| dc.contributor.author | Calatroni, Agustin | |
| dc.contributor.author | Tadigotla, Vasisht R. | |
| dc.contributor.author | Ruiter, Bert | |
| dc.contributor.author | Ma, Alex | |
| dc.contributor.author | Moon, James | |
| dc.contributor.author | Shreffler, Wayne G. | |
| dc.contributor.author | Patil, Sarita | |
| dc.contributor.author | Ogunniyi, Adebola Oluwakayode | |
| dc.contributor.author | Love, John C | |
| dc.date.accessioned | 2017-05-30T19:44:54Z | |
| dc.date.available | 2017-05-30T19:44:54Z | |
| dc.date.issued | 2015-05 | |
| dc.date.submitted | 2015-02 | |
| dc.identifier.issn | 0091-6749 | |
| dc.identifier.uri | http://hdl.handle.net/1721.1/109437 | |
| dc.description.abstract | Background
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 immunotherapy | en_US |
| dc.description.sponsorship | National Institute of Allergy and Infectious Diseases (U.S.) (NIAID U19 AI087881) | en_US |
| dc.description.sponsorship | National Institute of Allergy and Infectious Diseases (U.S.) (NIAID U19 AI095261) | en_US |
| dc.description.sponsorship | United States. National Institutes of Health (1S10RR023440-01A1) | en_US |
| dc.description.sponsorship | National Institute of Allergy and Infectious Diseases (U.S.) (NIAID F32 AI104182) | en_US |
| dc.description.sponsorship | United States. National Institutes of Health (UL1 TR001102) | en_US |
| dc.language.iso | en_US | |
| dc.publisher | Elsevier | en_US |
| dc.relation.isversionof | http://dx.doi.org/10.1016/j.jaci.2015.03.026 | en_US |
| dc.rights | Creative Commons Attribution-NonCommercial-NoDerivs License | en_US |
| dc.rights.uri | http://creativecommons.org/licenses/by-nc-nd/4.0/ | en_US |
| dc.source | PMC | en_US |
| dc.title | Peanut oral immunotherapy transiently expands circulating Ara h 2–specific B cells with a homologous repertoire in unrelated subjects | en_US |
| dc.type | Article | en_US |
| dc.identifier.citation | Patil, 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.department | Massachusetts Institute of Technology. Department of Chemical Engineering | en_US |
| dc.contributor.department | Koch Institute for Integrative Cancer Research at MIT | en_US |
| dc.contributor.mitauthor | Patil, Sarita | |
| dc.contributor.mitauthor | Ogunniyi, Adebola Oluwakayode | |
| dc.contributor.mitauthor | Love, John C | |
| dc.relation.journal | Journal of Allergy and Clinical Immunology | en_US |
| dc.eprint.version | Author's final manuscript | en_US |
| dc.type.uri | http://purl.org/eprint/type/JournalArticle | en_US |
| eprint.status | http://purl.org/eprint/status/PeerReviewed | en_US |
| dspace.orderedauthors | Patil, 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.terms | N | en_US |
| dc.identifier.orcid | https://orcid.org/0000-0002-2172-2286 | |
| dc.identifier.orcid | https://orcid.org/0000-0003-0921-3144 | |
| mit.license | PUBLISHER_CC | en_US |