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The DOI matches its Crossref record; 2 of the 2 references it cites were found in a registry or an index.

The TNFRs OX40, 4-1BB, and CD40 as targets for cancer immunotherapy

Open access
Moran, Amy E, Kovacsovics-Bankowski, Magdalena, Weinberg, Andrew D·2013·Current Opinion in Immunology

Abstract

T cell-mediated rejection of tumors requires signals from the T cell receptor and co-stimulatory molecules to license effector functions of tumor-antigen specific T cells. There is also an array of immune suppressive mechanisms within the tumor microenvironment that can suppress anti-tumor immunity. The use of monoclonal antibodies to overcome this suppression and/or enhance tumor-antigen specific T cell responses has shown promise in clinical trials. In particular, targeting co-stimulatory members of the tumor necrosis factor receptor (TNFR) family with agonist Abs enhances T cell function, which has led to encouraging therapeutic results in cancer-bearing hosts. These encouraging data establish TNFRs as important targets for enhancing tumor-specific immune responses in mice and man. This review will focus on agonists that target the TNFRs OX40, 4-1BB, and CD40.

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Metadata

Authors
Moran, A. E., Kovacsovics-Bankowski, M., & Weinberg, A. D.
Venue
Current Opinion in Immunology
Publisher
Elsevier BV
Published
2013-04
Volume
25
Issue
2
Pages
230-237
ISSN
0952-7915 (ISSN-L)
OpenAlex
W2012826189
Cited by
162
References
2
FWCI
1.07
Type
journal article
Language
en
Open access
green

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CoChat. (2026). Citation check: The TNFRs OX40, 4-1BB, and CD40 as targets for cancer immunotherapy. https://app.cochat.ai/papers/10.1016/j.coi.2013.01.004
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Moran, A. E., Kovacsovics-Bankowski, M., & Weinberg, A. D. (2013). The TNFRs OX40, 4-1BB, and CD40 as targets for cancer immunotherapy. Current Opinion in Immunology. https://doi.org/10.1016/j.coi.2013.01.004

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