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Innate Immune Landscape in Early Lung Adenocarcinoma by Paired Single-Cell Analyses

  • Yonit Lavin
  • , Soma Kobayashi
  • , Andrew Leader
  • , El-ad David Amir
  • , Naama Elefant
  • , Camille Bigenwald
  • , Romain Remark
  • , Robert Sweeney
  • , Christian D. Becker
  • , Jacob H. Levine
  • , Klaus Meinhof
  • , Andrew Chow
  • , Seunghee Kim-Shulze
  • , Andrea Wolf
  • , Chiara Medaglia
  • , Hanjie Li
  • , Julie A. Rytlewski
  • , Ryan O. Emerson
  • , Alexander Solovyov
  • , Benjamin D. Greenbaum
  • Catherine Sanders, Marissa Vignali, Mary Beth Beasley, Raja Flores, Sacha Gnjatic, Dana Pe'er, Adeeb Rahman, Ido Amit, Miriam Merad

Research output: Contribution to journalArticlepeer-review

Abstract

To guide the design of immunotherapy strategies for patients with early stage lung tumors, we developed a multiscale immune profiling strategy to map the immune landscape of early lung adenocarcinoma lesions to search for tumor-driven immune changes. Utilizing a barcoding method that allows a simultaneous single-cell analysis of the tumor, non-involved lung, and blood cells, we provide a detailed immune cell atlas of early lung tumors. We show that stage I lung adenocarcinoma lesions already harbor significantly altered T cell and NK cell compartments. Moreover, we identified changes in tumor-infiltrating myeloid cell (TIM) subsets that likely compromise anti-tumor T cell immunity. Paired single-cell analyses thus offer valuable knowledge of tumor-driven immune changes, providing a powerful tool for the rational design of immune therapies.

Original languageEnglish
Pages (from-to)750-765.e17
JournalCell
Volume169
Issue number4
DOIs
StatePublished - 4 May 2017

ASJC Scopus subject areas

  • General Biochemistry,Genetics and Molecular Biology

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