REY JURADO, EMMA
Preferred name
REY JURADO, EMMA
Main Affiliation
Email
emmarey@udd.cl
ORCID
0000-0003-4146-7785
Scopus Author ID
50562073000
10 results
Now showing 1 - 10 of 10
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Item type:Publication, Scopus© Citations 8 3 - Some of the metrics are blocked by yourconsent settings
Item type:Publication, Multicenter Study to Determine the Immune Response to the Vaccine Against SARS COV-2, in Patients With Chronic Kidney Disease on Dialysis and Kidney Transplants(2022) ;CAMILO ERNESTO ULLOA TESSER; ; ; 1 - Some of the metrics are blocked by yourconsent settings
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Item type:Publication, Multicenter analysis of neutrophil extracellular trap dysregulation in adult and pediatric COVID-19(2022) ;Carmelo Carmona-Rivera ;Yu Zhang ;Kerry Dobbs ;Tovah E. MarkowitzClifton L. Dalgard13Scopus© Citations 30 - Some of the metrics are blocked by yourconsent settings
Item type:Publication, Immunopathological signatures in multisystem inflammatory syndrome in children and pediatric COVID-19(2022) ;Keith Sacco ;Riccardo Castagnoli ;Svetlana Vakkilainen ;Can LiuOttavia M. DelmonteScopus© Citations 204 11 - Some of the metrics are blocked by yourconsent settings
Item type:Publication, Autoantibodies Against Proteins Previously Associated With Autoimmunity in Adult and Pediatric Patients With COVID-19 and Children With MIS-C(2022) ;Peter D. Burbelo ;Riccardo Castagnoli ;Chisato Shimizu ;Ottavia M. DelmonteKerry Dobbs<jats:p>The antibody profile against autoantigens previously associated with autoimmune diseases and other human proteins in patients with COVID-19 or multisystem inflammatory syndrome in children (MIS-C) remains poorly defined. Here we show that 30% of adults with COVID-19 had autoantibodies against the lung antigen KCNRG, and 34% had antibodies to the SLE-associated Smith-D3 protein. Children with COVID-19 rarely had autoantibodies; one of 59 children had GAD65 autoantibodies associated with acute onset of insulin-dependent diabetes. While autoantibodies associated with SLE/Sjögren’s syndrome (Ro52, Ro60, and La) and/or autoimmune gastritis (gastric ATPase) were detected in 74% (40/54) of MIS-C patients, further analysis of these patients and of children with Kawasaki disease (KD), showed that the administration of intravenous immunoglobulin (IVIG) was largely responsible for detection of these autoantibodies in both groups of patients. Monitoring <jats:italic>in vivo</jats:italic> decay of the autoantibodies in MIS-C children showed that the IVIG-derived Ro52, Ro60, and La autoantibodies declined to undetectable levels by 45-60 days, but gastric ATPase autoantibodies declined more slowly requiring &gt;100 days until undetectable. Further testing of IgG and/or IgA antibodies against a subset of potential targets identified by published autoantigen array studies of MIS-C failed to detect autoantibodies against most (16/18) of these proteins in patients with MIS-C who had not received IVIG. However, Troponin C2 and KLHL12 autoantibodies were detected in 2 of 20 and 1 of 20 patients with MIS-C, respectively. Overall, these results suggest that IVIG therapy may be a confounding factor in autoantibody measurements in MIS-C and that antibodies against antigens associated with autoimmune diseases or other human proteins are uncommon in MIS-C.</jats:p>Scopus© Citations 25 1 - Some of the metrics are blocked by yourconsent settings
Item type:Publication, Deep immunophenotyping reveals biomarkers of multisystemic inflammatory syndrome in children in a Latin American cohort(2022); ;Yazmin Espinosa ;Camila Astudillo; Scopus© Citations 16 8 - Some of the metrics are blocked by yourconsent settings
Item type:Publication, Partial loss-of-function mutations in GINS4 lead to NK cell deficiency with neutropenia(2022) ;Matilde I. Conte ;M. Cecilia Poli ;Angelo Taglialatela ;Giuseppe LeuzziIvan K. Chinn9Scopus© Citations 13 - Some of the metrics are blocked by yourconsent settings
Item type:Publication, A Third Dose of SARS-CoV-2 mRNA Vaccine Improves Immune Response in Chronic Kidney Disease Patients(2023); ; ; ;Natalia González<jats:p>Chronic kidney disease (CKD) patients have an increased risk of morbidity and mortality following SARS-CoV-2 infection. Vaccination in these patients is prioritized, and monitoring of the immune response is paramount to define further vaccination strategies. This prospective study included a cohort of 100 adult CKD patients: 48 with kidney transplant (KT) and 52 on hemodialysis without prior COVID-19. The patients were assessed for humoral and cellular immune responses after four months of an anti-SARS-CoV-2 primary two-dose vaccination scheme (CoronaVac or BNT162b2) and one month after a booster third dose of BNT162b2 vaccine. We identified poor cellular and humoral immune responses in the CKD patients after a primary vaccination scheme, and these responses were improved by a booster. Robust polyfunctional CD4+ T cell responses were observed in the KT patients after a booster, and this could be attributed to a higher proportion of the patients having been vaccinated with homologous BNT162b2 schemes. However, even after the booster, the KT patients exhibited lower neutralizing antibodies, attributable to specific immunosuppressive treatments. Four patients suffered severe COVID-19 despite three-dose vaccination, and all had low polyfunctional T-cell responses, underscoring the importance of this functional subset in viral protection. In conclusion, a booster dose of SARS-CoV-2 mRNA vaccine in CKD patients improves the impaired humoral and cellular immune responses observed after a primary vaccination scheme.</jats:p>8Scopus© Citations 5