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1.
J Med Virol ; 94(3): 1206-1211, 2022 03.
Article de Anglais | MEDLINE | ID: mdl-34647634

RÉSUMÉ

The Lambda variants of interest (VOI) (C37/GR/452Q.V1/21G) was initially reported in Lima, Peru but has gained rapid dissemination through other Latin American countries. Nevertheless, the dissemination and molecular epidemiology of the Lambda VOI in Brazil is unknown apart from a single case report. In this respect, we characterized the circulation of the SARS-CoV-2 Lambda VOI (C37/GR/452Q.V1/21G) in Sao Paulo State, Brazil. From March to June 2021, we identified seven Lambda isolates in a set of approximately 8000 newly sequenced genomes of the Network for Pandemic Alert of Emerging SARS-CoV-2 variants from Sao Paulo State. Interestingly, in three of the positive patients, the Lambda VOI infection was probably related to a contact transmission. These individuals were fully vaccinated to COVID-19 and presented mild symptoms. The remaining positive for Lambda VOI individuals showed different levels of COVID-19 symptoms and one of them needed hospitalization (score 5, WHO). In our study, we present a low level of Lambda VOI circulation in the Sao Paulo State. This reinforces the essential role of molecular surveillance for the effective SARS-CoV-2 pandemic response, especially in regard to circulating variants.


Sujet(s)
COVID-19 , SARS-CoV-2 , Brésil/épidémiologie , COVID-19/épidémiologie , Humains , SARS-CoV-2/génétique , Organisation mondiale de la santé
2.
J Med Virol, in press, p. 1-6, out. 2021
Article de Anglais | Sec. Est. Saúde SP, SESSP-IBPROD, Sec. Est. Saúde SP | ID: bud-3971

RÉSUMÉ

The Lambda variants of interest (VOI) (C37/GR/452Q.V1/21G) was initially reported in Lima, Peru but has gained rapid dissemination through other Latin American countries. Nevertheless, the dissemination and molecular epidemiology of the Lambda VOI in Brazil is unknown apart from a single case report. In this respect, we characterized the circulation of the SARS-CoV-2 Lambda VOI (C37/GR/452Q.V1/21G) in Sao Paulo State, Brazil. From March to June 2021, we identified seven Lambda isolates in a set of approximately 8000 newly sequenced genomes of the Network for Pandemic Alert of Emerging SARS-CoV-2 variants from Sao Paulo State. Interestingly, in three of the positive patients, the Lambda VOI infection was probably related to a contact transmission. These individuals were fully vaccinated to COVID-19 and presented mild symptoms. The remaining positive for Lambda VOI individuals showed different levels of COVID-19 symptoms and one of them needed hospitalization (score 5, WHO). In our study, we present a low level of Lambda VOI circulation in the Sao Paulo State. This reinforces the essential role of molecular surveillance for the effective SARS-CoV-2 pandemic response, especially in regard to circulating variants.

3.
Sci Rep ; 10(1): 20371, 2020 11 23.
Article de Anglais | MEDLINE | ID: mdl-33230132

RÉSUMÉ

Lymphoma is the most common type of canine hematological malignancy where the multicentric (cMCL) form accounts for 75% of all cases. The standard treatment is the CHOP chemotherapy protocols that include cyclophosphamide, doxorubicin, vincristine and prednisone, where the majority of dogs achieve complete/partial response; however, it is very important to predict non-responsive cases to improve treatment and to develop new targeted therapies. Here we evaluate a liquid biopsy approach based on serum Small Extracellular Vesicles enriched for exosomes (SEVs) to predict cMCL chemotherapy response. Nineteen dogs at the end of the 19-week chemotherapy protocol (8 Complete Response and 11 Progressive Disease) were evaluated for serum SEVs size, concentration and screened for 95 oncomirs. PD patients had higher SEVs concentration at the diagnosis than CR patients (P = 0.034). The ROC curve was significant for SEVs concentration to predict the response to CHOP (AUC = 0.8011, P = 0.0287). A potential molecular signature based on oncomirs from SEVs (caf-miR-205, caf-miR-222, caf-mir-20a and caf-miR-93) is proposed. To the best of our knowledge, this is the first study demonstrating the potential of a liquid biopsy based on SEVs and their miRNAs content to predict the outcome of chemotherapy for canine multicentric lymphomas.


Sujet(s)
Protocoles de polychimiothérapie antinéoplasique/pharmacologie , Marqueurs biologiques tumoraux/génétique , Maladies des chiens/traitement médicamenteux , Vésicules extracellulaires/génétique , Lymphomes/traitement médicamenteux , Lymphomes/médecine vétérinaire , microARN/génétique , Animaux , Marqueurs biologiques tumoraux/sang , Études cas-témoins , Cyclophosphamide/pharmacologie , Maladies des chiens/diagnostic , Maladies des chiens/génétique , Maladies des chiens/mortalité , Chiens , Doxorubicine/pharmacologie , Vésicules extracellulaires/métabolisme , Femelle , Régulation de l'expression des gènes tumoraux , Biopsie liquide , Lymphomes/génétique , Lymphomes/mortalité , Mâle , microARN/sang , Phosphatidylinositol 3-kinases/sang , Phosphatidylinositol 3-kinases/génétique , Prednisone/pharmacologie , Isoformes de protéines/sang , Isoformes de protéines/génétique , Protéines proto-oncogènes c-kit/sang , Protéines proto-oncogènes c-kit/génétique , Récepteur FGFR2/sang , Récepteur FGFR2/génétique , Récidive , Facteur de croissance des cellules souches/sang , Facteur de croissance des cellules souches/génétique , Analyse de survie , Résultat thérapeutique , Vincristine/pharmacologie
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