Transgenic B7-H3 therapy induces tumor-specific immune response in human oral squamous cell cancer: an in vitro study

Hong Y Yang1, Mei Chu, Li W Zheng

  • 1Department of Oral and Maxillofacial Surgery, Shenzhen Hospital, Peking University, Shenzhen, China. hyyang192@hotmail.com

Abstract

Insights

Genetically modified oral squamous cell cancer cells expressing B7-H3 can enhance anti-tumor immunity. This novel cancer vaccine strategy boosts T cell proliferation, interferon-gamma (IFN-γ) production, and cytotoxic activity against tumors.

Area of Science:

  • Immunology
  • Oncology
  • Molecular Biology

Background:

  • Tumors can evade immune detection by lacking essential costimulatory signals for T cell activation.
  • Oral squamous cell carcinoma (OSCC) presents a significant challenge due to immune evasion mechanisms.

Purpose of the Study:

  • To develop a tumor cell-based cancer vaccine using genetically modified OSCC cells.
  • To enhance anti-tumor immune responses by introducing the human B7-H3 gene into OSCC cells.

Main Methods:

  • The human B7-H3 gene was isolated from T lymphocytes.
  • Oral squamous cell cancer (OSCC) cell line Tca8113 was transfected with the B7-H3 gene or a mock vector to create a tumor cell vaccine (TCV-hB7-H3) and a control.
  • T cell responses, including proliferation, IFN-γ expression, and cytotoxicity, were measured after stimulation with the vaccine or control.

Main Results:

  • Tca8113 cells engineered to express human B7-H3 significantly improved T cell proliferation.
  • Enhanced interferon-gamma (IFN-γ) expression was observed in T cells stimulated with the B7-H3 modified cells.
  • Increased T cell cytotoxicity against tumor cells was demonstrated.

Conclusions:

  • Genetically modified OSCC cells expressing B7-H3 effectively enhance the induction of tumor-specific immune responses.
  • This approach holds promise for developing novel cancer vaccines against OSCC.

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