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食蟹猴静脉注射抗CD20功能人源化单克隆抗体SM09重复给药毒性研究 被引量:5

Toxicity of functionally humanized anti-CD20 monoclonal antibody SM09 for cynomolgus monkey following repeated intravenous administration
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摘要 目的:评价食蟹猴静脉重复给药抗CD20功能人源化单克隆抗体SM09的安全性。方法:将食蟹猴随机分为溶媒对照组,SM09低、高剂量组(25,50 mg.kg-1),每组6只,静脉注射给药,每周1次,连续8周,恢复期12周,进行各项毒理学指标检测。结果:除个别动物偶见呕吐外,体重、进食量、体温、尿、心电图、骨髓细胞计数等均未显示与供试品相关的改变。SM09给药后能够诱导动物产生快速深度的外周血B细胞清除,至恢复期结束,多数动物外周血中B细胞水平恢复正常。给药4周,动物血液白细胞及淋巴细胞下降,之后逐渐回升。给药结束时动物补体C4水平略有降低。组织病理学检查结果除药理学作用相关的改变外,未见其他与供试品相关的改变。结论:食蟹猴连续静脉注射SM09,总体上具有良好的剂量耐受性,除观察到与药理作用相关的效应外,未见其他毒性反应。 Objective: To evaluate the preclinical toxicity of a functionally humanized anti-CD20 monoclonal antibody SM09 for cynomolgus monkeys following repeated intravenous administration. Methods: Cynomol- gus monkeys were randomly divided into vehicle control, SM09 low dose and high dose groups (25, 50 mg.kg^- 1 ). All animals were intravenously given vehicle or SM09 once a week for 8 weeks followed by 12-week recovery. Toxicological parameters were determined. Results: There were no obvious abnormalities in body weight, food consumption, body temperature, electrocardiogram, bone marrow cell counts and urine that could be attributed to the administration of SM09, despite the observation of incidental vomitting in one of the animals tested. SM09 induced a rapid and in-depth peripheral B cell depletion in cynomolgus monkeys. Upon the cessation of SM09 administration, B cell counts in the peripheral blood in the majority of the treated animals returned to normal level, except for a few whose B cell counts remained partially depleted. Although transient decreases in white blood cell and lymphocyte counts were noted on week 4 after treatments, their levels returned to normal at the end of the study. Furthermore, the level of complement C4 in the SM09 group was found to be slightly lower than that of the control group Other than the d could be attribut ep ed letion of B cells and induction of lymphoid follicular atrophy, no histopathological findings that to SM09 were found. Conclusion: Repeated intravenous dosing of anti-CD20 monoclonal anti- body was well tolerated by cynomolgus monkeys. Except for pharmacologically-related reactions, as manifested in the form of peripheral CD20 positive B cell depletion and ses were found.
出处 《中国新药杂志》 CAS CSCD 北大核心 2012年第6期616-622,共7页 Chinese Journal of New Drugs
基金 国家"重大新药创制"科技重大专项(2008ZX09305-002)
关键词 抗CD20单克隆抗体 食蟹猴 临床前安全性 毒性 safety toxicity lymphoid follicular atrophy, no other toxicological respon- anti-CD20 functionally humanized monoclonal antibody Cynomolgus monkeys preclinical
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参考文献11

  • 1TEDDER TF,ENGEL P.CD20:a regulator of cell-cycle pro-gression of B lymphocytes[J].Immunol Today,1994,15(9):450-454.
  • 2HAINSWORTH JD,LITEHY S,BURRIS HA,et al.Rituximab asfirst-line and maintenance therapy for patients with indolent non-hodskin's lymphoma[J].J Clin Oncol,2002,20(20):4261-4267.
  • 3KEATING GM.Spotlight on rituximab in chronic lymphocyticleukemia,low-grade or follicular lymphoma,and diffuse large B-cell lymphoma[J].BioDrugs,2011,25(1):55-61.
  • 4CVETKOVIC'RS,PERRY CM.Rituximab:a review of its use innon-Hodgkin's lymphoma and chronic lymphocytic leukaemia[J].Drugs,2006,66(6):791-820.
  • 5PFREUNDSCHUH M,SCHUBERT J,ZIEPERT M,et al.Sixversus eight cycles of bi-weekly CHOP-14 with or without ritux-imab in elderly patients with aggressive CD20+B-cell lympho-mas:a randomised controlled trial(RICOVER-60)[J].LancetOncol,2008,9(2):105-116.
  • 6VAIDYANATHAN A,MCKEEVER K,ANAND B,et al.De-velopmental immunotoxicology assessment of rituximab in cyno-molgus monkeys[J].Toxicol Sci,2011,119(1):116-125.
  • 7梁瑞安,杨蕾,陈俊新,陈汉文,李正东,黄佩芬,张荣泰.应用抗体“框架重塑”技术构建人源化抗体fSM03[J].中国新药杂志,2006,15(21):1832-1836. 被引量:3
  • 8GENENTECH,BIOGEN IDEC,ROCHE.Investigator BrochureRituxian,MabThera,IDEC-C2B8(Rituximab)[EB/OL].[2011-09-20].http://prima.gela.org/studydoc/1_ETUDE/InvestigatorsBrochuref11e972e.pdf.
  • 9VUGMEYSTER Y,HOWELL K,BAKSHL A,et al.Effect ofanti-CD20 monoclonal antibody,Rituxan,on cynomolgus monkeyand human B cells in a whole blood matrix[J].Cytometry A,2003,52(2):101-109.
  • 10VUGMEYSTER Y,BEYER J,HOWELL K,et al.Depletion ofB cells by a humanized anti-CD20 antibody PRO70769 in Macacafascicularis[J].J Immunother,2005,28(3):212-219.

二级参考文献9

  • 1杨蕾,李德芬,冯晓茵,陈汉文,杨忠,李正东,张荣泰,梁瑞安.重组抗B细胞淋巴瘤嵌合抗体的构建及鉴定[J].中国新药杂志,2006,15(3):186-192. 被引量:4
  • 2KOHLER G,MILSTEIN C.Continuous Cultures of fused cells secreting antibody of predefined specificity[J].Nature.1975,256(5517):495 -497.
  • 3LEUNG SO,GOLDENBERG DM,DION AS,et al.Construction and characterization of a humanized,internalizing B-cell(CD22)-specific,leukemia/lymphoma antibody,LL2[J].Mol Immunol,1995,32(17/18):1413-1427.
  • 4LEUNG SO,SHEVITZ J,PELLEGRINI MC,et al.Chimerization of LL2,a rapidly internalizing antibody specific for B-cell lymphoma[J].Hybridoma,1994,13 (6):469-476.
  • 5SHIH LB,LU HHZ,XUAN H,et al.Internalization and intracellular processing of an anti-B-cell lymphoma monoclonal antibody,LL2[J].Int J Cancer,1994,56 (4):538-545.
  • 6The National Biomedical Research Foundation Protein identification Resource.Kabat Database[DB/OL].
  • 7AMIT AG,MARIUZZA RA,PHILLIPS SE,et al.Three-dimensional structure of an antigen-antibody complex at 2.8 A resolution[J].Science,1986,233 (4765):747-753.
  • 8PIRKER R,FITZGERALD DJP,HAMILTON TC,et al.Characterization of immunotoxins active against ovarian cancer cell lines[J].J Clin Invest,1985,76 (3):1261-1267.
  • 9KABAT EA,WU TT,REID-MILLER M,et al.Sequences of Proteins of Immunological Interest[M].5th ed.US Department of Health and Human Servcies,Washington,DC.1991.

共引文献2

同被引文献72

  • 1MUYLDERMANS S, BARAL T. N, RETAMOZZO V. C, et al. Camelid immunoglobulins and nanobody technology[ J]. Vet lm- munol lmmunopathol, 2009, 128( 1 -3) : 178 - 183.
  • 2WESOLOWSKI J, ALZOGARAY V, REYELT J, et al. Single domain antibodies: promising experimental and therapeutic tools in infection and immunity [ J ]. Med Microbiol Immunol, 2009, 198(3) : 157 -174.
  • 3KOLKMAN JA, LAW DA. Nanobodies-from llamas to therapeu- tic proteins[J]. Drug Discov Today: Technol, 2010, 7 (2) : e139 - e146.
  • 4STIJLEMANS B, CALJON G, Natesan SKA, et al. High affinity nanobodies against the trypanosome brucei VSG are potenttrypanolytic agents that block endocytosis [ J]. PLoS Pathog, 2011,7 (6) : el002072.
  • 5HMILA I, SAERENS D, BEN ABDERRAZEK R,et al. A bispe- cific nanobody to provide full protection against lethal scorpion envenoming[ J]. FASEB J, 2010,24(9) :3479 - 3489.
  • 6KLOOSTER R, EMAN MR, LE DUC Q,et al. Selection and characterization of KDEL-specific VHH antibody fragments and their application in the study of ER resident protein expression [ J]. J lmmunol Methods,2009, 342 ( 1 - 2) : 1 - 12.
  • 7SERRUYS B, VAN HOUTTE F, FARHOUDI-MOGHADAM A, et al. Production, characterization and in vitro testing of HBcAg- specific VHH intrabodies [ J ]. J Gen Virol, 2010,91 ( Pt 3 ) : 643 - 652.
  • 8VAN DEN ABBEELE A, DE CLERCQ S, DE GANCK A, et al. A llamaderived gelsolin single-domain antibody blocks gelsolin-G- actin interaction[ J]. Cell Mol Life Sci, 2010,67(9) :1519 -1535.
  • 9VAN BOCKSTAELE F, HOLZ JB, REVETS H. The development of nanobodies for therapeutic applications [ J ]. urr Opin Investig Drugs,2009,10( 11 ) :1212 - 1224.
  • 10ULRICHTS H, SILENCE K, SCHOOLMEESTER A, et al. An- tithrombotic drug candidate ALX-0081 shows superior preclinical efficacy and safety compared with currently marketed antiplatelet drugs[J]. Blood, 2011,118(3) :757 -765.

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