Evidence map›Paper›PMID 27292946›Full record

ArticleNature communications2016

Efficient generation of monoclonal antibodies against peptide in the context of MHCII using magnetic enrichment.

Justin A Spanier, Daniel R Frederick, Justin J Taylor, James R Heffernan, Dmitri I Kotov, Tijana Martinov, Kevin C Osum, Jenna L Ruggiero, Blake J Rust, Samuel J Landry and 3 more

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
1.9field-weighted citation impact, top 15% 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

25 citing papers in PubMed, 31 citations in OpenAlex.

  1. Trial
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  5. CD4Immunity · 2024
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  6. Review
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  11. Review
  12. TARP as antigen in cancer immunotherapy.Cancer immunology, immunotherapy : CII · 2021
    Review
  13. Article
  14. Review
  15. Monoclonal Antibodies Counteract Opioid-Induced Behavioral and Toxic Effects in Mice and Rats.The Journal of pharmacology and experimental therapeutics · 2020
    Article
  16. Review
  17. Article
  18. Review
  19. Programmed Death-1 Restrains the Germinal Center in Type 1 Diabetes.Journal of immunology (Baltimore, Md. : 1950) · 2019
    Article
  20. Targeting the MHC Ligandome by Use of TCR-Like Antibodies.Antibodies (Basel, Switzerland) · 2019
    Review
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

13 authors at 2 institutions in 1 country.

Justin A SpanierDepartment of Medicine, Center for Immunology, University of Minnesota Medical School, Minneapolis, Minnesota 55455, USA.
Daniel R FrederickDepartment of Microbiology and Immunology, Tulane University School of Medicine, New Orleans, Louisiana 70112, USA.
Justin J TaylorDepartment of Microbiology and Immunology, Center for Immunology, University of Minnesota Medical School, Minneapolis, Minnesota 55455, USA.
James R HeffernanDepartment of Medicine, Center for Immunology, University of Minnesota Medical School, Minneapolis, Minnesota 55455, USA.
Dmitri I KotovDepartment of Microbiology and Immunology, Center for Immunology, University of Minnesota Medical School, Minneapolis, Minnesota 55455, USA.
Tijana MartinovDepartment of Medicine, Center for Immunology, University of Minnesota Medical School, Minneapolis, Minnesota 55455, USA.
Kevin C OsumDepartment of Medicine, Center for Immunology, University of Minnesota Medical School, Minneapolis, Minnesota 55455, USA.
Jenna L RuggieroDepartment of Medicine, Center for Immunology, University of Minnesota Medical School, Minneapolis, Minnesota 55455, USA.
Blake J RustDepartment of Biochemistry, Tulane University School of Medicine, New Orleans, Louisiana 70112, USA.
Samuel J LandryDepartment of Biochemistry, Tulane University School of Medicine, New Orleans, Louisiana 70112, USA.
Marc K JenkinsDepartment of Microbiology and Immunology, Center for Immunology, University of Minnesota Medical School, Minneapolis, Minnesota 55455, USA.
James B McLachlanDepartment of Microbiology and Immunology, Tulane University School of Medicine, New Orleans, Louisiana 70112, USA.
Brian T FifeDepartment of Medicine, Center for Immunology, University of Minnesota Medical School, Minneapolis, Minnesota 55455, USA.ORCID 0000-0001-9826-5637
University of Minnesota Medical Center · USTulane University · US

Funding

Women's CancerP30CA077598 · NCI · UNIVERSITY OF MINNESOTA TWIN CITIES · PI HEATHER Hammond NELSON · 1998 to 2026
$100.4M
Type I interferons in tolerance in the steady stateP01AI035296 · NIAID · UNIVERSITY OF MINNESOTA TWIN CITIES · PI JENKINS, MARC KEVIN · 1993 to 2023
$31.1M
IMMUNOLOGY TRAINING PROGRAMT32AI007313 · NIAID · UNIVERSITY OF MINNESOTA TWIN CITIES · PI Carla Rothlin · 1989 to 2026
$5.7M
TRAINING GRANT IN DIABETES, ENDOCRINOLOGY, &METABOLISMT32DK007203 · NIDDK · UNIVERSITY OF MINNESOTA TWIN CITIES · PI LISA Senye CHOW, Douglas G Mashek · 1986 to 2026
$4.3M
Multiplex immune analysis of antigen specific CD4+ T cells in autoimmune diabetesU24AI118635 · NIAID · UNIVERSITY OF MINNESOTA · PI FIFE, BRIAN T · 2015 to 2019
$2.3M
Mechanisms of immune tolerance in autoimmune diabetesR01AI106791 · NIAID · UNIVERSITY OF MINNESOTA · PI FIFE, BRIAN T · 2014 to 2018
$1.9M
Organ-specific CD4 T cell responses regulate Salmonella persistenceR01AI103343 · NIAID · TULANE UNIVERSITY OF LOUISIANA · PI MCLACHLAN, JAMES B · 2013 to 2016
$1.5M
NCI NIH HHS P30 CA077598NIAID NIH HHS P01 AI035296NIAID NIH HHS R01 AI103343NIAID NIH HHS R01 AI106791NIAID NIH HHS T32 AI007313NIAID NIH HHS U24 AI118635NIDDK NIH HHS T32 DK007203
6 · The paper itself

Abstract

Monoclonal antibodies specific for foreign antigens, auto-antigens, allogeneic antigens and tumour neo-antigens in the context of major histocompatibility complex II (MHCII) are highly desirable as novel immunotherapeutics. However, there is no standard protocol for the efficient generation of monoclonal antibodies that recognize peptide in the context of MHCII, and only a limited number of such reagents exist. In this report, we describe an approach for the generation and screening of monoclonal antibodies specific for peptide bound to MHCII. This approach exploits the use of recombinant peptide:MHC monomers as immunogens, and subsequently relies on multimers to pre-screen and magnetically enrich the responding antigen-specific B cells before fusion and validation, thus saving significant time and reagents. Using this method, we have generated two antibodies enabling us to interrogate antigen presentation and T-cell activation. This methodology sets the standard to generate monoclonal antibodies against the peptide-MHCII complexes.

Indexed as

AnimalsAntibodies, MonoclonalAntibody AffinityCell ProliferationHistocompatibility Antigens Class IIHumansHybridomasMagneticsMice, Inbred C57BLPeptidesPhenotypeReproducibility of ResultsAntibodies, MonoclonalHistocompatibility Antigens Class IIPeptides

Identifiers

PMID27292946
PMCPMC4909947
OpenAlexW2427409766

What OpenQuestion holds

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LicenceCC BY
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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.