Journal Article DKFZ-2023-02285

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CMTM6 shapes antitumor T cell response through modulating protein expression of CD58 and PD-L1.

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2023
Elsevier New York, NY

Cancer cell 41(10), 1817 - 1828.e9 () [10.1016/j.ccell.2023.08.008]
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Abstract: The dysregulated expression of immune checkpoint molecules enables cancer cells to evade immune destruction. While blockade of inhibitory immune checkpoints like PD-L1 forms the basis of current cancer immunotherapies, a deficiency in costimulatory signals can render these therapies futile. CD58, a costimulatory ligand, plays a crucial role in antitumor immune responses, but the mechanisms controlling its expression remain unclear. Using two systematic approaches, we reveal that CMTM6 positively regulates CD58 expression. Notably, CMTM6 interacts with both CD58 and PD-L1, maintaining the expression of these two immune checkpoint ligands with opposing functions. Functionally, the presence of CMTM6 and CD58 on tumor cells significantly affects T cell-tumor interactions and response to PD-L1-PD-1 blockade. Collectively, these findings provide fundamental insights into CD58 regulation, uncover a shared regulator of stimulatory and inhibitory immune checkpoints, and highlight the importance of tumor-intrinsic CMTM6 and CD58 expression in antitumor immune responses.

Classification:

Note: DKFZ-ZMBH Alliance / #EA:D250#LA:D250# / #DKFZ-MOST-Ca208#

Contributing Institute(s):
  1. NWG Krebs-Immunregulation (D250)
  2. A240 Molekulare Neurogenetik (A240)
  3. NWG Erworbene Immunität und Lymphome (D180)
  4. T-Zell-Metabolismus (D192)
Research Program(s):
  1. 314 - Immunologie und Krebs (POF4-314) (POF4-314)

Appears in the scientific report 2023
Database coverage:
Medline ; BIOSIS Previews ; Biological Abstracts ; Clarivate Analytics Master Journal List ; Current Contents - Clinical Medicine ; Current Contents - Life Sciences ; Ebsco Academic Search ; Essential Science Indicators ; IF >= 50 ; JCR ; SCOPUS ; Science Citation Index Expanded ; Web of Science Core Collection
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 Record created 2023-11-07, last modified 2025-11-19



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