt=Abstract">Link to Article in PubMed</a> | |
| dc.rights | <p>Copyright 2013 Libraty et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.</p> | |
| dc.subject | Immunity | |
| dc.subject | Immunology of Infectious Disease | |
| dc.title | Toll-like receptor induced pro-interleukin-1beta and interleukin-6 in monocytes are lower in healthy infants compared to adults | |
| dc.type | Journal Article | |
| dc.source.journaltitle | PloS one | |
| dc.source.volume | 8 | |
| dc.source.issue | 10 | |
| dc.identifier.legacyfulltext | https://escholarship.umassmed.edu/cgi/viewcontent.cgi?article=3403&context=oapubs&unstamped=1 | |
| dc.identifier.legacycoverpage | https://escholarship.umassmed.edu/oapubs/2403 | |
| dc.identifier.contextkey | 5082683 | |
| refterms.dateFOA | 2022-08-23T16:40:05Z | |
| html.description.abstract | <p>Infants have long been known to have higher infectious diseases morbidity and mortality and suboptimal vaccination responses compared to older children and adults. A variety of differences in innate and adaptive immune responses have been described between these two groups. We compared Toll-like receptor (TLR)-induced production of pro-interleukin (IL)-1beta, IL-6, and tumor necrosis factor (TNF)-alpha between 2-month-old infants and adults. TLR 7/8-induced production of pro-IL-1beta and IL-6 in monocytes was lower in 2-month-old infants compared to adults. There was no difference in TLR 7/8-induced production of TNF-alpha. Lower TLR-induced production of pro-IL-1beta and IL-6 in innate immune cells during early infancy likely contributes to suboptimal vaccine responses and infectious diseases susceptibility.</p> | |
| dc.identifier.submissionpath | oapubs/2403 | |
| dc.contributor.department | Department of Medicine, Division of Infectious Diseases and Immunology | |
| dc.source.pages | e78018 |
