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Preclinical support for tumor protein D52 as a cancer vaccine antigen

Journal

HUMAN VACCINES & IMMUNOTHERAPEUTICS
Volume 19, Issue 3, Pages -

Publisher

TAYLOR & FRANCIS INC
DOI: 10.1080/21645515.2023.2273699

Keywords

TPD52 (D52); mD52 (murine orthologue TPD52); hD52 (human orthologue TPD52); overexpressed tumor-self antigen; oncogenic; shared; universal; vaccine

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Overexpressed tumor-associated antigens (TAAs) include proteins found at increased levels in tumors. Tumor Protein D52 (TPD52) is an overexpressed TAA that plays a role in tumor transformation, proliferation, and metastasis. Preclinical studies have shown that vaccine-induced immunity against mD52 is effective against multiple cancers in murine models without inducing autoimmunity against healthy tissues and cells.
Overexpressed tumor-associated antigens (TAAs) are a large group that includes proteins found at increased levels in tumors compared to healthy cells. Universal tumor expression can be defined as overexpression in all cancers examined as has been shown for Tumor Protein D52. TPD52 is an over expressed TAA actively involved in transformation, leading to increased proliferation and metastasis. TPD52 overexpression has been demonstrated in many human adult and pediatric malignancies. The murine orthologue of TPD52 (mD52) parallels normal tissue expression patterns and known functions of human TPD52 (hD52). Here in we present our preclinical studies over the past 15 years which have demonstrated that vaccine induced immunity against mD52 is effective against multiple cancers in murine models, without inducing autoimmunity against healthy tissues and cells.

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