The Immune Checkpoint BTLA in Oral Cancer: Expression Analysis and Its Correlation to Other Immune Modulators

Jutta Ries1,2, Leah Trumet2,3, Alina Hahn1

  • 1Department of Oral and Cranio-Maxillofacial Surgery, Friedrich-Alexander-Universität Erlangen-Nürnberg (FAU), 91054 Erlangen, Germany.

Insights

Oral squamous cell carcinoma (OSCC) shows increased expression of the immune checkpoint BTLA (B and T lymphocyte-associated antigen). BTLA, along with PD1 and CD96, may serve as biomarkers and targets for novel combination immunotherapies in OSCC.

Area of Science:

  • Immunology
  • Oncology
  • Biomarker Discovery

Background:

  • Oral squamous cell carcinoma (OSCC) exhibits an immunotolerant microenvironment, often driven by immune checkpoints (ICPs).
  • Current immune checkpoint inhibitors (ICIs) targeting the PD1/PD-L axis show limited response rates and acquired resistance, necessitating novel therapeutic strategies.
  • The B and T lymphocyte-associated antigen (BTLA) is identified as a novel negative immune checkpoint with potential as a biomarker and therapeutic target.

Purpose of the Study:

  • To investigate the expression levels of BTLA in OSCC tissues compared to normal oral mucosa (NOM).
  • To evaluate BTLA as a potential diagnostic biomarker and immunological target for OSCC treatment.
  • To analyze the correlation between BTLA expression and other immune checkpoints (PD1, PD-L1/2, CD96) to assess the utility of combination therapies.

Main Methods:

  • Quantitative analysis of BTLA (two isoforms), PD1, PD-L1/2, and CD96 expression using RT-qPCR in 102 OSCC tissues and 105 NOM tissues.
  • Immunohistochemistry (IHC) was employed to detect BTLA and CD96 protein expression.
  • Statistical analysis was performed to compare expression levels between groups and to determine correlations between checkpoints.

Main Results:

  • BTLA expression (both isoforms and protein) was significantly elevated in OSCC tissues compared to NOM (p < 0.003).
  • Expression of PD1, PD-L1, PD-L2, and CD96 was also significantly increased in OSCC tissues (p ≤ 0.001).
  • A strong positive correlation was observed between BTLA expression and the expression of PD1, PD-L1/2, and CD96 (p < 0.001; ρ ≥ 0.5).

Conclusions:

  • BTLA is significantly overexpressed in OSCC, indicating its role as a relevant local immune checkpoint.
  • BTLA represents a promising target for antibody-based immunotherapies in OSCC.
  • Combination therapies involving anti-BTLA antibodies, potentially with anti-PD1/PD-L1 and anti-CD96 agents, may enhance treatment efficacy in OSCC.

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