Use and specificity of breast cancer antigen/milk protein BA46 for generating anti-self-cytotoxic T lymphocytes by recombinant adeno-associated virus-based gene loading of dendritic cells

被引:22
作者
Liu, Y
Chiriva-Internati, M
You, CX
Luo, RC
You, H
Prasad, CK
Grizzi, F
Cobos, E
Klimberg, VS
Kay, H
Mehta, JL
Hermonat, PL
机构
[1] Univ Arkansas Med Sci, Dept Obstet & Gynecol, Little Rock, AR 72205 USA
[2] Univ Arkansas Med Sci, Dept Internal Med, Little Rock, AR 72205 USA
[3] Texas Tech Univ, Dept Microbiol & Immunol, Lubbock, TX 79430 USA
[4] Nanfang Hosp, Dept Oncol, Guangzhou, Peoples R China
[5] Inst Clin Human, Sci Direct, Milan, Italy
关键词
adeno-associated virus; dendritic cell; BA46; breast cancer; cytotoxic T lymphocyte; immunology;
D O I
10.1038/sj.cgt.7700785
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
Antigen-targeted immunotherapy is an emerging treatment for breast cancer. However, useful breast cancer antigens are only found in a subset of cancer patients. BA46, also known as lactadherin, is a membrane-associated glycoprotein that is expressed in most breast cancer cells but not in general hematopoietic cell populations. Moreover, it is much more difficult to generate CTLs against self-antigens. We wished to determine if the use of recombinant adeno-associated virus (rAAV) type 2 vectors for gene-loading of dendritic cells (DCs) could generate rapid, effective cytotoxic T lymphocytes (CTLs) against BA46. We were able to demonstrate that AAV/BA46/Neo-loading of DCs resulted in: (1) BA46 expression in DCs, (2) chromosomal integration of the AAV/BA46/Neo vector within DCs, (3) strong, rapid BA46-specific, MHC class I-restricted CTLs in only 1 week, (4) T-cell populations with significant interferon-gamma (IFN-gamma) expression but low IL-4 expression, (5) high CD80 and CD86 expression in DCs, and (6) high CD8:CD4 and CD8:CD56 T cell ratios. These data suggest that rAAV-loading of DCs may be useful for immunotherapeutic protocols against self-antigens in addition to viral antigens and that the BA46 antigen is potentially appropriate for cell-mediated immunotherapeutic protocols addressing ductal breast cancer.
引用
收藏
页码:304 / 312
页数:9
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