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1.
Parasitol Res ; 114(3): 809-21, 2015 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-25518818

RESUMO

Toxocariasis is a globally distributed parasitic infection caused by the larval stage of Toxocara spp. The typical natural hosts of the parasite are dogs and cats, but humans can be infected by the larval stage of the parasite after ingesting embryonated eggs in soil or from contaminated hands or fomites. The migrating larvae are not adapted to complete their life cycle within accidental or paratenic hosts like humans and laboratory animals, respectively, but they are capable of invading viscera or other tissues where they may survive and induce disease. In order to characterize hamsters (Mesocricetus auratus) as a model for Toxocara canis infection, histopathological and immunohistochemistry procedures were used to detect pathological lesions and the distribution of toxocaral antigens in the liver, lungs, and kidneys of experimentally infected animals. We also attempted to characterize the immunological parameters of the inflammatory response and correlate them with the histopathological findings. In the kidney, a correlation between glomerular changes and antigen deposits was evaluated using immunoelectron microscopy. The hamster is an adequate model of experimental toxocariasis for short-term investigations and has a good immunological and pathological response to the infection. Lung and liver manifestations of toxocariasis in hamsters approximated those in humans and other experimental animal models. A mixed Th2 immunological response to T. canis infection was predominant. The hamster model displayed a progressive rise of anti-toxocaral antibodies with the formation of immune complexes. Circulating antigens, immunoglobulin, and complement deposits were detected in the kidney without the development of a definite immune complex nephropathy.


Assuntos
Toxocara/parasitologia , Toxocaríase/patologia , Toxocaríase/parasitologia , Animais , Antígenos de Helmintos/análise , Proteínas do Sistema Complemento/análise , Cricetinae , Modelos Animais de Doenças , Imunoglobulinas/análise , Imuno-Histoquímica , Rim/imunologia , Rim/parasitologia , Rim/patologia , Larva/crescimento & desenvolvimento , Estágios do Ciclo de Vida , Fígado/imunologia , Fígado/parasitologia , Fígado/patologia , Pulmão/imunologia , Pulmão/parasitologia , Pulmão/patologia , Mesocricetus , Microscopia Imunoeletrônica , Toxocara/imunologia , Toxocaríase/imunologia
2.
J Clin Virol ; 75: 16-20, 2016 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-26741825

RESUMO

Acute kidney injury is an unusual complication during dengue infection. The objective of this study was to better identify the characteristics of glomerular changes focusing on in situ immune cells and cytokines. An immunohistochemical assay was performed on 20 kidney specimens from fatal human cases of dengue hemorrhagic fever (DHF). It was observed a lymphomononuclear infiltrate, neutrophils and nuclear fragmentation in the glomeruli, hydropic degeneration, nuclear retraction, eosinophilic tubules and intense acute congestion. Sickle erythrocytes were frequent in glomeruli and inflammatory infiltrate. The glomeruli presented endothelial swelling and mesangial proliferation. Lymphocytes CD4+ predominated over CD8+ T cells, B cells and natural killer cells. There were also an expressive number of macrophagic CD68+ cells. S100, Foxp3 and CD123 cells were not identified. Cells expressing IL17 and IL18+ cytokines predominated in the renal tissues, while IL4, IL6, IL10, IL13, TNF-alpha and IFN-gamma were rarely visualized. The high number of cells expressing IL17 and IL18+ could reflect the acute inflammatory response and possibly contribute to the local lesion. CD8+ T cells could play a role in the cytotoxic response. DHF is a multifactorial disease of capillary leakage associated with a "Tsunami of cytokines expression". The large numbers of cells expressing IL17 seems to play a role favoring the increased permeability.


Assuntos
Injúria Renal Aguda/etiologia , Interleucina-17/imunologia , Necrose do Córtex Renal/etiologia , Dengue Grave/complicações , Injúria Renal Aguda/imunologia , Injúria Renal Aguda/fisiopatologia , Linfócitos B/imunologia , Linfócitos T CD4-Positivos/imunologia , Linfócitos T CD8-Positivos/imunologia , Citocinas/imunologia , Humanos , Imuno-Histoquímica , Necrose do Córtex Renal/imunologia , Necrose do Córtex Renal/fisiopatologia , Células Matadoras Naturais/imunologia , Dengue Grave/imunologia , Dengue Grave/fisiopatologia
3.
PLoS Negl Trop Dis ; 8(9): e3162, 2014 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-25233082

RESUMO

BACKGROUND: Chromoblastomycosis is a chronic fungal infection that affects skin and subcutaneous tissue. Lesions can be classified in tumorous, verrucous, cicatricial and plaque type. The cellular immune response in the severe form of the disease seems to correlate with a Th2 pattern of cytokines. The humoral immune response also seems to play a role. We intended to explore the populations of regulatory T cells and the Th17 pattern. METHODOLOGY: Twenty-three biopsies of verrucous form were obtained from patients with clinical, culture and histopathological diagnostic of chromoblastomycosis, without treatment. It was performed an immunohistochemistry method to detect Foxp3, CD25, TGF-ß, IL-6, IL-17 and IL-23. PRINCIPAL FINDINGS: IL-17 was the only cytokine with high expression in CBM when compared to normal skin. The expression of Treg cells, TGF- ß, IL-6 and IL-23 were similar to normal skin. CONCLUSIONS/SIGNIFICANCE: The constitution of a local immune response with high expression of IL-17 and low expression of other cytokines could be at least in part, an attempt to help the immune system against fungal infection. On the other hand, high levels of local immune response mediated by Th17 profile could overcome the role of Treg cells. The inefficient immunomodulation as a consequence of the unbalance by Treg/Th17 cells seems to corroborate with the less effective immune response against fungi.


Assuntos
Cromoblastomicose/imunologia , Células Th17/imunologia , Idoso , Biópsia , Cromoblastomicose/patologia , Estudos de Coortes , Feminino , Humanos , Interleucina-17/biossíntese , Interleucina-17/imunologia , Masculino , Pessoa de Meia-Idade
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