Salamone Frank N, Gleich Lyon L, Li Ya-Qin, Stambrook Peter J
Departments of Otolaryngology-Head and Neck Surgery, The University of Cincinnati Medical Center, Cincinnati, Ohio, U.S.A.
Laryngoscope. 2004 Apr;114(4):612-5. doi: 10.1097/00005537-200404000-00004.
OBJECTIVES/HYPOTHESIS: Alloantigen gene therapy with the genes for the Class I major histocompatibility complex (MHC) HLA-B7 and beta 2-microglobulin in HLA-B7-negative patients has potential efficacy in the treatment of head and neck cancer, although the mechanism of response is unclear. Whether tumor regression is due to a response to HLA-B7 in HLA-B7-negative patients (i.e., due to "foreign" antigen) or simply to MHC overexpression is unknown. Therefore, a mouse model was used to compare tumor growth following syngeneic MHC transfection to alloantigenic MHC transfection. The importance of the beta 2-microglobulin gene was also evaluated.
Prospective animal study.
The head and neck cancer cell line SCC-VII that grows in immunocompetent C3H mice, which are MHC haplotype H2-K, was used. Stable transfections were made with H2-K, H2-K, and beta 2-microglobulin in the SCC-VII cells. To test the importance of MHC "foreignness," mice were injected with SCC-VII cells, SCC-VII plus H2-K plus beta 2-microglobulin transfected cells, and SCC-VII plus H2-K plus beta 2-microglobulin transfected cells. To evaluate beta 2-microglobulin, mice were injected with SCC-VII cells, SCC-VII plus H2-K plus beta 2-microglobulin transfected cells, SCC-VII plusH2-K transfected cells, and SCC-VII plus beta 2-microglobulin transfected cells. Tumor growth in all groups was compared statistically.
Major histocompatibility complex foreignness was a part of the antitumor response. Foreign MHC routinely abrogated tumor growth, whereas syngeneic MHC only slowed tumor growth. beta 2-microglobulin aided the MHC tumor inhibition but did not inhibit tumor without the MHC.
The antitumor response was greater when the MHC gene used was foreign. beta 2-microglobulin increased the efficacy of MHC gene therapy. Both of these findings are important when designing clinical trials of immunologically based gene therapies for head and neck cancer.
目的/假设:在HLA - B7阴性患者中,采用I类主要组织相容性复合体(MHC)HLA - B7和β2 - 微球蛋白基因进行同种异体抗原基因治疗对头颈部癌可能具有潜在疗效,尽管其反应机制尚不清楚。肿瘤消退是由于HLA - B7阴性患者对HLA - B7的反应(即由于“外来”抗原)还是仅仅由于MHC过表达尚不清楚。因此,使用小鼠模型比较同基因MHC转染与同种异体抗原MHC转染后的肿瘤生长情况。还评估了β2 - 微球蛋白基因的重要性。
前瞻性动物研究。
使用在具有免疫活性的C3H小鼠(MHC单倍型为H2 - K)中生长的头颈部癌细胞系SCC - VII。在SCC - VII细胞中进行H2 - K、H2 - K和β2 - 微球蛋白的稳定转染。为了测试MHC“异源性”的重要性,给小鼠注射SCC - VII细胞、SCC - VII加H2 - K加β2 - 微球蛋白转染细胞,以及SCC - VII加H2 - K加β2 - 微球蛋白转染细胞。为了评估β2 - 微球蛋白,给小鼠注射SCC - VII细胞、SCC - VII加H2 - K加β2 - 微球蛋白转染细胞、SCC - VII加H2 - K转染细胞,以及SCC - VII加β2 - 微球蛋白转染细胞。对所有组的肿瘤生长进行统计学比较。
主要组织相容性复合体的异源性是抗肿瘤反应的一部分。外来的MHC通常能消除肿瘤生长,而同基因MHC仅能减缓肿瘤生长。β2 - 微球蛋白有助于MHC对肿瘤的抑制作用,但在没有MHC时不能抑制肿瘤。
当使用的MHC基因是外来的时,抗肿瘤反应更强。β2 - 微球蛋白提高了MHC基因治疗的疗效。在设计基于免疫的头颈部癌基因治疗临床试验时,这两个发现都很重要。