Jul 2026· International Journal of Infectious Diseases· Vol 171, pp.
109008
· 0 citations· 17 references
Medicine
Abstract
Background
Enterovirus D68 (EV-D68) causes acute respiratory illnesses and has also implicated in acute flaccid myelitis. Neutralizing antibodies (NtAbs) represent key components of the adaptative immunity. However, the dynamics of EV-D68 NtAbs in adults remain poorly characterized. We evaluated EV-D68 NtAb levels in retail workers in Canada during the COVID-19 pandemic.
Methods
NtAbs were measured in paired serum samples (N=194), from retail workers (≥ 18 years) enrolled in a prospective SARS-CoV-2 cohort at the Centre Hospitalier Universitaire de Québec-Université Laval, in Quebec City. Samples collected 48 weeks apart, between June 2021 to October 2022, were tested by microneutralization assays.
Results
EV-D68 NtAb seroprevalence was high (>85%). Over the 48-weeks follow-up, the vast majority of patients (97%) had stable or reduced titers with a statistically significant overall reduction in geometric mean titer (GMT), p<0.001. Furthermore, a small subset of participants 6/194 (3%) showed a marked increase of titers (≥4-fold) with the GMT rising from 21 (10-57) at the first visit to 593 (57-7241) at follow-up visit.
Conclusions
Neutralizing antibody titers declined in most participants over 48 weeks. However, six individuals had significantly increased NtAb titers during the study period, which is consistent with potential ongoing EV-D68 or other enterovirus circulation in Quebec following sequential non-pharmaceutical interventions lift. This is in line with documented EV-D68 resurgence in the United States at the same period. Our work complements pediatric data on EV-D68 immunity and highlights the serological surveillance importance in adults.
The identification of a novel A2–B3 recombinant lineage provides evidence of ongoing viral evolution through recombination, a mechanism that may alter transmissibility, virulence, or immune responses, and underscores the importance of whole-genome surveillance for accurate viral characterization.
Amary Fall, C. Morris, Omar Elgazayerly et al.· Microbiology spectrum· 0 citations
BACKGROUND
Enterovirus D68 (EV-D68) causes cyclical outbreaks worldwide. Though EV-D68 can rarely cause acute flaccid myelitis, it commonly causes respiratory disease. In particular, EV-D68 causes outbreaks of severe asthma-like respiratory disease, but few systems have the capability to detect EV-D68 cases.
METHODS...
Hai Nguyen-Tran, Molly Butler, Dennis Simmons et al.· The Pediatric Infectious Dis...· 0 citations
Enterovirus D68 (EV-D68) primarily causes respiratory illness in children but is also associated with serious neurological outcomes. Although EV-D68 circulation has historically demonstrated a biennial pattern, with peaks during summer and fall, infections can occur year-round, with unpredictable outbreaks. Notab...
Haya Hayek, J. Amarin, Olla Hamdan et al.· Journal of the Pediatric Inf...· 0 citations
While most ARD patients demonstrated a detectable response, gender appeared to influence antibody levels, with females exhibiting a weaker response, which is consistent with the literature suggesting that vaccine efficacy may be reduced in immunocompromised populations.
Reza Farrokhseresht, Hanieh Roghanian, H. Samimagham et al.· Acta Medica Iranica· 0 citations
Background The COVID-19 pandemic and associated containment measures could have influenced children’s immune system development through reduced microbial exposure and lifestyle changes. Hematological parameters and immunoglobulin E (IgE) are key indicators for immune status, but large-scale, age-stratified studies are...
Findings highlight variant-specific limitations of anti-Spike IgG as a universal marker of protection and support the need for integrated serological and virological assessment to guide antiviral and monoclonal antibody strategies in vulnerable populations.
Matteo Domenico Marsiglia, Roberta Rovito, A. Amendola et al.· Journal of microbiology, imm...· 0 citations
We use cookies to run the site and, with your consent, for analytics and to show ads.
See our Cookie Policy.