Antibodies Against Epstein-Barr Virus Glycoprotein gp42 for the Diagnosis of Nasopharyngeal Carcinoma

التفاصيل البيبلوغرافية
العنوان: Antibodies Against Epstein-Barr Virus Glycoprotein gp42 for the Diagnosis of Nasopharyngeal Carcinoma
المؤلفون: Wan Li Liu, Mu Sheng Zeng, Yong Du, Xiaoming Huang, Qian Zhong, Hua Zhang, Lin Quan Tang, Rui Chen Li, Yan Li, Qiu Yao Zeng
المصدر: Clinical Laboratory. 62
بيانات النشر: Clinical Laboratory Publications, 2016.
سنة النشر: 2016
مصطلحات موضوعية: Adult, Male, 0301 basic medicine, Immunoglobulin A, Nasopharyngeal neoplasm, Antibodies, Viral, medicine.disease_cause, General Biochemistry, Genetics and Molecular Biology, Virus, Viral Proteins, 03 medical and health sciences, Antigen, Glycoprotein complex, otorhinolaryngologic diseases, medicine, Humans, Glycoproteins, Nasopharyngeal Carcinoma, biology, business.industry, Carcinoma, Nasopharyngeal Neoplasms, Middle Aged, medicine.disease, Epstein–Barr virus, Virology, stomatognathic diseases, Logistic Models, 030104 developmental biology, ROC Curve, Nasopharyngeal carcinoma, Immunology, biology.protein, Capsid Proteins, Female, Antibody, business, Biomarkers
الوصف: BACKGROUND Assessment of immunoglobulin A (IgA) antibody responses to Epstein-Barr virus (EBV) antigen is important for the early diagnosis of nasopharyngeal carcinoma (NPC). EBV glycoprotein gp42 has been shown to play an essential role in membrane fusion with B cells. The aim of the present study was to assess whether the antibodies to EBV glycoprotein gp42 in serum could be a novel marker for diagnosis of NPC. METHODS EBV glycoprotein gp42 expressed in the recombinant baculovirus system was used in an enzyme-linked immunosorbent assay (ELISA) to detect antibodies to gp42 in serum. The blood samples were obtained from 406 participants (n = 208 patients with NPC and 198 healthy controls). Receiver operating characteristics (ROC) was used to calculate diagnostic accuracy. RESULTS The ROC curves showed that IgA-gp42 ELISA had a sensitivity of 76.4%, specificity of 78.3% and an area under the curve (AUC) of 0.856 (95% CI, 0.82 - 0.891) to diagnose NPC. Furthermore, gp42 maintained diag- nostic capacity in NPC patients who were IgA-viral capsid antigen (VCA) negative (87.5%, 64.1% and 0.844 [95% CI, 0.776 - 0.912]). Combining gp42 and VCA improved the diagnostic capacity compared with the individual tests (89.9%, 94.4% and 0.973 [95% CI, 0.959 - 0.9871). CONCLUSIONS The EBV glycoprotein complex gp42 acts as a novel biomarker for diagnosis of NPC and improves identification of patients with VCA-negative NPC.
تدمد: 1433-6510
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::27e999c84155d1833d01c4813fbd3af7Test
https://doi.org/10.7754/clin.lab.2015.150723Test
رقم الانضمام: edsair.doi.dedup.....27e999c84155d1833d01c4813fbd3af7
قاعدة البيانات: OpenAIRE