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1.
Rheumatology, v. 57, n. 10, p. 1721-1725, out. 2018
Article in English | Sec. Est. Saúde SP, SESSP-IBPROD, Sec. Est. Saúde SP | ID: bud-2575

ABSTRACT

Abstract Objective To assess the possible effect of therapy, disease subtype and severity on H1N1 immunogenicity in patients with SSc. Methods Ninety-two patients and 92 age- and gender-matched healthy controls received adjuvant-free influenza A/California/7/2009 (pH1N1) vaccine. Blood samples were collected immediately before and 3 weeks after vaccination to evaluate antibody responses to the H1N1 virus. Efficacy was assessed by seroprotection (SP) and seroconversion (SC) rates and the factor increase in geometric mean antibody titre. Participants received a 21-day symptom diary card and were instructed to report local and systemic adverse events. Results SSc patients were predominantly females (91%) and 61% had limited SSc, 12% had severe skin involvement and 57.6% were on immunosuppressive (IS) therapy. SSc patients and controls presented comparable overall SP (P = 0.20) and SC (P = 0.61) rates. Further evaluation of the possible effect of disease and therapy revealed similar rates of SP and SC in patients with dcSSc vs lcSSc (SP P = 0.62 and SC P = 0.66), severe vs mild/moderate skin involvement (SP P = 1 and SC P = 0.45) and with vs without IS (SP P = 0.26 and SC P = 0.10). The frequency of mild local and minor systemic reactions was similar in patients with dcSSC vs lcSSc (P = 0.70 vs 0.32) and in those with and without severe skin involvement (P = 0.59 vs 0.28). Conclusion The non-adjuvanted influenza H1N1 virus vaccine proved to be safe and effective, independent of SSc clinical subtype, disease severity or therapy. These latter factors do not seem to contribute to mild adverse events observed in SSc. Our data support the annual influenza vaccination recommendation for these patients.

2.
Exp Mol Pathol ; 99(2): 253-61, 2015 Oct.
Article in English | MEDLINE | ID: mdl-26148929

ABSTRACT

BACKGROUND: Overproduction of pro-inflammatory cytokines and chemokines is frequently associated with severe clinical manifestations in patients infected with influenza A/H1N1 virus. Micro-RNAs (miRNAs) are highly conserved small non-coding RNA molecules that post-transcriptionally regulate gene expression and are potential biomarkers and therapeutic targets in different inflammatory conditions. METHODS: We studied the circulating and miRNA profiles in critically ill A/H1N1 patients, A/H1N1 patients with milder disease, asymptomatic housemates and healthy controls. Cytokine, chemokine and growth factors that were potential targets of differentially expressed miRNAs were assessed. Kyoto Encyclopedia of Genes and Genomes (KEGG) pathway enrichment and interactome analysis of these miRNAs were also performed. RESULTS: Critically ill patients exhibited a significant over-expression of circulating miR-150 (p<0.005) when compared to patients with milder disease. miR-29c, miR-145 and miR-22 were differentially expressed in patients with severe A/H1N1 disease whereas miR-210, miR-126 and miR-222 were downregulated in individuals exposed to the A/H1N1 virus. Significant correlations (p<0.05) between circulating levels of miR-150 with IL-1ra, IL-2, IL-6, CXCL8, IFN-γ, CXCL10 and G-CSF were detected, particularly in critically ill patients. CONCLUSION: The up-regulation of miR-150 is associated with poorer outcomes of A/H1N1 infection. The differential expression of miRNAs related with immune processes in severe A/H1N1 disease supports the potential role of these miRNAs as biomarkers of disease progression.


Subject(s)
Biomarkers/blood , Influenza A Virus, H1N1 Subtype/genetics , Influenza, Human/genetics , MicroRNAs/genetics , Severity of Illness Index , Adult , Case-Control Studies , Cells, Cultured , Cytokines/blood , Enzyme-Linked Immunosorbent Assay , Female , Gene Expression Profiling , Humans , Influenza, Human/blood , Influenza, Human/virology , Male , MicroRNAs/blood , Oligonucleotide Array Sequence Analysis , RNA, Messenger/genetics , Real-Time Polymerase Chain Reaction , Reverse Transcriptase Polymerase Chain Reaction
3.
Rev. chil. salud pública ; 18(2): 173-182, 2014. tab
Article in Spanish | LILACS | ID: biblio-836058

ABSTRACT

Objetivo. Determinar los factores asociados a la mortalidad por influenzapA(H1N1) en los pacientes hospitalizados por infección respiratoria agudagrave (IRAG) confirmada por reacción en cadena de la polimerasa (PCR)en el Instituto Mexicano del Seguro Social (IMSS).Material y métodos. En el IMSS en la delegación de Nuevo León entre el1 de junio de 2009 y 9 de marzo de 2010 se realizó un estudio observacionalretrospectivo de casos y controles, utilizando la base de datos del Sistemade Información en Línea para la Vigilancia Epidemiológica de Influenza(SINOLAVE). Se incluyeron 278 pacientes hospitalizados con IRAG (controles)y 50 pacientes con IRAG que fallecieron (casos) debido a la infecciónpor virus influenza pA(H1N1).Resultados. Los factores asociados a la mortalidad en los pacientes hospitalizadospor IRAG debida a influenza pA(H1N1) fueron la edad (OR: 1,03IC95% 1,01-1,05) y la obesidad (OR: 4,44 IC95% 1,85-1,6), utilizando unmodelo de regresión logística.Conclusión. Podemos concluir que en la delegación de Nuevo León delIMSS, la influenza pA(H1N1) afectó principalmente a adultos jóvenes, sinembargo las muertes se presentaron en mayor número en los pacientes alincrementar la edad y en pacientes con alguna comorbilidad.Palabras clave: Influenza pandémica A(H1N1), mortalidad, infección respiratoriaaguda grave, factores de riesgo, razón de probabilidad.


Objective. To determine factors associated with mortality from pAinfluenzA(H1N1) – confirmed by polymerase chain reaction (PCR) – Inhospitalized patients with severe acute respiratory infection (SARI) in theMexican Social Security Institute (IMSS). Methods. In the IMSS in the Delegation of Nuevo Leon between June 1, 2009 and March9, 2010 a retrospective observational case-control study was conducted using the database ofOnline Information System for Epidemiological Surveillance of Influenza (SINOLAVE). 278inpatients with SARI (controls) and 50 SARI patients who died (cases) due to infection withinfluenza virus pA(H1N1) were included.Results. In the logistic regression model factors associated with mortality in patientshospitalized due to SARI pA influenzA(H1N1) were age (OR: 1.03 95% CI 1.01-1.05) andobesity (OR: 4.44 95 1.85 to 1%, 0.6).Conclusion. We can conclude that the delegation of Nuevo León of the IMSS, pAinfluenzA(H1N1) affects mainly young adults, though the deaths occurred in greater numbersin patients with increasing age and in patients with comorbidities.


Subject(s)
Humans , Male , Female , Middle Aged , Influenza, Human/mortality , Influenza A Virus, H1N1 Subtype , Hospitalization , Respiratory Tract Infections/mortality , Logistic Models , Mexico/epidemiology , Observational Study , Odds Ratio , Pandemics , Retrospective Studies , Risk Factors
4.
Rev. Soc. Bras. Med. Trop ; Rev. Soc. Bras. Med. Trop;46(3): 348-351, May-Jun/2013. tab, graf
Article in English | LILACS | ID: lil-679515

ABSTRACT

Introduction This paper describes adverse events (AEs) temporally associated to the pandemic influenza A (H1N1) vaccine observed in a reference center in São Paulo, Brazil, during a 2010 mass vaccination campaign. Methods A retrospective study involving persons who sought medical care for AEs following influenza vaccination. Data were retrieved from medical records, vaccine AE notification forms, and a computerized system for immunobiological registration. Results Sixty-six vaccinees sought medical care for AEs after immunization. The most frequent AEs were fever, headache, myalgia, and pain at the injection site. No serious AEs were reported. Conclusions Few vaccinees spontaneously reported AEs to influenza A (H1N1) vaccine at this center. .


Subject(s)
Adolescent , Adult , Aged , Child , Female , Humans , Male , Middle Aged , Young Adult , Influenza A Virus, H1N1 Subtype , Influenza Vaccines/adverse effects , Influenza, Human/prevention & control , Pandemics , Brazil/epidemiology , Influenza, Human/epidemiology , Injections, Intradermal/adverse effects , Mass Vaccination , Retrospective Studies
5.
Rev. Soc. Bras. Med. Trop ; Rev. Soc. Bras. Med. Trop;46(2): 135-140, Mar-Apr/2013. tab, graf
Article in English | LILACS | ID: lil-674656

ABSTRACT

Introduction The objetctive of this study was to evaluate the 2009 Pandemic Influenza A (H1N1) in the elderly and identify the clinical characteristics, mortality and prognostic factors of the infection in these patients. Methods This was an observational, retrospective study. Data were collected from the National Notifiable Diseases (SINAN), from the Brazilian Ministry of Health. Only patients 60 years old or more that had laboratory confirmed infections were included. The socio-demographic and clinical variables and outcomes were evaluated to compare mortality rates in the presence or absence of these factors. Results We included 93 patients in the study, 16.1% of whom died. The symptoms of cough and dyspnea, the use of the antiviral oseltamivir, influenza vaccine and comorbidities influenced the outcomes of cure or death. Chest radiography can aid in diagnosis. Conclusions Although relatively few elderly people were infected, this population presented high lethality that can be justified by the sum of clinical, physical and immunological factors in this population. Treatment with oseltamivir and vaccination against seasonal influenza have significantly reduced rates of hospitalization and mortality. .


Subject(s)
Adolescent , Adult , Aged , Aged, 80 and over , Child , Child, Preschool , Female , Humans , Male , Middle Aged , Young Adult , Influenza A Virus, H1N1 Subtype , Influenza, Human/mortality , Pandemics , Age Distribution , Age Factors , Brazil/epidemiology , Influenza, Human/virology , Prognosis , Retrospective Studies , Risk Factors , Sex Distribution , Socioeconomic Factors
6.
Influenza Other Respir Viruses ; 7(5): 629-33, 2013 Sep.
Article in English | MEDLINE | ID: mdl-23136977

ABSTRACT

The trends of influenza infection in Suriname were assessed from February 2010 through February 2011. Testing of 393 patients with symptoms of acute respiratory infection (ARI) revealed 15.3% Influenza B and 18.6% could be identified as influenza A positive, consisting of 56% influenza A(H1N1)pdm09 and 44% seasonal A(H3N2). Influenza infection occurred throughout the year, and all three influenza types affected young children as the primary population. The annual incidence of A(H1N1)pdm09 was 6.88 per 100,000 inhabitants [CI] 4.87-9.45. The spread of influenza could neither be linked to tourist flow from the Netherlands nor to contact rates related to school schedules.


Subject(s)
Influenza A Virus, H1N1 Subtype/isolation & purification , Influenza A Virus, H3N2 Subtype/isolation & purification , Influenza B virus/isolation & purification , Influenza, Human/epidemiology , Adolescent , Adult , Age Distribution , Aged , Child , Child, Preschool , Female , Humans , Infant , Influenza A Virus, H1N1 Subtype/classification , Influenza A Virus, H1N1 Subtype/genetics , Influenza A Virus, H1N1 Subtype/physiology , Influenza A Virus, H3N2 Subtype/classification , Influenza A Virus, H3N2 Subtype/genetics , Influenza A Virus, H3N2 Subtype/physiology , Influenza B virus/classification , Influenza B virus/genetics , Influenza B virus/physiology , Influenza, Human/virology , Male , Middle Aged , Pandemics , Seasons , Suriname/epidemiology , Young Adult
7.
Rev. cuba. med. trop ; 63(1): 15-20, ene.-abr. 2011.
Article in Spanish | LILACS | ID: lil-584965

ABSTRACT

INTRODUCCIÓN: entre marzo y abril de 2009 se produjeron en México brotes de enfermedad respiratoria, debido a un nuevo virus de influenza proveniente del cerdo, el cual se diseminó rápidamente mediante la transmisión humano-humano. Los métodos moleculares usados en la actualidad eran inadecuados, porque la composición del genoma del nuevo virus era muy diferente del virus influenza A (H1N1) que había circulado hasta el momento. En su composición, estaba formado por segmentos de genes de origen aviar, humano y cerdo. OBJETIVO: teniendo en cuenta las secuencias publicadas, se diseñó un juego de cebadores específicos para el gen de la hemaglutinina, con la finalidad de evaluar un nuevo ensayo de TR-RCP para detectar el nuevo virus pandémico en Cuba. MÉTODOS: se procesó un total de 3 197 muestras clínicas de casos sospechosos de infección por el virus influenza A (H1N1) pandémico (pdm) mediante un ensayo de transcripción reversa-reacción en cadena de la polimerasa. RESULTADOS: el ensayo optimizado permitió obtener una banda de 292 pb, sin reacciones inespecíficas. El nuevo método resultó ser útil en el diagnóstico y subtipado del virus de influenza H1N1 pdm. El producto amplificado fue analizado por secuenciación nucleotídica y se confirmó la identificación del virus. CONCLUSIONES: con la introducción de este nuevo ensayo para la vigilancia de influenza, se fortalece la capacidad diagnóstica del Laboratorio Nacional de Referencia.


INTRODUCTION: from March through April of 2009, Mexico notified outbreaks of respiratory illness, due to a new influenza virus of swine origin, which spread over rapidly via human-to-human transmission. The molecular methods currently in use were not suitable because the genome composition based on gene segments of swine, avian and human origin was quite different from the influenza A virus (H1N1) circulating at that time. OBJECTIVE: based on the published sequences, a set of specific primers for the HA gene was designed to evaluate a new RT-PCR assay. METHODS: the RT-PCR assay processed 3 197 clinical samples from suspected cases of pandemic influenza A (H1N1) infection. RESULTS: the novel optimized method obtained a 262 pb segment, without unspecific reactions. The new method proved to be useful in the diagnosis and subtyping of pandemic HINI influenza virus. The amplified product was verified by nucleotide sequencing, thus confirming the virus. CONCLUSIONS: the introduction of this new assay for the laboratory surveillance of influenza virus strengthens the diagnostic capacity of the National Reference Laboratory.


Subject(s)
Humans , Influenza A Virus, H1N1 Subtype/genetics , Influenza A Virus, H1N1 Subtype/isolation & purification , Influenza, Human/diagnosis , Influenza, Human/virology , Cuba , Molecular Diagnostic Techniques/methods
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