» Articles » PMID: 39054343

CD28 Co-stimulation: Novel Insights and Applications in Cancer Immunotherapy

Overview
Journal Nat Rev Immunol
Date 2024 Jul 25
PMID 39054343
Authors
Affiliations
Soon will be listed here.
Abstract

Substantial progress in understanding T cell signalling, particularly with respect to T cell co-receptors such as the co-stimulatory receptor CD28, has been made in recent years. This knowledge has been instrumental in the development of innovative immunotherapies for patients with cancer, including immune checkpoint blockade antibodies, adoptive cell therapies, tumour-targeted immunostimulatory antibodies, and immunostimulatory small-molecule drugs that regulate T cell activation. Following the failed clinical trial of a CD28 superagonist antibody in 2006, targeted CD28 agonism has re-emerged as a technologically viable and clinically promising strategy for cancer immunotherapy. In this Review, we explore recent insights into the molecular functions and regulation of CD28. We describe how CD28 is central to the success of current cancer immunotherapies and examine how new questions arising from studies of CD28 as a clinical target have enhanced our understanding of its biological role and may guide the development of future therapeutic strategies in oncology.

Citing Articles

NI-3201 Is a Bispecific Antibody Mediating PD-L1-Dependent CD28 Co-stimulation on T Cells for Enhanced Tumor Control.

Majocchi S, Lloveras P, Nouveau L, Legrand M, Viandier A, Malinge P Cancer Immunol Res. 2025; 13(3):365-383.

PMID: 39760515 PMC: 11876958. DOI: 10.1158/2326-6066.CIR-24-0298.


Tumor Microenvironment Drives the Cross-Talk Between Co-Stimulatory and Inhibitory Molecules in Tumor-Infiltrating Lymphocytes: Implications for Optimizing Immunotherapy Outcomes.

Franzese O Int J Mol Sci. 2024; 25(23).

PMID: 39684559 PMC: 11641238. DOI: 10.3390/ijms252312848.

References
1.
Castellani P, Angelini G, Delfino L, Matucci A, Rubartelli A . The thiol redox state of lymphoid organs is modified by immunization: role of different immune cell populations. Eur J Immunol. 2008; 38(9):2419-25. DOI: 10.1002/eji.200838439. View

2.
Laszlo G, Gudgeon C, Harrington K, Walter R . T-cell ligands modulate the cytolytic activity of the CD33/CD3 BiTE antibody construct, AMG 330. Blood Cancer J. 2015; 5:e340. PMC: 4558592. DOI: 10.1038/bcj.2015.68. View

3.
Augustin R, Bao R, Luke J . Targeting Cbl-b in cancer immunotherapy. J Immunother Cancer. 2023; 11(2). PMC: 9906388. DOI: 10.1136/jitc-2022-006007. View

4.
Spranger S, Dai D, Horton B, Gajewski T . Tumor-Residing Batf3 Dendritic Cells Are Required for Effector T Cell Trafficking and Adoptive T Cell Therapy. Cancer Cell. 2017; 31(5):711-723.e4. PMC: 5650691. DOI: 10.1016/j.ccell.2017.04.003. View

5.
He S, Liu Y, Meng L, Sun H, Wang Y, Ji Y . Ezh2 phosphorylation state determines its capacity to maintain CD8 T memory precursors for antitumor immunity. Nat Commun. 2017; 8(1):2125. PMC: 5730609. DOI: 10.1038/s41467-017-02187-8. View