J4 ›› 2010, Vol. 36 ›› Issue (5): 841-846.

• 基础研究 • 上一篇    下一篇

抗Peroxiredoxin Ⅰ 肺腺癌噬菌体抗体的筛选及其在荷瘤裸鼠体内的分布

 李淑杰1, 罗弋1, 庞华2, 李少林1, 樊春波1, 王洁2   

  1. 1. |重庆医科大学基础医学院放射医学教研室|重庆 400016;2. 重庆医科大学附属第一医院核医学科|重庆400016
  • 收稿日期:2010-04-13 出版日期:2010-09-28 发布日期:2010-09-28
  • 通讯作者: 李少林( Tel:023-68485060,E-mail:shaolinli202@sina.com) E-mail:shaolinli202@sina.com
  • 作者简介:李淑杰(1981-),女,辽宁省沈阳市人,医师,在读医学硕士,主要从事肿瘤放射治疗的研究。
  • 基金资助:

     国家自然科学基金青年基金资助课题(30700672) 

Screening and radioimmunoimaging of novel fully human phage display recombinant antibodies against lung adenocarcinoma cell line overexpressing Peroxiredoxin Ⅰ

LI Chu-Jie1, LUO Yi1, PANG Hua2, LI Shao-Lin1, FAN Chun-Bo1, WANG Jie2   

  1. 1. Department of Radiation Medicine,Chongqing Medical University,Chongqing 400016,China;2. Department of Nuclear Medicine,First Affiliated Hospital,Chongqing Medical University,Chongqing 400016,China
  • Received:2010-04-13 Online:2010-09-28 Published:2010-09-28

摘要:

目的:通过对已构建的肺腺癌相关人源单链抗体库进行筛选,得到抗过氧化物酶Peroxiredoxin Ⅰ (Prx Ⅰ)肺腺癌单链抗体,评价抗体在动物模型体内分布及靶向显像作用。方法:PCR法检测大肠杆菌TG1中单链抗体single-chain variable fragment (scFv) 基因插入率;凝胶电泳鉴定Sfi Ⅰ和Not Ⅰ双酶切质粒结果;以肺腺癌细胞株A549和在肺癌中高表达的抗氧化蛋白Prx Ⅰ为靶抗原,对抗体库进行富集筛选。阳性克隆用IPTG诱导表达并检测。放射性核素131I标记纯化抗体,进行荷瘤裸鼠体内分布及SPECT放射免疫显像研究。结果:scFv基因插入率为77%(23/30),双酶切鉴定证实目的条带。通过亲和筛选,肺腺癌单链抗体得到富集,收获率逐轮提高,第6轮是第1轮的180倍。选取10个克隆经ELISA法检测,其中6个克隆与A549细胞呈阳性反应,阳性率60%(6/10)。SDS-PAGE及ELISA检测证实得到人源抗Prx Ⅰ肺腺癌单链抗体。竞争ELISA显示抗〖JP3〗体能有效结合A549细胞。核素标记抗体的放射化学纯度为(95.6±3.7)%,比活度为(2.8±0.2) TBq/g体内分布研究显示抗体与肺腺癌组织有效结合。尾静脉注射48 h后,瘤/血和瘤/肌肉放射性比值均达最大值,分别为(4.06±0.13)和(5.17±0.97) %ID/g。SPECT示抗体与肿瘤有效结合。抗体注射后48 h的T/NT值(3.73±0.20)明显高于12 h(1.26±0.15)、24 h(2.18±0.16)和72 h(2.85±0.18)(均P<0.01)。结论:利用肺腺癌细胞A549和Prx Ⅰ为靶抗原,从噬菌体抗体库中筛选获得具有较高特异性的抗Prx Ⅰ肺腺癌单链抗体。在体内抗体能与肺腺癌组织特异性结合。

关键词: 噬菌体抗体库;单链抗体;Peroxiredoxin Ⅰ;放射免疫显像;腺瘤病,

Abstract:

Abstract:Objective
To sieve out the fully human,Peroxiredoxin Ⅰ (Prx Ⅰ) -specific single chain variable fragment (scFv) antibodies from the lung adenocarcinoma-related phage antibody library and analysis the biodistribution of the antibodies in vivo. Methods The insert ratio of scFv antibodies library was identified by polymerase chain reaction (PCR) and the products digested by Sfi Ⅰ/ Not Ⅰ were analyzed on 1% agarose gel. Panning against lung adenocarcinoma cell line A549 and Prx Ⅰ were performed three rounds,separately. The positive clones were chosen for soluble expression and analyzed by sodium dodecyl sulfate polyacrylamide gel electropheresis (SDS-PAGE),enzyme-linked immunosorbent assay (ELISA) and competition ELISA. The tumor-beared athymic mice were injected via the tail vein with purified 131I-labeled scFv. The biodistribution analysis and radioimmunoimaging were taken to evaluate the specificity and distribution of antibodies in vivo. Results The ratio of recombinant bacteria inserted with scFv was 77% (23/30) and the enzyme digest reaction showed the aim products on 1% agarose gel. From the first to the sixth round of panning,the obtained phages number increased 180 times. The positive reactions to A549 cells were detected in 6 of 10 clones. The positive ratio was 60% (6/10). The human scFv vs  against Prx Ⅰ of lung adenocarcinoma were confirmed by SDS-PAGE and ELISA. Competition ELISA showed significant,concentration-dependent affinity of scFv antibodies to A549 cells. The radiochemical purity of 131I-labeled scFv was (95.6±3.7)% and the specific activity was (2.8±0.2) TBq/g. The radiolocalization indexes (RI) of tumor/serum and tumor/muscle were gradually increased,reaching its peak (4.06±0.13 and 5.17±0.97,respectively) at 48 h postadministration. The radioactivity was aggregated in tumor locations and the tumor imaging was clearly observed by single photon emission computed tomography (SPECT) imaging. The T/NT value at 48 h (3.73±0.20) was significantly higher than those at 12 h (1.26±0.15),24 h (2.18±0.16) and 72 h (2.85±0.18) (all P<0.01). Conclusion The scFv fragments against Prx Ⅰ of lung adenocarcinoma are acquired by screening the phage antibody library successfully. The soluble scFv antibodies have bonding avidity specifically in vivo.

Key words: phage antibody library;single chain variable fragment;Peroxiredoxin Ⅰ;radioimmunoimaging;adenomatosis,pulmonary

中图分类号: 

  • Q782