Determinants of Antibody Levels and Protection against Omicron BQ.1/XBB Breakthrough Infection DOI Creative Commons

Carla Martín Pérez,

Anna Ramírez‐Morros, Alfons Jiménez

et al.

medRxiv (Cold Spring Harbor Laboratory), Journal Year: 2024, Volume and Issue: unknown

Published: Oct. 11, 2024

Abstract The ongoing evolution of SARS-CoV-2, particularly through the emergence new variants, continues to challenge our understanding immune protection. While antibody levels correlate with protection against earlier variants like Alpha and Delta, their relationship Omicron sub-variants remains unclear. To investigate role neutralizing activity in preventing breakthrough infections, we analyzed longitudinal SARS-CoV-2 humoral responses ancestral virus major emerging a well-characterized cohort healthcare workers Spain (N = 405). We found that neutralization titers are key indicators including BQ.1 XBB variants. Higher IgG IgA were associated over three 6-month follow-up periods sequentially dominated by BA.1, BA.2, BA.5, BQ.1, sub-variants, although strength association between declined time. Our findings demonstrate binding valid more evasive this Additionally, results underscore importance continuous monitoring updating vaccination strategies maintain effective

Language: Английский

XBB.1.5 monovalent vaccine induces lasting cross-reactive responses to SARS-CoV-2 variants such as HV.1 and JN.1, as well as SARS-CoV-1, but elicits limited XBB.1.5 specific antibodies DOI Creative Commons
Juan Manuel Carreño,

Brian Lerman,

Gagandeep Singh

et al.

mBio, Journal Year: 2025, Volume and Issue: unknown

Published: March 5, 2025

The evolution of the antibody response to severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) is impacted by nature and number antigenic exposures. First-generation disease 2019 (COVID-19) vaccines encoded an ancestral spike protein. Updated bivalent breakthrough infections have shaped intricate diversity polyclonal specificity individual clones. We others previously showed that containing Omicron (BA.5) spikes induce high levels cross-reactive antibodies but undetectable BA.5-specific in serum. Here, we assessed sera collected before as well 1 3 months following administration updated XBB.1.5 monovalent vaccine individuals with diverse infection vaccination histories. Vaccination increased neutralization against recent variants concern, including HV.1, JN.1, vaccine-homologous XBB.1.5. Antibody binding avidity antigens significantly after vaccination. However, depletion experiments most was spike, only low XBB.1.5-specific or receptor-binding domain were detected. Importantly, still detectable circulation post-vaccination cross-reacted (SARS-CoV-1) measured pseudovirus assays. Overall, our data suggest predominantly elicits a imprinted viral encountered early during pandemic.IMPORTANCEUpdated COVID-19 formulations SARS-CoV-2 exposure history affect SARS-CoV-2. High titers are induced serum reveal majority despite increasing recently circulating variants. Vaccine-induced cross-react SARS-CoV-1 remain bloodstream for at least immunization.

Language: Английский

Citations

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Recurrent waning of anti-SARS-CoV-2 neutralizing antibodies despite multiple antigen encounters DOI Creative Commons
Edwards Pradenas, Víctor Urrea, Sílvia Marfil

et al.

Research Square (Research Square), Journal Year: 2025, Volume and Issue: unknown

Published: March 13, 2025

Abstract Background: SARS-CoV-2 neutralizing antibodies may protect against symptomatic infection in immunized individuals. However, vaccine-induced antibody levels wane over time, reducing vaccine efficacy. The definition of the waning kinetics SARS-CoV-2 responses and potential impact sequential antigen encounters are still poorly defined. Methods: Plasma activity was determined longitudinally collected samples from infected, primo-vaccinated boosted Neutralizing decay were modeled time using Log-Log biexponential models. Results:Neutralizing after an initial peak all groups vaccinated individuals with half-life ranging 29 to 60 days. Exponential models showed a subsequent stabilization titers plateau. Both response plateau values depended on type, status severity infection. Booster immunization by either vaccines or breakthrough infections did not modify peak, rate values. Conclusions:Our results indicate that recurrent even several encounters. Repeated immunizations would be required maintain high vulnerable

Language: Английский

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0

Immune Imprinting, Non-Durable Hybrid Immunity, and Hybrid Immune Damping Following SARS-CoV-2 Primary Vaccination with BNT162b2 and Boosting with mRNA-1273 DOI Creative Commons
Alejo Erice,

Néstor Nuño,

María Dolores Prieto

et al.

Vaccines, Journal Year: 2025, Volume and Issue: 13(3), P. 310 - 310

Published: March 13, 2025

Background/Objectives: Long-term studies on the immune response following multiple doses of SARS-CoV-2 mRNA vaccines remain limited. Methods: Secondary analyses data from a cohort non-immunocompromised subjects who received two BNT162b2 (primary vaccination) and booster with mRNA-1273 nine months later. Antibodies targeting receptor-binding domain S1 subunit spike (anti-RBD) were measured at eight time points during follow-up; SARS-CoV-2-specific T cell was 16 25 after primary vaccination using an interferon-γ release assay. Results: During 9-month follow up period before booster, anti-RBD significantly higher all in documented infection first study point (previously infected subjects; n = 50) compared to naïve (n 208; p < 0.05). 16-month lower previously 21) 109), although differences non-significant. Breakthrough infections increased over both groups, particularly booster. Most participants had persistent specific regardless prior infection. Conclusions: These findings suggest modulating effect previous humoral vaccination, non-durable hybrid immunity subjects, attenuation (immune damping) repeated exposure antigens through and/or

Language: Английский

Citations

0

Protection and waning of vaccine-induced, natural and hybrid immunity to SARS-CoV-2 in Hong Kong DOI Creative Commons
Jialiang Jiang, Kwok Fai Lam, Eric H. Y. Lau

et al.

Expert Review of Vaccines, Journal Year: 2025, Volume and Issue: unknown

Published: March 26, 2025

As the COVID-19 pandemic transitions into its fourth year, understanding dynamics of immunity is critical for implementing effective public health measures. This study examines vaccine-induced, natural, and hybrid to SARS-CoV-2 in Hong Kong, focusing on their protective effectiveness waning characteristics against infection during Omicron BA.1/2 dominant period. We conducted a territory-wide retrospective cohort using vaccination records from Kong Department Health. The analysis included over 6.5 million adults, applying Andersen-Gill model estimate while addressing selection bias through inverse probability weighting. Vaccine-induced peaked one month after first dose but waned rapidly, boosters significantly prolonged protection. Infection-induced showed higher initial declined faster than vaccine-induced immunity. Hybrid provided most durable mRNA vaccines (Comirnaty) demonstrated greater slower compared inactivated (CoronaVac). represents strategy sustained protection SARS-CoV-2. Public policies should emphasize booster campaigns pathways enhance population-level guide future management Kong.

Language: Английский

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Estimation of trajectory of COVID-19 vaccines effectiveness against infection DOI Creative Commons
Jialiang Jiang, Kwok Fai Lam, Eric H. Y. Lau

et al.

Vaccine, Journal Year: 2025, Volume and Issue: 55, P. 127067 - 127067

Published: March 31, 2025

Language: Английский

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0

Viral and host factors associated with SARS-CoV-2 disease severity in Georgia, USA DOI Creative Commons

Ludy R Carmola,

Allison Dorothy Roebling,

Dara Khosravi

et al.

PLoS ONE, Journal Year: 2025, Volume and Issue: 20(4), P. e0317972 - e0317972

Published: April 1, 2025

While SARS-CoV-2 vaccines have shown strong efficacy, the continued emergence of new viral variants raises concerns about ongoing and future public health impact COVID-19, especially in locations with suboptimal vaccination uptake. We investigated host factors, including status, that were associated disease severity a setting low rates. analyzed clinical demographic data from 1,957 individuals state Georgia, USA, coupled genome sequencing 1,185 samples. found no specific mutations severity. Compared to those who unvaccinated, vaccinated experienced less severe disease, effect was similar for both variants. Vaccination within prior 3-9 months decreased odds moderate death. Older age underlying conditions, immunosuppression renal increased Overall, this study provides insights into variants/mutations, factors on infection when rates are low. Understanding these associations will help refine reinforce messaging around crucial importance mitigating disease.

Language: Английский

Citations

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Long-lasting antibody B-cell responses to SARS-CoV-2 three years after the onset of the pandemic DOI Creative Commons
Luis M. Molinos‐Albert, Rocío Rubio,

Carla Martín-Pérez

et al.

Cell Reports, Journal Year: 2025, Volume and Issue: 44(4), P. 115498 - 115498

Published: April 1, 2025

Immune memory is essential for the effectiveness of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) vaccination. In current context pandemic, with a diminished vaccine efficacy against emerging variants, it remains crucial to perform long-term studies evaluate durability and quality immune responses. Here, we examined antibody B-cell responses in cohort 113 healthcare workers distinct exposure histories over 3-year period. Previously infected naive participants developed comparable humoral by 17 months after receiving full three-dose mRNA addition, both maintained substantial SARS-CoV-2-reactive pool, associated lower incidence breakthrough infections participants. Of note, previously an expanded CD27-CD21- atypical population that remained stable throughout follow-up Thus, previous SARS-CoV-2 infection differentially imprints compartment without compromising development long-lasting

Language: Английский

Citations

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Phenotypic heterogeneity defines B cell responses to repeated SARS-CoV-2 exposures through vaccination and infection DOI Creative Commons

Lela Kardava,

James Lim, Clarisa M. Buckner

et al.

Cell Reports, Journal Year: 2025, Volume and Issue: 44(4), P. 115557 - 115557

Published: April 1, 2025

Language: Английский

Citations

0

Beyond the Pandemic Era: Recent Advances and Efficacy of SARS-CoV-2 Vaccines Against Emerging Variants of Concern DOI Creative Commons
Ankita Saha, Sounak Ghosh Roy, Richa Dwivedi

et al.

Vaccines, Journal Year: 2025, Volume and Issue: 13(4), P. 424 - 424

Published: April 17, 2025

Vaccination has been instrumental in curbing the transmission of SARS-CoV-2 and mitigating severity clinical manifestations associated with COVID-19. Numerous COVID-19 vaccines have developed to this effect, including BioNTech-Pfizer Moderna’s mRNA vaccines, as well adenovirus vector-based such Oxford–AstraZeneca. However, emergence new variants subvariants SARS-CoV-2, characterized by enhanced transmissibility immune evasion, poses significant challenges efficacy current vaccination strategies. In review, we aim comprehensively outline landscape emerging concern (VOCs) sub-lineages that recently surfaced post-pandemic years. We assess effectiveness existing their booster doses, against these subvariants, BA.2-derived sub-lineages, XBB BA.2.86 (Pirola). Furthermore, discuss latest advancements vaccine technology, multivalent pan-coronavirus approaches, along development several next-generation coronavirus exosome-based, virus-like particle (VLP), mucosal, nanomaterial-based vaccines. Finally, highlight key critical areas for future research address evolving threat develop strategies combating viral threats, thereby improving preparedness pandemics.

Language: Английский

Citations

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Impact of Pre-Existing Comorbidities and Multimorbidities, Demography and Viral Variants on Post-Acute Sequelae of COVID-19 (‘Long COVID’) in Dutch Primary Care: A Retrospective Cohort Study DOI Creative Commons
Matthijs S. Berends, Maarten Homburg, Thijmen Kupers

et al.

International Journal of Infectious Diseases, Journal Year: 2025, Volume and Issue: unknown, P. 107912 - 107912

Published: April 1, 2025

Language: Английский

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