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dc.contributor.authorMesin, Luka
dc.contributor.authorVictora, Gabriel D.
dc.contributor.authorAmitai, Assaf
dc.contributor.authorKardar, Mehran
dc.contributor.authorChakraborty, Arup K
dc.date.accessioned2017-12-29T20:25:19Z
dc.date.available2017-12-29T20:25:19Z
dc.date.issued2017-09
dc.date.submitted2017-05
dc.identifier.issn1664-302X
dc.identifier.urihttp://hdl.handle.net/1721.1/112995
dc.description.abstractGerminal centers (GCs) are micro-domains where B cells mature to develop high affinity antibodies. Inside a GC, B cells compete for antigen and T cell help, and the successful ones continue to evolve. New experimental results suggest that, under identical conditions, a wide spectrum of clonal diversity is observed in different GCs, and high affinity B cells are not always the ones selected. We use a birth, death and mutation model to study clonal competition in a GC over time. We find that, like all evolutionary processes, diversity loss is inherently stochastic. We study two selection mechanisms, birth-limited and death limited selection. While death limited selection maintains diversity and allows for slow clonal homogenization as affinity increases, birth limited selection results in more rapid takeover of successful clones. Finally, we qualitatively compare our model to experimental observations of clonal selection in mice.en_US
dc.description.sponsorshipNational Science Foundation (U.S.) (Grant DMR-1708280)en_US
dc.publisherFrontiers Research Foundationen_US
dc.relation.isversionofhttp://dx.doi.org/10.3389/fmicb.2017.01693en_US
dc.rightsCreative Commons Attribution 4.0 Internationalen_US
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/en_US
dc.titleA Population Dynamics Model for Clonal Diversity in a Germinal Centeren_US
dc.typeArticleen_US
dc.identifier.citationAmitai, Assaf et al. “A Population Dynamics Model for Clonal Diversity in a Germinal Center.” Frontiers in Microbiology 8 (September 2017): 1603 © 2017 Amitai, Mesin, Victora, Kardar and Chakrabortyen_US
dc.contributor.departmentMassachusetts Institute of Technology. Institute for Medical Engineering & Scienceen_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Biological Engineeringen_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.mitauthorAmitai, Assaf
dc.contributor.mitauthorKardar, Mehran
dc.contributor.mitauthorChakraborty, Arup K
dc.relation.journalFrontiers in Microbiologyen_US
dc.type.urihttp://purl.org/eprint/type/JournalArticleen_US
eprint.statushttp://purl.org/eprint/status/PeerRevieweden_US
dc.date.updated2017-12-29T20:11:36Z
dspace.orderedauthorsAmitai, Assaf; Mesin, Luka; Victora, Gabriel D.; Kardar, Mehran; Chakraborty, Arup K.en_US
dspace.embargo.termsNen_US
dc.identifier.orcidhttps://orcid.org/0000-0002-8594-6529
dc.identifier.orcidhttps://orcid.org/0000-0002-1112-5912
dc.identifier.orcidhttps://orcid.org/0000-0003-1268-9602
mit.licensePUBLISHER_CCen_US


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