Cited by 3,207CAR-T cell therapy researchImmunotherapy and Immune ResponsesCancer Immunotherapy and Biomarkers

Car t cell immunotherapy for human cancer

June, Carl H., O’Connor, Roddy S., Kawalekar, Omkar U., Ghassemi, Saba, Milone, Michael C.·2018·Science

Abstract

Adoptive T cell transfer (ACT) is a new area of transfusion medicine involving the infusion of lymphocytes to mediate antitumor, antiviral, or anti-inflammatory effects. The field has rapidly advanced from a promising form of immuno-oncology in preclinical models to the recent commercial approvals of chimeric antigen receptor (CAR) T cells to treat leukemia and lymphoma. This Review describes opportunities and challenges for entering mainstream oncology that presently face the CAR T field, with a focus on the challenges that have emerged over the past several years.

Integrity signals

Registry

Crossref · 10.1126/science.aar6711

Cites

68 of 68 references verified0 citation errors · 0 not checkable

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  • CAR-T cytokine storm is triggered by the activation of CAR-T cells that recognize cognate antigens expressed by tumor cells, leading to the release of cytokines and chemokines, including IL-6, in parallel with the release of pro-inflammatory cytokines and chemokines by monocytes and/or macrophages.

    “It is triggered by the activation of CAR-T cells that recognize cognate antigens expressed by tumor cells, leading to the release of cytokines and chemokines, including IL-6 in parallel with the release of pro-inflammatory cytokines and chemokines by monocytes and/or macrophages (351, 352).”

    From IL-6 in inflammation, autoimmunity and cancer (2021) · cites this paper as [351]

  • Reinstructing cytotoxic T cells to identify specific antigens on cancer cells using either a modified T-cell receptor or a chimeric antigen receptor (CAR) has been successfully used for specific cancer therapies.

    “Reinstructing cytotoxic T cells to identify specific antigens on cancer cells using either a modified T-cell receptor or a chimeric antigen receptor (CAR) has been successfully used for specific cancer therapies [156].”

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Authors
June, C. H., O’Connor, R. S., Kawalekar, O. U., Ghassemi, S., & Milone, M. C.
Affiliations
University of Pennsylvania (US)
Corresponding author
June, Carl H.
Venue
Science
Published
2018-03-23
Volume
359
Issue
6382
Pages
1361-1365
ISSN
  • 0036-8075 (ISSN-L)
  • 1095-9203
OpenAlex
W2792588868
Cited by
3,207
References
67
Citations by year
2026: 377 · 2025: 447 · 2024: 410 · 2023: 447 · 2022: 363 · 2021: 423 · 2020: 358 · 2019: 275 · 2018: 104
FWCI
30.38
Type
journal article
Language
en
Open access
closed
Locations
  • Science (publishedVersion)
  • PubMed (publishedVersion)
Funders
National Cancer Institute (RO1CA226983, 5R01CA165206, 1P01CA214278)
Topics
  • Health Sciences › Medicine › Oncology › CAR-T cell therapy research
  • Life Sciences › Immunology and Microbiology › Immunology › Immunotherapy and Immune Responses
  • Health Sciences › Medicine › Oncology › Cancer Immunotherapy and Biomarkers
Keywords
CAR T-cell therapy, chimeric antigen receptor, adoptive T cell therapy, cancer immunotherapy, leukemia, lymphoma, clinical translation, commercialization
MeSH terms
Clinical Trials as Topic, Genetic Engineering, Humans, Neoplasms, Receptors, Antigen, T-Cell, T-Lymphocytes, Immunotherapy, Adoptive, Mutant Chimeric Proteins, Cell Engineering, Cell- and Tissue-Based Therapy

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