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Veterans health administration hepatitis B testing and treatment with anti-CD20 antibody administration 被引量:1
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作者 Christine M Hunt Lauren A Beste +7 位作者 Elliott Lowy Ayako Suzuki Cynthia A Moylan Hans L Tillmann George N Ioannou Joseph K Lim Michael J Kelley Dawn Provenzale 《World Journal of Gastroenterology》 SCIE CAS 2016年第19期4732-4740,共9页
AIM: To evaluate pretreatment hepatitis B virus(HBV) testing, vaccination, and antiviral treatment rates in Veterans Affairs patients receiving anti-CD20 Ab for quality improvement.METHODS: We performed a retrospectiv... AIM: To evaluate pretreatment hepatitis B virus(HBV) testing, vaccination, and antiviral treatment rates in Veterans Affairs patients receiving anti-CD20 Ab for quality improvement.METHODS: We performed a retrospective cohort study using a national repository of Veterans Health Administration(VHA) electronic health record data. We identified all patients receiving anti-CD20 Ab treatment(2002-2014). We ascertained patient demographics, laboratory results, HBV vaccination status(from vaccination records), pharmacy data, and vital status. The high risk period for HBV reactivation is during antiCD20 Ab treatment and 12 mo follow up. Therefore, we analyzed those who were followed to death or for at least 12 mo after completing anti-CD20 Ab. Pretreatment serologic tests were used to categorize chronic HBV(hepatitis B surface antigen positive or HBs Ag+), past HBV(HBs Ag-, hepatitis B core antibody positive or HBc Ab+), resolved HBV(HBs Ag-, HBc Ab+, hepatitis B surface antibody positive or HBs Ab+), likely prior vaccination(isolated HBs Ab+), HBV negative(HBs Ag-, HBc Ab-), or unknown. Acute hepatitis B was defined by the appearance of HBs Ag+ in the high risk period in patients who were pretreatment HBV negative. We assessed HBV antiviral treatment and the incidence of hepatitis, liver failure, and death during the high risk period. Cumulative hepatitis, liver failure, and death after anti-CD20 Ab initiation were compared by HBV disease categories and differences compared using the χ2 test. Mean time to hepatitis peak alanine aminotransferase, liver failure, and death relative to anti-CD20 Ab administration and follow-up were also compared by HBV disease group.RESULTS: Among 19304 VHA patients who received anti-CD20 Ab, 10224(53%) had pretreatment HBs Ag testing during the study period, with 49% and 43% tested for HBs Ag and HBc Ab, respectively within 6 mo pretreatment in 2014. Of those tested, 2%(167/10224) had chronic HBV, 4%(326/7903) past HBV, 5%(427/8110) resolved HBV, 8%(628/8110) likely prior HBV vaccination, and 76%(6022/7903) were HBV negative. In those with chronic HBV infection, ≤ 37% received HBV antiviral treatment during the high risk period while 21% to 23% of those with past or resolved HBV, respectively, received HBV antiviral treatment. During and 12 mo after anti-CD20 Ab, the rate of hepatitis was significantly greater in those HBV positive vs negative(P = 0.001). The mortality rate was 35%-40% in chronic or past hepatitis B and 26%-31% in hepatitis B negative. In those pretreatment HBV negative, 16(0.3%) developed acute hepatitis B of 4947 tested during anti-CD20 Ab treatment and followup. CONCLUSION: While HBV testing of Veterans has increased prior to anti-CD20 Ab, few HBV+ patients received HBV antivirals, suggesting electronic health record algorithms may enhance health outcomes. 展开更多
关键词 HEPATITIS B HEPATITIS B REACTIVATION anticd20 ANTIBODY RITUXIMAB LYMPHOMA Chemotherapy HEPATITIS B a
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三步法制备级纯化抗CD20(Fab′)_2
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作者 王金宏 杨铭 +3 位作者 范冬梅 许元生 熊冬生 杨纯正 《中国医学科学院学报》 CAS CSCD 北大核心 2008年第5期622-625,共4页
目的在小规模蛋白纯化系统AKTA prime上建立制备级纯化抗CD20(Fab′)2的方法。方法将通过高渗溶液提取的周质腔蛋白抗CD20(Fab′)2依次经过离子柱、疏水柱和亲和柱纯化,采用蛋白电泳和高效液相色谱法分析检测其分离效果及纯度,同时测定... 目的在小规模蛋白纯化系统AKTA prime上建立制备级纯化抗CD20(Fab′)2的方法。方法将通过高渗溶液提取的周质腔蛋白抗CD20(Fab′)2依次经过离子柱、疏水柱和亲和柱纯化,采用蛋白电泳和高效液相色谱法分析检测其分离效果及纯度,同时测定其与Raji细胞的结合活性。结果在该纯化条件下一次可获得8mg纯度为96.678%的抗CD20(Fab′)2,其与CD20+Raji细胞的结合活性与采用亲和柱联合分子筛柱得到的抗体活性基本一致。结论三步法制备级纯化抗CD20(Fab′)2操作简单,能获得制备级高纯度抗CD20(Fab′)2。 展开更多
关键词 抗CD20(Fab′)2 三步法纯化 高效液相色谱分析
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