Repository logo
Log in(current)
Repository logoMIT Open ScholarshipDSpace@MIT
  1. Home
  2. MIT Open Access Articles
  3. MIT Open Access Articles
  4. IFNγ-Dependent Tissue-Immune Homeostasis Is Co-opted in the Tumor Microenvironment

IFNγ-Dependent Tissue-Immune Homeostasis Is Co-opted in the Tumor Microenvironment

Thumbnail Image
Download
Name

nihms885203.pdf

Size

1.25 MB

Format

Adobe PDF

Checksum (MD5)

7115f35fc5abb0b42d7595c0e0481a23

Download all files submitted through automated deposit
sword-2018-07-02.original.zip (1.07 MB)
Author(s)
Nirschl, Christopher J.
•
Suárez-Fariñas, Mayte
•
Izar, Benjamin
•
Dannenfelser, Ruth
•
Tirosh, Itay
•
Liu, Yong
•
Zhu, Qian
•
Devi, K. Sanjana P.
•
Chau, David
•
Rezaee, Melika
more
Date Issued
June 2017
Journal
Cell
Publisher
Elsevier
Citation
Nirschl, Christopher J. et al. “IFNγ-Dependent Tissue-Immune Homeostasis Is Co-Opted in the Tumor Microenvironment.” Cell 170, 1 (June 2017): 127–141 © 2017 Elsevier Inc
Version
Author's final manuscript
Abstract
Homeostatic programs balance immune protection and self-tolerance. Such mechanisms likely impact autoimmunity and tumor formation, respectively. How homeostasis is maintained and impacts tumor surveillance is unknown. Here, we find that different immune mononuclear phagocytes share a conserved steady-state program during differentiation and entry into healthy tissue. IFNγ is necessary and sufficient to induce this program, revealing a key instructive role. Remarkably, homeostatic and IFNγ-dependent programs enrich across primary human tumors, including melanoma, and stratify survival. Single-cell RNA sequencing (RNA-seq) reveals enrichment of homeostatic modules in monocytes and DCs from human metastatic melanoma. Suppressor-of-cytokine-2 (SOCS2) protein, a conserved program transcript, is expressed by mononuclear phagocytes infiltrating primary melanoma and is induced by IFNγ. SOCS2 limits adaptive anti-tumoral immunity and DC-based priming of T cells in vivo, indicating a critical regulatory role. These findings link immune homeostasis to key determinants of anti-tumoral immunity and escape, revealing co-opting of tissue-specific immune development in the tumor microenvironment. Keywords: dendritic cells; homeostasis; differentiation; IFNγ; tumor microenvironment; melanoma tolerance; immunotherapy; suppressor-of-cytokine-signaling 2 (SOCS2); tissue mononuclear phagocytes
MIT Department
Massachusetts Institute of Technology. Institute for Medical Engineering & Science
Massachusetts Institute of Technology. Department of Biology
Massachusetts Institute of Technology. Department of Chemistry
Koch Institute for Integrative Cancer Research at MIT
Terms of Use
Creative Commons Attribution-NonCommercial-NoDerivs License
http://creativecommons.org/licenses/by-nc-nd/4.0/
Persistent DSpace Link
http://hdl.handle.net/1721.1/116738
DOI of Published Version
https://doi.org/10.1016/J.CELL.2017.06.016
Repository logo
PrivacyPermissionsAccessibilityContact us
Repository logo
Notify us about copyright concerns.