1.Clinical research on application of adjustable sutures in glaucoma filtering operation
International Eye Science 2014;(10):1868-1870
AIM:To discuss the application effect of adjustable sutures in glaucoma filtering operation after trabecular resection.
METHODS: Seventy-eight cases ( 101 eyes ) suffered from glaucoma were randomly divided into two groups, observation group and control group. Thirty-nine cases ( 51 eyes ) in the observation group underwent trabeculectomy with adjustable sutures, the control group (39 cases, 50 eyes) only adopted trabeculectomy.RESULTS: Compared Preoperative IOP in two groups, the difference was not statistically significant (P>0. 05). After 6mo, IOP were decreased compared with preoperative in two groups, and that in observation group was lower than control group, the difference was statistically significant ( P < 0. 05 ). Six months after operation, there were 1 eye with shallow anterior chamber Ⅰ and 2 eyes with non- functional bleb in observation group, and the complication rate was 5. 9%. While there were of 6 eyes with shallow anterior chamber, in which 4 eyes at gradeⅠ, each one at gradeII and Ⅲ. Non-functional blebs in 5 eyes and a scleral flap adhesion complications rate in the control group was 24. 0%, significantly higher than that in the observation group, the difference was statistically significant ( P<0.01).
CONCLUSION: The adjustable sutures combined with trabeculectomy for glaucoma can significantly reduce the postoperative complications. The curative effect is exact and clinically applicable.
4.Effect of Budesonide on Dendritic Cells in Asthmatic Mice
Journal of Applied Clinical Pediatrics 2006;0(16):-
Objective To explore the effect of budesonide(BUD) on dendritic cell(DC) and airway inflammation in the asthmatic mice.Methods Forty female Kunming mice were divided into 4 groups:asthmatic model group,therapeutic control group,BUD treated group,and normal control group,with 10 mice in each group.Mice were sensitized by an intraperitoneal injection of 50 ?g ovalbumin(OVA) adsorbed to 1 mg aluminum hydroxide dissolved in 0.2 mL saline.Animals were boosted on the 14th day in the same way.From the 21th to 35th days,and mice were challenged with 10 g/L aerosolized OVA for 30 min a day to establish a murine model of asthma.To evaluate the effect of BUD,60 minutes prior to OVA exposure,the mice were treated with 1 mg aerosolized BUD or placebo(saline).Control animals were sensitized intraperitoneally with saline and challenged with aerosolized saline alone.Eosinophil(EOS) count,degree of mucus secretion and DC count around the airways were measured by haematoxylin and eosin staining,periodic acid schiff's staining,immunochemistry technique and computerized image analysis system.Results In asthmatic model group,EOS count,DC count and the degree of mucus secretion around the airways were increased compared with nomal control group(P_a0.05).In BUD treated group,EOS count,DC count and the degree of mucus secretion around the airways were decreased compared with the asthmatic model group(P_a
6.Proliferation and identification of dendritic cells from peripheral blood of patients with bladder cancer in vitro
Dan CAI ; Zhi-Hua WANG ; Zhi-Quan HU ; Xu ZHANG ; Si-Wei ZHOU ; Zhang-Qun YE
Chinese Journal of Urology 2001;0(07):-
Objective To investigate the proliferation and identification of dendritic cells(DC)de- rived from peripheral blood of patients with bladder cancer in vitro.Methods The mononuclear cells were prepared from peripheral blood of patients with bladder cancer by Ficoll-Hypaque centrifugation method,and were induced by the recombinant cytokines hGM-CSF(50 ng/ml),hlL-4(10 ng/ml)and hTNF-?(50 ng/ ml)for 2 weeks.The growth and morphology of DC were observed through the phase contrast or electron mi- croscope,and their pheuotypes were determined by flow cytometry.The capacity of DC to activate T cell-de- pendent anti-tumor immune responses was tested by MTT method.Results The DC cultured in vitro turned into suspensive growth from adhesive situation on the 6th day,then the number of DC increased con- tinuously and the cells showed the irregular morphologic appearance of DC with veiled edges on the 8th day. Flow cytometry showed that the mature DC expressed high levels of specific markers such as CD_(1a),CD_(83), CD_(86)and HLA-DR.T cells activated by DC showed strong cytotoxicity to bladder cancer cell line BIU87 with a killing rate of(48.8?3.7)%,while the killing rate of T cells which were not activated by DC was(25.7?1.5)%;the difference of the rate between them was significant(P<0.01). Conclusions The DC can be cultured from peripheral blood of patients with bladder cancer by induction of rhGM-CSF,rhIL-4 and hT- NF-?in vitro.This may lay an experimental foundation for further research on DC vaccine.
8.Killing effect of IL-12-activated A-NK cells on human hepatocellular carcinoma HepG-2 cells in vitro.
Zhi-Hua WANG ; Dong-Lu ZHAO ; Chun-Yan ZHANG
Chinese Journal of Oncology 2007;29(6):423-424
Animals
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Carcinoma, Hepatocellular
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blood supply
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pathology
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therapy
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Cell Line, Tumor
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Cells, Cultured
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Cytotoxicity, Immunologic
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immunology
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Female
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Humans
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Interleukin-12
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pharmacology
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Interleukin-2
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pharmacology
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Killer Cells, Natural
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cytology
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drug effects
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immunology
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Liver Neoplasms, Experimental
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blood supply
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pathology
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therapy
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Lymphocyte Activation
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drug effects
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immunology
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Male
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Mice
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Mice, Inbred BALB C
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Mice, Inbred C57BL
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Microcirculation
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drug effects
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Random Allocation
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Xenograft Model Antitumor Assays
9.Advance in biomarkers of lung cancer in diagnosis and targeted therapy.
Jing ZHANG ; Zhi-yong LIANG ; Xuan ZENG ; Tong-hua LIU
Chinese Journal of Pathology 2009;38(8):564-567
Acid Anhydride Hydrolases
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metabolism
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Apoptosis
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Biomarkers, Tumor
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metabolism
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Caspases
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metabolism
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Cell Adhesion Molecules
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metabolism
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Chromosome Deletion
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Drug Delivery Systems
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GPI-Linked Proteins
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metabolism
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Humans
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Hyaluronoglucosaminidase
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metabolism
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In Situ Hybridization, Fluorescence
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methods
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Lung Neoplasms
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diagnosis
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drug therapy
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genetics
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metabolism
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Neoplasm Proteins
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metabolism
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Neoplasm Staging
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Receptor, Epidermal Growth Factor
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metabolism
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Vascular Endothelial Growth Factor A
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metabolism