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异体鳞状细胞肿瘤树突状细胞融合杂交细胞的免疫治疗。

Immunotherapy using allogeneic squamous cell tumor-dendritic cell fusion hybrids.

机构信息

Division of Otolaryngology-Head and Neck Surgery, Duke University Medical Center, Durham, North Carolina, USA.

出版信息

Head Neck. 2010 Sep;32(9):1209-16. doi: 10.1002/hed.21323.

Abstract

BACKGROUND

Tumor-associated antigens (TAAs) are known to be immunotherapy targets; thus tumor-sharing TAA may be used as a fusion hybrid partner to confer protection against subsequent tumor challenge.

METHODS

The squamous cell carcinomas (SCCs), SCCVII and B4B8, were used in C3H/HEN mice: SCCVII (H-2(k)) is syngeneic, B4B8 (H-2(d)) is allogeneic. Experiments using tumor alone included hyperimmunization schedule, subdermal and intranodal routes. Mice were challenged 2 weeks later. Fusion hybrids were created from both SCC tumor cell lines and syngeneic dendritic cells (DCs). These were delivered intranodally for immunization, and mice were challenged with tumor 2 weeks later.

RESULTS

Only syngeneic tumor given subdermally was able to protect after tumor challenge 2 weeks later. Hyperimmunization schedule did not alter these findings. However, fusion hybrid immunization from both allogeneic and syngeneic SCCs conferred protection after tumor challenge.

CONCLUSIONS

Allogeneic tumor-DC fusion hybrids targeting TAA can protect against subsequent tumor challenge.

摘要

背景

肿瘤相关抗原(TAAs)是已知的免疫治疗靶点;因此,肿瘤共享 TAA 可被用作融合杂交伙伴,以提供对随后的肿瘤挑战的保护。

方法

使用 C3H/HEN 小鼠中的鳞状细胞癌(SCC)SCCVII 和 B4B8:SCCVII(H-2(k))是同基因的,B4B8(H-2(d))是同种异体的。单独使用肿瘤的实验包括超免疫方案、皮下和淋巴结内途径。两周后对小鼠进行挑战。融合杂种由两种 SCC 肿瘤细胞系和同源树突状细胞(DC)创建。将这些通过淋巴结内途径进行免疫接种,两周后用肿瘤对小鼠进行挑战。

结果

只有皮下给予同基因肿瘤才能在两周后的肿瘤挑战后提供保护。超免疫方案并未改变这些发现。然而,来自同种异体和同基因 SCC 的融合杂交免疫接种在肿瘤挑战后提供了保护。

结论

针对 TAA 的同种异体肿瘤-DC 融合杂交体可以提供对随后的肿瘤挑战的保护。

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