Show simple item record

dc.contributor.authorKaczorowski, Kevin J.
dc.contributor.authorShekhar, Karthik
dc.contributor.authorNkulikiyimfura, Dieudonné
dc.contributor.authorDekker, Cornelia L.
dc.contributor.authorMaecker, Holden
dc.contributor.authorDavis, Mark M.
dc.contributor.authorChakraborty, Arup K.
dc.contributor.authorBrodin, Petter
dc.contributor.authorKaczorowski, Kevin John
dc.contributor.authorChakraborty, Arup K
dc.date.accessioned2018-05-01T18:35:23Z
dc.date.available2018-05-01T18:35:23Z
dc.date.issued2017-06
dc.date.submitted2017-04
dc.identifier.issn0027-8424
dc.identifier.issn1091-6490
dc.identifier.urihttp://hdl.handle.net/1721.1/115140
dc.description.abstractThe immune system consists of many specialized cell populations that communicate with each other to achieve systemic immune responses. Our analyses of various measured immune cell population frequencies in healthy humans and their responses to diverse stimuli show that human immune variation is continuous in nature, rather than characterized by discrete groups of similar individuals. We show that the same three key combinations of immune cell population frequencies can define an individual’s immunotype and predict a diverse set of functional responses to cytokine stimulation. We find that, even though interindividual variations in specific cell population frequencies can be large, unrelated individuals of younger age have more homogeneous immunotypes than older individuals. Across age groups, cytomegalovirus seropositive individuals displayed immunotypes characteristic of older individuals. The conceptual framework for defining immunotypes suggested by our results could guide the development of better therapies that appropriately modulate collective immunotypes, rather than individual immune components. Keywords: human immune variation; immune cell composition; systems immunology; agingen_US
dc.description.sponsorshipNational Institutes of Health (U.S.) (Grant R01 HL120724)en_US
dc.publisherNational Academy of Sciences (U.S.)en_US
dc.relation.isversionofhttp://dx.doi.org/10.1073/PNAS.1705065114en_US
dc.rightsArticle is made available in accordance with the publisher's policy and may be subject to US copyright law. Please refer to the publisher's site for terms of use.en_US
dc.sourceNational Academy of Sciencesen_US
dc.titleContinuous immunotypes describe human immune variation and predict diverse responsesen_US
dc.typeArticleen_US
dc.identifier.citationKaczorowski, Kevin J. et al. “Continuous Immunotypes Describe Human Immune Variation and Predict Diverse Responses.” Proceedings of the National Academy of Sciences 114, 30 (July 2017): E6097–E6106 © 2017 National Academy of Sciencesen_US
dc.contributor.departmentMassachusetts Institute of Technology. Institute for Medical Engineering & Scienceen_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Chemical Engineeringen_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Chemistryen_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Physicsen_US
dc.contributor.mitauthorKaczorowski, Kevin John
dc.contributor.mitauthorChakraborty, Arup K
dc.relation.journalProceedings of the National Academy of Sciencesen_US
dc.eprint.versionFinal published versionen_US
dc.type.urihttp://purl.org/eprint/type/JournalArticleen_US
eprint.statushttp://purl.org/eprint/status/PeerRevieweden_US
dc.date.updated2018-04-13T19:03:07Z
dspace.orderedauthorsKaczorowski, Kevin J.; Shekhar, Karthik; Nkulikiyimfura, Dieudonné; Dekker, Cornelia L.; Maecker, Holden; Davis, Mark M.; Chakraborty, Arup K.; Brodin, Petteren_US
dspace.embargo.termsNen_US
dc.identifier.orcidhttps://orcid.org/0000-0003-2936-6551
dc.identifier.orcidhttps://orcid.org/0000-0003-1268-9602
mit.licensePUBLISHER_POLICYen_US


Files in this item

Thumbnail

This item appears in the following Collection(s)

Show simple item record