Combination cancer immunotherapy targeting PD-1 and GITR can rescue CD8 + T cell dysfunction and maintain memory phenotype
Abstract
Synergistic CD8 + T cell activation by antibodies to PD-1 and GITR in cancer immunotherapy depends on the CD226 costimulatory pathway.
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A series of preclinical studies showed that co-stimulatory molecule agonists improved α-PD-1/PD-L1 efficacy.
“A series of preclinical studies showed that co-stimulatory molecule agonists improved α-PD-1/PD-L1 efficacy [170–176].”
From Combination strategies with PD-1/PD-L1 blockade: current advances and future directions (2022) · cites this paper as [175]
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References 51 · Cited by 167
- Authors
- Wang, B., Zhang, W., Jankovic, V., Golubov, J., Poon, P., Oswald, E. M., Gurer, C., Wei, J., Ramos, I., Wu, Q., Waite, J., Ni, M., Adler, C., Wei, Y., Macdonald, L., Rowlands, T., Brydges, S., Siao, J., Poueymirou, W., MacDonald, D., Yancopoulos, G. D., Sleeman, M. A., Murphy, A. J., & Skokos, D.
- Affiliations
- Regeneron (United States) (US)
- Regeneron Pharmaceuticals,Tarrytown, New York, NY 10591, USA.
- Corresponding author
- Wang, Bei
- Zhang, Wen
- Skokos, Dimitris
- ORCID
- Venue
- Science Immunology
- Published
- 2018-11-30
- Volume
- 3
- Issue
- 29
- ISSN
- 2470-9468 (ISSN-L)
- OpenAlex
- W2899058237
- Cited by
- 167
- References
- 51
- Citations by year
- 2026: 8 · 2025: 13 · 2024: 19 · 2023: 25 · 2022: 19 · 2021: 32 · 2020: 34 · 2019: 15 · 2018: 2
- FWCI
- 7.84
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Science Immunology (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Health Sciences › Medicine › Oncology › Cancer Immunotherapy and Biomarkers
- Life Sciences › Immunology and Microbiology › Immunology › T-cell and B-cell Immunology
- Life Sciences › Immunology and Microbiology › Immunology › Immunotherapy and Immune Responses
- Keywords
- PD-1, GITR, cancer immunotherapy, CD8+ T cell dysfunction, memory T cells, CD226, TIGIT, antitumor immunity
- MeSH terms
- T Lineage-Specific Activation Antigen 1, Animals, Antigens, Differentiation, T-Lymphocyte, Female, Immunologic Memory, Immunotherapy, Mice, Inbred BALB C, Mice, Inbred C57BL, Neoplasms, Phenotype, Mice, Knockout, CD8-Positive T-Lymphocytes, Mice, Glucocorticoid-Induced TNFR-Related Protein, Programmed Cell Death 1 Receptor
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