Construction of a Human Immune Library from Gallbladder Cancer Patients for the Single-Chain Fragment Variable (scFv) Antibody Selection against Claudin 18.2 via Phage Display

被引:0
|
作者
Effer, Brian [1 ]
Ulloa, Daniel [2 ]
Dappolonnio, Camila [2 ]
Munoz, Francisca [2 ]
Iturrieta-Gonzalez, Isabel [1 ,3 ]
Cotes, Loraine [4 ]
Rojas, Claudio [5 ,6 ]
Leal, Pamela [1 ,7 ]
机构
[1] Univ La Frontera, Ctr Excellence Translat Med CEMT & Sci & Technol B, Temuco 4811230, Chile
[2] Univ La Frontera, Fac Ciencias Agr & Medioambiente, Carrera Biotecnol, Temuco 4811230, Chile
[3] Univ La Frontera, Med Fac, Dept Preclin Sci, Temuco 4810296, Chile
[4] Univ Magdalena, Fac Ingn, Carrera Ingn Pesquera, Carrera 32 2208 Sect San Pedro Alejandrino, Santa Marta 470001, Colombia
[5] Univ La Frontera, Programa Doctorado Ciencias Med, Temuco 4811230, Chile
[6] Univ La Frontera, Ctr Estudios Morfol & Quirurg, Temuco 4811230, Chile
[7] Univ La Frontera, Fac Agr & Forestry Sci, Dept Agr Sci & Nat Resources, Temuco 4810296, Chile
关键词
immune library; phage display; monoclonal antibody; gallbladder cancer; claudin; 18.2; TARGET; RECOMBINATION; NAIVE;
D O I
10.3390/antib13010020
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Gallbladder cancer (GBC) is a very aggressive malignant neoplasm of the biliary tract with a poor prognosis. There are no specific therapies for the treatment of GBC or early diagnosis tools; for this reason, the development of strategies and technologies that facilitate or allow an early diagnosis of GBC continues to be decisive. Phage display is a robust technique used for the production of monoclonal antibodies (mAbs) involving (1) the generation of gene libraries, (2) the screening and selection of isoforms related to an immobilized antigen, and (3) the in vitro maturation of the affinity of the antibody for the antigen. This research aimed to construct a human immune library from PBMCs of GBC patients and the isolation of scFv-phage clones with specificity against the larger extracellular loop belonging to claudin 18.2, which is an important biomarker overexpressed in GBC as well as gastric cancer. The immune-library-denominated GALLBLA1 was constructed from seven GBC patients and has a diversity of 6.12 x 10(10) pfu mL(-1). After three rounds of panning, we were able to identify clones with specificity against claudin 18.2. GALLBLA1 can contribute to the selection, isolation, and recombinant production of new human mAbs candidates for the treatment of gastrointestinal cancers.
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页数:15
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