Literature DB >> 31758539

Cancer Immunotherapy Targeting Co-signal Molecules.

Masao Nakajima1, Koji Tamada2.   

Abstract

Great success of immune checkpoint blockade represented by anti-PD-1 monoclonal antibodies (mAbs) has changed a landscape of cancer immunotherapy. There is no doubt about an importance of co-signal molecules as one of the most promising targets in anti-cancer drugs. However, it should be noted that the proportion of patients who have objective and durable responses to immune checkpoint blockade remains less than 30% in majority of cancers. Thus, in addition to refine the usage of existing drugs for checkpoint blockade, identification and characterization of novel checkpoint molecules other than CTLA-4 and PD-1 is a highly anticipated research subject. In addition, agonists of stimulatory co-signal molecules have a potential to further improve anti-tumor effects, rendering them attractive in research and drug development. In this chapter, functions of co-signal molecules in anti-tumor immunity in terms of pre-clinical animal models as well as clinical trials are described.

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Keywords:  Agonistic antibody; Immune checkpoint blockade; Inhibitory co-signals; Stimulatory co-signals; T cell exhaustion

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Year:  2019        PMID: 31758539     DOI: 10.1007/978-981-32-9717-3_11

Source DB:  PubMed          Journal:  Adv Exp Med Biol        ISSN: 0065-2598            Impact factor:   2.622


  1 in total

1.  Editorial: Strategies for Modulating T Cell Responses in Autoimmunity and Infection.

Authors:  María Fernanda Pascutti; Gustavo Javier Martinez; Maria Florencia Quiroga
Journal:  Front Immunol       Date:  2020-02-20       Impact factor: 7.561

  1 in total

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