Your browser doesn't support javascript.
loading
Mostrar: 20 | 50 | 100
Resultados 1 - 12 de 12
Filtrar
Más filtros












Base de datos
Intervalo de año de publicación
1.
Biologics ; 11: 65-69, 2017.
Artículo en Inglés | MEDLINE | ID: mdl-28579754

RESUMEN

Currently, anti-TNFα antibodies are used to treat Crohn's disease. We report on a 45-year-old Japanese female with Crohn's disease developing SAPHO (synovitis, acne, pustulosis, hyperostosis, and osteitis) syndrome following exposure to the anti-TNFα antibody adalimumab. Initially, adalimumab induced remission, but the patient showed SAPHO syndrome 11 weeks following the start of adalimumab therapy for the first time. Cutaneous and articular involvement were exacerbating the condition, so adalimumab was discontinued and the patient was put on low-dose methotrexate to control her symptoms. To our knowledge, this is the first report of SAPHO syndrome occurring during anti-TNF therapy, which is thought to be a paradoxical response to adalimumab.

2.
Intern Med ; 52(17): 1855-62, 2013.
Artículo en Inglés | MEDLINE | ID: mdl-23994973

RESUMEN

OBJECTIVE: To investigate the short- and long-term efficacy and safety of infliximab (IFX) in intestinal Behçet's disease (BD) patients in a retrospective cohort study. METHODS: Among 43 consecutive patients with intestinal BD presenting at the same clinic, 15 with active disease and receiving standard treatment were given IFX infusions (5 mg/kg body weight) every eight weeks. The patients were clinically and endoscopically evaluated before treatment, then assessed after 10 weeks, 12 months and 24 months for a clinical response, defined as a significant improvement in intestinal symptoms and a reduced C-reactive protein (CRP) level. RESULTS: At week 10, 12 patients (80%) exhibited a response to IFX, with eight (53%) in remission with no intestinal symptoms and normal CRP levels. A response to IFX was maintained in seven of the 11 patients (64%) available at 12 months and in four of the eight patients (50%) available at 24 months. Of the seven patients receiving prednisolone at entry, five responders had their steroid doses reduced. Fulminant intestinal BD was predictive of an absence of response to IFX. The adverse effects comprised one infusion reaction and one case of fever, most likely related to IFX. CONCLUSION: IFX is effective and safe in patients with refractory intestinal BD.


Asunto(s)
Anticuerpos Monoclonales/uso terapéutico , Síndrome de Behçet/diagnóstico , Síndrome de Behçet/tratamiento farmacológico , Fármacos Gastrointestinales/uso terapéutico , Enfermedades Intestinales/diagnóstico , Enfermedades Intestinales/tratamiento farmacológico , Adolescente , Adulto , Anciano , Estudios de Cohortes , Femenino , Estudios de Seguimiento , Humanos , Infliximab , Masculino , Persona de Mediana Edad , Estudios Retrospectivos , Resultado del Tratamiento , Adulto Joven
3.
Med Sci Monit ; 17(5): CR235-40, 2011 May.
Artículo en Inglés | MEDLINE | ID: mdl-21525804

RESUMEN

BACKGROUND: Pretreatment with a proton pump inhibitor (PPI) reportedly decreases the efficacy of Helicobacter pylori (H. pylori) eradication, however, the effect of pretreatment with an H2 receptor antagonist (H2RA) on H. pylori eradication has not yet been studied. We compared the efficacy of eradication regimen (lansoprazole/amoxicillin/clarithromycin) in patients with H. pylori infection with or without H2RA pretreatment. MATERIAL/METHODS: In this retrospective study conducted at three centers, 310 patients with H. pylori infection were treated. The diagnosis of H. pylori infection was made using the rapid urease test, bacterial cultures and histological examination of endoscopic biopsy specimens. The patients were assigned to receive an eradication regimen first or following pretreatment with H2RA. Eradication was assessed using the 13C-urea breath test more than 4 weeks after the completion of therapy. RESULTS: Overall, H. pylori was eradicated in 79.7% of the cases: the eradication rate was 81.6% in the pretreatment group, and 77.6% in the eradication first group (p=0.3799, chi-square test). No significant difference in the eradication rate was observed between the two groups. CONCLUSIONS: Pretreatment with H2RA had no significant influence on the efficacy of H. pylori eradication therapy.


Asunto(s)
Helicobacter pylori/efectos de los fármacos , Antagonistas de los Receptores H2 de la Histamina/farmacología , Adulto , Anciano , Anciano de 80 o más Años , Femenino , Antagonistas de los Receptores H2 de la Histamina/administración & dosificación , Humanos , Modelos Logísticos , Masculino , Persona de Mediana Edad , Insuficiencia del Tratamiento , Adulto Joven
4.
Clin Res Hepatol Gastroenterol ; 35(4): 315-20, 2011 Apr.
Artículo en Inglés | MEDLINE | ID: mdl-21435967

RESUMEN

BACKGROUND AND OBJECTIVE: The incidence of Clostridium difficile infection (CDI) has increased throughout the world and patients with ulcerative colitis (UC) are at a high risk for CDI. Potentially, CDI can exacerbate UC. Therefore, knowledge on the prevalence of CDI should contribute to better management of UC patients. METHODS: The presence of toxin A antigen was defined as CDI, and the outcome of the test in patients with active UC during 2006-2009 was reviewed for identifying patients with CDI. Demographic data (disease profile, clinical response to medications and the need for colectomy) in UC patients with CDI were compared with the data from CDI free UC patients. RESULTS: Fifty-five of 137 patients (40.1%) were CDI positive. Univariate and multivariate analyses revealed that CDI was not associated with any demographic factor. Intensive antibiotic therapy spared five of 17 (29.4%) steroid refractory patients with CDI from steroids. CDI was not a predictor of colectomy although this could be an outcome of efficient eradication strategy. CONCLUSION: CDI was not associated with any demographic factor or colectomy rate. However, CDI eradication therapy allowed some refractory patients to withdraw from steroids. Patients with active UC benefit from regular CDI test and eradication treatment for CDI.


Asunto(s)
Antibacterianos/uso terapéutico , Colitis Ulcerosa/complicaciones , Enterocolitis Seudomembranosa/complicaciones , Enterocolitis Seudomembranosa/tratamiento farmacológico , Adolescente , Corticoesteroides/uso terapéutico , Adulto , Anciano , Anciano de 80 o más Años , Colectomía , Colitis Ulcerosa/cirugía , Enterocolitis Seudomembranosa/epidemiología , Femenino , Humanos , Masculino , Persona de Mediana Edad , Prevalencia , Factores de Riesgo , Insuficiencia del Tratamiento , Adulto Joven
6.
Hepatogastroenterology ; 57(104): 1645-9, 2010.
Artículo en Inglés | MEDLINE | ID: mdl-21443136

RESUMEN

BACKGROUND/AIMS: Pretreatment with a proton pump inhibitor (PPI) has been reported to decrease the efficacy of Helicobacter pylori (H. pylori) eradication. We compared the efficacy of an eradication regimen (lansoprazole/amoxicillin/clarithromycin) first or following pretreatment with a PPI. METHODOLOGY: In this retrospective study conducted at three centers, 353 patients infected with H. pylori were treated. The H. pylori status was determined using the rapid urease test, bacterial cultures, and the histological examination of endoscopic biopsy specimens, The patients were assigned to receive an eradication regimen first or following pretreatment with a PPI. Eradication was assessed using the 13C-urea breath test more than 4 weeks after the completion of therapy. RESULTS: Overall, H. pylori was eradicated in 78.8% of the cases: 79.6% in the pretreatment group, and 77.6% in the eradication first group (p = 0.6541 by chi square test). No significant difference in the eradication rates was observed between the two groups. CONCLUSIONS: This retrospective study indicated that pretreatment with a PPI does not significantly reduce the efficacy of eradication therapy in patients infected with H. pylori.


Asunto(s)
Infecciones por Helicobacter/tratamiento farmacológico , Helicobacter pylori , Inhibidores de la Bomba de Protones/administración & dosificación , 2-Piridinilmetilsulfinilbencimidazoles/administración & dosificación , Adolescente , Adulto , Anciano , Anciano de 80 o más Años , Amoxicilina/administración & dosificación , Distribución de Chi-Cuadrado , Claritromicina/administración & dosificación , Quimioterapia Combinada , Femenino , Humanos , Lansoprazol , Modelos Logísticos , Masculino , Persona de Mediana Edad , Premedicación , Estudios Retrospectivos , Estadísticas no Paramétricas
7.
Inflamm Bowel Dis ; 15(3): 328-34, 2009 Mar.
Artículo en Inglés | MEDLINE | ID: mdl-18942752

RESUMEN

BACKGROUND: Cytokines have validated roles in the immunopathogenesis of inflammatory bowel disease (IBD). This study was to investigate the expressions of tumor necrosis factor (TNF)-alpha, interleukin (IL)-6, IL-8, and IL-10 mRNAs in the colonic mucosa of patients with ulcerative colitis (UC) during active and quiescent UC. METHODS: At colonoscopy, biopsies were taken from inflamed and non-inflamed mucosa of patients with steroid-naive UC (n = 15), non-IBD inflammatory colitis controls (ICC, n = 6), and non-colitis controls (NCC, n = 14). The presence of extensive mononuclear cells and neutrophils infiltrate in the lamina propria, cryptitis, and epithelial damage defined an inflammatory lesion in the mucosa. Quantitative cytokine mRNA expressions in biopsies were measured by real-time polymerase chain reaction (PCR). RESULTS: Of 15 UC patients, 3 remitted with 5-aminosalicylate and 11 received granulocytapheresis; of these, 10 remitted. At baseline, IL-6, IL-8, TNF-alpha, and IL-10 mRNAs were high in inflamed mucosa compared with NCC (P < 0.01). In active UC, IL-6, IL-8 and IL-10 mRNAs were high compared with non-inflamed mucosa (P = 0.03, P = 0.03, P < 0.05, respectively). Both TNF-alpha mRNA (P = 0.03) and IL-6 mRNA (P = 0.04) were higher in UC compared with ICC. Even in non-inflamed mucosa, IL-8 and TNF-alpha mRNA expressions were high compared with NCC. Both IL-6 and IL-8 mRNAs decreased to normal levels after granulocytapheresis. CONCLUSIONS: During active UC, all 4 cytokine mRNA levels were high; only IL-6 and IL-8 mRNAs decreased to normal levels during remission. IL-8 mRNA was high even at sites of endoscopically quiescent UC during active disease. Steroid naïve patients respond well to granulocytapheresis.


Asunto(s)
Colitis Ulcerosa/genética , Colon/metabolismo , Citocinas/genética , Resistencia a Medicamentos/genética , Regulación de la Expresión Génica , Mesalamina/uso terapéutico , ARN Mensajero/genética , Administración Oral , Adulto , Antiinflamatorios no Esteroideos/administración & dosificación , Antiinflamatorios no Esteroideos/uso terapéutico , Biopsia , Colitis Ulcerosa/metabolismo , Colitis Ulcerosa/terapia , Colon/patología , Colonoscopía , Citocinas/biosíntesis , Relación Dosis-Respuesta a Droga , Femenino , Estudios de Seguimiento , Granulocitos , Humanos , Interleucina-6/biosíntesis , Interleucina-6/genética , Interleucina-8/biosíntesis , Interleucina-8/genética , Mucosa Intestinal/metabolismo , Mucosa Intestinal/patología , Leucaféresis/métodos , Masculino , Mesalamina/administración & dosificación , Persona de Mediana Edad , Reacción en Cadena de la Polimerasa , Pronóstico , ARN Mensajero/biosíntesis , Inducción de Remisión/métodos , Estudios Retrospectivos , Factor de Necrosis Tumoral alfa/biosíntesis , Factor de Necrosis Tumoral alfa/genética , Adulto Joven
8.
Microbiol Immunol ; 50(8): 629-35, 2006.
Artículo en Inglés | MEDLINE | ID: mdl-16924148

RESUMEN

We have followed 15 HIV-1 chronically infected patients during prolonged highly active antiretroviral treatment (HAART) and subsequent long term structured treatment interruption (STI). We analyzed Nef, Tat, and p24 specific cellular immunity using IFN-gamma enzyme-linked immunospot assays and T cell proliferation assays. Eight HAART patients showed IFN-gamma responses to at least one antigen, but no positive responses were seen during STI. We observed retained or increased p24 specific IFN-gamma responses in most patients during HAART with viral suppression. These results showed persisting HIV-1 specific cellular immunity during HAART; however, in prolonged STI with viral rebound this immunity declined.


Asunto(s)
Fármacos Anti-VIH/administración & dosificación , Terapia Antirretroviral Altamente Activa/métodos , Infecciones por VIH/tratamiento farmacológico , Infecciones por VIH/inmunología , VIH-1/inmunología , Fármacos Anti-VIH/uso terapéutico , Recuento de Linfocito CD4 , Linfocitos T CD8-positivos/inmunología , Esquema de Medicación , Ensayo de Inmunoadsorción Enzimática , Productos del Gen nef/inmunología , Productos del Gen tat/inmunología , Proteína p24 del Núcleo del VIH/inmunología , Humanos , Inmunidad Celular , Interferón gamma/inmunología , Activación de Linfocitos , Linfocitos T/inmunología , Carga Viral , Productos del Gen nef del Virus de la Inmunodeficiencia Humana , Productos del Gen tat del Virus de la Inmunodeficiencia Humana
9.
Eur Arch Otorhinolaryngol ; 263(4): 305-7, 2006 Apr.
Artículo en Inglés | MEDLINE | ID: mdl-16177918

RESUMEN

Metastatic hepatocellular carcinoma in the nasal cavity and paranasal sinuses is rare. We report the case of a 71-year-old male afflicted with hepatocellular carcinoma with metastasis in the maxillary sinus and nasal cavity. He underwent radiation therapy with a total dose of 36 Gy, but he died of terminal liver failure. The possible metastatic route and prognosis of metastatic hepatocellular carcinoma in the sinonasal tract are discussed.


Asunto(s)
Carcinoma Hepatocelular/secundario , Neoplasias Hepáticas/patología , Neoplasias del Seno Maxilar/secundario , Cavidad Nasal , Neoplasias Nasales/secundario , Anciano , Carcinoma Hepatocelular/diagnóstico por imagen , Carcinoma Hepatocelular/radioterapia , Resultado Fatal , Humanos , Neoplasias Hepáticas/radioterapia , Masculino , Neoplasias del Seno Maxilar/diagnóstico por imagen , Neoplasias del Seno Maxilar/radioterapia , Cavidad Nasal/patología , Neoplasias Nasales/radioterapia , Dosificación Radioterapéutica , Tomografía Computarizada por Rayos X
10.
Helicobacter ; 10(4): 307-11, 2005 Aug.
Artículo en Inglés | MEDLINE | ID: mdl-16104946

RESUMEN

BACKGROUND: In a previous cross-sectional study, we reported no significant differences between dentists and controls in the seroprevalence of Helicobacter pylori. The aim of the present study is to determine the risk and the risk factors for new infection of H. pylori. This is the first report designed to assess the seroprevalence of H. pylori infection over a 6-year period in a cohort of dental professionals. MATERIALS AND METHODS: We collected blood samples from employees of Kanagawa Dental College to test for serum anti-H. pylori IgG. We collected 566 samples in 1997 and another 551 samples in 2003. Questionnaires completed by participants provided information about risk factors of H. pylori infection. RESULTS: A total of 236 employees were tested on both occasions. Of the 170 who were seronegative in 1997, we randomly selected 59 from among the dental professionals (dentists and dental nurses). As controls, we selected 59 from among the nonclinical staff who were matched for sex and age. The risk of new infection of H. pylori for dental professionals is 1.12%/year and the relative risk is 4.0. We determined the risk factors for acquiring H. pylori using logistic regression. Adjusted odds ratio being a dental professionals was 2.68 (95% confidence interval [CI]: 0.55-19.67), having upper gastrointestinal family history was 4.84 (95% CI: 0.83-26.72), and age over 40 was 8.83 (95% CI: 1.36-177.24). CONCLUSION: This 6-year prospective study shows that dental professionals are at greater risk of being infected by H. pylori than are controls.


Asunto(s)
Anticuerpos Antibacterianos/sangre , Auxiliares Dentales , Odontólogos , Infecciones por Helicobacter/epidemiología , Helicobacter pylori/inmunología , Adulto , Estudios de Cohortes , Femenino , Infecciones por Helicobacter/microbiología , Humanos , Inmunoglobulina G/sangre , Masculino , Estudios Prospectivos , Factores de Riesgo , Estudios Seroepidemiológicos
11.
Vaccine ; 22(13-14): 1683-91, 2004 Apr 16.
Artículo en Inglés | MEDLINE | ID: mdl-15068851

RESUMEN

The aim of this study was to monitor the immune responses in HIV-infected patients previously immunized with gp160 or DNA vaccines to analyze whether the introduction of highly active antiretroviral treatment (HAART) would affect the persistence of immunity. The immune responses were evaluated in patients who had participated in randomized trials of therapeutic vaccination. Immunization in conjunction with antiretroviral therapy was effective in inducing HIV-specific T-cell responses. Therapeutic immunizations with recombinant gp160 had a modest effect on CD4-cell counts, the treatment alone lead to a transient clinical benefit in the form of an improved survival after two years of immunization. Immunizations with HIV DNA during HAART treatment permitted persistence or development of innate (NK), CD4+ and/or CD8+ immune responses. HIV specific T-helper cell responses induced by immunization with gp160 were maintained at high levels up to 7 years after the last injection. Cells with HIV-specific interferon-gamma (IFN-gamma) production were retained or increased in long-term HAART treated patients. The impact of a single structured therapy interruption (STI) was analyzed in a small group of patients showing no obvious increase or decrease in the HIV-specific immune response during or after STI. The possibility to induce very long-term strong and persistent immune responses in HIV-infected individuals raises hopes that vaccination preceding therapy interruption might prolong the symptom-free period without HAART.


Asunto(s)
Vacunas contra el SIDA/uso terapéutico , Terapia Antirretroviral Altamente Activa , Infecciones por VIH/terapia , Inmunoterapia , Adulto , Recuento de Linfocito CD4 , Terapia Combinada , Estudios de Seguimiento , Anticuerpos Anti-VIH/biosíntesis , Proteínas gp160 de Envoltorio del VIH/inmunología , Infecciones por VIH/tratamiento farmacológico , Infecciones por VIH/inmunología , VIH-1/inmunología , Humanos , Inmunización , Proteínas Recombinantes/inmunología , Linfocitos T Colaboradores-Inductores/inmunología , Vacunas de ADN/inmunología
12.
J Gastroenterol ; 37(4): 255-9, 2002.
Artículo en Inglés | MEDLINE | ID: mdl-11993508

RESUMEN

BACKGROUND: The infection mode of Helicobacter pylori is not well known. In order to prove that frequent exposure to saliva and dental plaque does not constitute a risk for acquiring H. pylori infection, we tested the hypothesis that the prevalence of H. pylori in dentists in Japan is the same as that in controls. We also studied factors associated with H. pylori prevalence by multivariate analysis. METHODS: We examined serum anti-H. pylori-IgG in 232 Japanese subjects (116 dentists and 116 age- and sex-matched nonclinical controls). Participants were given a questionnaire that included demographic data, life style, past history, and gastrointestinal symptoms, and dental practice. RESULTS: We analyzed the results for 111 dentists and 111 controls after exclusion of those who had an equivocal titer. The seroprevalence of H. pylori was 42.3% in dentists and 40.0% in controls. With multiple logistic regression, age was selected as the only independent variable correlated with seroprevalence (P = 0.0002; coefficient of determination 0.11). Factors associated with dental practice were not significant. CONCLUSIONS: We conclude that dental practice in Japan does not increase the risk of H. pylori infection for dentists.


Asunto(s)
Odontólogos , Infecciones por Helicobacter/epidemiología , Helicobacter pylori , Adulto , Anciano , Anticuerpos Antibacterianos/sangre , Femenino , Helicobacter pylori/inmunología , Humanos , Japón/epidemiología , Modelos Logísticos , Masculino , Persona de Mediana Edad , Análisis Multivariante , Oportunidad Relativa , Factores de Riesgo , Estudios Seroepidemiológicos
SELECCIÓN DE REFERENCIAS
DETALLE DE LA BÚSQUEDA
...