4-1BBL-B7-H3基因对免疫重建重症联合免疫缺陷荷瘤鼠的抑瘤作用

目的通过建立人免疫重建重症联合免疫缺陷(SCID)荷瘤鼠嵌合模型来探讨4-1BBL—B7-H3基因在非特异性抗肿瘤免疫中的作用。方法将40只SCID鼠随机分为5组,A组(对照组)行免疫重建加注射Tca8113细胞;B组(Ad4-1BBL-B7-H3组)行免疫重建加注射含有人4-1BBL-B7-H3基因腺病毒转染的Tca8113细胞;C组(空载组)行免疫重建加注射含有空载体腺病毒转染的Tca8113细胞;D组(非免疫重建组)不给予小鼠免疫重建,注射Tca8113细胞;E组(非肿瘤组)行免疫重建加注射PBS。每周定期测量肿瘤体积;酶联免疫吸附法检测人IgG蛋白含量;流式细胞仪检测外周血中人CD3^...

Full description

Saved in:
Bibliographic Details
Published in华西口腔医学杂志 Vol. 32; no. 2; pp. 190 - 195
Main Author 邬腊梅 杨宏宇 罗娟 苏铭扬
Format Journal Article
LanguageChinese
Published 北京大学深圳医院口腔颌面外科,深圳 518036 2014
汕头大学医学院,汕头 515041%北京大学深圳医院口腔颌面外科,深圳,518036
Subjects
Online AccessGet full text
ISSN1000-1182
DOI10.7518/hxkq.2014.02.019

Cover

More Information
Summary:目的通过建立人免疫重建重症联合免疫缺陷(SCID)荷瘤鼠嵌合模型来探讨4-1BBL—B7-H3基因在非特异性抗肿瘤免疫中的作用。方法将40只SCID鼠随机分为5组,A组(对照组)行免疫重建加注射Tca8113细胞;B组(Ad4-1BBL-B7-H3组)行免疫重建加注射含有人4-1BBL-B7-H3基因腺病毒转染的Tca8113细胞;C组(空载组)行免疫重建加注射含有空载体腺病毒转染的Tca8113细胞;D组(非免疫重建组)不给予小鼠免疫重建,注射Tca8113细胞;E组(非肿瘤组)行免疫重建加注射PBS。每周定期测量肿瘤体积;酶联免疫吸附法检测人IgG蛋白含量;流式细胞仪检测外周血中人CD3^+、CD56^+淋巴细胞比例;免疫组织化学法观察自然杀伤细胞2族成员D(NKG2D)和Toll样受体2(TLR2)在肿瘤中的表达;逆转录聚合酶链反应(RT-PCR)检测4-1BBL-B7-H3 mRNA的表达,实时定量聚合酶链反应(RT-qPCR)检测主要组织相容性复合体1类相关分子(M1C)A、B及TLR2的表达。结果1)B组小鼠肿瘤体积最小(P〈0.05);2)A、B、C、E组小鼠外周血中检测到人IgG、CD3^+、CD56^+淋巴细胞,B组淋巴细胞比例高于A、C和E组(P〈0.05);3)B组NKG2D和TLR2的表达较其余各组明显增强;4)人4-1BBL-B7-H3基因在B组小鼠肿瘤中稳定表达;5)B组M1CA、M1CB和TLR2的表达高于A、C、D组(P〈0.05)。结论4-1BBL—B7-H3基因在肿瘤组织中的高表达能成功诱导人CD3^+、CD56^+细胞增殖,直接或间接活化TLR2,上调NKG2D及其配体M1CA、M1CB的表达,从而产生有效的抗肿瘤免疫应答。
Bibliography:51-1169/R
4-1BBL-B7-H3 gene; severe combined immunodeficient mice; oral squamous cell carcinoma line; an- titumor immunity
Objective The non-specific antitumor immunity effect of4-1BBL-B7-H3 gene was investigated by establishing an oral squamous cell carcinoma human peripheral blood lymphocyte-severe combined immunodeficient (SCID) mice chimeric model. Methods Forty mice were randomly divided into five groups. All groups, except the non-immune reconstitution group (group D), had reconstructed human partial immune system. The control group (group A) was injected with Tca8113 cells. The Ad4-1BBL-B7-H3 group (group B) was injected with Tca8113 cells transfected by adenovirus containing 4-1BBL-B7-H3 gene. The empty vector group (group C) was injected with Tca8113 cells transfected by adenovirus containing an empty vector. The non-immune reconstitution group (group D) was injected with Tca8113 cells. The non-tumor group (group E) was injected with PBS. The tumor volumes in each group were measured weekly. Human IgG
ISSN:1000-1182
DOI:10.7518/hxkq.2014.02.019