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(Reference retrieved automatically from Web of Science through information on FAPESP grant and its corresponding number as mentioned in the publication by the authors.)

Boosting Antitumor Response by Costimulatory Strategies Driven to 4-1BB and OX40 T-cell Receptors

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Author(s):
Mascarelli, Daniele E. [1, 2] ; Rosa, Rhubia S. M. [1, 2] ; Toscaro, Jessica M. [1, 3] ; Semionatto, Isadora F. [1, 2] ; Ruas, Luciana P. [1] ; Fogagnolo, Carolinne T. [1, 4] ; Lima, Gabriel C. [1, 5] ; Bajgelman, Marcio C. [1, 2, 3]
Total Authors: 8
Affiliation:
[1] Brazilian Ctr Res Energy & Mat CNPEM, Brazilian Biosci Natl Lab LNBio, Campinas, SP - Brazil
[2] Univ Estadual Campinas, Fac Pharmaceut Sci, Campinas, SP - Brazil
[3] Univ Campinas UNICAMP, Med Sch, Campinas, SP - Brazil
[4] Univ Sao Paulo, Med Sch Ribeirao Preto FMRP, Ribeirao Preto - Brazil
[5] Univ Sao Paulo, Pro Rectory Grad, Sao Paulo - Brazil
Total Affiliations: 5
Document type: Review article
Source: FRONTIERS IN CELL AND DEVELOPMENTAL BIOLOGY; v. 9, JUN 30 2021.
Web of Science Citations: 0
Abstract

Immunotherapy explores several strategies to enhance the host immune system's ability to detect and eliminate cancer cells. The use of antibodies that block immunological checkpoints, such as anti-programed death 1/programed death 1 ligand and cytotoxic T-lymphocyte-associated protein 4, is widely recognized to generate a long-lasting antitumor immune response in several types of cancer. Evidence indicates that the elimination of tumors by T cells is the key for tumor control. It is well known that costimulatory and coinhibitory pathways are critical regulators in the activation of T cells. Besides blocking checkpoints inhibitors, the agonistic signaling on costimulatory molecules also plays an important role in T-cell activation and antitumor response. Therefore, molecules driven to costimulatory pathways constitute promising targets in cancer therapy. The costimulation of tumor necrosis factor superfamily receptors on lymphocytes surface may transduce signals that control the survival, proliferation, differentiation, and effector functions of these immune cells. Among the members of the tumor necrosis factor receptor superfamily, there are 4-1BB and OX40. Several clinical studies have been carried out targeting these molecules, with agonist monoclonal antibodies, and preclinical studies exploring their ligands and other experimental approaches. In this review, we discuss functional aspects of 4-1BB and OX40 costimulation, as well as the progress of its application in immunotherapies. (AU)

FAPESP's process: 19/13573-5 - Development of chimeric aptamers for inactivation of human regulatory T cells
Grantee:Carolinne Tomarchio Fogagnolo
Support Opportunities: Scholarships in Brazil - Scientific Initiation
FAPESP's process: 19/04458-8 - Development of biological nanoparticles to boost antitumor immunity
Grantee:Marcio Chaim Bajgelman
Support Opportunities: Regular Research Grants
FAPESP's process: 18/16449-0 - Engineering targeted multifunctional nanoparticles with antitumor activity
Grantee:Isadora Ferraz Semionatto
Support Opportunities: Scholarships in Brazil - Doctorate