Universal antigen encoding of T cell activation from high-dimensional cytokine dynamics

Author:

Achar Sooraj R.1ORCID,Bourassa François X. P.2ORCID,Rademaker Thomas J.2ORCID,Lee Angela1ORCID,Kondo Taisuke3ORCID,Salazar-Cavazos Emanuel1ORCID,Davies John S.4ORCID,Taylor Naomi3ORCID,François Paul2ORCID,Altan-Bonnet Grégoire1ORCID

Affiliation:

1. Immunodynamics Group, Laboratory of Integrative Cancer Immunology, Center for Cancer Research, National Cancer Institute, Bethesda, MD, USA.

2. Department of Physics, McGill University, Montréal, Québec, Canada.

3. Pediatric Oncology Branch, Center for Cancer Research, National Cancer Institute, Bethesda, MD, USA.

4. Genitourinary Malignancies Branch, Center for Cancer Research, National Cancer Institute, Bethesda, MD, USA.

Abstract

Systems immunology lacks a framework with which to derive theoretical understanding from high-dimensional datasets. We combined a robotic platform with machine learning to experimentally measure and theoretically model CD8 + T cell activation. High-dimensional cytokine dynamics could be compressed onto a low-dimensional latent space in an antigen-specific manner (so-called “antigen encoding”). We used antigen encoding to model and reconstruct patterns of T cell immune activation. The model delineated six classes of antigens eliciting distinct T cell responses. We generalized antigen encoding to multiple immune settings, including drug perturbations and activation of chimeric antigen receptor T cells. Such universal antigen encoding for T cell activation may enable further modeling of immune responses and their rational manipulation to optimize immunotherapies.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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