Evidence map›Paper›PMID 29200193›Full record

ArticleCellular & molecular immunology2019

Immunogenetic factors driving formation of ultralong VH CDR3 in Bos taurus antibodies.

Thaddeus C Deiss, Melissa Vadnais, Feng Wang, Patricia L Chen, Ali Torkamani, Waithaka Mwangi, Marie-Paule Lefranc, Michael F Criscitiello, Vaughn V Smider

Open access · bronzeAbstract read
In one paragraph

Article in Cellular & molecular immunology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 46 papers.

0numbers the graph read from it
0cells of the map it votes in
46citing 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

46 citing papers in PubMed, 76 citations in OpenAlex.

  1. A Synthetic Platform for Antibody Junctional Diversification Beyond Natural Constraints.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026
    Article
  2. IMGTAntibodies (Basel, Switzerland) · 2026
    Review
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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

9 authors at 6 institutions in 2 countries.

Thaddeus C DeissComparative Immunogenetics Laboratory, Department of Veterinary Pathobiology, College of Veterinary Medicine and Biomedical Sciences, Texas A&M University, College Station, TX, 77843, USA.
Melissa VadnaisDepartment of Molecular Medicine, The Scripps Research Institute, 92037, La Jolla, CA, USA.
Feng WangCalifornia Institute for Biomedical Research, 92037, La Jolla, CA, USA.
Patricia L ChenComparative Immunogenetics Laboratory, Department of Veterinary Pathobiology, College of Veterinary Medicine and Biomedical Sciences, Texas A&M University, College Station, TX, 77843, USA.
Ali TorkamaniDepartment of Integrative Structural and Computational Biology, The Scripps Research Institute, 92037, La Jolla, CA, USA.
Waithaka MwangiDepartment of Diagnostic Medicine and Pathobiology, College of Veterinary Medicine, Kansas State University, 66506, Manhattan, KS, USA.
Marie-Paule LefrancIMGT, the International ImMunoGeneTics information system, Laboratoire d'ImmunoGénétique Moléculaire, Institut de Génétique Humaine, CNRS, University of Montpellier, 34396, Montpellier, France.
Michael F CriscitielloComparative Immunogenetics Laboratory, Department of Veterinary Pathobiology, College of Veterinary Medicine and Biomedical Sciences, Texas A&M University, College Station, TX, 77843, USA. mcriscitiello@cvm.tamu.edu.
Vaughn V SmiderDepartment of Molecular Medicine, The Scripps Research Institute, 92037, La Jolla, CA, USA. mcriscitiello@cvm.tamu.edu.
Texas A&M University · USScripps Research Institute · USCalifornia Institute for Biomedical Research · USKansas State University · USScripps Memorial Hospital · USUniversité de Montpellier · FR

Funding

SCRIPPS TRANSLATIONAL SCIENCE INSTITUTE (UL1)UL1RR025774 · NCRR · SCRIPPS RESEARCH INSTITUTE, THE · PI TOPOL, ERIC JEFFREY · 2008 to 2011
$16.3M
Molecular and Structural Studies of Antibody Diversity MechanismsR01GM105826 · NIGMS · SCRIPPS RESEARCH INSTITUTE, THE · PI SMIDER, VAUGHN VASIL · 2014 to 2021
$3.1M
Defining clinically relevant viral epitopes with cow antibodiesR01HD088400 · NICHD · SCRIPPS RESEARCH INSTITUTE, THE · PI SMIDER, VAUGHN VASIL · 2017 to 2021
$1.8M
Cow ultralong CDR3 antibodies targeting HIV gp120R21AI120791 · NIAID · SCRIPPS RESEARCH INSTITUTE, THE · PI SMIDER, VAUGHN VASIL · 2016 to 2017
$525k
Antibody Fingerprinting of Triple Negative Breast Cancer by High Throughput FACSR21CA198595 · NCI · SCRIPPS RESEARCH INSTITUTE, THE · PI FELDING, BRUNIE H., SMIDER, VAUGHN VASIL · 2015 to 2016
$457k
NCI NIH HHS R21 CA198595NCRR NIH HHS UL1 RR025774NIAID NIH HHS R21 AI120791NICHD NIH HHS R01 HD088400NIGMS NIH HHS R01 GM105826
6 · The paper itself

Abstract

The antibody repertoire of Bos taurus is characterized by a subset of variable heavy (VH) chain regions with ultralong third complementarity determining regions (CDR3) which, compared to other species, can provide a potent response to challenging antigens like HIV env. These unusual CDR3 can range to over seventy highly diverse amino acids in length and form unique β-ribbon 'stalk' and disulfide bonded 'knob' structures, far from the typical antigen binding site. The genetic components and processes for forming these unusual cattle antibody VH CDR3 are not well understood. Here we analyze sequences of Bos taurus antibody VH domains and find that the subset with ultralong CDR3 exclusively uses a single variable gene, IGHV1-7 (VHBUL) rearranged to the longest diversity gene, IGHD8-2. An eight nucleotide duplication at the 3' end of IGHV1-7 encodes a longer V-region producing an extended F β-strand that contributes to the stalk in a rearranged CDR3. A low amino acid variability was observed in CDR1 and CDR2, suggesting that antigen binding for this subset most likely only depends on the CDR3. Importantly a novel, potentially AID mediated, deletional diversification mechanism of the B. taurus VH ultralong CDR3 knob was discovered, in which interior codons of the IGHD8-2 region are removed while maintaining integral structural components of the knob and descending strand of the stalk in place. These deletions serve to further diversify cysteine positions, and thus disulfide bonded loops. Hence, both germline and somatic genetic factors and processes appear to be involved in diversification of this structurally unusual cattle VH ultralong CDR3 repertoire.

Indexed as

Amino Acid SequenceAnimalsAntibodiesCattleComplementarity Determining RegionsGerm CellsImmunoglobulin Variable RegionMutation RateProtein Structure, SecondarySequence DeletionAntibodiesComplementarity Determining RegionsImmunoglobulin Variable Region

Identifiers

PMID29200193
PMCPMC6318308
OpenAlexW2774606440

What OpenQuestion holds

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Registered trials

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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.