The Potential of T Cell Immunoglobulin and Mucin-Domain Containing-3 (Tim-3) in Designing Novel Immunotherapy for Bladder Cancer

Author:

Mohsenzadegan Monireh1,Bavandpour Parizad2,Nowroozi Mohammad Reza3,Amini Erfan3,Kourosh-Arami Masoumeh4,Momeni Seyed Ali5,Bokaie Saied6,Sharifi Laleh3

Affiliation:

1. Department of Medical Laboratory Science, Faculty of Allied Medical Sciences,Iran

2. Department of Immunology, School of Medicine, Babol University of Medical Sciences, Babol,Iran

3. Uro-Oncology Research Center, Tehran University of Medical Sciences, Tehran,Iran

4. Department of Neuroscience, School of Advanced Technologies in Medicine, Iran University of Medical Sciences, Tehran,Iran

5. Uro-Oncology Research Center, Tehran University of Medical Sciences, Tehran, Iran

6. Department of Epidemiology, Faculty of Veterinary Medicine, University of Tehran, Tehran, Iran

Abstract

: Targeting inhibitory receptors on T cells in the tumor sites can promote effective anti-tumor immunity in bladder cancer. Unfortunately, the main dilemma is that a large number of patients remain refractory to CTLA-4, PD-1, and PD-L1 blockade therapies. T-cell immunoglobulin and mucin domain 3 (Tim-3) is an inhibitory receptor expressed on T cells and innate immune cells. Both in vivo and in vitro data from patients with advanced cancers support the role of Tim-3 inhibition in satisfactory anti-tumor immunity. In bladder cancer, the expression level of Tim-3 significantly increases with advanced pathological grade and T stage. Therefore, rationality implies that designing novel monoclonal antibodies reactive with Tim-3 alone or in combination with other checkpoint inhibitors may indicate a favorable response in bladder cancer. Here, we aimed to investigate the possibility of targeting Tim-3 as a novel anti-cancer treatment for bladder cancer.

Publisher

Bentham Science Publishers Ltd.

Subject

Immunology and Allergy,Endocrinology, Diabetes and Metabolism

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