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1.
Biologics ; 11: 65-69, 2017.
Article in English | MEDLINE | ID: mdl-28579754

ABSTRACT

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.
Article in English | MEDLINE | ID: mdl-23994973

ABSTRACT

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.


Subject(s)
Antibodies, Monoclonal/therapeutic use , Behcet Syndrome/diagnosis , Behcet Syndrome/drug therapy , Gastrointestinal Agents/therapeutic use , Intestinal Diseases/diagnosis , Intestinal Diseases/drug therapy , Adolescent , Adult , Aged , Cohort Studies , Female , Follow-Up Studies , Humans , Infliximab , Male , Middle Aged , Retrospective Studies , Treatment Outcome , Young Adult
3.
Med Sci Monit ; 17(5): CR235-40, 2011 May.
Article in English | MEDLINE | ID: mdl-21525804

ABSTRACT

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.


Subject(s)
Helicobacter pylori/drug effects , Histamine H2 Antagonists/pharmacology , Adult , Aged , Aged, 80 and over , Female , Histamine H2 Antagonists/administration & dosage , Humans , Logistic Models , Male , Middle Aged , Treatment Failure , Young Adult
4.
Clin Res Hepatol Gastroenterol ; 35(4): 315-20, 2011 Apr.
Article in English | MEDLINE | ID: mdl-21435967

ABSTRACT

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.


Subject(s)
Anti-Bacterial Agents/therapeutic use , Colitis, Ulcerative/complications , Enterocolitis, Pseudomembranous/complications , Enterocolitis, Pseudomembranous/drug therapy , Adolescent , Adrenal Cortex Hormones/therapeutic use , Adult , Aged , Aged, 80 and over , Colectomy , Colitis, Ulcerative/surgery , Enterocolitis, Pseudomembranous/epidemiology , Female , Humans , Male , Middle Aged , Prevalence , Risk Factors , Treatment Failure , Young Adult
6.
Hepatogastroenterology ; 57(104): 1645-9, 2010.
Article in English | MEDLINE | ID: mdl-21443136

ABSTRACT

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.


Subject(s)
Helicobacter Infections/drug therapy , Helicobacter pylori , Proton Pump Inhibitors/administration & dosage , 2-Pyridinylmethylsulfinylbenzimidazoles/administration & dosage , Adolescent , Adult , Aged , Aged, 80 and over , Amoxicillin/administration & dosage , Chi-Square Distribution , Clarithromycin/administration & dosage , Drug Therapy, Combination , Female , Humans , Lansoprazole , Logistic Models , Male , Middle Aged , Premedication , Retrospective Studies , Statistics, Nonparametric
7.
Inflamm Bowel Dis ; 15(3): 328-34, 2009 Mar.
Article in English | MEDLINE | ID: mdl-18942752

ABSTRACT

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.


Subject(s)
Colitis, Ulcerative/genetics , Colon/metabolism , Cytokines/genetics , Drug Resistance/genetics , Gene Expression Regulation , Mesalamine/therapeutic use , RNA, Messenger/genetics , Administration, Oral , Adult , Anti-Inflammatory Agents, Non-Steroidal/administration & dosage , Anti-Inflammatory Agents, Non-Steroidal/therapeutic use , Biopsy , Colitis, Ulcerative/metabolism , Colitis, Ulcerative/therapy , Colon/pathology , Colonoscopy , Cytokines/biosynthesis , Dose-Response Relationship, Drug , Female , Follow-Up Studies , Granulocytes , Humans , Interleukin-6/biosynthesis , Interleukin-6/genetics , Interleukin-8/biosynthesis , Interleukin-8/genetics , Intestinal Mucosa/metabolism , Intestinal Mucosa/pathology , Leukapheresis/methods , Male , Mesalamine/administration & dosage , Middle Aged , Polymerase Chain Reaction , Prognosis , RNA, Messenger/biosynthesis , Remission Induction/methods , Retrospective Studies , Tumor Necrosis Factor-alpha/biosynthesis , Tumor Necrosis Factor-alpha/genetics , Young Adult
8.
Microbiol Immunol ; 50(8): 629-35, 2006.
Article in English | MEDLINE | ID: mdl-16924148

ABSTRACT

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.


Subject(s)
Anti-HIV Agents/administration & dosage , Antiretroviral Therapy, Highly Active/methods , HIV Infections/drug therapy , HIV Infections/immunology , HIV-1/immunology , Anti-HIV Agents/therapeutic use , CD4 Lymphocyte Count , CD8-Positive T-Lymphocytes/immunology , Drug Administration Schedule , Enzyme-Linked Immunosorbent Assay , Gene Products, nef/immunology , Gene Products, tat/immunology , HIV Core Protein p24/immunology , Humans , Immunity, Cellular , Interferon-gamma/immunology , Lymphocyte Activation , T-Lymphocytes/immunology , Viral Load , nef Gene Products, Human Immunodeficiency Virus , tat Gene Products, Human Immunodeficiency Virus
9.
Eur Arch Otorhinolaryngol ; 263(4): 305-7, 2006 Apr.
Article in English | MEDLINE | ID: mdl-16177918

ABSTRACT

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.


Subject(s)
Carcinoma, Hepatocellular/secondary , Liver Neoplasms/pathology , Maxillary Sinus Neoplasms/secondary , Nasal Cavity , Nose Neoplasms/secondary , Aged , Carcinoma, Hepatocellular/diagnostic imaging , Carcinoma, Hepatocellular/radiotherapy , Fatal Outcome , Humans , Liver Neoplasms/radiotherapy , Male , Maxillary Sinus Neoplasms/diagnostic imaging , Maxillary Sinus Neoplasms/radiotherapy , Nasal Cavity/pathology , Nose Neoplasms/radiotherapy , Radiotherapy Dosage , Tomography, X-Ray Computed
10.
Helicobacter ; 10(4): 307-11, 2005 Aug.
Article in English | MEDLINE | ID: mdl-16104946

ABSTRACT

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.


Subject(s)
Antibodies, Bacterial/blood , Dental Auxiliaries , Dentists , Helicobacter Infections/epidemiology , Helicobacter pylori/immunology , Adult , Cohort Studies , Female , Helicobacter Infections/microbiology , Humans , Immunoglobulin G/blood , Male , Prospective Studies , Risk Factors , Seroepidemiologic Studies
11.
Vaccine ; 22(13-14): 1683-91, 2004 Apr 16.
Article in English | MEDLINE | ID: mdl-15068851

ABSTRACT

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.


Subject(s)
AIDS Vaccines/therapeutic use , Antiretroviral Therapy, Highly Active , HIV Infections/therapy , Immunotherapy , Adult , CD4 Lymphocyte Count , Combined Modality Therapy , Follow-Up Studies , HIV Antibodies/biosynthesis , HIV Envelope Protein gp160/immunology , HIV Infections/drug therapy , HIV Infections/immunology , HIV-1/immunology , Humans , Immunization , Recombinant Proteins/immunology , T-Lymphocytes, Helper-Inducer/immunology , Vaccines, DNA/immunology
12.
J Gastroenterol ; 37(4): 255-9, 2002.
Article in English | MEDLINE | ID: mdl-11993508

ABSTRACT

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.


Subject(s)
Dentists , Helicobacter Infections/epidemiology , Helicobacter pylori , Adult , Aged , Antibodies, Bacterial/blood , Female , Helicobacter pylori/immunology , Humans , Japan/epidemiology , Logistic Models , Male , Middle Aged , Multivariate Analysis , Odds Ratio , Risk Factors , Seroepidemiologic Studies
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