1.Clinical Study on Treatment of Iliac-Femoral Venous Thrombus Via Double Femoral Veins
Haozhou WANG ; Shanyan LIANG ; Shuhou WANG ; Wenbin ZHANG ; Junsheng KANG
Journal of Practical Radiology 2000;0(02):-
Objective To evaluate the efficiency of treatment of iliac-femoral venous thrombus(I-FVT)via double femoral veins.Methods Eighteen patients with I-FVT were treated with implantation of inferior vena caval filter,catheter-directed cut,balloon-directed extend and drag.Some patients were treated with ATD or OASIS catheter.After operation,the catheter was kept in iliac-femoral veins for one to six days.Meanwhile,strict anti-coagulation was necessary.Results The treatment was successful in seventeen patients,the iliac-femoral veins were patent after the opration.Swollen symptom of lower limb and pain disappeared in fifteen patients,swollen symptom of lower limb became better in two patients.The treatment was fail in one patient.Follow-up study showed no pulmonary embolization or recrudescence in all eighteen patients.Conclusion The treatment of I-FVT via double femoral veins is a safe and effective method,there are no serious complications.
2.Effect of induction therapy regimens on monocytic myeloid-derived suppressor cells in kidney transplantation recipients
Yihang JIANG ; Haozhou WANG ; Jing YANG ; Sujuan FENG ; Xiaodong ZHANG
Chinese Journal of Organ Transplantation 2016;37(7):385-391
Objective To investigate the effects of commonly used inductive agents on peripheral blood monocytic myeloid-derived suppressor cells (M-MDSCs) in renal transplantation recipients and to discuss their possible mechanism.Methods The enrolled patients received rabbit anti-thymocyte globulin (rATG) or basiliximab for induction therapy,with the maintenance immunosuppressive regimen of tacrolimus,mycophenolate mofetil and steroid.The number of CD11 b + CD33 + HLA-DR-CD14 + CD1 5-M-MDSCs and cytokine levels in peripheral blood,including interferon-γ(IFN-γ),interleukin-2 (IL-2),IL-4 and IL-6,were measured by flow cytometry before and 1 week,2 weeks,1 month,2 months,3 months after operation.Results A total of 47 recipients (29 given rATG 29,and 18 given basiliximab) were included in this study.Compared to the patients with basiliximab,asignificant increase in the frequency of M-MDSCs was observed in the rATG group at 2nd month after operation (5.5% ± 2.8% vs.3.8% ± 1.6%,P<0.001) and at 3rd month after operation (7.0 % ± 3.1%vs.4.1% ± 2.3 %,P< 0.001),while there was no significant difference in the cell number between the two groups.In the cytokine detection,levels of IL-2 and IL-4 in the rATG-treated recipients were significantly higher at 2nd weekpostoperation (Pr2 =0.032,and PIL-4 =0.019)and 1st month postoperation (PIL-2 =0.024,PIL-4 <0.001) than the basiliximab group.Conclusions ATG promotes the expansion of M-MDSCs,which is associated with the secretion of IL-2 and IL-4 due to the lymphocytes depletion.The synergistic immunosuppressive effect may contribute to the induction of immune tolerance.
3.Comparison of therapeutic efficacy between recombinant human brain natriuretic peptide and sodium nitroprusside in treatment of acute attack of chronic heart failure
Jingping WANG ; Yuean ZHANG ; Huixian WANG ; Jin DONG ; Xiaoxia ZENG ; Jianling WANG ; Haozhou ZHANG ; Bao LI
Chinese Journal of Geriatrics 2011;30(8):643-646
Objective To compare the curative effects between recombinant human brain natriuretic peptide (rhBNP) and sodium nitroprusside in treatment of the acute attack of elderly patients with chronic heart failure (CHF), and probe the impacts of rhBNP on the heart function,serum B-type natriuretic peptide (BNP), norepinephrine (NE), endothelin 1 (ET-1) and antidiuretic hormone (ADH) levels. Methods The 89 patients aged 65-85 years at acute attack stage of CHF were randomized into two therapy groups: rhBNP group (n= 47) and sodium nitroprusside group (n=42). The clinical effects, heart function, serum BNP, NE, ET-1 and ADH changes were observed before and after the treatment. Results After 24 hours of treatment, the efficacy rate and total effective rate were higher in rhBNP group than in sodium nitroprusside group (51.1% vs. 26.2 %,95.7% vs. 66. 7%, respectively, P<0. 05 and P<0. 01), and non-efficacy rate in rhBNP group was lower (4.3% vs. 33. 3%, P<0. 01). There was one death case in rhBNP group and three in sodium nitroprusside group. In rhBNP group, left ventricular ejection fraction values increased after 2 weeks of treatment [(46.2± 9.5)% vs. (38.1 ±6.0)%], P<0.05. Serum BNP level significantly decreased in rhlBNP group than in sodium nitroprusside group after 2 weeks of treatment (P<0.05).In rhBNP group, serum BNP and NE levels decreased 24 hours and 2 weeks after treatment (P<0. 01) and the levels furtherly reduced after 2 weeks (P<0.01). Serum ET-1 level decreased in rhBNP group than in sodium nitroprusside group 2 weeks after treatment (P<0.05). In rhBNP group, there was no significant difference in serum ET-1 level between baseline and 24 hours after treatment (P> 0. 05), but the ET-1 level decreased 2 weeks after treatment as compared with 24 hours after treatment (P<0.01). There were no significant differences between the two groups before and after treatment (P>0.05). Incidences of headache and hypotension were lower in rhBNP group than in sodium nitroprusside group (4.3% vs. 19.0%, 14.9% vs. 23.8%, both P<0.05),Conclusions RhBNP can be safely and effectively used for acute attack of CHF.
4.Validation and invalidation of SARS-CoV-2 main protease inhibitors using the Flip-GFP and Protease-Glo luciferase assays.
Chunlong MA ; Haozhou TAN ; Juliana CHOZA ; Yuyin WANG ; Jun WANG
Acta Pharmaceutica Sinica B 2022;12(4):1636-1651
SARS-CoV-2 main protease (Mpro) is one of the most extensively exploited drug targets for COVID-19. Structurally disparate compounds have been reported as Mpro inhibitors, raising the question of their target specificity. To elucidate the target specificity and the cellular target engagement of the claimed Mpro inhibitors, we systematically characterize their mechanism of action using the cell-free FRET assay, the thermal shift-binding assay, the cell lysate Protease-Glo luciferase assay, and the cell-based FlipGFP assay. Collectively, our results have shown that majority of the Mpro inhibitors identified from drug repurposing including ebselen, carmofur, disulfiram, and shikonin are promiscuous cysteine inhibitors that are not specific to Mpro, while chloroquine, oxytetracycline, montelukast, candesartan, and dipyridamole do not inhibit Mpro in any of the assays tested. Overall, our study highlights the need of stringent hit validation at the early stage of drug discovery.
5.Structural and molecular basis for foot-and-mouth disease virus neutralization by two potent protective antibodies.
Hu DONG ; Pan LIU ; Manyuan BAI ; Kang WANG ; Rui FENG ; Dandan ZHU ; Yao SUN ; Suyu MU ; Haozhou LI ; Michiel HARMSEN ; Shiqi SUN ; Xiangxi WANG ; Huichen GUO
Protein & Cell 2022;13(6):446-453