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1.
Pathol Res Pract ; 213(9): 1097-1101, 2017 Sep.
Artículo en Inglés | MEDLINE | ID: mdl-28778496

RESUMEN

Peri-implantitis is an infectious disease characterized by inflammation of the tissues surrounding the implant, bleeding on probing with or without suppuration, and bone loss. Peri-implant lesions contain a leukocyte infiltrate of plasma cells, lymphocytes, macrophages and neutrophils. A survey of the literature did not show any studies reporting an association between hypoxia and peri-implantitis. The aim of the present cross-sectional study was to evaluate histological changes and immunostaining for CD15, CD57 and HIF-1α in the peri-implant mucosa of patients with and without peri-implantitis. Mucosal biopsies were obtained from 18 patients with peri-implantitis and 10 control subjects without peri-implantitis at a private health care center between 2010 and 2012. The sections were fixed in 10% buffered formalin, processed and embedded in paraffin for histopathological and immunohistochemical study. Acanthosis, spongiosis and exocytosis were observed in both groups, with no significant difference between them. The peri-implantitis group showed increased immunostaining for CD15, a neutrophil marker, and HIF-1α, a tissue hypoxia marker, but no significant difference in immunostaining for CD57, a Natural Killer cell marker. The increase in neutrophil (CD15) and hypoxia (HIF-1α) markers in patients with peri-implantitis suggests an active participation of neutrophils and hypoxia in the pathogenesis of this disease. Since the present study was the first to evaluate the expression of CD15, CD57 and HIF-1α in peri-implant tissues, further studies should be performed to better understand the role of these molecules in peri-implantitis.


Asunto(s)
Implantes Dentales/efectos adversos , Periimplantitis/inmunología , Estomatitis/inmunología , Anciano , Biomarcadores/análisis , Biopsia , Antígenos CD57/análisis , Antígenos CD57/biosíntesis , Estudios Transversales , Femenino , Fucosiltransferasas/análisis , Fucosiltransferasas/biosíntesis , Humanos , Subunidad alfa del Factor 1 Inducible por Hipoxia/análisis , Subunidad alfa del Factor 1 Inducible por Hipoxia/biosíntesis , Antígeno Lewis X/análisis , Antígeno Lewis X/biosíntesis , Masculino , Persona de Mediana Edad
2.
Pathol Res Pract ; 213(9): 1207-1214, 2017 Sep.
Artículo en Inglés | MEDLINE | ID: mdl-28554765

RESUMEN

OBJECTIVE AND DESIGN: The aim of the present study was to evaluate the immunohistochemical expression of Gal-1, Gal-3 and Gal-9 in the colon of chronic chagasic patients compared to biopsied non-chagasic patients. MATERIAL OR SUBJECTS: Thirty-two colon fragments were selected from chagasic patients with megacolon (n=25) and nonchagasic patients without megacolon (n=7). METHODS: Immunohistochemistry for Gal-1, Gal-3 and Gal-9 was performed using a common light microscope and the results were scored 0-3 according to labeling intensity. Data were analyzed statistically by the chi-square test. RESULTS: Higher Gal-1, Gal-3 and Gal-9 expression was observed in the myenteric plexus ganglia of chagasic patients compared to non-chagasic patients, p=0.0487, p=0.0019 and p=0.0325, respectively, whereas no significant differences were observed between groups regarding the expression of Gal-1, Gal-3 and Gal-9 in the muscle layer. CONCLUSION: Since Gal-1, Gal-3 and Gal-9 galectin expression was higher in the myenteric plexus ganglia of chagasic patients, we believe that these lectins may be associated with ganglionitis in the chagasic megacolon. However, since the present study was the first to report the participation of Gal-9 in Chagas disease, further investigations are needed to elucidate the role of galectin 9 in this disease.


Asunto(s)
Enfermedad de Chagas/patología , Galectina 1/biosíntesis , Galectina 3/biosíntesis , Galectinas/biosíntesis , Anciano , Biomarcadores/análisis , Proteínas Sanguíneas , Femenino , Galectina 1/análisis , Galectina 3/análisis , Galectinas/análisis , Humanos , Inmunohistoquímica , Masculino , Megacolon/microbiología , Persona de Mediana Edad
3.
Clin Dev Immunol ; 2012: 361730, 2012.
Artículo en Inglés | MEDLINE | ID: mdl-22811738

RESUMEN

Chagas' disease is caused by the protozoan parasite Trypanosoma cruzi. The immune system plays an important role in the reduction of parasite load, but may also contribute to the development of lesions observed during the chronic phase of the disease. We analyzed cytokines produced by inflammatory heart cells in 21 autopsy samples obtained from patients with Chagas' disease divided according to the presence or absence of heart failure (HF). Left ventricular sections were analyzed by immunohistochemistry using antibodies against human IL-4, IFN-γ, TGF-ß, TNF-α, and NOS2. In situ mRNA expression was quantified by a Low Density Array. The number of IFN-γ-positive cells was significantly higher than IL-4 positive cells. TNF-α, TGF-ß and NOS2 were detected in 65%, 62% and 94% of samples respectively. There was an association between TNF-α-producing cells and the presence of HF. Subjects with HF presented higher levels of STAT4 mRNA, whereas FoxP3 and STAT6 levels were similar in the two groups. A Th1 cytokine pattern predominated in the cardiac inflammatory cell infiltrate of Chagas' disease patients associated with HF. High degree of fibrosis was associated with low NOS2 expression. These results support the idea that Th1 immune responses are involved in heart lesions of Chagas' disease patients.


Asunto(s)
Enfermedad de Chagas/complicaciones , Enfermedad de Chagas/inmunología , Citocinas/metabolismo , Insuficiencia Cardíaca/etiología , Insuficiencia Cardíaca/inmunología , Enfermedad de Chagas/genética , Citocinas/genética , Citocinas/inmunología , Fibrosis Endomiocárdica/inmunología , Fibrosis Endomiocárdica/patología , Insuficiencia Cardíaca/genética , Humanos , Interferón gamma/genética , Interferón gamma/metabolismo , Óxido Nítrico Sintasa de Tipo II/metabolismo , Células TH1/inmunología , Células TH1/metabolismo , Células Th2/inmunología , Células Th2/metabolismo , Factor de Necrosis Tumoral alfa/genética , Factor de Necrosis Tumoral alfa/metabolismo
4.
Quintessence Int ; 40(6): 491-6, 2009 Jun.
Artículo en Inglés | MEDLINE | ID: mdl-19587890

RESUMEN

OBJECTIVE: Restorative procedures of the dentin-pulp complex stimulate damages that, depending on the technique and materials used, may induce pulpal reactions. The purpose of this study was to evaluate immunochemistry, morphologic, and morphometric pulpal alterations of human teeth pulps capped with self-etching or total-etching adhesive systems. METHOD AND MATERIALS: Thirty human third molars were restored with a resin-based composite and adhesive system, either Clearfil (Kuraray; n = 10) or Scotchbond (3M ESPE; n = 10). After 7, 30, or 60 days, the teeth were extracted and longitudinally sectioned. The pulps were removed for histopathologic and immunochemistry evaluation for interferon (IFN)-gamma, tumor necrosis factor (TNF)-alpha, and inducible nitric oxide synthase (iNOS). RESULTS: The density of fibrous connective tissue was significantly higher after 30 days in both groups (P < .001). Congestion, hemorrhage, calcification, and swelling of the odontoblasts were similar in both groups. The total capillary area was significantly higher after 7 and 30 days in both groups. Positive immunoreactions for iNOS were found in 1 case (20%) of the 30-day Scotchbond group. Immunoreactions for IFN-gamma were positive in a few cells in 1 case (20%) of the 7-day Clearfil group. There were no positive immunoreactions for TNF-alpha in any case. CONCLUSION: No inflammatory reactions, necrotic areas, or severe immunoreactions for proinflammatory cytokines were found, suggesting biocompatibility of self-etching or total-etching adhesive systems when placed directly on dentin.


Asunto(s)
Resinas Compuestas , Recubrimiento de la Pulpa Dental/métodos , Pulpa Dental/efectos de los fármacos , Cementos de Resina/toxicidad , Pulpa Dental/química , Pulpa Dental/patología , Femenino , Humanos , Técnicas para Inmunoenzimas , Interferón gamma/análisis , Masculino , Óxido Nítrico Sintasa de Tipo II/análisis , Factor de Necrosis Tumoral alfa/análisis , Adulto Joven
5.
Microbes Infect ; 10(1): 29-37, 2008 Jan.
Artículo en Inglés | MEDLINE | ID: mdl-18078776

RESUMEN

Chagas' disease affects 16-18 million patients in South America and heart involvement is the major cause of morbidity and mortality. Heart failure is the most severe clinical manifestation of the chronic phase of infection with Trypanosoma cruzi. The intensity and nature of the immune response is associated with the clinical outcome of the disease. In murine models, a low proliferative response and T-cell apoptosis have been observed during acute infection. In the present study the immune response of patients in the chronic phase of infection was analyzed. Patients were divided into: (a) asymptomatic, i.e., without involvement of the heart or digestive system; and (b) with heart failure. Patients with heart failure presented a significantly lower peripheral blood mononuclear cell (PBMC) proliferative response to T. cruzi antigens compared to asymptomatic patients. This low response was associated with antigen-induced apoptosis. Apoptosis of PBMC and a low proliferative response were also associated with double Fas/Fas-L expression and high production of TNF-alpha, a cytokine known to induce programmed cell death. These results suggest that apoptosis of PBMC, probably triggered by double expression of Fas/Fas-L and TNF-alpha, is implicated in the immune regulatory mechanism during the chronic phase of Chagas' disease.


Asunto(s)
Apoptosis , Enfermedad de Chagas/inmunología , Proteína Ligando Fas/biosíntesis , Insuficiencia Cardíaca/inmunología , Linfocitos T/inmunología , Trypanosoma cruzi/inmunología , Receptor fas/biosíntesis , Animales , Proliferación Celular , Células Cultivadas , Enfermedad de Chagas/complicaciones , Humanos , Miocardio/patología , América del Sur , Factor de Necrosis Tumoral alfa/biosíntesis
6.
Clin Diagn Lab Immunol ; 10(5): 741-3, 2003 Sep.
Artículo en Inglés | MEDLINE | ID: mdl-12965897

RESUMEN

Endemic pemphigus foliaceus (EPF) is an autoimmune disease characterized by blister formation with a loss of cohesion and infiltration of inflammatory cells. We observed that supernatants of peripheral blood mononuclear cells from patients produced significantly more interleukin-1beta (IL-1beta) than those from stimulated healthy controls. Furthermore, a Th2 bias was observed in EPF patients when the IL-5/gamma interferon ratio was analyzed. These results indicate that cells from pemphigus patients react with a vigorous proinflammatory response.


Asunto(s)
Interleucina-1/biosíntesis , Leucocitos Mononucleares/metabolismo , Pénfigo/metabolismo , Enfermedades Autoinmunes/metabolismo , Citocinas/biosíntesis , Humanos , Interferón gamma/biosíntesis , Interleucina-5/biosíntesis , Células Th2/inmunología , Células Th2/metabolismo , Factor de Necrosis Tumoral alfa/biosíntesis
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