Pugnas políticas en el primer Imperio Mexicano

La amarga y dolorosa lucha sostenida en la Nueva España por lograr la autonomía de la península ibérica, se concretó en una novel patria llamada México, encabezada por un emperador, símbolo de una nueva etapa que se iniciaba con júbilo y gozo, pero que años después sólo provocaría lágrimas, anarquía y derramamiento de sangre.

Comentario del libro “Recuerdos del imperio”

Introducción El historiador costarricense Rodrigo Quesada al publicar su obra “Recuerdos del Imperio”, asunto que sigue vigente en nuestros días. Su trabajo busca cuestionar las nuevas vertientes historiográficas, si se les puede llamar así, que han tratado de borrar el impacto que ha tenido en América Latina y en especial en Centro América las políticas imperiales articuladas por España, Inglaterra y los Estados Unidos. Como muy bien señala en autor: “Porque hay que aclarar que la Pax Británica durante el último siglo, no fue un conjunto mal articulado de medidas expansionistas o de oportunismo colonialista, El imperialismo británico fue algo más que eso. Fue el producto del propio desarrollo capitalista de dicha nación lo que facilitó la estructura de una política económica, que sirvió como instrumento interventor en los países centroamericanos…

Comentario del libro de Georgina Meneses. “Tradición oral en el Imperio de los Incas Historia, religión y teatro”

IntroducciónEl Departamento Ecuménico de Investigaciones, DEI ha publicado la obra de Georgina Meneses titulada Tradición oral en el Imperio de los Incas. Historia, religión y teatro. Con este trabajo la autora se graduó como licenciada en Artes Dramáticas, con énfasis en teatrología, en la Universidad de Costa Rica, en 1984. Han pasado, por tanto, casi ocho años sin que este libro saliera a al liz pública, corriendo el riesgo de quedar desactualizado sin llegar a lectores. En este marco de la celebración del "Quinto Centenario del Encuentro de Dos Mundos" cuando se ha creido oportuno editar esta tesis, galardonada con la nota máxima y una recomendación de publicación...

Análise da sensibilidade do gosto umami em crianças com câncer

O câncer pediátrico possui alta incidência, principalmente a leucemia linfoide aguda e o linfoma não Hodgkin. A quimioterapia, devido a seus efeitos colaterais, diminui a ingestão de alimentos, por causar alteração do paladar, ressecamento da boca, náuseas e ou vômitos. A sensação do gosto é responsável pela detecção e resposta ao estímulo doce, salgado, azedo, amargo e umami, este último proveniente do glutamato monossódico, o qual está relacionado ao aumento da palatabilidade de preparações, fato que pode colaborar para a melhoria da aceitação alimentar em pacientes pediátricos com câncer. O objetivo deste estudo foi identificar os limiares de detecção do gosto umami em crianças portadoras de câncer que seguem os protocolos quimioterápicos: GBTLI LLA 97, 99 e 2009 e LNH 2000. Foi aplicado o teste de sensibilidade de Threshold em duplicata para determinação do limiar do gosto umami, utilizando seis concentrações crescentes de água deionizada e glutamato monossódico. Os dados foram analisados com auxílio do programa Epinfo 6.0. Foram avaliados 69 pacientes, 63,8por cento do sexo masculino; 69,6 por cento portadores de leucemia linfoide aguda e o restante de linfoma não Hodgkin. Em relação à idade, cerca de 69por cento estavam na faixa etária de 6 a 10 anos. A maioria da população (mais de 70 por cento) detectou o gosto umami a partir da segunda concentração oferecida no teste, nas duas aplicações, sendo sensíveis a este gosto. As crianças com câncer em tratamento quimioterápico mostraram-se sensíveis ao gosto umami. A utilização de forma moderada desse componente nas preparações e orientação alimentar adequada pode colaborar para a melhora do estado nutricional das crianças em tratamento quimioterápico

A Genome-Wide Association Study of Upper Aerodigestive Tract Cancers Conducted within the INHANCE Consortium

Genome-wide association studies (GWAS) have been successful in identifying common genetic variation involved in susceptibility to etiologically complex disease. We conducted a GWAS to identify common genetic variation involved in susceptibility to upper aero-digestive tract (UADT) cancers. Genome-wide genotyping was carried out using the Illumina HumanHap300 beadchips in 2,091 UADT cancer cases and 3,513 controls from two large European multi-centre UADT cancer studies, as well as 4,821 generic controls. The 19 top-ranked variants were investigated further in an additional 6,514 UADT cancer cases and 7,892 controls of European descent from an additional 13 UADT cancer studies participating in the INHANCE consortium. Five common variants presented evidence for significant association in the combined analysis (p <= 5 x 10(-7)). Two novel variants were identified, a 4q21 variant (rs1494961, p = 1 x 10(-8)) located near DNA repair related genes HEL308 and FAM175A (or Abraxas) and a 12q24 variant (rs4767364, p = 2 x 10(-8)) located in an extended linkage disequilibrium region that contains multiple genes including the aldehyde dehydrogenase 2 (ALDH2) gene. Three remaining variants are located in the ADH gene cluster and were identified previously in a candidate gene study involving some of these samples. The association between these three variants and UADT cancers was independently replicated in 5,092 UADT cancer cases and 6,794 controls non-overlapping samples presented here (rs1573496-ADH7, p = 5 x 10(-8); rs1229984-ADH1B, p = 7 x 10(-9); and rs698-ADH1C, p = 0.02). These results implicate two variants at 4q21 and 12q24 and further highlight three ADH variants in UADT cancer susceptibility.

Cellular Renewal and Improvement of Local Cell Effector Activity in Peritoneal Cavity in Response to Infectious Stimuli

The peritoneal cavity (PerC) is a singular compartment where many cell populations reside and interact. Despite the widely adopted experimental approach of intraperitoneal (i.p.) inoculation, little is known about the behavior of the different cell populations within the PerC. To evaluate the dynamics of peritoneal macrophage (Mempty set) subsets, namely small peritoneal Mempty set (SPM) and large peritoneal Mempty set (LPM), in response to infectious stimuli, C57BL/6 mice were injected i.p. with zymosan or Trypanosoma cruzi. These conditions resulted in the marked modification of the PerC myelo-monocytic compartment characterized by the disappearance of LPM and the accumulation of SPM and monocytes. In parallel, adherent cells isolated from stimulated PerC displayed reduced staining for beta-galactosidase, a biomarker for senescence. Further, the adherent cells showed increased nitric oxide (NO) and higher frequency of IL-12-producing cells in response to subsequent LPS and IFN-gamma stimulation. Among myelo-monocytic cells, SPM rather than LPM or monocytes, appear to be the central effectors of the activated PerC; they display higher phagocytic activity and are the main source of IL-12. Thus, our data provide a first demonstration of the consequences of the dynamics between peritoneal Mempty set subpopulations by showing that substitution of LPM by a robust SPM and monocytes in response to infectious stimuli greatly improves PerC effector activity.

The Spleen CD4(+) T Cell Response to Blood-Stage Plasmodium chabaudi Malaria Develops in Two Phases Characterized by Different Properties

The pivotal role of spleen CD4(+) T cells in the development of both malaria pathogenesis and protective immunity makes necessary a profound comprehension of the mechanisms involved in their activation and regulation during Plasmodium infection. Herein, we examined in detail the behaviour of non-conventional and conventional splenic CD4(+) T cells during P. chabaudi malaria. We took advantage of the fact that a great proportion of CD4(+) T cells generated in CD1d(-/-) mice are I-A(b)-restricted (conventional cells), while their counterparts in I-Ab(-/-) mice are restricted by CD1d and other class IB major histocompatibility complex (MHC) molecules (non-conventional cells). We found that conventional CD4(+) T cells are the main protagonists of the immune response to infection, which develops in two consecutive phases concomitant with acute and chronic parasitaemias. The early phase of the conventional CD4(+) T cell response is intense and short lasting, rapidly providing large amounts of proinflammatory cytokines and helping follicular and marginal zone B cells to secrete polyclonal immunoglobulin. Both TNF-alpha and IFN-gamma production depend mostly on conventional CD4(+) T cells. IFN-gamma is produced simultaneously by non-conventional and conventional CD4(+) T cells. The early phase of the response finishes after a week of infection, with the elimination of a large proportion of CD4(+) T cells, which then gives opportunity to the development of acquired immunity. Unexpectedly, the major contribution of CD1d-restricted CD4(+) T cells occurs at the beginning of the second phase of the response, but not earlier, helping both IFN-gamma and parasite-specific antibody production. We concluded that conventional CD4(+) T cells have a central role from the onset of P. chabaudi malaria, acting in parallel with non-conventional CD4(+) T cells as a link between innate and acquired immunity. This study contributes to the understanding of malaria immunology and opens a perspective for future studies designed to decipher the molecular mechanisms behind immune responses to Plasmodium infection.

Comparative Analysis of Activation Phenotype, Proliferation, and IFN-gamma Production by Spleen NK1.1(+) and NK1.1(-) T Cells During Plasmodium chabaudi AS Malaria

The NK1.1 molecule participates in NK, NKT, and T-cell activation, contributing to IFN-gamma production and cytotoxicity. To characterize the early immune response to Plasmodium chabaudi AS, spleen NK1.1(+) and NK1.1(-) T cells were compared in acutely infected C57BL/6 mice. The first parasitemia peak in C57BL/6 mice correlated with increase in CD4(+)NK1.1(+)TCR-alpha beta(+), CD8(+)NK1.1(+)TCR-alpha beta(+), and CD4(+)NK1.1(-)TCR-alpha beta(+) cell numbers per spleen, where a higher increment was observed for NK1.1(+) T cells compared to NK1.1(-) T cells. According to the ability to recognize the CD1d-alpha-GalCer tetramer, CD4(+)NK1.1(+) cells in 7-day infected mice were not predominantly invariant NKT cells. At that time, nearly all NK1.1(+) T cells and around 30% of NK1.1(-) T cells showed an experienced/activated (CD44(HI)CD69(HI)CD122(HI)) cell phenotype, with high expression of Fas and PD-L1 correlating with their low proliferative capacity. Moreover, whereas IFN-gamma production by CD4(+)NK1.1(+) cells peaked at day 4 p.i., the IFN-gamma response of CD4(+)NK1.1(-) cells continued to increase at day 5 of infection. We also observed, at day 7 p.i., 2-fold higher percentages of perforin(+) cells in CD8(+)NK1.1(+) cells compared to CD8(+)NK1.1(-) cells. These results indicate that spleen NK1.1(+) and NK1.1(-) T cells respond to acute P. chabaudi malaria with different kinetics in terms of activation, proliferation, and IFN-gamma production.

The Liver Plays a Major Role in Clearance and Destruction of Blood Trypomastigotes in Trypanosoma cruzi Chronically Infected Mice

Intravenous challenge with Trypanosoma cruzi can be used to investigate the process and consequences of blood parasite clearance in experimental Chagas disease. One hour after intravenous challenge of chronically infected mice with 5610 6 trypomastigotes, the liver constituted a major site of parasite accumulation, as revealed by PCR. Intact parasites and/or parasite remnants were visualized at this time point scattered in the liver parenchyma. Moreover, at this time, many of liver-cleared parasites were viable, as estimated by the frequency of positive cultures, which considerably diminished after 48 h. Following clearance, the number of infiltrating cells in the hepatic tissue notably increased: initially (at 24 h) as diffuse infiltrates affecting the whole parenchyma, and at 48 h, in the form of large focal infiltrates in both the parenchyma and perivascular spaces. Phenotypic characterization of liver-infiltrating cells 24 h after challenge revealed an increase in Mac1(+), CD8(+) and CD4(+) cells, followed by natural killer (NK) cells. As evidence that liver-infiltrating CD4(+) and CD8(+) cells were activated, increased frequencies of CD69(+) CD8(+), CD69(+) CD4(+) and CD25(+) CD122(+) CD4(+) cells were observed at 24 and 48 h after challenge, and of CD25(-)CD122(+)CD4(+) cells at 48 h. The major role of CD4(+) cells in liver protection was suggested by data showing a very high frequency of interferon (IFN)-gamma-producing CD4(+) cells 24 h after challenge. In contrast, liver CD8(+) cells produced little IFN-gamma, even though they showed an enhanced potential for secreting this cytokine, as revealed by in vitro T cell receptor (TCR) stimulation. Confirming the effectiveness of the liver immune response in blood parasite control during the chronic phase of infection, no live parasites were detected in this organ 7 days after challenge.

The characteristics of NDM-producing Klebsiella pneumoniae from Canada

After recent hospitalization in India (New Delhi and Mumbai), 2 patients, on their return to Canada, presented with lower urinary tract infections due to multiresistant Klebsiella pneumoniae that produced New Delhi metall-beta-lactamase and CTX-M-15. The organisms belonged to clones ST147 and ST340, and were positive for aac(6`)-Ib-cr, as well as for the ccdAB and vagCD addiction systems. The bla(NDM) plasmid was located on the IncFIIA and IncA/C replicon groups of plasmids. Clones ST147 and ST340 are also responsible for harbouring bla(KPC), and it is possible that they played an important role in the intercontinental spread of antimicrobial resistance. (C) 2011 Elsevier Inc. All rights reserved.

Programa de valoriza????o e reconhecimento ALGO+

H?? algum tempo a Coordena????o de Recursos Humanos do Instituto Nacional de C??ncer - INCA vem implementando a????es que procuram estabelecer uma pol??tica de Recursos Humanos moderna e participativa. Era not??rio, por??m, que os nossos colaboradores do INCA esperavam mais. Havia uma car??ncia do desafio e do reconhecimento efetivo, para que fossem estimulados a desempenhar suas tarefas com maior dedica????o e compet??ncia. Esta necessidade desencadeou o processo de elabora????o deste programa para que periodicamente identific??ssemos os colaboradores que fossem o ???ALGO+??? do INCA

Sistema de treinamento por cotas

O Sistema de Treinamento por Cotas foi elaborado para funcionar como uma "conta-corrente" para a????es de treinamento. A partir do planejamento estrat??gico e da disponibilidade or??ament??ria do Instituto para o ano, s??o estabelecidas cotas proporcionais para cada unidade, de acordo com o foco definido para atua????o. O Sistema ?? visto como uma ferramenta gerencial e proporciona a democratiza????o das a????es de treinamento pelos colaboradores em geral, visto alcan??ar desde o n??vel mais alto do Instituto ao mais operacional. Acima de tudo, por??m, destaca-se na melhoria do processo a otimiza????o da distribui????o da verba destinada a treinamento e o aumento de profissionais atendidos

Como promover e trabalhar em parceria

No Brasil, os procedimentos m??dicos de alta complexidade absorvem elevada parcela dos recursos do SUS, particularmente nas especialidades de nefrologia e oncologia, ao mesmo tempo em que atingem uma parcela reduzida da popula????o. A partir da percep????o das dificuldades existentes, foi elaborado e implantado um programa de controle e avalia????o em oncologia (atendimento ambulatorial em quimioterapia e radioterapia), mediante parceria entre o Inca/Pr??-onco e o SUS Campos. Com a iniciativa observou-se uma redu????o de mais de 50% nos gastos com quimioterapia, cujos custos exibem uma tend??ncia progressiva ao decl??nio. Os gastos com radioterapia exibem padr??o vari??vel, visto que os mecanismos de controle e avalia????o ainda se encontram em implanta????o. Houve ganho em qualidade das indica????es terap??uticas. Desenvolveu-se maior motiva????o entre os auditores e revisores, que passaram a dispor de instrumentos mais eficazes para realizar seu trabalho. Melhorou o entendimento e a organiza????o do fluxo de informa????es entre o SUS-Campos e os prestadores. Os prestadores reconheceram a necessidade de melhor organizar seus servi??os e de iniciar um registro adequado dos casos. Ocorreu uma melhoria generalizada na qualidade das informa????es. O SUS-Campos tomou a iniciativa de utilizar o registro de mortalidade e de programar outros tipos de registro que possam favorecer o controle e avalia????o em oncologia. Passou a ser desenvolvida uma metodologia de bases realistas para aplicar-se a um programa de controle e avalia????o em oncologia. Surgiu a possibilidade de acompanhamento dos casos e de avalia????o dos resultados dos tratamentos aplicados

Taxonomy of Apenesia Westwood (Hymenoptera, Bethylidae) from Paraná, Brazil

Apenesia quadrimera sp. n., A. rotunda sp. n. and A. clypeata sp. n. are described and illustrated. New geographic records and variation data of A. cusco Evans, 1966, A distinta Corrêa & Azevedo, 2001, A. funebris Evans, 1963, A. fusilis Corrêa & Azevedo, 2001, A. inca Evans, 1963 and A. transversa Evans, 1963 are added.