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Cited by 1,104

The DOI matches its Crossref record; 38 of the 38 references it cites were found in a registry or an index.

Cytokine release syndrome and associated neurotoxicity in cancer immunotherapy

Open access
Morris, Emma C., Neelapu, Sattva S., Giavridis, Theodoros, Sadelain, Michel·2022·Nature Reviews Immunology

Abstract

A paradigm shift has recently occurred in the field of cancer therapeutics. Traditional anticancer agents, such as chemotherapy, radiotherapy and small-molecule drugs targeting specific signalling pathways, have been joined by cellular immunotherapies based on T cell engineering. The rapid adoption of novel, patient-specific cellular therapies builds on scientific developments in tumour immunology, genetic engineering and cell manufacturing, best illustrated by the curative potential of chimeric antigen receptor (CAR) T cell therapy targeting CD19-expressing malignancies. However, the clinical benefit observed in many patients may come at a cost. In up to one-third of patients, significant toxicities occur that are directly associated with the induction of powerful immune effector responses. The most frequently observed immune-mediated toxicities are cytokine release syndrome and immune effector cell-associated neurotoxicity syndrome. This Review discusses our current understanding of their pathophysiology and clinical features, as well as the development of novel therapeutics for their prevention and/or management. This Review discusses our current understanding of the pathophysiological mechanisms of cytokine release syndrome and immune effector cell-associated neurotoxicity syndrome associated with chimeric antigen receptor (CAR) T cell therapies, and how this might be used for the prevention or management of these toxicities.

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Crossref · 10.1038/s41577-021-00547-6

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Metadata

Authors
Morris, E. C., Neelapu, S. S., Giavridis, T., & Sadelain, M.
Venue
Nature Reviews Immunology
Published
2021-05-17
Volume
22
Issue
2
Pages
85-96
ISSN
  • 1474-1733 (ISSN-L)
  • 1474-1741
OpenAlex
W3162374648
Cited by
1,104
References
38
FWCI
21.70
Type
journal article
Language
en
Open access
bronze

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