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

Author

Listed:
  • Justin A. Spanier

    (Center for Immunology, University of Minnesota Medical School)

  • Daniel R. Frederick

    (Tulane University School of Medicine)

  • Justin J. Taylor

    (Center for Immunology, University of Minnesota Medical School
    Present address: Vaccine and Infectious Disease Division, Fred Hutchinson Cancer Research Center, Seattle, Washington 98019, USA.)

  • James R. Heffernan

    (Center for Immunology, University of Minnesota Medical School)

  • Dmitri I. Kotov

    (Center for Immunology, University of Minnesota Medical School)

  • Tijana Martinov

    (Center for Immunology, University of Minnesota Medical School)

  • Kevin C. Osum

    (Center for Immunology, University of Minnesota Medical School)

  • Jenna L. Ruggiero

    (Center for Immunology, University of Minnesota Medical School)

  • Blake J. Rust

    (Tulane University School of Medicine)

  • Samuel J. Landry

    (Tulane University School of Medicine)

  • Marc K. Jenkins

    (Center for Immunology, University of Minnesota Medical School)

  • James B. McLachlan

    (Tulane University School of Medicine)

  • Brian T. Fife

    (Center for Immunology, University of Minnesota Medical School)

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.

Suggested Citation

  • 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 & Marc K. Jen, 2016. "Efficient generation of monoclonal antibodies against peptide in the context of MHCII using magnetic enrichment," Nature Communications, Nature, vol. 7(1), pages 1-11, September.
  • Handle: RePEc:nat:natcom:v:7:y:2016:i:1:d:10.1038_ncomms11804
    DOI: 10.1038/ncomms11804
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