Volume 3 Supplement 2

30th Annual Meeting and Associated Programs of the Society for Immunotherapy of Cancer (SITC 2015)

Open Access

Identification of novel immune regulators of tumor growth using RIPPS screening in vivo

  • Tom Brennan1,
  • David Bellovin1,
  • Jacqueline de la Torre1,
  • Nebiyu Wondyfraw1,
  • Servando Palencia1,
  • Kevin Hestir1 and
  • Ernestine Lee1
Journal for ImmunoTherapy of Cancer20153(Suppl 2):P66

https://doi.org/10.1186/2051-1426-3-S2-P66

Published: 4 November 2015

Identification of novel targets in cancer immunotherapy is needed to address the significant number of patients that either do not respond to current therapies or encounter unacceptable toxicities. The discovery of such targets, including novel checkpoint regulators and the counter-receptors for previously “orphan” checkpoints, has been limited by a lack of a comprehensive collection of proteins suitable for functional screening and methods for assessing their function in high-throughput.

We have generated a comprehensive library of substantially all human extracellular proteins, encompassing nearly every target for protein therapeutics. Our library contains more than 5700 proteins, including secreted protein ligands and the extracellular domains of membrane-bound receptors in soluble forms. The library proteins represent therapeutic targets and in some cases may act as therapeutics themselves. A portion of this library we call the immunome contains ~500 proteins with structural features characteristic of immune-activators and checkpoints that we selected.

RIPPSSM technology is a robust method whereby FivePrime's library of soluble secreted proteins can be tested in vivo in virtually any disease model. Each cDNA representing a unique protein is administered to a cohort of mice and results in high circulating levels of the encoded protein. RIPPSSM also allows us to rapidly confirm activity identified by other in vitro screening approaches. Here, we have exploited RIPPSSM technology to screen for new immuno-oncology therapeutics and targets for therapeutic development. As positive controls we performed RIPPSSM on CT-26 tumor-bearing mice using known agonists and antagonists of the immune response, which resulted in decreased or increased tumor growth, respectively. Subsequently, we screened over 250 immunome proteins by RIPPSSM in the CT-26 tumor model and have identified proteins that enhance and inhibit tumor growth and display changes in TIL (tumor-infiltrating lymphocyte) profiles. In addition, the immunome was screened in vitro for the ability to modulate anti-CD3-stimulated human T cell proliferation[1]. This screen identified a number of known checkpoint regulators, which validated the assay, and identified numerous novel co-inhibitory proteins – the majority of which have no published link to immune cell regulation. Proteins identified in the in vitro screens have been validated using RIPPSSM and other in vivo methods. These data demonstrate the power of our discovery platform to discover and validate novel therapeutic targets and protein therapeutics for immuno-oncology.

Authors’ Affiliations

(1)
FivePrime Therapeutics Inc.

References

  1. Sallee NA, et al: Discovery of Novel Immune Checkpoint Regulators in a Comprehensive Library of Human Extracellular Proteins. 2014, Poster presented at: SITC. Nov 7-9Google Scholar

Copyright

© Brennan et al. 2015

This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.

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