Adoptive immunotherapy for cancer: harnessing the T cell response
Open accessAbstract
Immunotherapy based on the adoptive transfer of naturally occurring or gene-engineered T cells can mediate tumour regression in patients with metastatic cancer. Here, we discuss progress in the use of adoptively transferred T cells, focusing on how they can mediate tumour cell eradication. Recent advances include more accurate targeting of antigens expressed by tumours and the associated vasculature, and the successful use of gene engineering to re-target T cells before their transfer into the patient. We also describe how new research has helped to identify the particular T cell subsets that can most effectively promote tumour eradication.
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Several proteins with potential roles in modifying immunotherapy response were strongly down-regulated exclusively in co-culture, including CXCR4, c-KIT, and KDR.
“there was strong down-regulation of several proteins with potential roles in modifying the response to immunotherapies exclusively in co-culture conditions, including CXCR4 (CD184), c-KIT (CD117) and KDR (CD309)23,24”
From Multimodal pooled Perturb-CITE-seq screens in patient models define mechanisms of cancer immune evasion (2021) · cites this paper as [24]
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“It exploit endogenous immune surveillance mechanisms to target and eliminate malignant cells, providing durable clinical responses with favorable toxicity profiles compared to conventional chemotherapeutic regimens ( 4 – 6 ).”
- Authors
- Restifo, N. P., Dudley, M. E., & Rosenberg, S. A.
- Affiliations
- National Institutes of Health (US)
- Corresponding author
- Restifo, Nicholas P.
- Rosenberg, Steven A.
- Venue
- Nature Reviews Immunology
- Published
- 2012-03-22
- Volume
- 12
- Issue
- 4
- Pages
- 269-281
- ISSN
- 1474-1733 (ISSN-L)
- 1474-1741
- PMC
- PMC6292222
- OpenAlex
- W2043904711
- Cited by
- 1,688
- References
- 166
- Citations by year
- 2026: 34 · 2025: 81 · 2024: 94 · 2023: 104 · 2022: 88 · 2021: 121 · 2020: 106 · 2019: 112 · 2018: 131 · 2017: 125 · 2016: 164 · 2015: 187 · 2014: 141 · 2013: 157 · 2012: 40
- FWCI
- 15.48
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Licence
- www.springer.com/tdm (tdm)
- Locations
- Nature reviews. Immunology (publishedVersion)
- PubMed (publishedVersion)
- Europe PMC (PubMed Central) (acceptedVersion)
- PubMed Central (acceptedVersion)
- Funders
- National Institutes of Health
- National Cancer Institute (Z01BC010984)
- Topics
- Life Sciences › Immunology and Microbiology › Immunology › Immunotherapy and Immune Responses
- Health Sciences › Medicine › Oncology › CAR-T cell therapy research
- Life Sciences › Immunology and Microbiology › Immunology › T-cell and B-cell Immunology
- Keywords
- adoptive T cell therapy, antitumor immunity, tumor-infiltrating T cells, T cell subsets, metastatic cancer, tumor regression
- MeSH terms
- Animals, Genetic Engineering, Humans, Neoplasms, T-Lymphocytes, Immunotherapy, Adoptive
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