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Detection of Circulating VZV-Glycoprotein E-Specific Antibodies by Chemiluminescent Immunoassay (CLIA) for Varicella–Zoster Diagnosis

Varicella and herpes zoster are mild symptoms-associated diseases caused by varicella–zoster virus (VZV). They often cause severe complications (disseminated zoster), leading to death when diagnoses and treatment are delayed. However, most commercial VZV diagnostic tests have low sensitivity, and th...

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Autores principales: Kombe Kombe, Arnaud John, Xie, Jiajia, Zahid, Ayesha, Ma, Huan, Xu, Guangtao, Deng, Yiyu, Nsole Biteghe, Fleury Augustin, Mohammed, Ahmed, Dan, Zhao, Yang, Yunru, Feng, Chen, Zeng, Weihong, Chang, Ruixue, Zhu, Keyuan, Zhang, Siping, Jin, Tengchuan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8778750/
https://www.ncbi.nlm.nih.gov/pubmed/35056014
http://dx.doi.org/10.3390/pathogens11010066
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author Kombe Kombe, Arnaud John
Xie, Jiajia
Zahid, Ayesha
Ma, Huan
Xu, Guangtao
Deng, Yiyu
Nsole Biteghe, Fleury Augustin
Mohammed, Ahmed
Dan, Zhao
Yang, Yunru
Feng, Chen
Zeng, Weihong
Chang, Ruixue
Zhu, Keyuan
Zhang, Siping
Jin, Tengchuan
author_facet Kombe Kombe, Arnaud John
Xie, Jiajia
Zahid, Ayesha
Ma, Huan
Xu, Guangtao
Deng, Yiyu
Nsole Biteghe, Fleury Augustin
Mohammed, Ahmed
Dan, Zhao
Yang, Yunru
Feng, Chen
Zeng, Weihong
Chang, Ruixue
Zhu, Keyuan
Zhang, Siping
Jin, Tengchuan
author_sort Kombe Kombe, Arnaud John
collection PubMed
description Varicella and herpes zoster are mild symptoms-associated diseases caused by varicella–zoster virus (VZV). They often cause severe complications (disseminated zoster), leading to death when diagnoses and treatment are delayed. However, most commercial VZV diagnostic tests have low sensitivity, and the most sensitive tests are unevenly available worldwide. Here, we developed and validated a highly sensitive VZV diagnostic kit based on the chemiluminescent immunoassay (CLIA) approach. VZV-glycoprotein E (gE) was used to develop a CLIA diagnostic approach for detecting VZV-specific IgA, IgG, and IgM. The kit was tested with 62 blood samples from 29 VZV-patients classified by standard ELISA into true-positive and equivocal groups and 453 blood samples from VZV-negative individuals. The diagnostic accuracy of the CLIA kit was evaluated by receiver-operating characteristic (ROC) analysis. The relationships of immunoglobulin-isotype levels between the two groups and with patient age ranges were analyzed. Overall, the developed CLIA-based diagnostic kit demonstrated the detection of VZV-specific immunoglobulin titers depending on sample dilution. From the ELISA-based true-positive patient samples, the diagnostic approach showed sensitivities of 95.2%, 95.2%, and 97.6% and specificities of 98.0%, 100%, and 98.9% for the detection of VZV-gE-specific IgA, IgG, and IgM, respectively. Combining IgM to IgG and IgA detection improved diagnostic accuracy. Comparative analyses on diagnosing patients with equivocal results displaying very low immunoglobulin titers revealed that the CLIA-based diagnostic approach is overall more sensitive than ELISA. In the presence of typical VZV symptoms, CLIA-based detection of high titer of IgM and low titer of IgA/IgG suggested the equivocal patients experienced primary VZV infection. Furthermore, while no difference in IgA/IgG level was found regarding patient age, IgM level was significantly higher in young adults. The CLIA approach-based detection kit for diagnosing VZV-gE-specific IgA, IgG, and IgM is simple, suitable for high-throughput routine analysis situations, and provides enhanced specificity compared to ELISA.
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spelling pubmed-87787502022-01-22 Detection of Circulating VZV-Glycoprotein E-Specific Antibodies by Chemiluminescent Immunoassay (CLIA) for Varicella–Zoster Diagnosis Kombe Kombe, Arnaud John Xie, Jiajia Zahid, Ayesha Ma, Huan Xu, Guangtao Deng, Yiyu Nsole Biteghe, Fleury Augustin Mohammed, Ahmed Dan, Zhao Yang, Yunru Feng, Chen Zeng, Weihong Chang, Ruixue Zhu, Keyuan Zhang, Siping Jin, Tengchuan Pathogens Article Varicella and herpes zoster are mild symptoms-associated diseases caused by varicella–zoster virus (VZV). They often cause severe complications (disseminated zoster), leading to death when diagnoses and treatment are delayed. However, most commercial VZV diagnostic tests have low sensitivity, and the most sensitive tests are unevenly available worldwide. Here, we developed and validated a highly sensitive VZV diagnostic kit based on the chemiluminescent immunoassay (CLIA) approach. VZV-glycoprotein E (gE) was used to develop a CLIA diagnostic approach for detecting VZV-specific IgA, IgG, and IgM. The kit was tested with 62 blood samples from 29 VZV-patients classified by standard ELISA into true-positive and equivocal groups and 453 blood samples from VZV-negative individuals. The diagnostic accuracy of the CLIA kit was evaluated by receiver-operating characteristic (ROC) analysis. The relationships of immunoglobulin-isotype levels between the two groups and with patient age ranges were analyzed. Overall, the developed CLIA-based diagnostic kit demonstrated the detection of VZV-specific immunoglobulin titers depending on sample dilution. From the ELISA-based true-positive patient samples, the diagnostic approach showed sensitivities of 95.2%, 95.2%, and 97.6% and specificities of 98.0%, 100%, and 98.9% for the detection of VZV-gE-specific IgA, IgG, and IgM, respectively. Combining IgM to IgG and IgA detection improved diagnostic accuracy. Comparative analyses on diagnosing patients with equivocal results displaying very low immunoglobulin titers revealed that the CLIA-based diagnostic approach is overall more sensitive than ELISA. In the presence of typical VZV symptoms, CLIA-based detection of high titer of IgM and low titer of IgA/IgG suggested the equivocal patients experienced primary VZV infection. Furthermore, while no difference in IgA/IgG level was found regarding patient age, IgM level was significantly higher in young adults. The CLIA approach-based detection kit for diagnosing VZV-gE-specific IgA, IgG, and IgM is simple, suitable for high-throughput routine analysis situations, and provides enhanced specificity compared to ELISA. MDPI 2022-01-05 /pmc/articles/PMC8778750/ /pubmed/35056014 http://dx.doi.org/10.3390/pathogens11010066 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Kombe Kombe, Arnaud John
Xie, Jiajia
Zahid, Ayesha
Ma, Huan
Xu, Guangtao
Deng, Yiyu
Nsole Biteghe, Fleury Augustin
Mohammed, Ahmed
Dan, Zhao
Yang, Yunru
Feng, Chen
Zeng, Weihong
Chang, Ruixue
Zhu, Keyuan
Zhang, Siping
Jin, Tengchuan
Detection of Circulating VZV-Glycoprotein E-Specific Antibodies by Chemiluminescent Immunoassay (CLIA) for Varicella–Zoster Diagnosis
title Detection of Circulating VZV-Glycoprotein E-Specific Antibodies by Chemiluminescent Immunoassay (CLIA) for Varicella–Zoster Diagnosis
title_full Detection of Circulating VZV-Glycoprotein E-Specific Antibodies by Chemiluminescent Immunoassay (CLIA) for Varicella–Zoster Diagnosis
title_fullStr Detection of Circulating VZV-Glycoprotein E-Specific Antibodies by Chemiluminescent Immunoassay (CLIA) for Varicella–Zoster Diagnosis
title_full_unstemmed Detection of Circulating VZV-Glycoprotein E-Specific Antibodies by Chemiluminescent Immunoassay (CLIA) for Varicella–Zoster Diagnosis
title_short Detection of Circulating VZV-Glycoprotein E-Specific Antibodies by Chemiluminescent Immunoassay (CLIA) for Varicella–Zoster Diagnosis
title_sort detection of circulating vzv-glycoprotein e-specific antibodies by chemiluminescent immunoassay (clia) for varicella–zoster diagnosis
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8778750/
https://www.ncbi.nlm.nih.gov/pubmed/35056014
http://dx.doi.org/10.3390/pathogens11010066
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