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1.
Fetal Pediatr Pathol ; 42(3): 355-366, 2023 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-36106665

RESUMO

Introduction: Pediatric DLBCL is considered a homogenous group and has superior outcomes compared to adults. This study investigated the clinical pathology and immunohistochemical distinction between adult and pediatric large B-cell lymphoma. Methods: A cross-sectional study of 314 NHLs with the morphology of diffuse pattern, large B-cell, and CD20 expression was investigated. Results: Of 314 cases, there were 6 cases of pleomorphic MCL (all in adults), 19 cases of Burkitt lymphoma (all in children), and 289 cases of DLBCL. Pediatric DLBCL had many striking differences: More frequency in extra-nodal sites; a higher proportion of centroblastic morphology; a predominance of GCB-type; a high proliferation rate; an infrequency of Bcl2 protein expression, and a lack of double-expresser lymphoma. Conclusions: Our study demonstrated the significant biological differences between adult and pediatric DLBCL.


Assuntos
Linfoma Difuso de Grandes Células B , Humanos , Adulto , Criança , Estudos Transversais , Linfoma Difuso de Grandes Células B/diagnóstico , Linfoma Difuso de Grandes Células B/metabolismo , Linfoma Difuso de Grandes Células B/patologia , Prognóstico
2.
Nat Med ; 12(10): 1203-7, 2006 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-16964257

RESUMO

Avian influenza A (H5N1) viruses cause severe disease in humans, but the basis for their virulence remains unclear. In vitro and animal studies indicate that high and disseminated viral replication is important for disease pathogenesis. Laboratory experiments suggest that virus-induced cytokine dysregulation may contribute to disease severity. To assess the relevance of these findings for human disease, we performed virological and immunological studies in 18 individuals with H5N1 and 8 individuals infected with human influenza virus subtypes. Influenza H5N1 infection in humans is characterized by high pharyngeal virus loads and frequent detection of viral RNA in rectum and blood. Viral RNA in blood was present only in fatal H5N1 cases and was associated with higher pharyngeal viral loads. We observed low peripheral blood T-lymphocyte counts and high chemokine and cytokine levels in H5N1-infected individuals, particularly in those who died, and these correlated with pharyngeal viral loads. Genetic characterization of H5N1 viruses revealed mutations in the viral polymerase complex associated with mammalian adaptation and virulence. Our observations indicate that high viral load, and the resulting intense inflammatory responses, are central to influenza H5N1 pathogenesis. The focus of clinical management should be on preventing this intense cytokine response, by early diagnosis and effective antiviral treatment.


Assuntos
Citocinas/sangue , Virus da Influenza A Subtipo H5N1/patogenicidade , Influenza Humana/sangue , Influenza Humana/mortalidade , RNA Viral/metabolismo , Adolescente , Adulto , Criança , Pré-Escolar , Citocinas/metabolismo , Citometria de Fluxo , Humanos , Lactente , Influenza Humana/virologia , Pessoa de Meia-Idade , Dados de Sequência Molecular , Linfócitos T/metabolismo , Resultado do Tratamento
3.
Clin Infect Dis ; 49(9): 1387-92, 2009 Nov 01.
Artigo em Inglês | MEDLINE | ID: mdl-19814625

RESUMO

Adjunctive treatment to improve outcome from bacterial meningitis has centered on dexamethasone. Among Vietnamese patients with bacterial meningitis, cerebrospinal fluid (CSF) opening pressure and CSF:plasma glucose ratios were significantly improved and levels of CSF cytokines interleukin (IL)-6, IL-8, and IL-10 and were all statistically significantly lower after treatment in patients who were randomized to dexamethasone, compared with levels in patients who received placebo.


Assuntos
Dexametasona/uso terapêutico , Meningites Bacterianas/líquido cefalorraquidiano , Meningites Bacterianas/tratamento farmacológico , Adolescente , Adulto , Anti-Inflamatórios/uso terapêutico , Povo Asiático , Criança , Feminino , Humanos , Interleucina-10/líquido cefalorraquidiano , Interleucina-6/líquido cefalorraquidiano , Interleucina-8/líquido cefalorraquidiano , Masculino , Pessoa de Meia-Idade , Vietnã , Adulto Jovem
4.
J Infect Dis ; 198(4): 516-24, 2008 Aug 15.
Artigo em Inglês | MEDLINE | ID: mdl-18598189

RESUMO

The pathogenesis of severe dengue is not well understood. Maternally derived subneutralizing levels of dengue virus-reactive IgG are postulated to be a critical risk factor for severe dengue during infancy. In this study, we found that, in healthy Vietnamese infants, there was a strong temporal association between the Fc-dependent, dengue virus infection-enhancing activity of neat plasma and the age-related epidemiology of severe dengue. We then postulated that disease severity in infants with primary infections would be associated with a robust immune response, possibly as a consequence of higher viral burdens in vivo. Accordingly, in infants hospitalized with acute dengue, the activation phenotype of peripheral-blood NK cells and CD8+ and CD4+ T cells correlated with overall disease severity, but HLA-A*1101-restricted NS3(133-142)-specific CD8+ T cells were not measurable until early convalescence. Plasma levels of cytokines/chemokines were generally higher in infants with dengue shock syndrome. Collectively, these data support a model of dengue pathogenesis in infants whereby antibody-dependent enhancement of infection explains the age-related case epidemiology and could account for antigen-driven immune activation and its association with disease severity. These results also highlight potential risks in the use of live attenuated dengue vaccines in infants in countries where dengue is endemic.


Assuntos
Linfócitos T CD8-Positivos/imunologia , Vírus da Dengue/imunologia , Dengue/epidemiologia , Dengue/imunologia , Antígenos HLA-A/imunologia , Imunidade Celular/imunologia , Fatores Etários , Dengue/sangue , Vírus da Dengue/genética , Antígenos HLA-A/genética , Humanos , Lactente , Índice de Gravidade de Doença
5.
J Infect Dis ; 195(8): 1097-107, 2007 Apr 15.
Artigo em Inglês | MEDLINE | ID: mdl-17357045

RESUMO

Responses by peripheral blood leukocytes may contribute to the pathogenesis of dengue hemorrhagic fever (DHF). We used DNA microarrays to reveal transcriptional patterns in the blood of 14 adults with DHF. Acute DHF was defined by an abundance of transcripts from cell cycle- and endoplasmic reticulum (ER)-related genes, suggesting a proliferative response accompanied by ER stress. Transcript-abundance levels for immunoresponse-associated genes, including cell surface markers, immunoglobulin, and innate response elements, were also elevated. Twenty-four genes were identified for which transcript abundance distinguished patients with dengue shock syndrome (DSS) from those without DSS. All the gene transcripts associated with DSS, many of which are induced by type I interferons, were less abundant in patients with DSS than in those without DSS. To our knowledge, these data provide the first snapshot of gene-expression patterns in peripheral blood during acute dengue and suggest that DSS is associated with attenuation of selected aspects of the innate host response.


Assuntos
Linfócitos B/imunologia , Vírus da Dengue/fisiologia , Regulação Viral da Expressão Gênica/fisiologia , Dengue Grave/virologia , Doença Aguda , Adolescente , Adulto , Linfócitos B/virologia , Linfócitos T CD4-Positivos/imunologia , Linfócitos T CD8-Positivos/imunologia , Criança , Convalescença , Citocinas/genética , Primers do DNA/química , Vírus da Dengue/genética , Vírus da Dengue/imunologia , Feminino , Perfilação da Expressão Gênica/métodos , Genes cdc/fisiologia , Humanos , Masculino , Família Multigênica/genética , Análise de Sequência com Séries de Oligonucleotídeos/métodos , RNA Mensageiro/sangue , RNA Viral/sangue , Dengue Grave/imunologia , Transcrição Gênica , Vietnã
6.
J Infect Dis ; 196(3): 416-24, 2007 Aug 01.
Artigo em Inglês | MEDLINE | ID: mdl-17597456

RESUMO

The pathogenesis of dengue in infants is poorly understood. We postulated that dengue severity in infants would be positively associated with markers of viral burden and that maternally derived, neutralizing anti-dengue antibody would have decayed before the age at which infants with dengue presented to the hospital. In 75 Vietnamese infants with primary dengue, we found significant heterogeneity in viremia and NS1 antigenemia at hospital presentation, and these factors were independent of disease grade or continuous measures of disease severity. Neutralizing antibody titers, predicted in each infant at the time of their illness, suggested that the majority of infants (65%) experienced dengue hemorrhagic fever when the maternally derived neutralizing antibody titer had declined to <1 : 20. Collectively, these data have important implications for dengue vaccine research because they suggest that viral burden may not solely explain severe dengue in infants and that neutralizing antibody is a reasonable but not absolute marker of protective immunity in infants.


Assuntos
Vírus da Dengue/classificação , Dengue/imunologia , Anticorpos Antivirais , Antígenos Virais/sangue , Vírus da Dengue/imunologia , Feminino , Humanos , Imunidade Materno-Adquirida , Lactente , Masculino , Testes de Neutralização , Fatores de Tempo , Carga Viral
7.
J Immunol ; 176(3): 2007-14, 2006 Feb 01.
Artigo em Inglês | MEDLINE | ID: mdl-16424233

RESUMO

Tuberculous meningitis (TBM) is the most devastating form of tuberculosis. Both intracerebral and peripheral blood immune responses may be relevant to pathogenesis, diagnosis, and outcome. In this study, the relationship between pretreatment host response, disease phenotype, and outcome in Vietnamese adults with TBM was examined. Before treatment, peripheral blood IFN-gamma ELISPOT responses to the Mycobacterium tuberculosis Ags ESAT-6, CFP-10, and purified protein derivative (PPD) were a poor diagnostic predictor of TBM. Cerebrospinal fluid IL-6 concentrations at presentation were independently associated with severe disease presentation, suggesting an immunological correlate of neurological damage before treatment. Surprisingly however, elevated cerebrospinal fluid inflammatory cytokines were not associated with death or disability in HIV-negative TBM patients at presentation. HIV coinfection attenuated multiple cerebrospinal fluid inflammatory indices. Low cerebrospinal fluid IFN-gamma concentrations were independently associated with death in HIV-positive TBM patients, implying that IFN-gamma contributes to immunity and survival. Collectively, these results reveal the effect of HIV coinfection on the pathogenesis of TBM and suggest that intracerebral immune responses, at least in HIV-negative cases, may not be as intimately associated with disease outcome as previously thought.


Assuntos
Telencéfalo/imunologia , Tuberculose Meníngea/diagnóstico , Tuberculose Meníngea/imunologia , Adolescente , Adulto , Idoso , Idoso de 80 Anos ou mais , Antígenos de Bactérias/sangue , Proteínas de Bactérias/sangue , Feminino , HIV/imunologia , Infecções por HIV/imunologia , Infecções por HIV/mortalidade , Humanos , Interferon gama/sangue , Masculino , Pessoa de Meia-Idade , Índice de Gravidade de Doença , Telencéfalo/irrigação sanguínea , Telencéfalo/metabolismo , Resultado do Tratamento , Tuberculose Meníngea/sangue , Tuberculose Meníngea/líquido cefalorraquidiano , Vietnã
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