Publications by authors named "Ana Marquez"

Giant cell arteritis (GCA) is a complex inflammatory disease affecting individuals over 50 suggesting a strong link with aging-related immune and vascular changes. However, the precise mechanisms underlying this age-related susceptibility remain poorly understood. Considering the relevance of aging in GCA, genetic factors influencing biological aging markers, such as telomere shortening and epigenetic age acceleration (EAA), might also contribute to its development.

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Erdheim-Chester Disease (ECD) is a rare histiocytosis characterized by a wide spectrum of clinical manifestations. Although somatic mutations have been involved in ECD, its etiology remains poorly understood. This study aimed to identify novel molecular mechanisms involved in ECD through the first integrated methylome and transcriptome analysis.

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Objectives: Giant cell arteritis (GCA) is a large-vessel vasculitis, potentially causing complications such as blindness and strokes. This study aims to gain insights into the pathogenesis of GCA by identifying specific DNA methylation signatures in the arterial tissue of patients with this vasculitis.

Methods: DNA methylation profiling was analyzed in 79 temporal artery biopsy samples (69 patients with GCA and 10 controls) by performing an epigenome-wide association study (EWAS).

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The COVID-19 pandemic, caused by SARS-CoV-2, highlighted the need for accurate and timely data on virus spread and immune responses at a population level. Serological surveys offer a comprehensive view of population-level immune response to SARS-CoV-2 post- infection and/or vaccination. Here, we performed a serial cross-sectional study from residual serum samples collected from pregnant individuals in British Columbia during their first trimester antenatal screening.

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There is a limited understanding of the immunological differences between children and adults that protect children from developing severe coronavirus disease 2019 (COVID-19) following SARS-CoV-2 infection. Previous infection with endemic human coronaviruses (HCoVs) has been suggested as a factor. In this study, we used 100 paired residual samples collected before and during the COVID-19 pandemic from children in Bangladesh.

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Objective: To explore the association of maternal characteristics, oxygenation, and mechanical ventilatory parameters with fetal and neonatal outcomes.

Methods: The present study was a multicenter, binational (Argentina/Colombia), prospective, cohort study, conducted in 21 intensive care units (ICUs) and including pregnant or postpartum patients with COVID-19 pneumonia requiring advanced respiratory support and their fetuses/neonates. Advanced respiratory support was defined as high-flow nasal cannula (HFNC), non-invasive ventilation (NIV) or invasive mechanical ventilation (IMV).

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  • Rugulopteryx okamurae is a brown alga that has spread invasively from its native habitat in the northwestern Pacific, first appearing in the southern Strait of Gibraltar in 2015 and covering much of the northern Alboran Sea by 2021.
  • Researchers used biogeographic modeling to analyze the yearly distribution of R. okamurae from 2016 to 2021, relying on a favourability function that incorporates various environmental factors to understand the algae's colonization patterns.
  • The models revealed that while initial spread was influenced by factors such as dispersion and ocean conditions, complete establishment relied on a combination of all studied factors, providing insights to help manage and mitigate the effects of this invasive species.
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  • The gut microbiome is crucial for our body's functioning, but the effects of non-nutritious food components on it are often ignored.
  • Certain food additives and microplastics may negatively impact the gut microbiome and human health, and understanding the mechanisms behind this is essential.
  • Recommendations include integrating gut microbiome research into food safety assessments to better evaluate the risks of food additives and contaminants.
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  • Human cytomegalovirus (HCMV) is the most common congenital infection, and while vaccines are being developed, none have been approved yet.
  • The salivary glands play a crucial role in the replication and spread of CMV, suggesting that the immune response in these glands may affect viral transmission.
  • Researchers studied the immune response and viral dynamics in mice infected with murine CMV, leading to the creation of mathematical models that highlight the significance of cellular immunity in different organs and the critical infection threshold in the salivary glands for viral spread.
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Background: Assessing refractive errors under cycloplegia is recommended for paediatric patients; however, this may not always be feasible. In these situations, refraction has to rely on measurements made under active accommodation which may increase measurements variability and error. Therefore, evaluating the accuracy and precision of non-cycloplegic refraction and biometric measurements is clinically relevant.

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  • * Genetic predisposition is significant, with evidence from family history, ethnicity differences, and genetic variants, primarily in the HLA region, playing critical roles in disease risk and severity.
  • * Future research should aim to identify specific genetic markers to improve early diagnosis, prognosis, and treatment strategies for systemic vasculitis.
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Human-wildlife conflicts (HWC) are increasing and are potentially harmful to both people and wildlife. Understanding the current and potential distribution of wildlife species involved in HWC, such as carnivores, is essential for implementing management and conservation measures for such species. In this study, we assessed both the current distribution and potential distribution (forecast) of the Egyptian mongoose (Herpestes ichneumon) in the central part of the Iberian Peninsula.

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Epidemiological studies report opposing influences of infection on childhood B-cell acute lymphoblastic leukemia (B-ALL). Although infections in the first year of life appear to exert the largest impact on leukemia risk, the effect of early pathogen exposure on the fetal preleukemia cells (PLC) that lead to B-ALL has yet to be reported. Using cytomegalovirus (CMV) infection as a model early-life infection, we show that virus exposure within 1 week of birth induces profound depletion of transplanted E2A-PBX1 and hyperdiploid B-ALL cells in wild-type recipients and in situ-generated PLC in Eμ-ret mice.

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Background: Giant cell arteritis (GCA) is an immune-mediated large-vessels vasculitis with complex etiology. Although the pathogenic mechanisms remain poorly understood, a central role for CD4 T cells has been demonstrated. In this context, understanding the transcriptome dysregulation in GCA CD4 T cells will yield new insights into its pathogenesis.

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Background: Giant cell arteritis is an age-related vasculitis that mainly affects the aorta and its branches in individuals aged 50 years and older. Current options for diagnosis and treatment are scarce, highlighting the need to better understand its underlying pathogenesis. Genome-wide association studies (GWAS) have emerged as a powerful tool for unravelling the pathogenic mechanisms involved in complex diseases.

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  • The study evaluated immune responses to COVID-19 vaccines in adults aged 50 and older by measuring antibody levels and T-cell responses after a two-dose series.
  • Vaccinated individuals with mRNA/mRNA and ChAdOx1-S/mRNA regimens showed higher antibody responses compared to those receiving the ChAdOx1-S/ChAdOx1-S regimen, peaking one month after the second dose.
  • It suggests that both antibody concentration and avidity should be factored in when assessing COVID-19 vaccine protection.
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  • * Two phases of serosurveys involved 2,864 participants and found that 4.4% of all ages and 8.8% of unvaccinated young children tested positive for antibodies, with higher rates observed in South Asian participants.
  • * The findings highlight a need for better diagnostic strategies that consider age-specific factors in understanding COVID-19’s impact on pediatric populations.
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  • This study analyzed how antibody levels decline over 11 months in paramedics who received two doses of mRNA vaccines, specifically looking for factors that accelerate this decline.* -
  • Researchers found that the highest antibody levels occurred 21 days post-vaccination, followed by a half-life of about 94 days, after which levels plateaued around day 295.* -
  • Factors such as older age, shorter time between vaccine doses, and receiving the BNT162b2 vaccine were linked to quicker antibody decay, which could help guide booster shot recommendations.*
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Giant cell arteritis (GCA) is a systemic vasculitis mediated by an aberrant immunological response against the blood vessel wall. Although the pathogenic mechanisms that drive GCA have not yet been elucidated, there is strong evidence that CD4 T cells are key drivers of the inflammatory process occurring in this vasculitis. The aim of this study was to further delineate the role of CD4 T cells in GCA by applying single-cell RNA sequencing and T cell receptor (TCR) repertoire profiling to 114.

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We sought to evaluate the rates and predictors of SARS-CoV-2 vaccination among members of a structurally-marginalized population of people who use drugs (PWUD) during a targeted, community-wide, vaccination campaign in Vancouver, Canada. Interviewer-administered data were collected from study participants between June 2021 and March 2022. Generalized estimating equation analysis was used to identify factors associated with SARS-CoV-2 vaccine uptake, ascertained through a province-wide vaccine registry.

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  • The study explored the use of Bayesian latent class models (BLCMs) to estimate the presence of anti-SARS-CoV-2 antibodies in blood donor samples, without relying on a definitive testing standard.
  • A total of 6,810 plasma samples from blood donors in Québec collected between May and July 2020 were tested with seven different serological assays, revealing a SARS-CoV-2 seroprevalence of 0.71%.
  • The research highlighted the variability in sensitivity among the assays used and emphasized that BLCMs can provide rapid updates on disease prevalence and assist public health efforts, especially when a gold standard test is unavailable.
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(rs11150612, rs11574637), rs17019602, rs4077515, (rs2738048, rs10086568), and rs2412971 are mucosal immune defence polymorphisms, that have an impact on IgA production, described as risk for IgA nephropathy (IgAN). Since IgAN and Immunoglobulin-A vasculitis (IgAV) share molecular mechanisms, with the aberrant deposit of IgA1 being the main pathophysiologic feature of both entities, we assessed the potential influence of the seven abovementioned polymorphisms on IgAV pathogenesis. These seven variants were genotyped in 381 Caucasian IgAV patients and 997 matched healthy controls.

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  • - The study investigates the genetic underpinnings of Erdheim-Chester disease (ECD), a rare condition characterized by abnormal immune cell activity, by conducting the first genome-wide association study to understand its inherited genetic factors.
  • - Researchers analyzed data from 255 ECD patients and 7,471 healthy individuals, identifying a significant genetic region (18q12.3) that could increase susceptibility to ECD, linked to the SETBP1 gene.
  • - The findings suggest that inherited genetic variants play a role in ECD development and point to new biological pathways that may contribute to the disease's progression.
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Background: Giant cell arteritis (GCA) causes severe inflammation of the aorta and its branches and is characterized by intense effector T-cell infiltration. The roles that immune checkpoints play in the pathogenesis of GCA are still unclear. Our aim was to study the immune checkpoint interplay in GCA.

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Objective: Emerging evidence indicates that longer SARS-CoV-2 vaccine dosing intervals results in an enhanced immune response. However, the optimal vaccine dosing interval for achieving maximum immunogenicity is unclear.

Methods: This study included samples from adult paramedics in Canada who received two doses of either BNT162b2 or mRNA-1273 vaccines and provided blood samples six months (170 to 190 days) after the first vaccine dose.

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