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Cited by 879

The DOI matches its Crossref record; 19 of the 19 references it cites were found in a registry or an index.

Therapeutic T cell engineering

Open access
Sadelain, Michel, Rivière, Isabelle, Riddell, Stanley·2017·Nature

Abstract

Genetically engineered T cells are powerful new medicines, offering hope for curative responses in patients with cancer. Chimaeric antigen receptors (CARs) are a class of synthetic receptors that reprogram lymphocyte specificity and function. CARs targeting CD19 have demonstrated remarkable potency in B cell malignancies. Engineered T cells are applicable in principle to many cancers, pending further progress to identify suitable target antigens, overcome immunosuppressive tumour microenvironments, reduce toxicities, and prevent antigen escape. Advances in the selection of optimal T cells, genetic engineering, and cell manufacturing are poised to broaden T-cell-based therapies and foster new applications in infectious diseases and autoimmunity.

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Crossref · 10.1038/nature22395

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Metadata

Authors
Sadelain, M., Rivière, I., & Riddell, S.
Venue
Nature
Published
2017-05-25
Volume
545
Issue
7655
Pages
423-431
ISSN
  • 0028-0836 (ISSN-L)
  • 1476-4687
OpenAlex
W2619886251
Cited by
879
References
19
FWCI
33.71
Type
journal article
Language
en
Open access
green

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CoChat. (2026). Citation check: Therapeutic T cell engineering. https://app.cochat.ai/papers/10.1038/nature22395
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Sadelain, M., Rivière, I., & Riddell, S. (2017). Therapeutic T cell engineering. Nature. https://doi.org/10.1038/nature22395

Data sources

Bibliographic data: Semantic Scholar, OpenAlex, Crossref.

Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).

Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.