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1.
Lancet ; 396(10249): 479-488, 2020 08 15.
Artigo em Inglês | MEDLINE | ID: mdl-32702299

RESUMO

BACKGROUND: This is the first randomised controlled trial for assessment of the immunogenicity and safety of a candidate non-replicating adenovirus type-5 (Ad5)-vectored COVID-19 vaccine, aiming to determine an appropriate dose of the candidate vaccine for an efficacy study. METHODS: This randomised, double-blind, placebo-controlled, phase 2 trial of the Ad5-vectored COVID-19 vaccine was done in a single centre in Wuhan, China. Healthy adults aged 18 years or older, who were HIV-negative and previous severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection-free, were eligible to participate and were randomly assigned to receive the vaccine at a dose of 1 × 1011 viral particles per mL or 5 × 1010 viral particles per mL, or placebo. Investigators allocated participants at a ratio of 2:1:1 to receive a single injection intramuscularly in the arm. The randomisation list (block size 4) was generated by an independent statistician. Participants, investigators, and staff undertaking laboratory analyses were masked to group allocation. The primary endpoints for immunogenicity were the geometric mean titres (GMTs) of specific ELISA antibody responses to the receptor binding domain (RBD) and neutralising antibody responses at day 28. The primary endpoint for safety evaluation was the incidence of adverse reactions within 14 days. All recruited participants who received at least one dose were included in the primary and safety analyses. This study is registered with ClinicalTrials.gov, NCT04341389. FINDINGS: 603 volunteers were recruited and screened for eligibility between April 11 and 16, 2020. 508 eligible participants (50% male; mean age 39·7 years, SD 12·5) consented to participate in the trial and were randomly assigned to receive the vaccine (1 × 1011 viral particles n=253; 5 × 1010 viral particles n=129) or placebo (n=126). In the 1 × 1011 and 5 × 1010 viral particles dose groups, the RBD-specific ELISA antibodies peaked at 656·5 (95% CI 575·2-749·2) and 571·0 (467·6-697·3), with seroconversion rates at 96% (95% CI 93-98) and 97% (92-99), respectively, at day 28. Both doses of the vaccine induced significant neutralising antibody responses to live SARS-CoV-2, with GMTs of 19·5 (95% CI 16·8-22·7) and 18·3 (14·4-23·3) in participants receiving 1 × 1011 and 5 × 1010 viral particles, respectively. Specific interferon γ enzyme-linked immunospot assay responses post vaccination were observed in 227 (90%, 95% CI 85-93) of 253 and 113 (88%, 81-92) of 129 participants in the 1 × 1011 and 5 × 1010 viral particles dose groups, respectively. Solicited adverse reactions were reported by 183 (72%) of 253 and 96 (74%) of 129 participants in the 1 × 1011 and 5 × 1010 viral particles dose groups, respectively. Severe adverse reactions were reported by 24 (9%) participants in the 1 × 1011 viral particles dose group and one (1%) participant in the 5 × 1010 viral particles dose group. No serious adverse reactions were documented. INTERPRETATION: The Ad5-vectored COVID-19 vaccine at 5 × 1010 viral particles is safe, and induced significant immune responses in the majority of recipients after a single immunisation. FUNDING: National Key R&D Programme of China, National Science and Technology Major Project, and CanSino Biologics.


Assuntos
Betacoronavirus/imunologia , Infecções por Coronavirus/prevenção & controle , Pandemias/prevenção & controle , Pneumonia Viral/prevenção & controle , Vacinas Virais/efeitos adversos , Vacinas Virais/imunologia , Adenoviridae , Adolescente , Adulto , Fatores Etários , Idoso , Idoso de 80 Anos ou mais , Anticorpos Neutralizantes/sangue , Anticorpos Antivirais/sangue , COVID-19 , Vacinas contra COVID-19 , China , Infecções por Coronavirus/imunologia , Método Duplo-Cego , Feminino , Vetores Genéticos , Humanos , Masculino , Pessoa de Meia-Idade , SARS-CoV-2 , Glicoproteína da Espícula de Coronavírus/imunologia , Linfócitos T/imunologia , Vacinas Virais/administração & dosagem , Adulto Jovem
2.
Ying Yong Sheng Tai Xue Bao ; 32(3): 1112-1118, 2021 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-33754579

RESUMO

Cotton is one of the most important crops in the world. With the increasing scarce of global water resources, irrigation water will become a major limiting factor in cotton production. Deficit irrigation is an irrigation method which consumes less water than the normal evapotranspiration of crops. It is an effective water-saving method due to improved water use efficiency without sacrificing cotton yield and fiber quality. We summarized the effects of deficit irrigation on the growth and water use efficiency of cotton. The results showed that deficit irrigation promoted the transformation from vegetative growth to reproductive growth, reduced plant height, leaf area, and total biomass of cotton, and subsequently improved the harvest index, stem diameter and water use efficiency. Finally, based on the current research and combined with cotton production reality, the application and future development of deficit irrigation were proposed, which might provide theoretical guidance for the sustainable development of cotton plantation in arid areas.


Assuntos
Irrigação Agrícola , Água , Biomassa , Produtos Agrícolas , Folhas de Planta
3.
PLoS One ; 7(2): e28839, 2012.
Artigo em Inglês | MEDLINE | ID: mdl-22363396

RESUMO

BACKGROUND: A recent genome-wide association study has identified a new susceptibility locus, kinesin family member 1B gene (KIF1B), strongly associated with progression from chronic hepatitis B (CHB) to hepatitis B virus-related hepatocellular carcinoma (HCC) in Chinese population, this study was carried out to explore the role of the genetic variants in KIF1B in the development of chronic hepatitis B. METHODOLOGY/PRINCIPAL FINDINGS: Three KIF1B polymorphisms (rs8019, rs17401924, and rs17401966) were selected and genotyped in 473 CHB patients and 580 controls with no history of CHB. Odds ratios (ORs) and 95% confidence intervals (CIs) were calculated by logistic regression model. None of these three SNPs showed association with CHBs after adjusting for age and gender. Equivalence-based method analysis confirmed the absence of association. In the further haplotype analysis, three common haplotypes were observed in this study population, but no significant effect was also found for haplotypes in the progression to CHB. CONCLUSIONS/SIGNIFICANCE: This study showed the new locus identified for HCC, KIF1B, was not associated with progression to CHB, implying distinct genetic susceptibility factor contributes to the progression from hepatitis B virus infection to HCC. Nevertheless, further comprehensive analyses are warranted to dissect the mechanism.


Assuntos
Carcinoma Hepatocelular/genética , Carcinoma Hepatocelular/virologia , Predisposição Genética para Doença , Vírus da Hepatite B/fisiologia , Hepatite B Crônica/genética , Hepatite B Crônica/virologia , Cinesinas/genética , Adulto , Povo Asiático/genética , Carcinoma Hepatocelular/complicações , Estudos de Casos e Controles , China , Feminino , Estudos de Associação Genética , Haplótipos/genética , Hepatite B Crônica/complicações , Humanos , Neoplasias Hepáticas/complicações , Neoplasias Hepáticas/genética , Neoplasias Hepáticas/virologia , Masculino , Razão de Chances , Polimorfismo de Nucleotídeo Único/genética , Reprodutibilidade dos Testes , Fatores de Risco
4.
PLoS One ; 6(11): e27301, 2011.
Artigo em Inglês | MEDLINE | ID: mdl-22087284

RESUMO

BACKGROUND: Metabolic syndrome traits play an important role in the development of colorectal cancer. Adipokines, key metabolic syndrome cellular mediators, when abnormal, may induce carcinogenesis. METHODOLOGY/PRINCIPAL FINDINGS: To investigate whether polymorphisms of important adipokines, adiponectin (ADIPOQ) and its receptors, either alone or in combination with environmental factors, are implicated in colorectal cancer, a two-stage case-control study was conducted. In the first stage, we evaluated 24 tag single nucleotide polymorphisms (tag SNPs) across ADIPOQ ligand and two ADIPOQ receptors (ADIPOR1 and ADIPOR2) among 470 cases and 458 controls. One SNP with promising association was then analyzed in stage 2 among 314 cases and 355 controls. In our study, ADIPOQ rs1063538 was consistently associated with increased colorectal cancer risk, with an odds ratio (OR) of 1.94 (95%CI: 1.48-2.54) for CC genotype compared with TT genotype. In two-factor gene-environment interaction analyses, rs1063538 presented significant interactions with smoking status, family history of cancer and alcohol use, with ORs of 4.52 (95%CI: 2.78-7.34), 3.18 (95%CI: 1.73-5.82) and 1.97 (95%CI: 1.27-3.04) for smokers, individuals with family history of cancer or drinkers with CC genotype compared with non-smokers, individuals without family history of cancer or non-drinkers with TT genotype, respectively. Multifactor gene-environment interactions analysis revealed significant interactions between ADIPOQ rs1063538, ADIPOR1 rs1539355, smoking status and BMI. Individuals carrying one, two and at least three risk factors presented 1.18-fold (95%CI:0.89-fold to 1.58-fold), 1.87-fold (95%CI: 1.38-fold to 2.54-fold) and 4.39-fold (95%CI: 2.75-fold to 7.01-fold) increased colorectal cancer risk compared with those who without risk factor, respectively (P(trend) <0.0001). CONCLUSIONS/SIGNIFICANCE: Our results suggest that variants in ADIPOQ may contribute to increased colorectal cancer risk in Chinese and this contribution may be modified by environmental factors, such as smoking status, family history of cancer and BMI.


Assuntos
Adiponectina/genética , Neoplasias Colorretais/etiologia , Interação Gene-Ambiente , Polimorfismo de Nucleotídeo Único , Receptores de Adiponectina/genética , Índice de Massa Corporal , Estudos de Casos e Controles , China/epidemiologia , Neoplasias Colorretais/genética , Família , Feminino , Predisposição Genética para Doença , Genótipo , Humanos , Masculino , Síndrome Metabólica/complicações , Pessoa de Meia-Idade , Fatores de Risco , Fumar
5.
Virology ; 375(1): 301-6, 2008 May 25.
Artigo em Inglês | MEDLINE | ID: mdl-18308361

RESUMO

Human astrovirus is one of the important causes for viral gastroenteritis in young children. In previous study where we examined the molecular epidemiology of human astrovirus (HAstV) infection in infants in Wuhan City, we isolated and identified a new subtype (WH1859) of HAstV genotype 3 from an infant with diarrhea. The sequence analysis of this strain showed that the complete region of ORF2 of WH1859 contains 2385-bp of nucleotides that encode 795 amino acids. Because WH1859 strain has the identity of less than 95% with the distance of more than 0.05 to the reference strains of HAstV-3, WH1859 represents a distinct subtype within HAstV-3 strains. Further studies are needed to determine the role of this new subtype strain of HAstV in viral gastroenteritis among young children.


Assuntos
Infecções por Astroviridae/virologia , Diarreia/virologia , Mamastrovirus/classificação , Mamastrovirus/genética , Sequência de Aminoácidos , China , Genótipo , Humanos , Lactente , Masculino , Mamastrovirus/isolamento & purificação , Dados de Sequência Molecular , Fases de Leitura Aberta , Filogenia , Alinhamento de Sequência , Análise de Sequência de DNA , Homologia de Sequência
6.
J Clin Microbiol ; 45(4): 1308-9, 2007 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-17301278

RESUMO

We report the molecular epidemiology of astrovirus infection in 335 infants with diarrhea in Wuhan City, China. Astrovirus RNA was detected in the stool specimens of 33 children (9.87%). Genotyping analysis indicated that 23 out of 24 astroviruses identified were classified as belonging to genotype 1, with highest identity (>98%) to a Mongolian strain.


Assuntos
Infecções por Astroviridae/virologia , Mamastrovirus/classificação , Mamastrovirus/genética , Infecções por Astroviridae/epidemiologia , China/epidemiologia , Diarreia/virologia , Fezes/virologia , Gastroenterite/virologia , Genótipo , Humanos , Lactente , Mamastrovirus/isolamento & purificação , Epidemiologia Molecular , Dados de Sequência Molecular , RNA Viral/análise , RNA Viral/genética , Análise de Sequência de DNA , Homologia de Sequência
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