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Detection of Cystic Fibrosis Serological Biomarkers Using a T7 Phage Display Library.


ABSTRACT: Cystic fibrosis (CF) is an autosomal recessive disorder affecting the cystic fibrosis transmembrane conductance regulator (CFTR). CF is characterized by repeated lung infections leading to respiratory failure. Using a high-throughput method, we developed a T7 phage display cDNA library derived from mRNA isolated from bronchoalveolar lavage (BAL) cells and leukocytes of sarcoidosis patients. This library was biopanned to obtain 1070 potential antigens. A microarray platform was constructed and immunoscreened with sera from healthy (n?=?49), lung cancer (LC) (n?=?31) and CF (n?=?31) subjects. We built 1,000 naïve Bayes models on the training sets. We selected the top 20 frequently significant clones ranked with student t-test discriminating CF antigens from healthy controls and LC at a False Discovery Rate (FDR)?

SUBMITTER: Talwar H 

PROVIDER: S-EPMC5735098 | biostudies-literature | 2017 Dec

REPOSITORIES: biostudies-literature

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Detection of Cystic Fibrosis Serological Biomarkers Using a T7 Phage Display Library.

Talwar Harvinder H   Hanoudi Samer Najeeb SN   Geamanu Andreea A   Kissner Dana D   Draghici Sorin S   Samavati Lobelia L  

Scientific reports 20171218 1


Cystic fibrosis (CF) is an autosomal recessive disorder affecting the cystic fibrosis transmembrane conductance regulator (CFTR). CF is characterized by repeated lung infections leading to respiratory failure. Using a high-throughput method, we developed a T7 phage display cDNA library derived from mRNA isolated from bronchoalveolar lavage (BAL) cells and leukocytes of sarcoidosis patients. This library was biopanned to obtain 1070 potential antigens. A microarray platform was constructed and im  ...[more]

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