Evidence map›Paper›PMID 37027017›Full record

ArticleJournal of immunology (Baltimore, Md. : 1950)2023

FLAIRR-Seq: A Method for Single-Molecule Resolution of Near Full-Length Antibody H Chain Repertoires.

Easton E Ford, David Tieri, Oscar L Rodriguez, Nancy J Francoeur, Juan Soto, Justin T Kos, Ayelet Peres, William S Gibson, Catherine A Silver, Gintaras Deikus and 9 more

Open access · bronzeAbstract read
In one paragraph

Article in Journal of immunology (Baltimore, Md. : 1950), 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
7.1field-weighted citation impact, top 2% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

22 citing papers in PubMed, 31 citations in OpenAlex.

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  19. Identification of IgG1 and IgG3 Allotypes by PCR and Sanger Sequencing.Methods in molecular biology (Clifton, N.J.) · 2024
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

19 authors at 3 institutions in 2 countries.

Easton E FordDepartment of Microbiology and Immunology, University of Louisville School of Medicine, Louisville, KY.ORCID 0000-0001-9812-6741
David TieriDepartment of Biochemistry and Molecular Genetics, University of Louisville School of Medicine, Louisville, KY.ORCID 0000-0003-1554-816X
Oscar L RodriguezDepartment of Biochemistry and Molecular Genetics, University of Louisville School of Medicine, Louisville, KY.
Nancy J FrancoeurDepartment of Genetics and Genomic Sciences, Icahn School of Medicine at Mount Sinai, New York City, NY.ORCID 0000-0003-1798-3587
Juan SotoDepartment of Genetics and Genomic Sciences, Icahn School of Medicine at Mount Sinai, New York City, NY.
Justin T KosDepartment of Biochemistry and Molecular Genetics, University of Louisville School of Medicine, Louisville, KY.ORCID 0000-0003-2645-3641
Ayelet PeresFaculty of Engineering, Bar Ilan University, Ramat Gan, Israel.ORCID 0000-0002-0188-7315
William S GibsonDepartment of Biochemistry and Molecular Genetics, University of Louisville School of Medicine, Louisville, KY.ORCID 0000-0003-4262-4893
Catherine A SilverDepartment of Biochemistry and Molecular Genetics, University of Louisville School of Medicine, Louisville, KY.
Gintaras DeikusDepartment of Genetics and Genomic Sciences, Icahn School of Medicine at Mount Sinai, New York City, NY.ORCID 0000-0002-4475-1186
Elizabeth HudsonDepartment of Biochemistry and Molecular Genetics, University of Louisville School of Medicine, Louisville, KY.
Cassandra R WoolleyDepartment of Microbiology and Immunology, University of Louisville School of Medicine, Louisville, KY.ORCID 0000-0003-2752-1351
Noam BeckmannDepartment of Genetics and Genomic Sciences, Icahn School of Medicine at Mount Sinai, New York City, NY.
Alexander CharneyDepartment of Genetics and Genomic Sciences, Icahn School of Medicine at Mount Sinai, New York City, NY.
Thomas C MitchellDepartment of Microbiology and Immunology, University of Louisville School of Medicine, Louisville, KY.ORCID 0000-0002-6493-2232
Gur YaariFaculty of Engineering, Bar Ilan University, Ramat Gan, Israel.
Robert P SebraDepartment of Genetics and Genomic Sciences, Icahn School of Medicine at Mount Sinai, New York City, NY.
Corey T WatsonDepartment of Biochemistry and Molecular Genetics, University of Louisville School of Medicine, Louisville, KY.ORCID 0000-0001-7248-8787
Melissa L SmithDepartment of Biochemistry and Molecular Genetics, University of Louisville School of Medicine, Louisville, KY.ORCID 0000-0001-7151-3207
University of Louisville · USIcahn School of Medicine at Mount Sinai · USBar-Ilan University · IL

Funding

The role of ECM-mediated mechanosignaling on regional immunosuppression in GBMP20GM135004 · NIGMS · UNIVERSITY OF LOUISVILLE · PI Sharmila Nair · 2020 to 2026
$21.1M
Mechanisms of successful vaccine adjuvantsR01AI127970 · NIAID · UNIVERSITY OF LOUISVILLE · PI MITCHELL, THOMAS C. · 2017 to 2021
$1.9M
NIAID NIH HHS R01 AI127970NIGMS NIH HHS P20 GM135004
6 · The paper itself

Abstract

Current Adaptive Immune Receptor Repertoire sequencing (AIRR-seq) using short-read sequencing strategies resolve expressed Ab transcripts with limited resolution of the C region. In this article, we present the near-full-length AIRR-seq (FLAIRR-seq) method that uses targeted amplification by 5' RACE, combined with single-molecule, real-time sequencing to generate highly accurate (99.99%) human Ab H chain transcripts. FLAIRR-seq was benchmarked by comparing H chain V (IGHV), D (IGHD), and J (IGHJ) gene usage, complementarity-determining region 3 length, and somatic hypermutation to matched datasets generated with standard 5' RACE AIRR-seq using short-read sequencing and full-length isoform sequencing. Together, these data demonstrate robust FLAIRR-seq performance using RNA samples derived from PBMCs, purified B cells, and whole blood, which recapitulated results generated by commonly used methods, while additionally resolving H chain gene features not documented in IMGT at the time of submission. FLAIRR-seq data provide, for the first time, to our knowledge, simultaneous single-molecule characterization of IGHV, IGHD, IGHJ, and IGHC region genes and alleles, allele-resolved subisotype definition, and high-resolution identification of class switch recombination within a clonal lineage. In conjunction with genomic sequencing and genotyping of IGHC genes, FLAIRR-seq of the IgM and IgG repertoires from 10 individuals resulted in the identification of 32 unique IGHC alleles, 28 (87%) of which were previously uncharacterized. Together, these data demonstrate the capabilities of FLAIRR-seq to characterize IGHV, IGHD, IGHJ, and IGHC gene diversity for the most comprehensive view of bulk-expressed Ab repertoires to date.

Indexed as

Complementarity Determining RegionsBase SequenceHumansComplementarity Determining Regions

Identifiers

PMID37027017
PMCPMC10152037
OpenAlexW4362692173

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.