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1.
Br J Dermatol ; 170(5): 1048-55, 2014 May.
Article in English | MEDLINE | ID: mdl-24372073

ABSTRACT

BACKGROUND: There have been extensive studies regarding which types of T lymphocytes are involved in psoriasis vulgaris (PV). However, it has remained unclear which types of T lymphocytes might directly contribute to psoriasiform epidermal and vascular hyperplasia. OBJECTIVES: To understand the role of T-cell receptor (TCR)Vα24+ invariant natural killer (iNK)T cells in the development of PV. METHODS: Seventeen patients were enrolled in this study. Using biopsy samples of PV plaques, TCRVα24(+) iNKT cells were investigated regarding their cytokine production to understand their roles in development of disease. RESULTS: The number of interferon (IFN)-γ+ iNKT cells correlated with the length of the psoriasiform hyperplasia rete ridge and the Psoriasis Area and Severity Index. IFN-γ+ iNKT cells in psoriatic skin exhibited higher C-C chemokine receptor (CCR)5 expression, and the amount of C-C chemokine ligand (CCL)5, a ligand for CCR5, was increased in capillary veins of psoriasis plaques. CCR5+ iNKT-cell numbers significantly correlated with the number of capillary vein endothelial cells expressing CCL5 in PV. Furthermore, the number of CCL5+ capillary veins correlated with the maximum rete ridge length. CONCLUSIONS: IFN-γ/CCR5 expression in iNKT cells and CCL5 expression in vessels of dermal papillae correlate with the development of psoriasiform hyperplasia and microabscess. We propose that these iNKT cells may become useful targets for development of novel therapeutic approaches to PV.


Subject(s)
Chemokine CCL5/metabolism , Interferon-gamma/immunology , Natural Killer T-Cells/immunology , Psoriasis/immunology , Receptors, Antigen, T-Cell, alpha-beta/immunology , Adult , Aged , Capillaries/metabolism , Case-Control Studies , Female , Humans , Male , Middle Aged
2.
J Vet Med Sci ; 63(8): 921-3, 2001 Aug.
Article in English | MEDLINE | ID: mdl-11558551

ABSTRACT

Anti-Borna disease virus (BDV) antibodies were detected from cats in Japan, Philippines and Indonesia by using electrochemiluminescence immunoassay. Positive rates were 3.1%, 3.8% and 2.0% in Japan, Philippines and Indonesia, respectively. There was no differences in the positive rate of anti-BDV antibodies between male and female cats and among habitats. While, a significantly (P<0.05) higher prevalence (6.5%) was found in the oldest age group (more than 6 years) cats.


Subject(s)
Antibodies, Viral/blood , Borna Disease/epidemiology , Borna disease virus/immunology , Cat Diseases/virology , Age Factors , Animals , Borna Disease/virology , Cat Diseases/epidemiology , Cats , Female , Immunoassay/methods , Immunoassay/veterinary , Indonesia/epidemiology , Japan/epidemiology , Luminescent Measurements , Male , Philippines/epidemiology , Seroepidemiologic Studies , Sex Factors
3.
Histochem J ; 33(11-12): 597-603, 2001.
Article in English | MEDLINE | ID: mdl-12197667

ABSTRACT

Mast cells from 15 different cat organs were examined in terms of distribution and protease activity. The number of mast cells in each site was found to vary when visualised by metachromatic staining using Alcian Blue. Enzyme histochemical analysis revealed the existence of two subtypes of mast cells. These were categorised based on protease content, i.e. whether the mast cells contained chymase or tryptase. Tryptase-positive mast cells were clearly identifiable in every organ examined, whereas chymase-containing mast cells were predominantly observed in the ear (skin), tongue, spleen, and submucosa of the stomach and rectum. The chymase-reactive cells were not detected in the heart, or in the muscularis or serosa of the duodenum, jejunum, ileum or rectum. In addition, we suggest the existence of another subtype of mast cell containing both chymase and tryptase and localised within the ear (skin), tongue, spleen and submucosa of the rectum.


Subject(s)
Mast Cells/enzymology , Serine Endopeptidases/metabolism , Alcian Blue , Animals , Cats , Cell Count , Chymases , Histocytochemistry , Male , Mast Cells/classification , Mast Cells/cytology , Staining and Labeling , Tryptases
4.
Am J Infect Control ; 27(4): 367-9, 1999 Aug.
Article in English | MEDLINE | ID: mdl-10433677

ABSTRACT

Handwashing is one of the most important factors in controlling the spread of bacteria and in preventing the development of infections. This simple procedure does not have a high compliance rate. The Association for Professionals in Infection Control and Epidemiology, Inc, guideline recommends that hands must be washed before and after patient contact. In our intensive care unit (ICU), we have made it a rule that everyone should wash their hands before entering the ICU. The purpose of this study was to ascertain the handwashing compliance of all personnel and visitors to the ICU. A ceiling-mounted video camera connected to a time-lapse video cassette recorder recorded each person's actions when they entered the ICU during a 7-day period. Handwashing compliance was assessed for 3 different categories: ICU personnel, non-ICU personnel, and visitors to patients. There were 1030 entries to the ICU during the observation period. ICU personnel complied with handwashing in 71% of entries, non-ICU personnel in 74% of entries, and visitors to patients in 94% of entries. Handwashing compliance by visitors to patients was significantly higher than among personnel (P <.001). Handwashing compliance among personnel before entering the ICU was low. Continuous effort is needed to raise awareness of the handwashing issue, not only to ensure compliance with APIC recommendations but also in our facility, to ensure that health care personnel wash their hands on entry to the ICU.


Subject(s)
Guideline Adherence/statistics & numerical data , Hand Disinfection , Intensive Care Units , Health Personnel , Humans , Japan , Videotape Recording , Visitors to Patients
5.
J Vet Med Sci ; 55(2): 237-9, 1993 Apr.
Article in English | MEDLINE | ID: mdl-8513003

ABSTRACT

The object of this study was to determine whether several washings with trypsin affected the survival and development of in vitro fertilized (IVF) bovine embryos. The embryos developed to blastocysts 7-8 days after insemination, were washed 12 times in washing medium (modified Dulbecco's phosphate-buffered saline (mPBS) containing 20% fetal bovine serum (FBS): 25 mM Hepes TCM199 with Earle's salts = 1:1), or in a series of three washes in the washing medium, two in mPBS containing 0.3% bovine serum albumin (BSA), two in 0.25% trypsin in Hank's solution (without Ca++ and Mg++) for a total time in the trypsin of 60 to 90 sec and five in the washing medium. After washing, the embryos were either cultured in vitro or cryopreserved. The fresh and frozen-thawed embryos were either cultured for 72 hr in vitro for evaluating development or transferred nonsurgically to recipient cows. Development of fresh and frozen-thawed embryos in vitro in control-washed and trypsin-washed embryos did not differ. Pregnancy rates did not differ (P > 0.05) among recipient cows receiving control-washed or trypsin-washed embryos, and transferring fresh or frozen-thawed embryos. These results indicate that the treatment of bovine IVF embryos with trypsin during washing did not have a positive effect on embryonic development.


Subject(s)
Blastocyst/drug effects , Fertilization in Vitro , Pregnancy, Animal , Trypsin/pharmacology , Animals , Blastocyst/cytology , Blastocyst/physiology , Cattle , Cell Survival/drug effects , Cryopreservation , Embryonic and Fetal Development/drug effects , Female , Organ Culture Techniques , Pregnancy
6.
Hiroshima J Med Sci ; 41(1): 1-5, 1992 Mar.
Article in English | MEDLINE | ID: mdl-1572805

ABSTRACT

Hydrogen peroxide was generated from creatinine by the sequential enzyme reactions of creatinine amidohydrolase, creatine amidinohydrolase and sarcosine oxidase. Hydrogen peroxide was, in turn, used stoichiometrically for the condensation of 4-aminoantipyrine and N-ethyl-N-(2-hydroxy-3-sulfopropyl)-m-toluidine catalyzed by horse-radish peroxidase, resulting in the formation of quinone dye with maximum absorbance at 546 nm. The optimized assay conditions for the enzymatic determination of creatinine in a HITACHI 7250 autoanalyzer was established. This system, which requires less than 5 microliters of sample, was found to be the most economical for laboratories equipped with autoanalyzers.


Subject(s)
Autoanalysis/methods , Clinical Enzyme Tests/methods , Creatinine/blood , Humans
7.
Acta Pathol Jpn ; 37(1): 141-54, 1987 Jan.
Article in English | MEDLINE | ID: mdl-3033987

ABSTRACT

An autopsy case of multiple myeloma, IgA kappa type, accompanying systemic crystal-storing histiocytosis and generalized amyloidosis, is reported. Besides multiple destructive lesions in the skeletal bones, nodular myeloma cell infiltrates were scattered in the liver, spleen, and both kidneys. Not only in these lesions but also in the reticuloendothelial organs, crystal-storing macrophages appeared dispersively or in clusters. Electron microscopically, numerous crystalline inclusions contained in the cytoplasm of macrophages were membrane-bound and of variable configuration, comprising of a homogeneous electron-lucid material. Enzyme cytochemically, almost all of the inclusions showed acid phosphatase activity. On the basis of the results obtained from the immunohistochemical, immunofluorescent and immunoelectron microscopic studies, it was considered that the crystalline inclusions stored in the macrophages were derived from IgA kappa immunoglobulin secreted from the myeloma cells and were formed within secondary lysosomes by crystallization during lysosomal digestion and degradation of the ingested immunoglobulin by macrophages. Generalized amyloidosis developed in different sites from those of the crystal-storing histiocytosis and were proven immunohistochemically to belong to AL amyloidosis probably derived from a certain group of A kappa precursor protein.


Subject(s)
Amyloidosis/etiology , Histiocytic Sarcoma/etiology , Multiple Myeloma/complications , Amyloidosis/complications , Fluorescent Antibody Technique , Histiocytic Sarcoma/complications , Histocytochemistry , Humans , Immunoenzyme Techniques , Immunoglobulin A/analysis , Immunoglobulin kappa-Chains/analysis , Inclusion Bodies/analysis , Inclusion Bodies/ultrastructure , Macrophages/ultrastructure , Male , Microscopy, Electron , Middle Aged , Multiple Myeloma/analysis , Multiple Myeloma/pathology , Multiple Myeloma/ultrastructure
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