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dc.contributor.authorCalatroni, Agustin
dc.contributor.authorTadigotla, Vasisht R.
dc.contributor.authorRuiter, Bert
dc.contributor.authorMa, Alex
dc.contributor.authorMoon, James
dc.contributor.authorShreffler, Wayne G.
dc.contributor.authorPatil, Sarita
dc.contributor.authorOgunniyi, Adebola Oluwakayode
dc.contributor.authorLove, John C
dc.date.accessioned2017-05-30T19:44:54Z
dc.date.available2017-05-30T19:44:54Z
dc.date.issued2015-05
dc.date.submitted2015-02
dc.identifier.issn0091-6749
dc.identifier.urihttp://hdl.handle.net/1721.1/109437
dc.description.abstractBackground Peanut oral immunotherapy (PNOIT) induces persistent tolerance to peanut in a subset of patients and induces specific antibodies that might play a role in clinical protection. However, the contribution of induced antibody clones to clinical tolerance in PNOIT is unknown. Objective We hypothesized that PNOIT induces a clonal, allergen-specific B-cell response that could serve as a surrogate for clinical outcomes. Methods We used a fluorescent Ara h 2 multimer for affinity selection of Ara h 2–specific B cells and subsequent single-cell immunoglobulin amplification. The diversity of related clones was evaluated by means of next-generation sequencing of immunoglobulin heavy chains from circulating memory B cells with 2x250 paired-end sequencing on the Illumina MiSeq platform. Results Expression of class-switched antibodies from Ara h 2–positive cells confirms enrichment for Ara h 2 specificity. PNOIT induces an early and transient expansion of circulating Ara h 2–specific memory B cells that peaks at week 7. Ara h 2–specific sequences from memory cells have rates of nonsilent mutations consistent with affinity maturation. The repertoire of Ara h 2–specific antibodies is oligoclonal. Next-generation sequencing–based repertoire analysis of circulating memory B cells reveals evidence for convergent selection of related sequences in 3 unrelated subjects, suggesting the presence of similar Ara h 2–specific B-cell clones. Conclusions Using a novel affinity selection approach to identify antigen-specific B cells, we demonstrate that the early PNOIT-induced Ara h 2–specific B-cell receptor repertoire is oligoclonal and somatically hypermutated and shares similar clonal groups among unrelated subjects consistent with convergent selection. Key words Immunotherapy; antigen-specific B cells; peanut allergy; food allergy; antibody repertoire Abbreviations used APC, Allophycocyanin; BCR, B-cell receptor; CDR, Complementarity-determining region; NGS, Next-generation sequencing; OIT, Oral immunotherapy; PNOIT, Peanut oral immunotherapyen_US
dc.description.sponsorshipNational Institute of Allergy and Infectious Diseases (U.S.) (NIAID U19 AI087881)en_US
dc.description.sponsorshipNational Institute of Allergy and Infectious Diseases (U.S.) (NIAID U19 AI095261)en_US
dc.description.sponsorshipUnited States. National Institutes of Health (1S10RR023440-01A1)en_US
dc.description.sponsorshipNational Institute of Allergy and Infectious Diseases (U.S.) (NIAID F32 AI104182)en_US
dc.description.sponsorshipUnited States. National Institutes of Health (UL1 TR001102)en_US
dc.language.isoen_US
dc.publisherElsevieren_US
dc.relation.isversionofhttp://dx.doi.org/10.1016/j.jaci.2015.03.026en_US
dc.rightsCreative Commons Attribution-NonCommercial-NoDerivs Licenseen_US
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/en_US
dc.sourcePMCen_US
dc.titlePeanut oral immunotherapy transiently expands circulating Ara h 2–specific B cells with a homologous repertoire in unrelated subjectsen_US
dc.typeArticleen_US
dc.identifier.citationPatil, Sarita U.; Ogunniyi, Adebola O.; Calatroni, Agustin; Tadigotla, Vasisht R.; Ruiter, Bert; Ma, Alex; Moon, James; Love, J. Christopher and Shreffler, Wayne G. “Peanut Oral Immunotherapy Transiently Expands Circulating Ara h 2–specific B Cells with a Homologous Repertoire in Unrelated Subjects.” Journal of Allergy and Clinical Immunology 136, no. 1 (July 2015): 125–134.e12 © 2015 American Academy of Allergy, Asthma & Immunology.en_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Chemical Engineeringen_US
dc.contributor.departmentKoch Institute for Integrative Cancer Research at MITen_US
dc.contributor.mitauthorPatil, Sarita
dc.contributor.mitauthorOgunniyi, Adebola Oluwakayode
dc.contributor.mitauthorLove, John C
dc.relation.journalJournal of Allergy and Clinical Immunologyen_US
dc.eprint.versionAuthor's final manuscripten_US
dc.type.urihttp://purl.org/eprint/type/JournalArticleen_US
eprint.statushttp://purl.org/eprint/status/PeerRevieweden_US
dspace.orderedauthorsPatil, Sarita U.; Ogunniyi, Adebola O.; Calatroni, Agustin; Tadigotla, Vasisht R.; Ruiter, Bert; Ma, Alex; Moon, James; Love, J. Christopher; Shreffler, Wayne G.en_US
dspace.embargo.termsNen_US
dc.identifier.orcidhttps://orcid.org/0000-0002-2172-2286
dc.identifier.orcidhttps://orcid.org/0000-0003-0921-3144
mit.licensePUBLISHER_CCen_US


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