4 resultados para PFU
em Scielo Saúde Pública - SP
Resumo:
The rhesus-human reassortant, tetravalent rotavirus vaccine (RRV-TV) was licensed for routine use in the United States of America but it was recently withdrawn from the market because of its possible association with intussusception as an adverse event. The protective efficacy of 3 doses of RRV-TV, in its lower-titer (4 x 10(4) pfu/dose) formulation, was evaluated according to the nutritional status of infants who participated in a phase III trial in Belém, Northern Brazil. A moderate protection conferred by RRV-TV was related to weight-for-age Z-scores (WAZ) greater than -1 only, with rates of 38% (p = 0.04) and 40% (p = 0.04) for all- and- pure rotavirus diarrhoeal cases, respectively. In addition, there was a trend for greater efficacy (43%, p = 0.05) among infants reaching an height-for-age Z-score (HAZ) of > -1. Taking WAZ, HAZ and weight-for-height Z-score (WHZ) indices <= -1 together, there was no significant protection (p > 0.05) if both placebo and vaccine groups are compared. There was no significant difference if rates of mixed and pure rotavirus diarrhoeal cases are compared in relation to HAZ, WAZ and weight-for-height Z-score (WHZ) indices. Although a low number of malnourished infants could be identified in the present study, our data show some evidence that malnutrition may interfere with the efficacy of rotavirus vaccines in developing countries.
Resumo:
The assessment of yellow fever vaccine thermostability both in lyophilized form and after reconstitution were analyzed. Two commercial yellow fever vaccines were assayed for their thermal stability. Vaccines were exposed to test temperatures in the range of 8 (graus) C to 45 (graus) C. Residual infectivity was measured by a plaque assay using Vero cells. The titre values were used in an accelerated degradation test that follows the Arrhenius equation and the minimum immunizing dose was assumed to be 10 (ao cubo) particles forming unit (pfu)/dose. Some of the most relevant results include that (i) regular culture medium show the same degradation pattern of a reconstituted 17D-204 vaccine; (ii) reconstituted YF-17D-204 showed a predictable half life of more than six days if kept at 0 (graus) C; (iii) there are differences in thermostability between different products that are probably due to both presence of stabilizers in the preparation and the modernization in the vaccine production; (iv) it is important to establish a proper correlation between the mouse infectivity test and the plaque assay since the last appears to be more simple, economical, and practical for small laboratories to assess the potency of the vaccine, and (v) the accelerated degradation test appears to be the best procedure to quantify the thermostability of biological products.
Resumo:
Aedes albopictus was responsible for transmission in the first outbreak of chikungunya (CHIK) on La Réunion Island, Indian Ocean, in 2005-2006. The magnitude of the outbreak on this island, which had been free of arboviral diseases for over 30 years, as well as the efficiency of Ae. albopictus as the main vector, raises questions about the maintenance of the CHIK virus (CHIKV) through vertical transmission mechanisms. Few specimens collected from the field as larvae were found to be infected. In this study, Ae. albopictus originating from La Réunion were orally infected with a blood-meal containing 10(8) pfu/mL of the CHIKV epidemic strain (CHIKV 06.21). Eggs from the first and second gonotrophic cycles were collected and raised to the adult stage. The infectious status of the progeny was checked (i) by immunofluorescence on head squashes of individual mosquitoes to detect the presence of viral particles or (ii) by quantitative RT-PCR on mosquito pools to detect viral RNA. We analysed a total of 1,675 specimens from the first gonotrophic cycle and 1,709 from the second gonotrophic cycle without detecting any viral particles or viral RNA. These laboratory results are compared to field records.
Resumo:
RESUMOO azevém é uma planta daninha de ciclo anual, encontrada em praticamente todas as lavouras de inverno, em pomares e vinhedos da região Sul do Brasil. A espécie é normalmente controlada pelo herbicida glyphosate, no entanto, o uso continuado desse produto selecionou biótipos resistentes. Diferenças na suscetibilidade do azevém a herbicidas têm sido atribuídas a características morfológicas, anatômicas e genéticas das plantas. Os objetivos deste trabalho foram realizar a caracterização morfoanatômica, adequar metodologia para a análise citológica de cromossomos e indicar corantes para testes de viabilidade polínica de biótipos de azevém suscetível e resistentes ao herbicida glyphosate. As sementes dos biótipos de azevém suspeitos de resistência provieram do município de São Valentin, RS (SVA 1 e SVA 4), e Passo Fundo, RS (PFU 5), e as do biótipo conhecidamente suscetível (SVA 2), de São Valentin. Os biótipos de azevém estudados que apresentam resistência ao herbicida glyphosate não podem ser diferenciados do biótipo suscetível através de aspectos morfológicos, não existindo diferenças anatômicas de folha e raiz que evidenciem possibilidade da absorção diferencial do herbicida glyphosate entre os biótipos de azevém. A metodologia para a análise citológica dos biótipos de azevém merece adequações para melhor nitidez dos cromossomos, podendo-se aumentar o tempo de hidrólise e de exposição ao agente antimitótico utilizado neste trabalho, bem como testar outros agentes. Todos os corantes apresentaram bom desempenho na determinação da viabilidade polínica frente aos biótipos avaliados, exceto o azul de tripan, que subestimou os resultados.