<?xml version="1.0" encoding="UTF-8"?>
<STUDY_SET xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
  <STUDY center_name="GEO" alias="GSE219087" accession="SRP410681">
    <IDENTIFIERS>
      <PRIMARY_ID>SRP410681</PRIMARY_ID>
      <EXTERNAL_ID namespace="BioProject" label="primary">PRJNA907008</EXTERNAL_ID>
      <EXTERNAL_ID namespace="GEO">GSE219087</EXTERNAL_ID>
    </IDENTIFIERS>
    <DESCRIPTOR>
      <STUDY_TITLE>Distant antimetastatic effect of enterotropic colon cancer-derived a4ß7 CD8 T cells [scRNA-seq]</STUDY_TITLE>
      <STUDY_TYPE existing_study_type="Transcriptome Analysis"/>
      <STUDY_ABSTRACT>Despite the high prognostic value of immune infiltrates in colorectal cancer (CRC), metastatic disease remains resistant to immunotherapy by immune checkpoint blockade (ICB). Here we show in a metastatic CRC multi-tumor preclinical model that orthotopically-implanted primary colon tumors can spontaneously exert a colon-specific and immune-dependent antimetastatic effect on distant hepatic lesions. An immune signature, integrating antitumor CD8 T cells, dendritic cells and protumor macrophages, that we called MicroEnvironment (ME)-score, was predictive of the antimetastatic effect. ScRNA-Seq and phenotypic analyses revealed that enterotropic a4ß7 integrin expressing tumor neoantigen-specific CD8 T cells were key components of the systemic immune response responsible for the antimetastatic effect. Accordingly, the presence of concomitant colon tumors improved the efficacy of proof-of-concept ICB on liver lesions and generated a protective memory immune response whereas antibody-mediated partial depletion of a4ß7+ cells abrogated the control of metastatic disease by the primary tumor. Finally, in a metastatic CRC patients' cohort, we show increased expression of genes encoding the a4ß7 integrin and of the ME-score in ICB responsive metastases concomitant with increased proportions of circulating a4ß7+ CD8 T cells. Our findings identify a systemic cancer immunosurveillance role for gut primed tumor-specific a4ß7+ CD8 T cells.  Overall design: Single-cell RNA sequencing was performed on sorted T cells from mice liver and colon tumors and blood samples, harvested at day 10 post tumor implantations (intra-hepatic (IH)+intra-colon (IC) concomitant injections (IH+IC group) or IH alone (al.) injections). Each sample corresponds to a pool of 18 (for IH+IC group) or 9 (for IH al. group) IH tumors; 18 (for IH+IC group) IC tumors; 18 (for IH+IC group) or 9 (for IH al. group) blood samples.</STUDY_ABSTRACT>
      <CENTER_PROJECT_NAME>GSE219087</CENTER_PROJECT_NAME>
    </DESCRIPTOR>
    <STUDY_ATTRIBUTES>
      <STUDY_ATTRIBUTE>
        <TAG>parent_bioproject</TAG>
        <VALUE>PRJNA796808</VALUE>
      </STUDY_ATTRIBUTE>
    </STUDY_ATTRIBUTES>
  </STUDY>
</STUDY_SET>
