Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Review
. 2020 Sep:137:260-271.
doi: 10.1016/j.ejca.2020.06.009. Epub 2020 Aug 18.

Chemokine biology on immune checkpoint-targeted therapies

Affiliations
Review

Chemokine biology on immune checkpoint-targeted therapies

Diane Letourneur et al. Eur J Cancer. 2020 Sep.

Abstract

The use of antagonistic immune checkpoint-targeted monoclonal antibodies has profoundly modified the standard of care and significantly increased the survival for many cancers. However, many patients still do not respond to those treatments. Biomarkers predictive for efficacy or failure of such immunotherapies would allow developing treatment stratification strategies which could further increase the survival rates of patients with cancer. Chemokines are a subset of the immune cell messenger molecules known as cytokines. Chemokines are key chemoattractant molecules which are essential for the homing of immune cells, notably within tumours. Therefore, they are good candidates for providing predictive biomarkers of the clinical response to checkpoint blockade immunotherapies. In this review, we summarise the recent advances in our understanding of the role of chemokines and how chemokine concentrations may set the tone for the efficacy of immune checkpoint-targeted immunotherapies.

Keywords: Biomarker; CTLA-4; Chemokine; Immune checkpoint blockade; PD-1; PD-L1.

PubMed Disclaimer

Conflict of interest statement

Conflict of interest statement The funding of research on chemokines in the laboratory of A.M. is partly funded by academic grants from Boehringer Ingelheim, Fondation MSDAvenir and CIC BT Inserm 1428. The other authors declare no conflicts of interest.

Publication types

MeSH terms

LinkOut - more resources