Evaluation of the sensitivity and specificity of GST-tagged recombinant antigens 2B2t, Ag5t and DIPOL in ELISA for the diagnosis and follow up of patients with cystic echinococcosis.


Journal

PLoS neglected tropical diseases
ISSN: 1935-2735
Titre abrégé: PLoS Negl Trop Dis
Pays: United States
ID NLM: 101291488

Informations de publication

Date de publication:
11 2020
Historique:
received: 12 12 2019
accepted: 14 10 2020
revised: 10 12 2020
pubmed: 1 12 2020
medline: 23 1 2021
entrez: 30 11 2020
Statut: epublish

Résumé

Cystic echinococcosis (CE) is a neglected zoonotic disease caused by Echinococcus granulosus sensu lato. Diagnosis and monitoring of CE rely primarily on imaging while serology is used as a confirmatory test. However, imaging is not always conclusive and currently available serological assays have suboptimal sensitivity and specificity, lack standardization, and are not useful for patients´ follow-up. Seroassays for CE are usually based on hydatid fluid (HF), a complex, variable antigenic mixture, and cross-reactivity exists especially with alveolar echinococcosis. Recombinant proteins based on immunogenic antigens most abundant in HF, such as AgB1, AgB2 and Ag5, have been used to overcome these limitations. None of them so far showed potential to replace HF; however, their performance have been largely tested on a limited number of samples, and comparison of different antigens using the same cohort has been rarely performed. The combination of several immunogenic epitopes in a single recombinant protein could enhance test sensitivity. For the diagnosis and follow-up of patients with CE, we compared the performance of the crude HF, previously described recombinant 2B2t antigen, and GST-tagged version of 2B2t, and novel designed recombinants (GST-Ag5t and the GST-DIPOL chimera containing AgB1, AgBB2 and Ag5 epitopes) by IgG-ELISA format. Samples belong to a retrospective cohort of 253 well-characterized patients with CE, previously described for the evaluation of the 2B2t antigen, 92 patients with alveolar echinococcosis, and 82 healthy donors. The reference standard for CE diagnosis was the presence of a CE lesion as diagnosed by ultrasonography. The highest sensitivity was obtained with HF [86.7%, 95% confidence interval (CI): 81.2-91.0], followed by GST-2B2t (70.0%, 95% CI: 63.1-76.2), 2B2t (65.5%, 95% CI: 58.5-72.0), GST-Ag5t (64.5%, 95% CI: 57.5-71.1) and GST-DIPOL (63.1%, 95% CI: 56.0-69.7). The GST-2B2t had the best specificity (95.8%, 95% CI: 88.3-99.1) and the lowest cross-reactivity (38.7%, 95% CI: 27.6-50.6). Good response to treatment also correlated to negative test results in the GST-2B2t ELISA. While none of the tested recombinant antigen appears suitable to replace HF for the diagnosis of CE, GST-2B2t should be further explored as a confirmation test, based on its high specificity and low cross-reactivity, and for the follow-up after treatment in those patients with positive serology for this antigen.

Identifiants

pubmed: 33253168
doi: 10.1371/journal.pntd.0008892
pii: PNTD-D-19-02022
pmc: PMC7728171
doi:

Substances chimiques

Antibodies, Helminth 0
Antigens, Helminth 0
Recombinant Proteins 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

e0008892

Déclaration de conflit d'intérêts

The authors have declared that no competing interests exist.

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Auteurs

Carlos Sánchez-Ovejero (C)

Sierrallana Hospital, Barrio de Ganzo s/n, Torrelavega, Spain.

Eylem Akdur (E)

Cukurova Univeristy, Department of Parasitology, Sarıçam/Adana, Turkey.

Raúl Manzano-Román (R)

Proteomic Unit, Center for Cancer Research, University of Salamanca, Campus Miguel de Unamuno, Salamanca.

Ana Hernández-González (A)

Instituto de Salud Carlos III, Centro Nacional de Microbiología, Majadahonda, Madrid, Spain.

María González-Sánchez (M)

Instituto de Recursos Naturales y Agrobiología de Salamanca (IRNASA-CSIC), Cordel de Merinas, Salamanca, Spain.

David Becerro-Recio (D)

Instituto de Recursos Naturales y Agrobiología de Salamanca (IRNASA-CSIC), Cordel de Merinas, Salamanca, Spain.

Javier González-Miguel (J)

Instituto de Recursos Naturales y Agrobiología de Salamanca (IRNASA-CSIC), Cordel de Merinas, Salamanca, Spain.

Okan Akhan (O)

Faculty of Medicine, Hacettepe University, Ankara, Turkey.

Carmen M Cretu (CM)

University of Medicine and Pharmacy, Colentina Clinical Hospital-Parasitology, Bucharest, Romania.

Kamenna Vutova (K)

Specialised Hospital of Infectious and Parasitic Diseases "Prof. Ivan Kirov", Department of Infectious, Parasitic and Tropical Diseases, Medical University, Sofia, Bulgaria.

Francesca Tamarozzi (F)

WHO Collaborating Centre for the epidemiology, detection and control of cystic and alveolar echinococcosis, Istituto Superiore di Sanità, Rome, Italy.

Mara Mariconti (M)

Department of Clinical Surgical Diagnostic and Paediatric Sciences, University of Pavia, Via Taramelli 5, Pavia, Italy.

Enrico Brunetti (E)

Department of Clinical Surgical Diagnostic and Paediatric Sciences, University of Pavia, and Division of Infectious and Tropical Diseases, San Matteo Hospital Foundation, Via Taramelli 5, Pavia, Italy.

Ambra Vola (A)

San Matteo Hospital Foundation, Via Taramelli 5, Pavia, Italy.

Massimo Fabiani (M)

Infectious Diseases Department, Istituto Superiore di Sanità, Rome, Italy.

Adriano Casulli (A)

WHO Collaborating Centre for the epidemiology, detection and control of cystic and alveolar echinococcosis, Istituto Superiore di Sanità, Rome, Italy.
European Reference Laboratory for Parasites (EURLP), Istituto Superiore di Sanità, Rome, Italy.

Mar Siles-Lucas (M)

Instituto de Recursos Naturales y Agrobiología de Salamanca (IRNASA-CSIC), Cordel de Merinas, Salamanca, Spain.

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Classifications MeSH