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2.
Am J Community Psychol ; 63(1-2): 153-167, 2019 03.
Artigo em Inglês | MEDLINE | ID: mdl-30801758

RESUMO

Little systematic information exists about how community-based prevention efforts at the state and local levels contribute to our knowledge of intimate partner violence (IPV) prevention. The Centers for Disease Control and Prevention's (CDC) DELTA FOCUS program funds ten state domestic violence coalitions to engage in IPV primary prevention through approaches addressing the outer layers of the social ecology. This paper explored the ways in which DELTA FOCUS recipients have contributed to a national-level dialogue on IPV prevention. Previously undefined, the authors define national-level dialogue and retrospectively apply the CDC Science Impact Framework (SIF) to describe contributions DELTA FOCUS recipients made to it. Authors conducted document review and qualitative content analysis of recipient semi-annual progress reports from 2014 to 2016 (N = 40) using NVivo. A semi-structured coding scheme was applied across the five SIF domains: Creating Awareness, Catalyzing Action, Effecting Change, Disseminating Science, and Shaping the Future. All recipients sought to promote IPV prevention by communicating and sharing with non-CDC-funded state coalitions, national partners, and other IPV stakeholders information and resources accumulated through practice-based prevention efforts. Through implementing and disseminating their prevention work in myriad ways, DELTA FOCUS recipients are building practice-based evidence on community-based IPV prevention.


Assuntos
Relações Comunidade-Instituição , Violência por Parceiro Íntimo/prevenção & controle , Prevenção Primária/métodos , Centers for Disease Control and Prevention, U.S. , Humanos , Relações Interinstitucionais , Relações Interprofissionais , Prevenção Primária/organização & administração , Avaliação de Programas e Projetos de Saúde , Estados Unidos
4.
J Infect Dis ; 197(7): 981-9, 2008 Apr 01.
Artigo em Inglês | MEDLINE | ID: mdl-18419534

RESUMO

The amino terminal sequence of the Candida albicans cell wall protein Int1 exhibited partial identity with the major histocompatibility complex (MHC) class II binding site of the Mycoplasma arthritidis superantigen MAM. Int1-positive C. albicans blastospores activated human T lymphocytes and expanded Vbeta subsets 2, 3, and/or 14; Int1-negative strains were inactive. Release of interferon-gamma (IFN-gamma) but not of tumor necrosis factor-alpha or interleukin-6 was Int1 dependent; interleukin-4 and interleukin-10 were not detected. T lymphocyte activation, Vbeta expansion, and IFN-gamma release were associated with a soluble polypeptide that encompassed the first 263 amino acids of Int1 (Pep(263)). Monoclonal antibody 163.5, which recognizes an Int1 epitope that overlaps the region of identity with MAM, significantly inhibited these activities when triggered by Int1-positive blastospores or Pep(263) but not by staphylococcal enterotoxin B. Histidine(263) was required. Pep(263) bound to T lymphocytes and MHC class II and was detected in the urine of a patient with C. albicans fungemia. These studies identify a candidal protein that displays superantigen-like activities.


Assuntos
Candida albicans/imunologia , Moléculas de Adesão Celular/imunologia , Proteínas Fúngicas/imunologia , Superantígenos/imunologia , Candida albicans/genética , Moléculas de Adesão Celular/genética , Moléculas de Adesão Celular/metabolismo , Citocinas/metabolismo , Proteínas Fúngicas/genética , Proteínas Fúngicas/metabolismo , Deleção de Genes , Antígenos de Histocompatibilidade Classe II/metabolismo , Humanos , Ativação Linfocitária , Mycoplasma arthritidis/genética , Ligação Proteica , Superantígenos/genética , Subpopulações de Linfócitos T/imunologia , Urina/química
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