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Temporal evolution of the humoral antibody response after Ebola virus disease in Guinea: a 60-month observational prospective cohort study

Authors :
Mamadou Saliou Kalifa Diallo, MSc
Ahidjo Ayouba, PhD
Alpha Kabinet Keita, PhD
Guillaume Thaurignac, MSc
Mamadou Saliou Sow, MD
Cécé Kpamou, MSc
Thierno Alimou Barry, MD
Philippe Msellati, PhD
Jean-François Etard, PhD
Martine Peeters, PhD
René Ecochard, ProfPhD
Eric Delaporte, ProfPhD
Abdoulaye Toure, PhD
Ahidjo Ayouba
Sylvain Baize
Kaba Bangoura
Alimou Barry
Moumié Barry
Mamoudou Cissé
Mohammed Cissé
Eric Delaporte
Jean-François Delfraissy
Christelle Delmas
Alice Desclaux
Saliou Bella Diallo
Mamadou Safiatou Diallo
Mariama Sadjo Diallo
Jean-François Étard
Cécile Etienne
Ousmane Faye
Ibrahima Fofana
Bruno Granouillac
Suzanne Izard
Djenaba Kassé
Alpha Kabinet Keita
Sakoba Keita
Lamine Koivogui
Cécé Kpamou
Christine Lacarabaratz
Sandrine Leroy
Claire Levy Marchal
Yves Levy
N'Fally Magassouba
Laura March
Vincent Mendiboure
Philippe Msellati
Harissatou Niane
Martine Peeters
Yves-Marie Pers
Hervé Raoul
Sidi Lamine Sacko
Ibrahima Savané
Mamadou Saliou Sow
Bernard Taverne
Abdoulaye Touré
Fodé Amara Traoré
Falaye Traoré
Yamoussa Youla
Yazdan Yazdanpanah
Source :
The Lancet Microbe, Vol 2, Iss 12, Pp e676-e684 (2021)
Publication Year :
2021
Publisher :
Elsevier, 2021.

Abstract

Summary: Background: Insufficient long-term data are available on antibody kinetics in survivors of Ebola virus disease (EVD). Likewise, few studies, with very small sample sizes, have investigated cross-reactions between Ebolavirus spp. In this study, we aimed to assess the humoral antibody response and its determinants in survivors of EVD and assess cross-reactivity of antibodies between diverse Ebolavirus spp. Methods: In this observational, prospective cohort study, we collected blood samples from patients from three recruitment sites in Guinea included in the Postebogui study, and we assessed IgG antibody binding to recombinant glycoprotein, nucleoprotein, and 40-kDa viral protein (VP40) of Zaire (EBOV), Bundibugyo (BDBV), and Sudan (SUDV) Ebolaviruses. Participants from the PostEbogui study, from whom we had at least one blood sample that could be tested for the presence of antibodies, were eligible for this analysis. Patients in the PostEbogui study were assessed clinically at inclusion, 1 month and 3 months later, and subsequently every 6 months for up to 60 months after discharge from the Ebola treatment centre. We explored predictors of glycoprotein, nucleoprotein, and VP40 antibody concentrations through a linear mixed model. A logistic mixed model was done to estimate the probability of seropositivity and associated determinants. We assessed cross-reactivity by use of hierarchical cluster analysis. Findings: Of the 802 patients included in the Postebogui study, 687 were included in our analyses. 310 (45%) patients were men and 377 (55%) were women, with an overall median age at the time of the first blood sample of 27·3 years (IQR 19·5–38·2). We observed an overall significant decrease over time of EBOV antibodies, with antibodies against nucleoproteins decreasing more rapidly. At 60 months after discharge from the Ebola treatment centre, the probability of having antibodies against glycoproteins was 76·2% (95% CI 67·2–83·3), against nucleoproteins was 59·4% (46·3–71·3), and against VP40 was 60·9% (51·4–69·8). Persistence of EBOV RNA in semen was associated with higher concentrations of IgG antibodies against nucleoprotein EBOV antigens. Individually, we observed in some survivors an antibody wax-and-wane pattern. The proportion of cross-reactions was highest between glycoproteins from Kissidougou and Mayinga EBOV strains (94·5%, 95% CI 92·5–96·1), followed by EBOV VP40 and BDBV VP40 (88·3%, 85·7–90·6), and EBOV VP40 and SUDV VP40 (83·3%, 80·3–86·1). Interpretation: The probability for survivors of EVD to have antibodies against one or more EBOV antigens remained high, although approximately 25% of survivors had undetectable antibodies, which could have implications, such as a possible decreasing population immunity, for future Ebola outbreaks in the same region. Funding: Reacting–Institut National de la Santé et de la Recherche Médicale, Institut de Recherche pour le Developpement, and Montpellier Université d'Excellence.

Details

Language :
English
ISSN :
26665247
Volume :
2
Issue :
12
Database :
Directory of Open Access Journals
Journal :
The Lancet Microbe
Publication Type :
Academic Journal
Accession number :
edsdoj.708b31ffbff24a4484bb0cc539035b8c
Document Type :
article
Full Text :
https://doi.org/10.1016/S2666-5247(21)00170-1