PMID- 23627026 OWN - NLM STAT- MEDLINE DCOM- 20130628 LR - 20130430 IS - 1003-9279 (Print) IS - 1003-9279 (Linking) VI - 26 IP - 6 DP - 2012 Dec TI - [Effect of kurarinol on peripheral blood CTL surface PD-1 expression of patients with chronic hepatitis B]. PG - 446-9 AB - OBJECTIVE: To explore the anti-viral mechanism of kurarinol through studying its influence on cytotoxic T lymphocyte (CTL) surface program death receptor-1 (PD-1) expression of patients with chronic hepatitis B (CHB). METHODS: 69 cases of CHB, HBV DNA > or = 10(4) copies/ml, HBeAg positive, human leukocyte antigen (HLA)-A2 positive, alanine aminotransferase (ALT) > 2 x upper limit of normal value(ULN).69 cases were randomly divided into two groups:34 cases in treatment group,600 mg of kurarinol glucose injection was used for intravenous dripping, once a day, one month later, 200 mg of kurarinol capsule was used orally,three times a day and 200 mg of silybin meglumine tablet was used orally, three times a day. 35 cases in control group, only silibin meglumine tablet was used, method and dosage were the same as those of treatment group. Three months later, their peripheral blood HBV specific CTL surface PD-1 expression, non-specific CTL surface PD-1 expression and level of HBV specific CTL,HBV DNA and HBeAg negative rate and liver functions were analyzed and compared. RESULTS: 3 months after treatment, peripheral blood HBV specific CTL surface PD-1 expression of the treatment group decreased compared with that before treatment (t = 2.39, P < 0.05), it also decreased compared with that of the control group 3 months after treatment (t = 2.26, P < 0.05), HBV specific CTL increased compared with that before treatment( t = 3.01, P < 0.01), it also increased compared with that of the control group after treatment (t = 2.65, P < 0.05). There was no significant difference of non-specific CTL surface PD-1 expression compared with that before treatment (P > 0.05), and there was no significant difference compared with that of the control group after treatment (P > 0.05). HBV DNA of 11 cases (32.5%) turned negative ( HBV DNA < 500 copies/ ml), higher than that of the control group after treatment (2 cases, 5.71%) chi2 = 7.99, P < 0.01, HBeAg of 9 cases (26.47%) turned negative, higher than that of the control group after treatment (1 case, 2.86%), chi2 = 7.75, P < 0.01. CONCLUSION: Kurarinol can increase level of HBV specific CTL by down-regulating peripheral blood HBV specific CTL surface PD-1 expression of CHB patients, which may be one of the possible mechanisms that kurarinol can remove or inhibit HBV of CHB patients. FAU - Zhu, Yin-Fang AU - Zhu YF AD - Wuxi Hospital for Infectious Diseases, China. FAU - Gu, Xi-Bing AU - Gu XB FAU - Yang, Xiao-Juan AU - Yang XJ FAU - Hua, Zhong AU - Hua Z FAU - Lu, Zhong-Hua AU - Lu ZH FAU - Zang, Bo AU - Zang B FAU - Wu, Hang-Yuan AU - Wu HY FAU - Jiang, Yi-Ming AU - Jiang YM FAU - Chen, Hao-Kun AU - Chen HK FAU - Pei, Hao AU - Pei H FAU - Xu, Yue-Qin AU - Xu YQ LA - chi PT - English Abstract PT - Journal Article PT - Randomized Controlled Trial PT - Research Support, Non-U.S. Gov't PL - China TA - Zhonghua Shi Yan He Lin Chuang Bing Du Xue Za Zhi JT - Zhonghua shi yan he lin chuang bing du xue za zhi = Zhonghua shiyan he linchuang bingduxue zazhi = Chinese journal of experimental and clinical virology JID - 9602873 RN - 0 (Drugs, Chinese Herbal) RN - 0 (Flavonoids) RN - 0 (PDCD1 protein, human) RN - 0 (Programmed Cell Death 1 Receptor) RN - 0 (kurarinol) SB - IM MH - Adult MH - Drugs, Chinese Herbal/*administration & dosage MH - Flavonoids/*administration & dosage MH - Gene Expression/*drug effects MH - Hepatitis B virus/physiology MH - Hepatitis B, Chronic/*drug therapy/*genetics/immunology/virology MH - Humans MH - Male MH - Middle Aged MH - Programmed Cell Death 1 Receptor/*genetics/immunology MH - T-Lymphocytes, Cytotoxic/*drug effects/*immunology MH - Treatment Outcome MH - Young Adult EDAT- 2013/05/01 06:00 MHDA- 2013/07/03 06:00 CRDT- 2013/05/01 06:00 PHST- 2013/05/01 06:00 [entrez] PHST- 2013/05/01 06:00 [pubmed] PHST- 2013/07/03 06:00 [medline] PST - ppublish SO - Zhonghua Shi Yan He Lin Chuang Bing Du Xue Za Zhi. 2012 Dec;26(6):446-9.