Preclinical support for tumor protein D52 as a cancer vaccine antigen

被引:0
|
作者
Bright, Robert K. [1 ,2 ,3 ,4 ]
机构
[1] Texas Tech Univ Hlth Sci Ctr, Dept Immunol & Mol Microbiol, Sch Med, Lubbock, TX 79430 USA
[2] Texas Tech Univ Hlth Sci Ctr, Canc Ctr, Lubbock, TX 79430 USA
[3] Texas Tech Univ Hlth Sci Ctr, Dept Immunol & Mol Microbiol, Sch Med, 3601 4th St, STOP 6591, Lubbock, TX 79430 USA
[4] Texas Tech Univ Hlth Sci Ctr, Canc Ctr, 3601 4th St, STOP 6591, Lubbock, TX 79430 USA
关键词
TPD52 (D52); mD52 (murine orthologue TPD52); hD52 (human orthologue TPD52); overexpressed tumor-self antigen; oncogenic; shared; universal; vaccine; DIFFERENTIAL GENE-EXPRESSION; REACTIVE T-CELLS; PHASE-II TRIAL; BREAST-CANCER; PROSTATE-CANCER; PEPTIDE VACCINATION; COPY NUMBER; TPD52; GENE; TELOMERASE; TARGET;
D O I
10.1080/21645515.2023.2273699
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
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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页数:11
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