The DOI matches its Crossref record; 2 of the 2 references it cites were found in a registry or an index.
Treg Cells Survive and Thrive in Inhospitable Environments
Open accessAbstract
Immune responses are dangerous by nature and require regulation to prevent inflammatory and/or autoimmune sequelae and allow healing. CD4+Foxp3+ T cells (Treg cells) play a crucial role in this process, and in this edition of Cell Metabolism, Angelin et al. (2017) describe how these cells are metabolically adapted to the job.
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The majority of patients do not respond to checkpoint therapies as a result of heightened immunosuppression in the tumor microenvironment or inadequate non-self antigenic load within the tumor.
“the majority of patients do not respond as a result of heightened immunosuppression in the tumor microenvironment or inadequate non-self antigenic load within the tumor”
From LXR/ApoE Activation Restricts Innate Immune Suppression in Cancer (2018) · cites this paper as Grzes et al., 2017
No passage from our copy matched the claim. Searches for checkpoint-therapy nonresponse, tumor immunosuppression, and non-self antigenic load also returned no passages, so the attributed explanation cannot be verified from this copy. (LLM, conf=0.68)
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A Special Population of Regulatory T Cells Potentiates Muscle Repair
Burzyn, D., Kuswanto, W., Kolodin, D., Shadrach, J. L., Cerletti, M., Jang, Y., Sefik, E., Tan, T. G., Wagers, A. J., Benoist, C., et al. (2013) · Cell · doi:10.1016/j.cell.2013.10.054 · Cited by 1,234 · cited 1×
“…and function in tissues with limited glucose concentrations or high lactate concentrations is reinforced by other studies where Treg cells have been shown to play a crucial role in the repair of renal ischemia-reperfusion injury (Gandolfo et al., 2009) or muscle damage (Burzyn et al., 2013).”
BackgroundScharping, N. E., Menk, A. V., Moreci, R. S., Whetstone, R. D., Dadey, R. E., Watkins, S. C., Ferris, R. L., & Delgoffe, G. M. (2016) · Immunity · doi:10.1016/j.immuni.2016.07.009 · Cited by 848
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Research works printed but not linked: 8
- Angelin, 2017, Cell Metab., 25, 1282, 10.1016/j.cmet.2016.12.018 · DOI
- De Rosa, 2015, Nat. Immunol., 16, 1174, 10.1038/ni.3269 · DOI
- Gandolfo, 2009, Kidney Int., 76, 717, 10.1038/ki.2009.259 · DOI
- Gerriets, 2016, Nat. Immunol., 17, 1459, 10.1038/ni.3577 · DOI
- Howie, 2017, JCI Insight, 2, e89160, 10.1172/jci.insight.89160 · DOI
- Michalek, 2011, J. Immunol., 186, 3299, 10.4049/jimmunol.1003613 · DOI · Paper page
- Preston, 2015, EMBO J., 34, 2008, 10.15252/embj.201490252 · DOI
- Wang, 2011, Immunity, 35, 871, 10.1016/j.immuni.2011.09.021 · DOI · Paper page
Cited by
Sorted by citations
LXR/ApoE Activation Restricts Innate Immune Suppression in Cancer
Tavazoie, M. F., Pollack, I., Tanqueco, R., Ostendorf, B. N., Reis, B. S., Gonsalves, F. C., Kurth, I., Andreu-Agullo, C., Derbyshire, M. L., Posada, J., et al. (2018) · Cell · doi:10.1016/j.cell.2017.12.026 · Cited by 476
“Although the clinical responses to these therapies in multiple common cancer types can be remarkably prolonged, the majority of patients do not respond as a result of heightened immunosuppression in the tumor microenvironment or inadequate non-self-antigenic load within the tumor (Grzes et al., 2017; Sharma et al., 20…”
Metadata
- Authors
- Grzes, K. M., Field, C. S., & Pearce, E. J.
- Affiliations
- Max Planck Institute of Immunobiology and Epigenetics (DE)
- University of Freiburg (DE)
- Corresponding author
- Pearce, Edward J.
- Venue
- Cell Metabolism
- Publisher
- Elsevier BV
- Published
- 2017-06
- Volume
- 25
- Issue
- 6
- Pages
- 1213-1215
- ISSN
- 1550-4131 (ISSN-L)
- OpenAlex
- W2623945663
- Cited by
- 16
- References
- 2
- Citations by year
- 2026: 2 · 2025: 2 · 2024: 1 · 2023: 1 · 2022: 4 · 2021: 2 · 2020: 1 · 2018: 3
- FWCI
- 0.50
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Licence
- Locations
- Cell Metabolism (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Life Sciences › Immunology and Microbiology › Immunology › T-cell and B-cell Immunology
- Life Sciences › Immunology and Microbiology › Immunology › Psoriasis: Treatment and Pathogenesis
- Health Sciences › Medicine › Oncology › Cancer Immunotherapy and Biomarkers
- Keywords
- regulatory T cells, CD4+ Foxp3+ T cells, metabolic adaptation, immune regulation, inflammation, autoimmunity
- MeSH terms
- Glucose, CD4-Positive T-Lymphocytes, Lactic Acid, T-Lymphocytes, Regulatory, Forkhead Transcription Factors
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