1.Screening of Marine Mold Activity and Having Antifungi Primary Research
Shu-Bin LI ; Guang-Xin LU ; Ru-Mei LIN ; Jin-Jie WU ; Weng-De CAI ;
Microbiology 1992;0(02):-
More than one hundred strains of marine molds have been isolated from the sediment and the sample of seawater collected from the South China Sea. By the first screening, more than 30 strains of marine molds which can inhibit tested fungi such as Candida albicans and Fursarium sp. were obtained.The results of the second screening showed those strains designed as B 4#-6、B 4#-3、1-B 6-6、1-B 6-10-5、1-B 6-22、C 2#-5、A 2-9 and 1-B 6-10 can produced extracelluar antifungi metabolic products and the crude extract of the strains 1-B 6-10-5 and B 4#-3 can inhibit the growth of many other species of fungi.
2.Comparison of continuous and discontinuous density gradient centrifugation for purification of human pancreatic islets.
Guo-hong WEI ; Wei-ping SUN ; Jian ZHANG ; De-hong CAI ; Long-yi ZENG ; Gui-hua CHEN ; Jian-ping WENG
Journal of Southern Medical University 2007;27(9):1352-1354
OBJECTIVETo compare the effect of continuous and discontinuous density gradient centrifugation for purification of human pancreatic islets with COBE 2991 cell processor.
METHODSHuman pancreases were obtained from brain-dead donors and stored in cold UW solution. The connective tissues were removed from the pancreases, and the pancreatic ducts were perfused with a cold enzyme (Liberase). The islets were then separated by gentle mechanical dissociation and purified with discontinuous (10 pancreases) or continuous (8 pancreases) gradients of HCA-Ficoll in COBE 2991 cell processor. Samples were collected in duplicate for determination of the quantity of islets, islet equivalents (IEQ), and the purity.
RESULTSThe weights of the pancreases before and after connective tissue removal and pancreas duct perfusion, and the quantity of islets obtained (including islets quantity of different diameters and total IEQ) after dissociation were not significantly different. Continuous gradient of HCA-Ficoll, compared with discontinuous gradient, resulted in significantly greater final islet quantity (55,000 IEQ vs 206,000 IEQ, P=0.000) and islet purity (58.0%-/+8.0% vs 33.5%-/+10.3%, P=0.000) and also greater number of islets with a diameter lager than 200 microm (P<0.01).
CONCLUSIONContinuous density gradient centrifugation can be more effective than discontinuous gradient in islet purification.
Cell Count ; Cell Separation ; methods ; Centrifugation, Density Gradient ; methods ; Humans ; Islets of Langerhans ; cytology ; Organ Size
3.Isolation and purification of human islet cells with semi-automated digestion.
Hua ZHANG ; De-hong CAI ; Jun-ling HAN ; Guo-hong WEI ; Jia SUN ; Wei-ping SUN ; Jian ZHANG ; Hong CHEN ; Long-yi ZENG ; Jian-ping WENG
Journal of Southern Medical University 2007;27(6):824-826
OBJECTIVETo establish an semi-automated effective method for large-scale purification of islet cells from human pancreas.
METHODSHuman pancreas tissue was digested with collagenase P using a semi-automated pancreas-digestion system followed by purification in a HCA-Ficoll continuous gradient using Cobe2991 cell separator. After isolation, the islet cell yield and purity was evaluated with light microscope with DTZ staining, and the islet function assessed by insulin release assay in vitro.
RESULTSThe number of the islets collected from each pancreas averaged 38 6201-/+78 219 islet equivalents (IEQ) before purification, and 231 420-/+28 054 IEQ after the purification with discontinuous gradient centrifugation. From each gram of the pancreatic tissue, 3148-/+317 IEQ were obtained with an average purity of (62.81-/+2.68) %. The purified islets responded well to high-concentration (16.7 mmol/L) glucose stimulation with a 2.53-fold increase of insulin secretion over the basal level (3.3 mmol/l, P<0.001).
CONCLUSIONThe established semi-automated method can be applicable for large-scale purification of fully functional islet cells from human pancreas.
Cell Count ; Cell Separation ; instrumentation ; methods ; Cell Survival ; Glucose ; pharmacology ; Humans ; Insulin ; secretion ; Islets of Langerhans ; cytology ; drug effects ; metabolism ; Reproducibility of Results
4.Study on etiology and pathology of severe acute respiratory syndrome.
Yan-qing DING ; Hui-jun WANG ; Hong SHEN ; Zu-guo LI ; Jian GENG ; Hui-xia HAN ; Jun-jie CAI ; Xin LI ; Wei KANG ; De-sheng WENG ; Yao-dan LU ; Kai-tai YAO
Chinese Journal of Pathology 2003;32(3):195-200
OBJECTIVETo investigate the clinicopathologic characteristics of severe acute respiratory syndrome (SARS).
METHODSThree autopsy cases were studied retrospectively. Routine HE stain was used to study all the cases. Part of the lung tissue specimens were studied further with Macchiavello's stain, viral inclusion body stain, reticulin and PAS stains, immunohistochemistry, thin sections with staining, light microscopy and transmission electronic microscope investigation.
RESULTSThe earliest symptom of all 3 cases was hyperpyrexia and followed by progressive dyspnea and appearance of lung field shadows in X rays findings. Pulmonary lesions included: bilateral and extensive consolidation, localized hemorrhage and necrosis, desquamative alveolitis and bronchitis, alveolar proliferation and desquamation, accumulation of protein exudates, mononuclear cells, lymphocytes, and plasma cells as well as hyaline membrane formation in alveoli and viral inclusion bodies were seen in the alveolus epithelial cells. The exudated organization tended to become glomeruloid organizing pneumonitis in a few avaoli. Lesions of the immune organs included: large patchy necrosis in the spleens and localized necrosis in the lymph nodes were seen. Bone marrow became restrained. There were lesions of systemic small vasculitis including edema of the perivascular tissue and vascular wall of the small veins with localized fibrinoid necrosis distributing in the heart, lungs, kidneys, adrenal glands and the striated muscles accompanying with mononuclear cells and lymphocytes infiltration. Thrombosis was seen in part of the small veins. In addition, there were also the systemic poisonous changes including: degeneration and necrosis of the parenchyma cells in lungs, liver, kidneys, heart and adrenals. Electronic microscopy demonstrated clusters of virus particles seen in the lung tissue.
CONCLUSIONSARS is a systemic disease. Lungs, immune system and systemic small vessels are the main target organs attacked by the virus. Extensive consolidation of lungs, formation of hyaline membrane to a large extent, respiratory distress and decrease of immune function are the main causes of death.
Adult ; Cause of Death ; Female ; Humans ; Male ; Microscopy, Electron, Scanning ; Middle Aged ; Severe Acute Respiratory Syndrome ; etiology ; pathology
5.Inadequate glycaemic control and antidiabetic therapy among inpatients with type 2 diabetes in Guangdong Province of China.
Yan BI ; Jin-hua YAN ; Zhi-hong LIAO ; Yan-bing LI ; Long-yi ZENG ; Kuan-xiao TANG ; Yao-ming XUE ; Hua-zhang YANG ; Lu LI ; De-hong CAI ; Ge WU ; Fan ZHANG ; Shao-da LIN ; Zheng-hua XIAO ; Da-long ZHU ; Jian-ping WENG
Chinese Medical Journal 2008;121(8):677-681
BACKGROUNDDiabetes mellitus has become epidemic in recent years in China. We investigated the prevalence of hyperglycaemia and inadequate glycaemic control among type 2 diabetic inpatients from ten university teaching hospitals in Guangdong Province, China.
METHODSInadequate glycaemic control in diabetic patients was defined as HbA1c = 6.5%. Therapeutic regimens included no-intervention, lifestyle only, oral antiglycemic agents (OA), insulin plus OA (insulin + OA), or insulin only. Antidiabetic managements included monotherapy, double therapy, triple or quadruple therapy.
RESULTSAmong 493 diabetic inpatients with known history, 75% had HbA1c = 6.5%. Inadequate glucose control rates were more frequently seen in patients on insulin + OA regimen (97%) than on OA regimen (71%) (P < 0.001), and more frequent in patients on combination therapy (81% - 96%) than monotherapy (75%) (P < 0.05). Patients on insulin differed significantly from patients on OA by mean HbA1c, glycemic control rate, diabetes duration, microvascular complications, and BMI (P < 0.01).
CONCLUSIONSThis study showed that glycaemic control of type 2 diabetic patients deteriorated for patients who received insulin and initiation time of insulin was usually delayed. It is up to clinicians to move from the traditional stepwise therapy to a more active and early combination antidiabetic therapy to provide better glucose control.
Aged ; China ; epidemiology ; Diabetes Mellitus, Type 2 ; blood ; drug therapy ; Female ; Glycated Hemoglobin A ; analysis ; Humans ; Hyperglycemia ; epidemiology ; Hypoglycemic Agents ; administration & dosage ; Inpatients ; Male ; Middle Aged
6.Safety of in vitro amplified HLA-haploidentical donor immune cell infusions for childhood malignancies.
Fei ZHANG ; Xiao-Fei SUN ; Yong-Qiang LI ; Zi-Jun ZHEN ; Hai-Xia ZHENG ; Jia ZHU ; Qi-Jing WANG ; Su-Ying LU ; Jia HE ; Juan WANG ; Ke PAN ; Rui-Qing CAI ; Yan CHEN ; De-Sheng WENG ; Fei-Fei SUN ; Jian-Chuan XIA
Chinese Journal of Cancer 2013;32(12):661-666
In vitro amplified human leukocyte antigen (HLA)-haploidentical donor immune cell infusion (HDICI) is not commonly used in children. Therefore, our study sought to evaluate its safety for treating childhood malignancies. Between September 2011 and September 2012, 12 patients with childhood malignancies underwent HDICI in Sun Yat-sen University Cancer Center. The median patient age was 5.1 years (range, 1.7-8.4 years). Of the 12 patients, 9 had high-risk neuroblastoma (NB) [7 showed complete response (CR), 1 showed partial response (PR), and 1 had progressive disease (PD) after multi-modal therapies], and 3 had Epstein-Barr virus (EBV)-positive lymphoproliferative disease (EBV-LPD). The 12 patients underwent a total of 92 HDICIs at a mean dose of 1.6×10(8) immune cells/kg body weight: 71 infusions with natural killer (NK) cells, 8 with cytokine-induced killer (CIK) cells, and 13 with cascade primed immune cells (CAPRIs); 83 infusions with immune cells from the mothers, whereas 9 with cells from the fathers. Twenty cases (21.7%) of fever, including 6 cases (6.5%) accompanied with chills and 1 (1.1%) with febrile convulsion, occurred during infusions and were alleviated after symptomatic treatments. Five cases (5.4%) of mild emotion changes were reported. No other adverse events occurred during and after the completion of HDIDIs. Neither acute nor chronic graft versus host disease (GVHD) was observed following HDICIs. After a median of 5.0 months (range, 1.0-11.5 months) of follow-up, the 2 NB patients with PR and PD developed PD during HDICIs. Of the other 7 NB patients in CR, 2 relapsed in the sixth month of HDICIs, and 5 maintained CR with disease-free survival (DFS) ranging from 4.5 to 11.5 months (median, 7.2 months). One EBV-LPD patient achieved PR, whereas 2 had stable disease (SD). Our results show that HDICI is a safe immunotherapy for childhood malignancies, thus warranting further studies.
Child
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Child, Preschool
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Cytokine-Induced Killer Cells
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immunology
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Epstein-Barr Virus Infections
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therapy
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Female
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Follow-Up Studies
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Graft vs Host Disease
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etiology
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Hematopoietic Stem Cell Transplantation
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adverse effects
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Humans
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Immunotherapy, Adoptive
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Infant
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Killer Cells, Natural
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immunology
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Lymphoproliferative Disorders
;
therapy
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virology
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Male
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Neuroblastoma
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therapy
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Transplantation, Homologous
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Treatment Outcome