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CCR Translations

A Tumor-Localized Approach to Bypass Anti-4-1BB Immuno-Toxicity

Tina Tianjiao Su, Xiaobin Gao and Jun Wang
Tina Tianjiao Su
1Department of Immunobiology, Yale University School of Medicine, New Haven, Connecticut.
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Xiaobin Gao
2Department of Pathology, Yale University School of Medicine, New Haven, Connecticut.
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Jun Wang
1Department of Immunobiology, Yale University School of Medicine, New Haven, Connecticut.
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  • ORCID record for Jun Wang
  • For correspondence: jwang133@gmail.com
DOI: 10.1158/1078-0432.CCR-19-1799 Published October 2019
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Abstract

4-1BB (CD137) is an important costimulatory molecule upregulated on antigen-experienced T cells, however, clinical development of 4-1BB agonists has stalled because of significant liver immuno-toxicity. Using rational protein engineering, a next-generation anticalin-antibody–based therapy achieved localized 4-1BB activation triggered by tumor-expressed antigen, helping to revitalize this pathway in immuno-oncology.

See related article by Hinner et al., p. 5878

Footnotes

  • Clin Cancer Res 2019;25:5732–4

  • Received June 21, 2019.
  • Revision received July 8, 2019.
  • Accepted July 26, 2019.
  • Published first July 31, 2019.
  • ©2019 American Association for Cancer Research.
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Clinical Cancer Research: 25 (19)
October 2019
Volume 25, Issue 19
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A Tumor-Localized Approach to Bypass Anti-4-1BB Immuno-Toxicity
Tina Tianjiao Su, Xiaobin Gao and Jun Wang
Clin Cancer Res October 1 2019 (25) (19) 5732-5734; DOI: 10.1158/1078-0432.CCR-19-1799

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A Tumor-Localized Approach to Bypass Anti-4-1BB Immuno-Toxicity
Tina Tianjiao Su, Xiaobin Gao and Jun Wang
Clin Cancer Res October 1 2019 (25) (19) 5732-5734; DOI: 10.1158/1078-0432.CCR-19-1799
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Clinical Cancer Research
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