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1.
Intern Med ; 55(22): 3337-3340, 2016.
Article in English | MEDLINE | ID: mdl-27853079

ABSTRACT

We herein describe a patient with Behçet's disease in whom we followed the development and resolution of pulmonary artery aneurysms. He presented with intermittent hemoptysis, pulmonary thromboembolism was initially diagnosed, and anticoagulant therapy was started. Over the next several months, the expansion of pulmonary arteries was noted. Five months after his initial admission, he was readmitted for massive hemoptysis, and further examinations revealed that he had Behçet's disease. Corticosteroids and intravenous cyclophosphamide were started. Over the next five months, the pulmonary artery aneurysms and thrombosis resolved. The development of pulmonary artery aneurysms led to the diagnosis of Behçet's disease, and they resolved after immunosuppressive therapy.


Subject(s)
Aneurysm/etiology , Behcet Syndrome/complications , Behcet Syndrome/diagnosis , Pulmonary Artery , Pulmonary Embolism/etiology , Adult , Aneurysm/diagnostic imaging , Behcet Syndrome/drug therapy , Cyclophosphamide/therapeutic use , Glucocorticoids/therapeutic use , Hemoptysis/etiology , Humans , Immunosuppressive Agents/therapeutic use , Male , Pulmonary Embolism/diagnostic imaging
2.
BMC Infect Dis ; 16: 31, 2016 Jan 27.
Article in English | MEDLINE | ID: mdl-26818764

ABSTRACT

BACKGROUND: Although the isolation of clarithromycin (CAM)-resistant Mycobacterium avium complex (MAC) indicates a poor treatment outcome and increased mortality, there have been only a few reports on drug treatment for CAM-resistant MAC lung disease. We aimed to reveal the effectiveness of the continuation of a macrolide and the use of a multidrug regimen in the treatment of CAM-resistant MAC lung disease. METHODS: Among patients with MAC pulmonary disease as defined by the 2007 criteria of the American Thoracic Society and the Infectious Diseases Society of America statement, those with CAM-resistant MAC (minimum inhibitory concentration ≥32 µg/ml) isolated, newly diagnosed and treated from January 2009 to June 2013 were analysed in this study. Effectiveness was measured based on culture conversion rate and improvement of radiological findings. RESULTS: Thirty-three HIV-negative patients were analysed in this study. Twenty-six were treated with a regimen containing CAM or azithromycin (AZM), and 21 patients were treated with three or more drugs except macrolide. The median duration to be evaluated was 10.4 months after beginning the treatment regimen. Sputum conversion (including cases of inability to expectorate sputum) was achieved in 12 (36%) patients. Radiological effectiveness improved in 4 (12%) patients, was unchanged in 11 (33%) patients and worsened in 18 (55%) patients. In the multivariate analysis, CRP <1.0 mg/dl (p = 0.017, odds ratio 12, 95% confidence interval (CI) 1.6-95) was found to be the only significant risk factor for radiological non-deterioration, and no significant risk factors for microbiological improvement were found. CONCLUSIONS: Our results suggested that continuation of macrolides or the addition of a new quinolone or injectable aminoglycoside to therapy with rifampicin and ethambutol would not improve clinical outcome after the emergence of CAM-resistant MAC. However, further prospective study is required to evaluate the precise clinical efficacy and effectiveness of these drugs.


Subject(s)
Anti-Bacterial Agents/therapeutic use , Clarithromycin/therapeutic use , Lung Diseases/drug therapy , Mycobacterium avium Complex/isolation & purification , Mycobacterium avium-intracellulare Infection/drug therapy , Aged , Anti-Bacterial Agents/pharmacology , Azithromycin/pharmacology , Azithromycin/therapeutic use , C-Reactive Protein/analysis , Drug Resistance, Bacterial , Female , Humans , Lung Diseases/microbiology , Male , Microbial Sensitivity Tests , Middle Aged , Multivariate Analysis , Mycobacterium avium Complex/drug effects , Mycobacterium avium-intracellulare Infection/microbiology , Retrospective Studies , Risk Factors , Serum Albumin/analysis , Sputum/microbiology , Tomography, X-Ray Computed , Treatment Outcome
3.
J Orthop Sci ; 18(1): 54-60, 2013 Jan.
Article in English | MEDLINE | ID: mdl-23114856

ABSTRACT

BACKGROUND: Pre- and postoperative knee kinematics in unicompartmental knee arthroplasty (UKA) can be theoretically related to clinical outcome and longevity after UKA with regard to ligament function and the degree of arthritic changes. However, the preoperative knee kinematics of patients indicated for UKA remain to be elucidated, and it is also unclear whether the preoperative kinematics can be maintained by the UKA procedure. The objective of this study was to examine the in vivo pre- and postoperative three-dimensional knee kinematics in UKA while referencing the normal knee kinematics reported in our previous study. METHODS: We analyzed the knee kinematics in 17 knees (14 patients) undergoing UKA via a three-dimensional to two-dimensional registration technique employing femoral condylar translation and femoral axial rotation. The pre- and postoperative knee kinematics during squat motion were evaluated in the same subjects, employing consistent evaluation parameters. RESULTS: On average, both pre- and postoperative knee kinematics in the range 10-100° of knee flexion demonstrated near-consistent femoral external rotation and anterior translation of the medial condyle and posterior translation of the lateral condyle. However, the mean femoral external rotation angle and the posterior translation of the lateral condyle postoperatively were significantly smaller than the values observed preoperatively. DISCUSSION: Although the patterns of preoperative knee motion were similar to those seen in normal knees, the magnitude of this motion varied widely between patients, so it was not necessarily representative of normal knees. These variations may be due to the varying degrees of arthritic changes caused by osteoarthritis. Although the patterns of knee kinematics were largely maintained by the UKA procedure, the causes of the significant reductions in the magnitude of motion upon performing the UKA procedure should be investigated in subsequent studies with a larger number of patients.


Subject(s)
Arthroplasty, Replacement, Knee/methods , Imaging, Three-Dimensional , Knee Joint/physiopathology , Knee Prosthesis , Osteoarthritis, Knee/surgery , Range of Motion, Articular/physiology , Tomography, X-Ray Computed/methods , Aged , Aged, 80 and over , Algorithms , Arthroscopy , Biomechanical Phenomena , Female , Fluoroscopy , Follow-Up Studies , Humans , Knee Joint/diagnostic imaging , Knee Joint/surgery , Male , Middle Aged , Osteoarthritis, Knee/diagnostic imaging , Osteoarthritis, Knee/physiopathology , Postoperative Period , Preoperative Period , Prosthesis Design , Reproducibility of Results
4.
Cancer Immunol Immunother ; 59(10): 1503-9, 2010 Oct.
Article in English | MEDLINE | ID: mdl-20582589

ABSTRACT

BACKGROUND: Cancer immunotherapy with NKT cells is a potential new treatment strategy for advanced head and neck cancer. NKT cell therapy is promising due to its unique anti-tumor activity and higher degree of safety compared to current therapies. Radiotherapy is indispensable as a standard treatment for advanced head and neck cancer. To elucidate the possibility of using NKT cells as an adjuvant immunotherapy with radiotherapy, we examined the effect of radiotherapy on NKT cells in patients with head and neck cancer. METHODS: The number, IFN-gamma production and proliferation capacity of NKT cells were analyzed before and after 50 Gy radiation therapy in 12 patients with stage IV head and neck squamous cell carcinoma. The cytotoxic activity of NKT cells was examined in vitro. RESULTS: The number of NKT cells in the blood varied widely between patients. After radiation therapy, the population of CD3 T cells decreased significantly, while the NKT cell population remained stable. The number of NKT cells was the same after radiation therapy as before. IFN-gamma production from NKT cells collected just after radiotherapy was impaired after stimulation with exogenous ligand, but the proliferative responses of these NKT cells was enhanced in comparison to those collected before radiation therapy. Furthermore, the proliferated NKT cells displayed a significant level of anti-tumor activity. CONCLUSION: NKT cells are relatively resistant to radiation and might therefore be suitable for adjuvant immunotherapy to eradicate remnant cancer cells in patients who have undergone radiation therapy.


Subject(s)
Carcinoma, Squamous Cell/pathology , Carcinoma, Squamous Cell/radiotherapy , Head and Neck Neoplasms/pathology , Head and Neck Neoplasms/radiotherapy , Natural Killer T-Cells/radiation effects , Aged , Cell Count , Female , Humans , Interferon-gamma/metabolism , K562 Cells , Male , Middle Aged , Natural Killer T-Cells/immunology , Neoplasm Staging
5.
Allergy Asthma Proc ; 30(4): 397-405, 2009.
Article in English | MEDLINE | ID: mdl-19772761

ABSTRACT

Japanese cedar pollinosis is an important contributor to allergic rhinitis in Japan. Lactobacillus may be useful as an immunomodulator and is used widely as a foodstuff. The purpose of the study was to examine the effects of daily intake of the Lactobacillus paracasei strain KW3110 in patients with cedar pollinosis. The effects of daily intake of KW3110 in patients with cedar pollinosis were investigated in 126 patients who received KW3110 or a placebo in a double-blind study. The study began 1 month before the start of the pollen season and lasted for 3 months. A significant reduction of nasal symptoms and the serum level of eosinophil cationic protein and improvement of quality of life scores occurred in the patients who received KW3110 when pollen scattering was low. However, the effects were limited during the peak period of pollen scattering. Intake of KW3110 may reduce allergic inflammation, but the effect is limited.


Subject(s)
Eosinophil Cationic Protein/biosynthesis , Lactobacillus/immunology , Probiotics/administration & dosage , Rhinitis, Allergic, Seasonal/physiopathology , Rhinitis, Allergic, Seasonal/therapy , Adult , Cryptomeria/adverse effects , Double-Blind Method , Eating/immunology , Eosinophil Cationic Protein/blood , Eosinophil Cationic Protein/genetics , Humans , Immunomodulation , Male , Middle Aged , Nasal Obstruction , Probiotics/adverse effects , Rhinitis, Allergic, Seasonal/blood , Rhinitis, Allergic, Seasonal/immunology , Rhinitis, Allergic, Seasonal/microbiology , Seasons , Treatment Outcome
6.
J Clin Immunol ; 27(6): 598-604, 2007 Nov.
Article in English | MEDLINE | ID: mdl-17597385

ABSTRACT

Tumor-specific peptide-pulsed dendritic cells (DC) were administered via different routes to a group of patients with head and neck cancers. The migration and homing patterns of such antigen-stimulated cells was carefully studied employing single photon emission computed tomography (SPECT). The DC administered directly into the nasal submucosa quickly migrated very rapidly to the regional neck lymph nodes in the neck. However, after inoculation of the cells into the palatine tonsils, the DCs remained close to the site of administration and did not migrate to the regional lymph nodes or to other mucosal regions. After nasal submucosal administration of the DC, tumor-antigen-specific cytotoxic T cells were detected in the ipsilaterals but not in the contra lateral lymph nodes. These results suggest that after antigen processing, the regional lymph nodes serve as inductive sites for development of mucosal immune responses and for induction of memory cells during the local immunological responses in the nasopharyngeal-associated lymphoid tissue in man.


Subject(s)
Antigens, Neoplasm/administration & dosage , Cell Movement/immunology , Dendritic Cells/immunology , Nasal Mucosa/immunology , Administration, Intranasal , Aged , Antigens, Neoplasm/immunology , Antigens, Neoplasm/metabolism , Biomarkers/metabolism , Carcinoma, Squamous Cell/immunology , Carcinoma, Squamous Cell/pathology , Dendritic Cells/transplantation , Female , HLA-DR Antigens/biosynthesis , Head and Neck Neoplasms/immunology , Head and Neck Neoplasms/pathology , Humans , Immunophenotyping , Injections, Intravenous , Male , Maxillary Neoplasms/immunology , Maxillary Neoplasms/pathology , Middle Aged , Nasal Mucosa/pathology , Palatine Tonsil/immunology , Palatine Tonsil/metabolism , Palatine Tonsil/pathology , Pharyngeal Neoplasms/immunology , Pharyngeal Neoplasms/pathology
7.
Clin Cancer Res ; 12(1): 191-7, 2006 Jan 01.
Article in English | MEDLINE | ID: mdl-16397042

ABSTRACT

PURPOSE: To isolate cancer testis antigens that are expressed in pancreatic cancers and may be useful in clinical applications. EXPERIMENTAL DESIGN: To efficiently isolate cancer testis antigens, a testis cDNA library was immunoscreened (SEREX) with serum from a patient with pancreatic ductal adenocarcinoma. The expression of isolated antigens in various cancer cell lines and tissues was evaluated by reverse transcription-PCR and Northern blot analyses. The immunogenicity of the antigen in cancer patients was evaluated by detection of the IgG antibody in sera from patients with various cancers. RESULTS: Of the three clones isolated through screening of a total of 2 x 10(6) cDNA library clones, one clone (KU-CT-1) was found to be expressed in various cancers but only in testis among normal tissues, indicating that it was a novel cancer testis antigen. The KU-CT-1 gene is located on chromosome 10p12 and produces two splice variants, which encode proteins of 397 and 872 amino acids, respectively. KU-CT-1 was expressed in pancreatic cancer tissues (3 of 9, 33%), lung cancer tissues (9 of 24, 38%), and endometrial cancer tissues (7 of 11, 64%). Specific serum IgG antibodies were detected in 3 of 20 pancreatic cancer patients, 2 of 12 endometrial cancer patients, 1 of 18 colon cancer patients, and 1 of 10 prostate cancer patients but not detected in 30 healthy individuals. CONCLUSIONS: KU-CT-1 is a new cancer testis antigen that is expressed in pancreatic, lung, and endometrial cancers and may be useful for diagnosis and immunotherapy for patients with various cancers.


Subject(s)
Gene Library , Neoplasm Proteins/genetics , Neoplasms/genetics , Amino Acid Sequence , Base Sequence , Blotting, Northern , Cell Line, Tumor , Endometrial Neoplasms/genetics , Female , Humans , Lung Neoplasms/genetics , Male , Molecular Sequence Data , Pancreatic Neoplasms/genetics , Reverse Transcriptase Polymerase Chain Reaction , Testis/physiology
8.
Ann Allergy Asthma Immunol ; 94(2): 286-91, 2005 Feb.
Article in English | MEDLINE | ID: mdl-15765747

ABSTRACT

BACKGROUND: CD23 is the low-affinity receptor for IgE on B cells and is thought to play an important role in regulation of IgE production. OBJECTIVE: To measure the expression of membrane-bound CD23 in nasal B cells and examine its correlation with CD4 subtypes or serum IgE levels in patients with perennial allergic rhinitis. METHOD: We used flow cytometric analysis with double, direct immunofluorescence staining of the mucosal-infiltrating lymphocytes to examine the expression of CD23 in nasal mucosal B cells of patients with perennial allergic rhinitis. The expression of CD23 in nasal B cells of patients with nonatopic rhinosinusitis served as a control. RESULT: The ratio of CD23+ B cells to total B cells in patients with perennial allergic rhinitis was significantly higher than in nonatopic controls, whereas that of B cells to total lymphocytes was unchanged. The ratio of CCR4+ CD4 cells to total CD4 cells in allergic patients was significantly higher than in nonatopic controls, whereas the ratio of CXCR3+ CD4 cells to total CD4 cells was unchanged. There was no significant correlation between the percentages of CD23+ B cells and CCR4+ CD4 cells. In addition, the percentage of CD23+ B cells did not correlate with the total IgE level or with the specific IgE level. CONCLUSIONS: Our results indicate that nasal mucosal CD23-bearing B cells, as well as T(H)2 cells, increase in patients with perennial allergic rhinitis. However, the expression of CD23 did not directly correlate with the number of T(H)2 cells in the nasal mucosa.


Subject(s)
B-Lymphocytes/immunology , Cell Membrane/immunology , Nasal Mucosa/cytology , Nasal Mucosa/immunology , Receptors, IgE/biosynthesis , Rhinitis, Allergic, Perennial/immunology , Adult , Aged , Female , Flow Cytometry , Fluorescent Antibody Technique , Humans , Immunoglobulin E/blood , Male , Middle Aged , Receptors, CXCR3 , Receptors, Chemokine/biosynthesis , Rhinitis, Allergic, Perennial/blood , Th2 Cells/immunology
9.
Dent Mater J ; 23(3): 284-90, 2004 Sep.
Article in English | MEDLINE | ID: mdl-15510855

ABSTRACT

The purpose of this study was to develop a method to monitor the free-shrinkage vectors of a light-cured resin using laser speckle contrast measurement. The laser speckle contrast measurement system comprised a semiconductor laser, a speckle analyzer, and a computer-controlled data acquisition system. A light-cured resin was condensed into a glass tube and irradiated using a curing unit, the light intensity of which was adjusted to either 100 or 600 mW/cm2. The speckle patterns obtained from the lateral surface of the specimen were monitored using a CCD camera connected to a computer. The speckle images were analyzed using a phase-only correlation algorithm, and movements of the pattern were traced. The speckle pattern revealed rapid movement almost immediately after light exposure was initiated, and the orientation of free-shrinkage vectors is dependent on light intensity. When the specimens were irradiated at the lower light intensity, the free shrinkage vectors were oriented towards the light source. On the other hand, when irradiated at the higher light intensity, the free-shrinkage vectors of these specimens tended to orient towards the bottom surface. The effectiveness of the employed method to determine free-shrinkage vectors is thus proven through the results of this study.


Subject(s)
Composite Resins/radiation effects , Interferometry/methods , Algorithms , Dental Marginal Adaptation , Image Processing, Computer-Assisted/methods , Lasers , Light , Phase Transition
10.
J Lab Clin Med ; 142(2): 128-35, 2003 Aug.
Article in English | MEDLINE | ID: mdl-12960960

ABSTRACT

Although neutrophil depletion can reduce the level of acute lung injury (ALI) induced by Escherichia coli endotoxin, that induced by live E coli cannot be attenuated even in neutropenia. This suggests that live E coli cause ALI by way of an mechanism independent of circulating neutrophil. Tumor necrosis factor-alpha (TNF-alpha), which is released from monocytes and macrophages, is a proinflammatory cytokine that is recognized as a central mediator of several forms of inflammation. In this controlled experimental study, we examined the effects of an adenosine-receptor agonist, 2-chloroadenosine (2CA), that has suppressive effects on various cell types and TNF-alpha, on endotoxin plus latex particles, and on ALI induced by live E coli in the neutropenic state. We studied 42 guinea pigs rendered neutropenic by means of intraperitoneal cyclophosphamide administration. Experimental groups consisted of (1) a saline-solution control group; (2) an endotoxin (0.2 mg/kg)-treated group; (3) a group treated with endotoxin plus 2CA (10 micro g/kg); (4) a group treated with latex (2 x 10(9)/kg); (5) a group exposed to endotoxin and latex; (6) a group exposed to endotoxin, latex, and 2CA; (7) a group exposed to E coli (2 x 10(9)/kg); and (8) a group exposed to E coli and 2CA. The injection of endotoxin alone in neutropenic animals did not increase the indexes of ALI (lung tissue/plasma ratio [T/P] and lung wet weight/dry weight ratio [W/D], calculated with the use of iodine 125-labeled albumin). In contrast, these indexes were increased in the endotoxin-and-latex groups compared with those of the control group. ALI in the endotoxin-and-latex group was attenuated by intravenous 2CA. The intravenous injection of live E coli also caused increases in T/P, W/D, and plasma TNF-alpha, but thse were limited by 2CA. In summary, ALI induced by latex particles added to endotoxin and live E coli in the neutropenic state was attenuated by 2CA, suggesting a partial contribution of various cell types or humoral mediators as a neutrophil-independent pathway in its pathogenesis.


Subject(s)
2-Chloroadenosine/pharmacology , Escherichia coli Infections/immunology , Escherichia coli , Lung Diseases/drug therapy , Neutropenia/immunology , Acute Disease , Animals , Endotoxins/pharmacology , Guinea Pigs , Injections, Intravenous , Lung Diseases/immunology , Lung Diseases/microbiology , Microspheres , Neutropenia/microbiology , Specific Pathogen-Free Organisms , Tumor Necrosis Factor-alpha/metabolism
11.
Nihon Kokyuki Gakkai Zasshi ; 41(6): 386-91, 2003 Jun.
Article in Japanese | MEDLINE | ID: mdl-12833843

ABSTRACT

A 70-year-old man in whom nodular and reticular shadows had been noted on chest radiography since 1992 was admitted to our hospital with complaints of persistent cough and dyspnea on exertion in August, 2000. The definitive diagnosis of lung abnormalities was not confirmed by TBLB. He was re-admitted to our hospital to undergo a lung biopsy by video-assisted thoracoscopic surgery. Although desquamative interstitial pneumonia was diagnosed, respiratory failure developed rapidly after surgery. He responded well to high-dose steroid administration followed by maintenance therapy with a moderate dose of steroid, resulting in a considerable importance of the clinical condition associated with a significant decrease in the ground-glass opacities and infiltrative shadows. Although we could find no literature reporting acute exacerbation of DIP, our case demonstrates that DIP may also be acutely exacerbated when a severe insult is superimposed.


Subject(s)
Lung Diseases, Interstitial/drug therapy , Lung Diseases, Interstitial/pathology , Lung/pathology , Thoracic Surgery, Video-Assisted/adverse effects , Aged , Anti-Inflammatory Agents/administration & dosage , Biopsy , Humans , Male , Methylprednisolone/administration & dosage , Prednisolone/administration & dosage , Pulse Therapy, Drug
12.
Int J Cancer ; 100(5): 592-9, 2002 Aug 10.
Article in English | MEDLINE | ID: mdl-12124810

ABSTRACT

A blood assay for detection of lung cancer biomarkers could significantly improve cancer patient prognosis and survival rates. Amplified fragment length polymorphism-differential display (AFLP-DD) was used to identify gene transcripts found in lung cancer tissue and the peripheral blood of lung cancer patients. The clones were evaluated for gene expression in lung cancer tissue, peripheral blood of lung cancer patients and healthy volunteers' blood. The isolated gene transcript clones were found to be from the syndecan 1 gene, collagen 1 gene and 2 novel genes. All 4 transcripts were expressed in normal lung tissue, 4 cultured primary lung cells and 6 lung cancer cell lines. RNA was isolated from peripheral blood samples of 69 lung cancer patients. Reverse transcriptase polymerase chain reaction (RT-PCR) was used to test for the presence of cytokeratin 19 and the 4 gene mRNA transcripts in blood RNA. The positive detection rate of at least 1 of the 5 transcripts was 79% for lung adenocarcinoma and 62% for squamous carcinoma. Using RT-PCR, at least 1 of the markers was found in 53% of stage I patients, 100% of stage II, 71% of stage III and 81% of stage IV lung cancer patients. Blood samples from 20 healthy volunteers were also tested, but only 1 of the 5 transcripts was found in 1 patient. These new molecular markers may aid early detection, staging and follow-up of lung cancer patients by RNA isolated from blood.


Subject(s)
Biomarkers, Tumor/blood , Biomarkers, Tumor/genetics , Gene Expression Profiling/methods , Lung Neoplasms/diagnosis , Lung Neoplasms/genetics , Adult , Aged , Gene Expression Regulation, Neoplastic , Humans , Lung Neoplasms/blood , Lung Neoplasms/pathology , Male , Middle Aged , Neoplasm Staging , Polymorphism, Genetic , RNA, Neoplasm/genetics , RNA, Neoplasm/metabolism , Reverse Transcriptase Polymerase Chain Reaction
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