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Updated: May 29, 2026

Studying the Effects of Tumor-Secreted Paracrine Ligands on Macrophage Activation using Co-Culture with Permeable Membrane Supports
Published on: November 28, 2019
Hiding the road signs that lead to tumor immunity
David A Schaer1, Alexander M Lesokhin, Jedd D Wolchok
1Swim Across America Laboratory, Immunology Program, Sloan-Kettering Institute for Cancer Research, New York, NY, USA. schaerd@mskcc.org
Abstract:
Tumors exploit many strategies to evade T cell-mediated destruction. For example, tumors can prevent T cell infiltration by modifying gene expression in the endothelial cells and pericytes that form their vasculature. New work showing that the T cell-attracting chemokine CCL2 can be posttranslationally modified in the tumor microenvironment adds another mechanism to the already formidable arsenal of immunoevasion tactics used by solid tumors.
Insights
Solid tumors employ diverse immunoevasion tactics. A new study reveals that posttranslational modification of the T cell-attracting chemokine CCL2 within the tumor microenvironment represents an additional strategy tumors use to evade immune destruction.
Area of Science:
- Immunology
- Cancer Biology
- Tumor Microenvironment
Background:
- Tumors utilize numerous strategies to escape T cell-mediated killing.
- Tumor vasculature modification hinders T cell infiltration.
- The tumor microenvironment plays a critical role in immune evasion.
Purpose of the Study:
- To identify novel mechanisms of tumor immune evasion.
- To investigate the role of chemokine modification in T cell exclusion.
Main Methods:
- Analysis of posttranslational modifications of chemokines within the tumor microenvironment.
- Investigating the impact of modified chemokines on T cell trafficking.
Main Results:
- The T cell-attracting chemokine CCL2 undergoes posttranslational modification in the tumor microenvironment.
- This modification represents a newly identified mechanism of tumor immunoevasion.
Conclusions:
- Posttranslational modification of CCL2 is a significant contributor to tumor immune evasion.
- Targeting chemokine modification could enhance anti-tumor T cell responses.
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