Inmunogenicidad de la vacuna cubana recombitante contra HVB, en niños de 1 a 10 años

We evaluated the immunogenecity of the recombinant HBV Cuban vaccine, utilising the 012 months scheme in children between 1 to 10 years of age. Whith the second dose, 98% of after the vaccinated children developed seroprotection (values 210 IU/l) and after the third dose (75 days), 100% had antibody levels > 100 IU/l.Evaluamos la inmunogenicidad de la vacuna cubana recombinane contra la HBV aplicando el esquema 012 meses, en niños de 1 a 10 años, encontrándose que con la segunda dosis el 98% tienen seroprotección (valores 10 Ul/l) y después de la tercera dosis (75 días) el 100% de los vacunados tienen niveles de anticuerpos 100 Ul/l

Resultados al primer año de aplicada la vacuna recombinante cubana antiHVB en esquemas 012 y 016 meses

An immunoassay analysis of the seroprotection achieved one year after vaccination with the Cuban recombinant vaccine anti-VHB, revealed immunogenicity in 100% ofthose vaccinated with the schemes 012 and 016 months and reached values 100 lU/l in 97% for both schemes. The geometrical media showed a significan reductiion with the 016 scheme but not with the 012 scheme. Consequently, we propose the use of the levels 012 scheme because of its short latency, simmety and stability of the levels anti-HBs stability antibody.Los resultados obtenidos por el método inmunoenzimático cuantitativo de Abbott al primer año de completados los esquemas 012 y 016 meses, con la vacuna recombinante cubana contra la hepatitis viral B, muestran la inmunogenicidad en los vacunados con los dos esquemas, viéndose que el 100% tienen seroprotección y el 97% de estos tienen valores 100 Ul/l para ambos esquemas. En cuanto a los valores de las medias geométricas, observamos que no se evidencian disminuciones significativas con el esquema 012, pero sí con el esquema 016, por lo cual sugerimos el uso del esquema 012, debido a su corta latencia, simetría y estabilidad de los valores de anticuerpos anti-HBs

Antioxidant and anti-inflammatory extracts from sea cucumbers and tunicates induce a pro-osteogenic effect in Zebrafish Larvae

Bone metabolic disorders such as osteoporosis are characterized by the loss of mineral from the bone tissue leading to its structural weakening and increased susceptibility to fractures. A growing body of evidence suggests that inflammation and oxidative stress play an important role in the pathophysiological processes involved in the rise of these conditions. As the currently available therapeutic strategies are often characterized by toxic effects associated with their long-term use, natural antioxidants and anti-inflammatory compounds such as polyphenols promise to be a valuable alternative for the prevention and treatment of these disorders. In this scope, the marine environment is becoming an important source of bioactive compounds with potential pharmacological applications. Here, we explored the bioactive potential of three species of holothurians (Echinodermata) and four species of tunicates (Chordata) as sources of antioxidant and anti-inflammatory compounds with a particular focus on polyphenolic substances. Hydroethanolic and aqueous extracts were obtained from animals' biomass and screened for their content of polyphenols and their antioxidant and anti-inflammatory properties. Hydroethanolic fractions of three species of tunicates displayed high polyphenolic content associated with strong antioxidant potential and anti-inflammatory activity. Extracts were thereafter tested for their capacity to promote bone formation and mineralization by applying an assay that uses the developing operculum of zebrafish (Danio rerio) to assess the osteogenic activity of compounds. The same three hydroethanolic fractions from tunicates were characterized by a strong in vivo osteogenic activity, which positively correlated with their anti-inflammatory potential as measured by COX-2 inhibition. This study highlights the therapeutic potential of polyphenol-rich hydroethanolic extracts obtained from three species of tunicates as a substrate for the development of novel drugs for the treatment of bone disorders correlated to oxidative stress and inflammatory processes.info:eu-repo/semantics/publishedVersio

Genetic Evidence of Importation of Drug-Resistant Plasmodium falciparum to Guatemala from the Democratic Republic of the Congo

Molecular markers and population genetics were effective tracking tools.Imported malaria threatens control and elimination efforts in countries that have low rates of transmission. In 2010, an outbreak of Plasmodium falciparum malaria was reported among United Nations peacekeeping soldiers from Guatemala who had recently returned from the Democratic Republic of the Congo (DRC). Epidemiologic evidence suggested that the soldiers were infected in the DRC, but local transmission could not be ruled out in all cases. We used population genetic analyses of neutral microsatellites to determine the outbreak source. Genetic relatedness was compared among parasites found in samples from the soldiers and parasite populations collected in the DRC and Guatemala; parasites identified in the soldiers were more closely related to those from the DRC. A phylogenetic clustering analysis confirms this identification with >99.9% confidence. Thus, results support the hypothesis that the soldiers likely imported malaria from the DRC. This study demonstrates the utility of molecular genotyping in outbreak investigations

Estudio de inmunogenicidad para dos vacunas recombinantes contra hepatitis B

This study compares the immunogenicity (seroconversion, seroprotection and hiperesponse) produced by two hepatitis B recombinant vaccines (Engerix- B Belge and Cuban). For this purpose two sketches were used (012 and 016 months). The anti-HBs quantification was performed by using Abbott and Organon methods in order to compare its results. In the study 257 volunteers were distributed in four groups to the hapazard (two vaccines and two sketches). Results: the Abbott and Organon methods did not show any statistically significant difference. The Cuban vaccine shows greater immunogenous response for two doses and 012 sketch. There are no differences between sketch 012 and 016 with the Cuban vaccine. The scheme 016 did not show statistically significant difference for the Engerix-B Belge vaccine. The last mentioned vaccine showed to be better with the 016 scheme.Este estudio compara la inmunogenicidad (seroconversión, seroprotección e Hiperrespuesta), producida por dos vacunas recombinantes contra la hepatitis B (Engerix-B de Bélgica y Cubana), en dos esquemas (012 y 016 meses), empleando los métodos de cuantificación para Anti-HBsAg (Abbott y Organón), los cuales fueron también comparados. En el estudio participaron 257 voluntarios,  divididos al azar en 4 grupos (dos vacunas, dos esquemas). Resultados: los dos métodos de Abbon y Organon, no presentan diferencias estadísticas significativas. La vacuna cubana muestra una mayor respuesta inmunogénica para dos dosis de vacuna y para el esquema 012. No hay diferencia entre los esquemas 012 y 016 y en el esquema 016 no se ven diferencias estadísticamente significativas con la vacuna Engerix-B. En esta Última el esquema 016 muestra mejores resultados que el 012

First Colombian Multicentric Newborn Screening for Congenital Toxoplasmosis

Congenital toxoplasmosis can result in permanent sequel as blindness or neurological damage in children and it seems to be more severe in South America than in other continents. There is a lack of information about this frequency in Colombia, where no control program is established, although it is a recognized cause of potentially preventable congenital blindness. We propose the first Colombian multicentric study to determine the frequency and impact of congenital toxoplasmosis. More than 15,000 newborns in seven cities were studied. Newborns were tested at birth by doing a cord blood test for toxoplasmosis. Additionally, children from mothers with history of toxoplasmosis acquired during pregnancy were recalled for a follow-up. The program identified fifteen children otherwise undiagnosed; three of these children died as consequence of congenital toxoplasmosis. The frequency of the congenital infection varied significantly between cities, being higher in Armenia and Florencia, intermediate in Bogota, Bucaramanga and Barranquilla and very low in western cities such as Cucuta and Riohacha. For the first time a significant correlation was found between mean rainfall at the city and the incidence of this congenital infection

The Complete Genome Sequence of the Pathogenic Intestinal Spirochete Brachyspira pilosicoli and Comparison with Other Brachyspira Genomes

Background: The anaerobic spirochete Brachyspira pilosicoli colonizes the large intestine of various species of birds and mammals, including humans. It causes ''intestinal spirochetosis'', a condition characterized by mild colitis, diarrhea and reduced growth. This study aimed to sequence and analyse the bacterial genome to investigate the genetic basis of its specialized ecology and virulence. Methodology/Principal Findings: The genome of B. pilosicoli 95/1000 was sequenced, assembled and compared with that of the pathogenic Brachyspira hyodysenteriae and a near-complete sequence of Brachyspira murdochii. The B. pilosicoli genome was circular, composed of 2,586,443 bp with a 27.9 mol% G+C content, and encoded 2,338 genes. The three Brachyspira species shared 1,087 genes and showed evidence of extensive genome rearrangements. Despite minor differences in predicted protein functional groups, the species had many similar features including core metabolic pathways. Genes distinguishing B. pilosicoli from B. hyodysenteriae included those for a previously undescribed bacteriophage that may be useful for genetic manipulation, for a glycine reductase complex allowing use of glycine whilst protecting from oxidative stress, and for aconitase and related enzymes in the incomplete TCA cycle, allowing glutamate synthesis and function of the cycle during oxidative stress. B. pilosicoli had substantially fewer methyl-accepting chemotaxis genes than B. hyodysenteriae and hence these species are likely to have different chemotactic responses that may help to explain their different host range and colonization sites. B. pilosicoli lacked the gene for a new putative hemolysin identified in B. hyodysenteriae WA1. Both B. pilosicoli and B. murdochii lacked the rfbBADC gene cluster found on the B. hyodysenteriae plasmid, and hence were predicted to have different lipooligosaccharide structures. Overall, B. pilosicoli 95/1000 had a variety of genes potentially contributing to virulence. Conclusions/Significance: The availability of the complete genome sequence of B. pilosicoli 95/1000 will facilitate functional genomics studies aimed at elucidating host-pathogen interactions and virulence