Evidence map›Paper›PMID 28818634›Full record

ArticleJournal of molecular biology2017

Mining Naïve Rabbit Antibody Repertoires by Phage Display for Monoclonal Antibodies of Therapeutic Utility.

Haiyong Peng, Thomas Nerreter, Jing Chang, Junpeng Qi, Xiuling Li, Pabalu Karunadharma, Gustavo J Martinez, Mohammad Fallahi, Jo Soden, Jim Freeth and 4 more

Open access · greenAbstract read
In one paragraph

Article in Journal of molecular biology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed
4.3field-weighted citation impact, top 5% 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

29 citing papers in PubMed, 45 citations in OpenAlex.

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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

14 authors at 3 institutions in 3 countries.

Haiyong PengDepartment of Immunology and Microbiology, The Scripps Research Institute, Jupiter, FL 33458, USA.
Thomas NerreterMedizinische Klinik und Poliklinik II, Universitätsklinikum Würzburg, 97080 Würzburg, Germany.
Jing ChangDepartment of Immunology and Microbiology, The Scripps Research Institute, Jupiter, FL 33458, USA.
Junpeng QiDepartment of Immunology and Microbiology, The Scripps Research Institute, Jupiter, FL 33458, USA.
Xiuling LiDepartment of Immunology and Microbiology, The Scripps Research Institute, Jupiter, FL 33458, USA.
Pabalu KarunadharmaGenomics Core, The Scripps Research Institute, Jupiter, FL 33458, USA.
Gustavo J MartinezGenomics Core, The Scripps Research Institute, Jupiter, FL 33458, USA.
Mohammad FallahiInformatics Core, The Scripps Research Institute, Jupiter, FL 33458, USA.
Jo SodenRetrogenix Ltd, Whaley Bridge, High Peak, SK23 7LY, United Kingdom.
Jim FreethRetrogenix Ltd, Whaley Bridge, High Peak, SK23 7LY, United Kingdom.
Roger R BeerliNBE-Therapeutics AG, 4057 Basel, Switzerland.
Ulf GrawunderNBE-Therapeutics AG, 4057 Basel, Switzerland.
Michael HudecekMedizinische Klinik und Poliklinik II, Universitätsklinikum Würzburg, 97080 Würzburg, Germany.
Christoph RaderDepartment of Immunology and Microbiology, The Scripps Research Institute, Jupiter, FL 33458, USA. Electronic address: crader@scripps.edu.
Scripps Research Institute · USNBE Therapeutics (Switzerland) · CHUniversitätsklinikum Würzburg · DE

Funding

Novel Enediyne-Based Antibody-Drug Conjugates for CancersR01CA204484 · NCI · UNIVERSITY OF FLORIDA · PI Natarajan Muthusamy, Ben Shen · 2017 to 2026
$4.6M
Chemically Programmed Bispecific Antibodies for Cancer TherapyR01CA181258 · NCI · SCRIPPS FLORIDA · PI RADER, CHRISTOPH · 2014 to 2018
$2.0M
A Drug Delivery Strategy for Targeted Therapy of Chronic Lymphocytic LeukemiaU01CA174844 · NCI · SCRIPPS FLORIDA · PI RADER, CHRISTOPH · 2013 to 2015
$1.4M
NCI NIH HHS R01 CA181258NCI NIH HHS R01 CA204484NCI NIH HHS U01 CA174844
6 · The paper itself

Abstract

Owing to their high affinities and specificities, rabbit monoclonal antibodies (mAbs) have demonstrated value and potential primarily as basic research and diagnostic reagents, but, in some cases, also as therapeutics. To accelerate access to rabbit mAbs bypassing immunization, we generated a large naïve rabbit antibody repertoire represented by a phage display library encompassing >10 billion independent antibodies in chimeric rabbit/human Fab format and validated it by next-generation sequencing. Panels of rabbit mAbs selected from this library against two emerging cancer targets, ROR1 and ROR2, revealed high diversity, affinity, and specificity. Moreover, ROR1- and ROR2-targeting rabbit mAbs demonstrated therapeutic utility as components of chimeric antigen receptor-engineered T cells, further corroborating the value of the naïve rabbit antibody library as a rich and virtually unlimited source of rabbit mAbs.

Indexed as

AnimalsAntibodies, MonoclonalAntigens, NeoplasmCell Line, TumorCell ProliferationCytokinesCytotoxicity Tests, ImmunologicHumansImmunoglobulin Fab FragmentsImmunologic FactorsImmunotherapyPeptide LibraryRabbitsReceptor Tyrosine Kinase-like Orphan ReceptorsRecombinant ProteinsT-LymphocytesAntibodies, MonoclonalAntigens, NeoplasmCytokinesImmunoglobulin Fab FragmentsImmunologic FactorsPeptide LibraryReceptor Tyrosine Kinase-like Orphan ReceptorsRecombinant ProteinsROR1 protein, humanROR2 protein, humanantibody engineeringcancer therapychimeric antigen receptorsROR1ROR2

Identifiers

PMID28818634
PMCPMC5610937
OpenAlexW2747369917

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.