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1.
Sci Rep ; 14(1): 13702, 2024 06 14.
Artigo em Inglês | MEDLINE | ID: mdl-38871789

RESUMO

Coronavirus disease 2019 (COVID-19) is caused by Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2). Recent research has demonstrated how epigenetic mechanisms regulate the host-virus interactions in COVID-19. It has also shown that microRNAs (miRNAs) are one of the three fundamental mechanisms of the epigenetic regulation of gene expression and play an important role in viral infections. A pilot study published by our research group identified, through next-generation sequencing (NGS), that miR-4433b-5p, miR-320b, and miR-16-2-3p are differentially expressed between patients with COVID-19 and controls. Thus, the objectives of this study were to validate the expression of these miRNAs using quantitative real-time polymerase chain reaction (qRT-PCR) and to perform in silico analyses. Patients with COVID-19 (n = 90) and healthy volunteers (n = 40) were recruited. MiRNAs were extracted from plasma samples and validated using qRT-PCR. In addition, in silico analyses were performed using mirPath v.3 software. MiR-320b was the only miRNA upregulated in the case group com-pared to the control group. The in silico analyses indicated the role of miR-320b in the regulation of the KITLG gene and consequently in the inflammatory process. This study confirmed that miR-320b can distinguish patients with COVID-19 from control participants; however, further research is needed to determine whether this miRNA can be used as a target or a biomarker.


Assuntos
COVID-19 , MicroRNAs , SARS-CoV-2 , Humanos , COVID-19/genética , COVID-19/sangue , COVID-19/virologia , MicroRNAs/sangue , MicroRNAs/genética , Masculino , Feminino , SARS-CoV-2/genética , Pessoa de Meia-Idade , Adulto , Idoso , Estudos de Casos e Controles
2.
Oncol Res ; 32(4): 597-605, 2024.
Artigo em Inglês | MEDLINE | ID: mdl-38560564

RESUMO

Bladder cancer (BC) is the 10th most common cancer worldwide, with about 0.5 million reported new cases and about 0.2 million deaths per year. In this scoping review, we summarize the current evidence regarding the clinical implications of single-cell sequencing for bladder cancer based on PRISMA guidelines. We searched PubMed, CENTRAL, Embase, and supplemented with manual searches through the Scopus, and Web of Science for published studies until February 2023. We included original studies that used at least one single-cell technology to study bladder cancer. Forty-one publications were included in the review. Twenty-nine studies showed that this technology can identify cell subtypes in the tumor microenvironment that may predict prognosis or response to immune checkpoint inhibition therapy. Two studies were able to diagnose BC by identifying neoplastic cells through single-cell sequencing urine samples. The remaining studies were mainly a preclinical exploration of tumor microenvironment at single cell level. Single-cell sequencing technology can discriminate heterogeneity in bladder tumor cells and determine the key molecular properties that can lead to the discovery of novel perspectives on cancer management. This nascent tool can advance the early diagnosis, prognosis judgment, and targeted therapy of bladder cancer.


Assuntos
Carcinoma de Células de Transição , Neoplasias da Bexiga Urinária , Humanos , Carcinoma de Células de Transição/tratamento farmacológico , Carcinoma de Células de Transição/patologia , Neoplasias da Bexiga Urinária/diagnóstico , Neoplasias da Bexiga Urinária/genética , Neoplasias da Bexiga Urinária/terapia , Prognóstico , Microambiente Tumoral/genética
3.
Front Pharmacol ; 14: 1278720, 2023.
Artigo em Inglês | MEDLINE | ID: mdl-38035025

RESUMO

Introduction: Several polymorphisms altering the NAT2 activity have already been identified. The geographical distribution of NAT2 variants has been extensively studied and has been demonstrated to vary significantly among different ethnic population. Here, we describe the genetic variability of human N-acetyltransferase 2 (NAT2) gene and the predominant genotype-deduced acetylation profiles of Brazilians. Methods: A total of 964 individuals, from five geographical different regions, were genotyped for NAT2 by sequencing the entire coding exon. Results: Twenty-three previously described NAT2 single nucleotide polymorphisms (SNPs) were identified, including the seven most common ones globally (c.191G>A, c.282C>T, c.341T>C, c.481C>T, c.590G>A, c.803A>G and c.857G>A). The main allelic groups were NAT2*5 (36%) and NAT2*6 (18.2%), followed to the reference allele NAT2*4 (20.4%). Combined into genotypes, the most prevalent allelic groups were NAT2*5/*5 (14.6%), NAT2*5/*6 (11.9%) and NAT2*6/*6 (6.2%). The genotype deduced NAT2 slow acetylation phenotype was predominant but showed significant variability between geographical regions. The prevalence of slow acetylation phenotype was higher in the Northeast, North and Midwest (51.3%, 45.5% and 41.5%, respectively) of the country. In the Southeast, the intermediate acetylation phenotype was the most prevalent (40.3%) and, in the South, the prevalence of rapid acetylation phenotype was significantly higher (36.7%), when compared to other Brazilian states (p < 0.0001). Comparison of the predicted acetylation profile among regions showed homogeneity among the North and Northeast but was significantly different when compared to the Southeast (p = 0.0396). The Southern region was significantly different from all other regions (p < 0.0001). Discussion: This study contributes not only to current knowledge of the NAT2 population genetic diversity in different geographical regions of Brazil, but also to the reconstruction of a more accurate phenotypic picture of NAT2 acetylator profiles in those regions.

4.
Vaccine ; 41(44): 6599-6606, 2023 Oct 20.
Artigo em Inglês | MEDLINE | ID: mdl-37743116

RESUMO

OBJECTIVES: Healthcare workers (HCWs) may have different response to Bacillus Calmette-Guérin (BCG) vaccination due to previous occupational exposure to Mycobacterium particles. We report subgroup analysis of the BATTLE trial, comparing BCG effects in HCWs vs non-HCWs. This was a secondary analysis of a trial. METHODS: The BATTLE trial was a double-blind placebo-controlled phase III clinical trial that investigated BCG revaccinating adults who were recently infected with SARS-CoV-2 virus. BCG and placebo recipients were sub-grouped based on regular occupational contact with patients into HCWs (48 BCG and 50 placebo) and non-HCWs (124 BCG and 134 placebo). Weekly COVID-19 symptom progression and injection site reactions were compared between subgroups on weeks one, two, three, and six follow-ups. RESULTS: HCWs were more likely to complain of itching on the injection site early after injection (OR = 2.5, p = 0.049). They developed peeling and crusting on the site of injection faster than non-HCWs (during the second week, p = 0.033 and 0.040, OR = 3.3 and 2.7, respectively). HCWs were also more likely to maintain their papule or develop a late onset pustule during later weeks (weeks four and six, p = 0.024 and 0.006, OR = 2.2 and 8.6, respectively). In terms of COVID-19 symptom progression, recovery from anosmia was more likely in the non-HCWs who received BCG (week six, pHolm's corrected = 0.002, OR = 3.3). CONCLUSION: HCWs' local reaction to BCG injection was slightly more rapid and more intense, possibly due to their occupational exposure. BCG may also ameliorate COVID-19 induced inflammation and anosmia in non-HCWs but not HCWs. Therefore, HCWs might be less likely to benefit from BCG vaccination. CLINICALTRIALS: gov register number NCT04369794.

5.
Immunotherapy ; 15(1): 9-15, 2023 01.
Artigo em Inglês | MEDLINE | ID: mdl-36628594

RESUMO

Aim: We previously published results of the BATTLE trial, showing that patients recently infected with SARS-CoV-2 can benefit from receiving Bacillus Calmette-Guérin (BCG) with minimal adverse effects. The study incorporated two strains of this vaccine. In this study, patient outcomes were compared based on the strain of BCG because different strains have been shown to have different immunogenicity. Methods: BATTLE was a double-blind controlled trial of COVID-19 convalescent patients; symptom progression, injection-site lesion characteristics and adverse effects were compared between recipients of placebo, Russian BCG strain or Brazilian BCG strains. Results: There was no statistically significant difference between the two BCG strains in terms of symptom progression, lesion-size or type. Conclusion: The two strains have similar clinical outcomes in COVID-19 convalescent patients.


We previously published results of the BATTLE trial, showing that patients recently infected with SARS-CoV-2 virus can benefit from receiving BCG with minimal adverse effects. This article shows that the two BCG strains, Russian and Brazilian, have similar clinical outcomes in COVID-19 convalescent patients.


Assuntos
COVID-19 , Humanos , COVID-19/terapia , Vacina BCG/uso terapêutico , SARS-CoV-2 , Federação Russa , Ensaios Clínicos Controlados Aleatórios como Assunto
6.
Int J Gen Med ; 15: 8583-8592, 2022.
Artigo em Inglês | MEDLINE | ID: mdl-36545246

RESUMO

Aim: To find whether an emergent airborne infection is more likely to spread among healthcare workers (HCW) based on data of SARS-CoV-2 and whether the number of new cases of such airborne viral disease can be predicted using a method traditionally used in weather forecasting called Autoregressive Fractionally Integrated Moving Average (ARFIMA). Methods: We analyzed SARS-CoV-2 spread among HCWs based on outpatient nasopharyngeal swabs for real-time polymerase chain reaction (RT-PCR) tests and compared it to non-HCW in the first and the second wave of the pandemic. We also generated an ARFIMA model based on weekly case numbers from February 2020 to April 2021 and tested it on data from May to July 2021. Results: Our analysis of 8998 tests in the 15 months period showed a rapid rise in positive RT-PCR tests among HCWs during the first wave of pandemic. In the second wave, however, positive patients were more commonly non-HCWs. The ARFIMA model showed a long-memory pattern for SARS-CoV-2 (seven months) and predicted future new cases with an average error of ±1.9 cases per week. Conclusion: Our data indicate that the virus rapidly spread among HCWs during the first wave of the pandemic. Review of published literature showed that this was the case in multiple other areas as well. We therefore suggest strict policies early in the emergence of a new infection to protect HCWs and prevent spreading to the general public. The ARFIMA model can be a valuable forecasting tool to predict the number of new cases in advance and assist in efficient planning.

7.
Rev Bras Med Trab ; 20(1): 27-35, 2022.
Artigo em Inglês | MEDLINE | ID: mdl-36118062

RESUMO

Introduction: Health professionals are at high or very high risk of being infected with COVID-19, making it essential to adopt control and protection measures. The World Health Organization developed a risk assessment instrument to identify possible protection failures and to guide corrective actions. Objectives: To test an adapted version of this instrument among health care workers with a suspected case of COVID-19. Methods: The World Health Organization instrument was translated and adapted with the participation of health care workers. The adapted version was inserted into Google Forms® and applied to 211 health care workers with a suspected case of COVID-19 in three public hospitals. Results: Fifty-five percent of workers were nursing professionals. The main risk factors for exposure to the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) were failures in training, in donning and doffing, and in the use and maintenance of personal and collective protective equipment; problems in cleaning rooms and equipment; and changes in work organization. The assessment instrument fulfilled its purpose of assessing risk factors for exposure to SARS-CoV-2 and helped adopt the corrective and preventive measures required to prevent COVID-19 among health care workers. Conclusions: The adapted instrument proved to be an important support tool to improve risk management and protection of these workers.

8.
Vaccine ; 40(32): 4603-4608, 2022 07 30.
Artigo em Inglês | MEDLINE | ID: mdl-35738969

RESUMO

INTRODUCTION: The safety of BCG revaccination is uncertain and there is no data on its use in patients with COVID-19. METHODS: COVID-19 convalescent adults confirmed by SARS-CoV-2 RT-PCR in South-America were 1:1 randomized in the first 14 days of symptoms to BCG intradermal vaccine or placebo and evaluated for adverse events on days 7, 14, 21, and beyond 40 days. CLINICAL TRIAL REGISTRATION: NCT04369794. RESULTS: 151 placebo and 148 BCG patients were included in the final analysis, with an average age of 40.7 years. No severe adverse event to BCG was reported. On day 7, 130 (87.8%) of the BCG recipients had local reaction, average size of 10.6 ± 6.4 mm, compared to only 2 (1.3%) placebos. Lesions gradually shrunk in size (mean 10.5 mm, 9.7 mm, and 6.8 mm at 14, 21, and beyond 40 days, respectively. The number of symptoms in any of the visits was not different between groups, and anosmia resolved earlier (25.7% vs. 37.1% at 7 days, OR = 1.70, 1.01-2.89, p = 0.035) in the BCG recipients. CONCLUSION: The BCG revaccination is safe in convalescent COVID-19 adults of a tuberculosis endemic region, regardless of tuberculin or IGRA test results. Local adverse events were similar though occurred earlier to that previously reported in children.


Assuntos
Vacina BCG , COVID-19 , Tuberculose , Adulto , Vacina BCG/efeitos adversos , Vacina BCG/uso terapêutico , Método Duplo-Cego , Humanos , Imunização Secundária , Tuberculose/prevenção & controle
9.
J Intern Med ; 292(4): 654-666, 2022 10.
Artigo em Inglês | MEDLINE | ID: mdl-35599154

RESUMO

BACKGROUND: The Bacillus Calmette-Guérin (BCG) vaccine may confer cross-protection against viral diseases in adults. This study evaluated BCG vaccine cross-protection in adults with convalescent coronavirus disease 2019 (COVID-19). METHOD: This was a multicenter, prospective, randomized, placebo-controlled, double-blind phase III study (ClinicalTrials.gov: NCT04369794). SETTING: University Community Health Center and Municipal Outpatient Center in South America. PATIENTS: a total of 378 adult patients with convalescent COVID-19 were included. INTERVENTION: single intradermal BCG vaccine (n = 183) and placebo (n = 195). MEASUREMENTS: the primary outcome was clinical evolution. Other outcomes included adverse events and humoral immune responses for up to 6 months. RESULTS: A significantly higher proportion of BCG patients with anosmia and ageusia recovered at the 6-week follow-up visit than placebo (anosmia: 83.1% vs. 68.7% healed, p = 0.043, number needed to treat [NNT] = 6.9; ageusia: 81.2% vs. 63.4% healed, p = 0.032, NNT = 5.6). BCG also prevented the appearance of ageusia in the following weeks: seven in 113 (6.2%) BCG recipients versus 19 in 126 (15.1%) placebos, p = 0.036, NNT = 11.2. BCG did not induce any severe or systemic adverse effects. The most common and expected adverse effects were local vaccine lesions, erythema (n = 152; 86.4%), and papules (n = 111; 63.1%). Anti-severe acute respiratory syndrome coronavirus 2 humoral response measured by N protein immunoglobulin G titer and seroneutralization by interacting with the angiotensin-converting enzyme 2 receptor suggest that the serum of BCG-injected patients may neutralize the virus at lower specificity; however, the results were not statistically significant. CONCLUSION: BCG vaccine is safe and offers cross-protection against COVID-19 with potential humoral response modulation. LIMITATIONS: No severely ill patients were included.


Assuntos
Ageusia , COVID-19 , Adulto , Enzima de Conversão de Angiotensina 2 , Anosmia , Vacina BCG/efeitos adversos , COVID-19/prevenção & controle , Método Duplo-Cego , Humanos , Imunidade Humoral , Imunoglobulina G , Estudos Prospectivos
10.
Emerg Infect Dis ; 27(6): 1737-1740, 2021.
Artigo em Inglês | MEDLINE | ID: mdl-33871331

RESUMO

We documented 4 cases of severe acute respiratory syndrome coronavirus 2 reinfection by non-variant of concern strains among healthcare workers in Campinas, Brazil. We isolated infectious particles from nasopharyngeal secretions during both infection episodes. Improved and continued protection measures are necessary to mitigate the risk for reinfection among healthcare workers.


Assuntos
COVID-19/diagnóstico , Pessoal de Saúde , Reinfecção/diagnóstico , Reinfecção/virologia , SARS-CoV-2/isolamento & purificação , Eliminação de Partículas Virais , Adulto , Brasil/epidemiologia , COVID-19/epidemiologia , Feminino , Humanos , Pessoa de Meia-Idade , Reinfecção/terapia
11.
Saúde debate ; 44(126): 640-655, jul.-set. 2020. tab
Artigo em Português | LILACS-Express | LILACS, Sec. Est. Saúde SP | ID: biblio-1139574

RESUMO

RESUMO Trata-se da avaliação de um programa de prevenção e tratamento de Doenças Crônicas Não Transmissíveis (DCNT) oferecido à comunidade de uma universidade pública por ambulatório localizado em suas dependências. O processo avaliativo teve como objetivo apreender a dinâmica e compreender a forma de interação entre os atores envolvidos no cotidiano do programa, partindo do entendimento dos seus grupos de interesse, formados pela equipe, usuários, gestores e profissionais encaminhadores. Realizou-se pesquisa qualitativa de caráter participativo e com dimensão formativa para ampliar a possibilidade de aperfeiçoamento do programa pelos sujeitos envolvidos a partir de elementos oriundos de sua prática. A Avaliação de Quarta Geração de Guba e Lincoln e o Método Paideia de Campos foram norteadores metodológicos da pesquisa. A análise do material empírico foi agrupada em três núcleos temáticos: método de trabalho, equipe e gestão do programa. Constatou-se que uma escuta reflexiva dos profissionais é fator decisivo para ampliar a autonomia dos usuários e sua adesão terapêutica; a realização de grupos educativos no local de trabalho favoreceu a captação para tratamento e participação dos usuários, especialmente os do gênero masculino; e os encontros dos grupos possibilitam diversos ganhos objetivos e subjetivos, como a interação social entre pessoas de diferentes áreas da universidade.


ABSTRACT This work concerns the evaluation of a program for the prevention and treatment of Chronic Non-Communicable Diseases (NCD) offered to the community assisted by a public university by means of its outpatient health facility. The evaluation process sought to apprehend the dynamics and to understand the form of interaction between the actors involved in the daily routine of the Program grounded on the understanding of its interest groups, composed of staff, users, managers and referral professionals. A qualitative, participatory and formative research was conducted to broaden the Program possibilities of improvement by the stakeholders based on elements derived from their experience. Guba' and Lincoln' Fourth Generation Evaluation and Paideia' Method of Campos guided the research methodology. The empirical material analysis was grouped into three thematic clusters: working method, team, and program management. It was revealed that a reflective listening by professionals is a deciding factor to extend the autonomy of users and their therapeutic adherence; that the gathering of educational groups in the work premises favored the participation of users and their capture for treatment, especially as for males; and that the group meetings allow for various objective and subjective gains, such as social interaction among people from different areas of the University.

12.
Eng. sanit. ambient ; 24(5): 993-1002, set.-out. 2019. tab
Artigo em Português | LILACS-Express | LILACS | ID: biblio-1056098

RESUMO

RESUMO O objetivo deste trabalho é identificar quais características das instituições de educação superior (IES) atuam como facilitadoras ou barreiras no desenvolvimento de ações de gestão ambiental. A análise de regressão beta de 38 relatórios de sustentabilidade elaborados conforme as diretrizes da Global Reporting Initiative (GRI) mostrou que a facilidade de acesso a recursos financeiros, a existência de plano ou política ambiental/de sustentabilidade e a natureza pública da instituição podem ser consideradas facilitadoras para o desenvolvimento da gestão ambiental em IES, enquanto a alta complexidade da estrutura administrativa e a existência de diversos campi podem ser entendidas como barreiras para seu desenvolvimento. O estudo auxilia tomadores de decisão a entender como as particularidades das IES e o contexto em que se inserem impactam no desenvolvimento das ações de gestão ambiental.


ABSTRACT This research aims at exploring which characteristics of Higher Education Institutions act as enablers or barriers in the development of environmental management actions. The beta regression analysis of 38 sustainability reports prepared in accordance with the Global Reporting Initiative (GRI) guidelines showed that the institution's ease of access to financial resources, the existence of an environmental/sustainability plan or policy and the public nature can be considered as enablers for the development of environmental management in HEI, while high complexity of the administrative structure and the existence of several campuses can be understood as barriers to its development. The study helps decision makers understand how the particularities of HEIs and the context in which they operate impact the development of environmental management actions.

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