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Cited by 284

The DOI matches its Crossref record; 138 of the 138 references it cites were found in a registry or an index.

An early history of T cell-mediated cytotoxicity

Open access
Golstein, Pierre, Griffiths, Gillian M.·2018·Nature Reviews Immunology

Abstract

After 60 years of intense fundamental research into T cell-mediated cytotoxicity, we have gained a detailed knowledge of the cells involved, specific recognition mechanisms and post-recognition perforin–granzyme-based and FAS-based molecular mechanisms. What could not be anticipated at the outset was how discovery of the mechanisms regulating the activation and function of cytotoxic T cells would lead to new developments in cancer immunotherapy. Given the profound recent interest in therapeutic manipulation of cytotoxic T cell responses, it is an opportune time to look back on the early history of the field. This Timeline describes how the early findings occurred and eventually led to current therapeutic applications. This Timeline looks back at the past 60 years of fundamental research into the mechanisms of T cell-mediated cytotoxicity, which has culminated in recent interest in the therapeutic manipulation of cytotoxic T cell responses for cancer immunotherapy.

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Metadata

Authors
Golstein, P., & Griffiths, G. M.
Venue
Nature Reviews Immunology
Published
2018-04-16
Volume
18
Issue
8
Pages
527-535
ISSN
  • 1474-1733 (ISSN-L)
  • 1474-1741
OpenAlex
W2799753096
Cited by
284
References
138
FWCI
2.17
Type
journal article
Language
en
Open access
green

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CoChat. (2026). Citation check: An early history of T cell-mediated cytotoxicity. https://app.cochat.ai/papers/10.1038/s41577-018-0009-3
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Golstein, P., & Griffiths, G. M. (2018). An early history of T cell-mediated cytotoxicity. Nature Reviews Immunology. https://doi.org/10.1038/s41577-018-0009-3

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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.