» Articles » PMID: 23890064

Deciphering and Reversing Tumor Immune Suppression

Overview
Journal Immunity
Publisher Cell Press
Date 2013 Jul 30
PMID 23890064
Citations 296
Authors
Affiliations
Soon will be listed here.
Abstract

Generating an anti-tumor immune response is a multi-step process that is executed by effector T cells that can recognize and kill tumor targets. However, tumors employ multiple strategies to attenuate the effectiveness of T-cell-mediated attack. They achieve this by interfering with nearly every step required for effective immunity, from deregulation of antigen-presenting cells to establishment of a physical barrier at the vasculature that prevents homing of effector tumor-rejecting cells and the suppression of effector lymphocytes through the recruitment and activation of immunosuppressive cells such as myeloid-derived suppressor cells, tolerogenic monocytes, and T regulatory cells. Here, we review the ways in which tumors exert immune suppression and highlight the new therapies that seek to reverse this phenomenon and promote anti-tumor immunity. Understanding anti-tumor immunity, and how it becomes disabled by tumors, will ultimately lead to improved immune therapies and prolonged survival of patients.

Citing Articles

Finding the right HARMONi-A.

Cordeiro de Lima V, Carioca Freitas H Transl Lung Cancer Res. 2025; 13(12):3835-3837.

PMID: 39830738 PMC: 11736612. DOI: 10.21037/tlcr-24-864.


Multiplexed inhibition of immunosuppressive genes with Cas13d for combinatorial cancer immunotherapy.

Zhang F, Chow R, He E, Dong C, Xin S, Mirza D Nat Biotechnol. 2025; .

PMID: 39820813 DOI: 10.1038/s41587-024-02535-2.


Preliminary characterisation of the spatial immune and vascular environment in triple negative basal breast carcinomas using multiplex fluorescent immunohistochemistry.

Takano E, Jana M, Lara Gonzalez L, Pang J, Salgado R, Loi S PLoS One. 2025; 20(1):e0317331.

PMID: 39792888 PMC: 11723538. DOI: 10.1371/journal.pone.0317331.


Analysis of the benefit of anti-PD-1 monotherapy according to NGS-diagnosed genetic alterations in patients with non-small cell lung cancer.

De Saint Basile H, Elaidi R, Maaradji Z, Blons H, BenDhiab R, Gibault L Explor Target Antitumor Ther. 2025; 5(6):1435-1449.

PMID: 39764418 PMC: 11702263. DOI: 10.37349/etat.2024.00283.


A Pvr-AP-1-Mmp1 signaling pathway is activated in astrocytes upon traumatic brain injury.

Li T, Shi W, Ho M, Zhang Y Elife. 2024; 12.

PMID: 39480704 PMC: 11527428. DOI: 10.7554/eLife.87258.


References
1.
Zang X, Sullivan P, Soslow R, Waitz R, Reuter V, Wilton A . Tumor associated endothelial expression of B7-H3 predicts survival in ovarian carcinomas. Mod Pathol. 2010; 23(8):1104-12. PMC: 2976590. DOI: 10.1038/modpathol.2010.95. View

2.
Frebel H, Nindl V, Schuepbach R, Braunschweiler T, Richter K, Vogel J . Programmed death 1 protects from fatal circulatory failure during systemic virus infection of mice. J Exp Med. 2012; 209(13):2485-99. PMC: 3526355. DOI: 10.1084/jem.20121015. View

3.
Frommer K, Muller-Ladner U . Expression and function of ETA and ETB receptors in SSc. Rheumatology (Oxford). 2008; 47 Suppl 5:v27-8. DOI: 10.1093/rheumatology/ken274. View

4.
Loser K, Apelt J, Voskort M, Mohaupt M, Balkow S, Schwarz T . IL-10 controls ultraviolet-induced carcinogenesis in mice. J Immunol. 2007; 179(1):365-71. DOI: 10.4049/jimmunol.179.1.365. View

5.
Vignali D, Collison L, Workman C . How regulatory T cells work. Nat Rev Immunol. 2008; 8(7):523-32. PMC: 2665249. DOI: 10.1038/nri2343. View