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  3. Supplementary Figure 5 from Engineering T Cells with a Tumor-Reactive Chimeric T-cell Receptor Reduces Exhaustion and Promotes Persistence to Elicit Enhanced Antitumor Responses
  1. Home
  2. Publications
  3. Supplementary Figure 5 from Engineering T Cells with a Tumor-Reactive Chimeric T-cell Receptor Reduces Exhaustion and Promotes Persistence to Elicit Enhanced Antitumor Responses

Supplementary Figure 5 from Engineering T Cells with a Tumor-Reactive Chimeric T-cell Receptor Reduces Exhaustion and Promotes Persistence to Elicit Enhanced Antitumor Responses

Authors:
  • JMJoey C. Magno
    Joey C. Magno
  • JGJitao Guo
    Jitao Guo
  • SHSpencer C. Hall
    Spencer C. Hall
  • JLJing Liu
    Jing Liu
  • GAGabriella K. Albert
    Gabriella K. Albert
  • JCJake D. Carter
    Jake D. Carter
  • ADAndres S. Davalos
    Andres S. Davalos
  • PCPhoebe Cao
    Phoebe Cao
  • ABAmandip Bangar
    Amandip Bangar
  • ZDZoe Drigot
    Zoe Drigot
  • HHHannah Hudson
    Hannah Hudson
  • TGTaylor Geluck
    Taylor Geluck

Open Access
Publisher website
Google Scholar
  • 1 June 2026
    • other
    • Published by American Association for Cancer Research (AACR)
    • DOI:10.1158/0008-5472.32530406
Abstract
The β:CD3ζ:MyD88 pMel-1 TCR augments pMel-1 T cell cytokine production but not cytotoxicity ability
Keywords
  • IMMUNOLOGY
  • T CELL EXHAUSTION
  • TUMOR ANTIGENS/NEOANTIGENS
  • TUMOR IMMUNOLOGY ANIMAL MODELS
  • TUMOR RESISTANCE TO IMMUNE RESPONSE
  • IMMUNOTHERAPY
  • CELLULAR IMMUNOTHERAPY
  • SKIN CANCERS
  • MELANOMA
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