CN108948195B - 一种抗egfr/pd-l1双靶向抗体、其制备方法及用途 - Google Patents

一种抗egfr/pd-l1双靶向抗体、其制备方法及用途 Download PDF

Info

Publication number
CN108948195B
CN108948195B CN201710369198.4A CN201710369198A CN108948195B CN 108948195 B CN108948195 B CN 108948195B CN 201710369198 A CN201710369198 A CN 201710369198A CN 108948195 B CN108948195 B CN 108948195B
Authority
CN
China
Prior art keywords
ser
val
thr
leu
pro
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Active
Application number
CN201710369198.4A
Other languages
English (en)
Other versions
CN108948195A (zh
Inventor
胡毅
赵磊
张帆
姬时宇
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Chinese PLA General Hospital
Original Assignee
Individual
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Individual filed Critical Individual
Priority to CN201710369198.4A priority Critical patent/CN108948195B/zh
Publication of CN108948195A publication Critical patent/CN108948195A/zh
Application granted granted Critical
Publication of CN108948195B publication Critical patent/CN108948195B/zh
Active legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Images

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07KPEPTIDES
    • C07K16/00Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies
    • C07K16/18Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from animals or humans
    • C07K16/28Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from animals or humans against receptors, cell surface antigens or cell surface determinants
    • C07K16/2863Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from animals or humans against receptors, cell surface antigens or cell surface determinants against receptors for growth factors, growth regulators
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07KPEPTIDES
    • C07K16/00Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies
    • C07K16/18Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from animals or humans
    • C07K16/28Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from animals or humans against receptors, cell surface antigens or cell surface determinants
    • C07K16/2803Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from animals or humans against receptors, cell surface antigens or cell surface determinants against the immunoglobulin superfamily
    • C07K16/2827Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from animals or humans against receptors, cell surface antigens or cell surface determinants against the immunoglobulin superfamily against B7 molecules, e.g. CD80, CD86
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K39/00Medicinal preparations containing antigens or antibodies
    • A61K2039/505Medicinal preparations containing antigens or antibodies comprising antibodies
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07KPEPTIDES
    • C07K2317/00Immunoglobulins specific features
    • C07K2317/30Immunoglobulins specific features characterized by aspects of specificity or valency
    • C07K2317/31Immunoglobulins specific features characterized by aspects of specificity or valency multispecific
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07KPEPTIDES
    • C07K2317/00Immunoglobulins specific features
    • C07K2317/50Immunoglobulins specific features characterized by immunoglobulin fragments
    • C07K2317/52Constant or Fc region; Isotype

Landscapes

  • Health & Medical Sciences (AREA)
  • Immunology (AREA)
  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • General Health & Medical Sciences (AREA)
  • Biophysics (AREA)
  • Biochemistry (AREA)
  • Genetics & Genomics (AREA)
  • Medicinal Chemistry (AREA)
  • Molecular Biology (AREA)
  • Proteomics, Peptides & Aminoacids (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Peptides Or Proteins (AREA)

Abstract

本发明提供了一种EGFR/PD‑L1双靶向抗体、其制备方法及其在制备抗肿瘤药物中的应用。所述EGFR/PD‑L1双靶向抗体是以Cetuximab抗体和RG7446抗体为亲本,采用knob‑into‑hole技术制备而成。所述双靶向抗体抗体具有比Cetuximab抗体和RG7446抗体联合使用都更强的抗肿瘤效果,应用前景巨大。

Description

一种抗EGFR/PD-L1双靶向抗体、其制备方法及用途
技术领域
本发明属于生物技术领域,更具体地,本发明公开了一种EGFR/PD-L1双靶向抗体、其制备方法及其在制备抗肿瘤药物中的应用。
背景技术
肿瘤尤其是恶性肿瘤是当今世界严重危害人类健康的疾病,其致死率居各种疾病致死率的前列。而且近年来,其发病率呈明显上升趋势。恶性肿瘤治疗效果差,晚期转移率高,预后多不佳。目前临床上所采用的常规治疗方法如放疗、化疗和手术治疗虽然在很大程度上缓解了病痛,延长了生存时间,但这些方法均存在很大的局限性,其疗效难以进一步提高。
抗体靶向性药物具有特异性好、副作用小、半衰周期长等优点,已广泛的应用于肿瘤的临床治疗。目前,已经发现了多种能够作为肿瘤靶向治疗较好的靶点:EGFR家族是一组跨膜蛋白,参与调节许多生物学关键过程,如细胞增殖、分裂、迁移和分化等。EGFR在多种肿瘤细胞上均高表达,并通过与配体结合,激活许多下游信号传导通路,进而参与肿瘤细胞的增殖、黏附、侵袭、迁移、凋亡及肿瘤血管生成等。因此,EGFR已经成为肿瘤靶向治疗的一个理想靶点。
程序性死亡分子1(programmed death 1,PD-1)是免疫球蛋白B7-CD28家族成员之一,可表达于活化的CD4+T细胞、CD8+T细胞、B细胞、自然杀伤T细胞、单核细胞和树突状细胞上,目前已经证实其与效应性T细胞应答活性密切相关。PD-L1是PD-1的主要配体,在包括NSCLC、黑色素瘤、肾细胞癌等许多恶性肿瘤中高表达。PD-1/PD-L1信号通路的激活可导致免疫抑制性肿瘤微环境形成,使肿瘤细胞逃避机体免疫监视和杀伤,而阻断PD-1/PD-L1信号通路可以逆转肿瘤免疫微环境,增强抗肿瘤免疫效应。目前,靶向PD-1、PD-L1的抗体药物在多种肿瘤的临床试验中都取得较好的疗效。这些结果为后续肿瘤靶向治疗指明了方向。然而即使是目前疗效较好的肿瘤靶向抗体,其反应率和疗效依然有待提高,大部分患者在治疗过程中也逐渐产生耐受。众所周知,肿瘤在发生、发展过程中的异质性和复杂性决定了,仅仅依靠单一靶点的抗体靶向药物很难更加有效杀伤肿瘤细胞、激活抗肿瘤免疫,进而避免肿瘤复发。因此,多靶向抗体是目前抗体靶向药物研究的一个热点。
发明内容
为了解决上述问题,发明人进行了长期研究,经大量试验,利用基因工程技术构建了一类具有类似全抗体结构与功能的EGFR/PD-L1双靶向抗体,该双靶向抗体既可以靶向、杀伤EGFR阳性的肿瘤细胞,又能够阻断PD-1/PD-L1免疫抑制信号。
因此,本发明一个目的是,提供一种EGFR/PD-L1双靶向抗体及其相应的药物制剂,所述EGFR/PD-L1双靶向抗体是由4条肽链构成的全抗体,其既可以靶向、杀伤EGFR阳性的肿瘤细胞,又能够阻断PD-1/PD-L1免疫抑制信号。
本发明的另一个目的是,提供一种EGFR/PD-L1双靶向抗体的制备方法。
根据本发明的一个方面,以EGFR的抗体Cetuximab和PD-L1的抗体RG7446为亲本,运用基因工程技术获得双靶向抗体,所述双靶向抗体的结构如图1所示。
所述双靶向抗体包括4条肽链,分别为如SEQ ID NO:20所示的RG7446HV-CL-Hinge-CH2-CH3、如SEQ ID NO:22所示的RG7446LV-CH1、如SEQ IDNO:18所示的Cetuximab重链knob突变体、如SEQ ID NO:26所示的Cetuximab轻链。
进一步地,上述双靶向抗体可应用于抗肿瘤药物的制备;
上述双靶向抗体,可以和药学上可以接受的辅料一起组成药物制剂从而更稳定地发挥疗效,这些制剂可以保证本发明公开的双靶向抗体氨基酸核心序列的结构完整性,同时还要保护蛋白质的多官能团防止其降解(包括但不限于凝聚、脱氨或氧化)。所述制剂可以是各种形态,通常情况下,对于液体制剂,通常可以在2℃-8℃条件下至少稳定保存一年,对于冻干制剂,在30℃至少六个月保持稳定。在这里制剂可为制药领域常用的混悬、水针、冻干等制剂,优选水针或冻干制剂。
对于本发明公开的双功能融合蛋白(双靶向抗体)的水针或冻干制剂,其中药学上可以接受的辅料包括表面活性剂、溶液稳定剂、等渗调节剂和缓冲液之一或其组合,其中表面活性剂包括非离子型表面活性剂如聚氧乙烯山梨醇脂肪酸酯(吐温20或80);poloxamer(如poloxamer 188);Triton;十二烷基硫酸钠(SDS);月桂硫酸钠;十四烷基、亚油基或十八烷基肌氨酸;Pluronics;MONAQUATTM等,其加入量应使双功能融合蛋白的颗粒化趋势最小,溶液稳定剂可以为糖类,包括还原性糖和非还原性糖,氨基酸类包括谷氨酸单钠或组氨酸,醇类包括三元醇、高级糖醇、丙二醇、聚乙二醇之一或其组合,溶液稳定剂的加入量应该使最后形成的制剂在本领域的技术人员认为达到在稳定的时间内保持稳定状态,等渗调节剂可以为氯化钠、甘露醇之一,缓冲液可以为TRIS、组氨酸缓冲液、磷酸盐缓冲液之一。
使用上述双靶向抗体及其药物制剂在对包括人在内的动物给药时,给药剂量因病人的年龄和体重、疾病特性和严重性、以及给药途径而异,可以参考动物实验的结果和种种情况,总给药量不能超过一定范围。具体讲静脉注射的剂量是0.1~3000mg/天。
本发明所称的抗肿瘤药物,指具有抑制和/或治疗肿瘤的药物,可以包括伴随肿瘤生长相关症状发展的延迟和/或这些症状严重程度的降低,它进一步还包括已存在的肿瘤生长伴随症状的减轻并防止其他症状的出现,还也减少或防止转移。
上述双靶向抗体及其药物制剂还可以和其他的抗肿瘤药联合给药,用于肿瘤的治疗,这些用于联合给药的抗肿瘤药包括:1、细胞毒类药物(1)作用于DNA化学结构的药物:烷化剂如氮芥类、亚硝尿类、甲基磺酸酯类;铂类化合物如顺铂、卡铂和草酸铂等;丝裂霉素(MMC);(2)影响核酸合成的药物:二氢叶酸还原酶抑制剂如甲氨喋呤(MTX)和Alimta等;胸腺核苷合成酶抑制剂如氟尿嘧啶类(5FU、FT-207、卡培他滨)等;嘌呤核苷合成酶抑制剂如6-巯基嘌呤(6-MP)和6-TG等;核苷酸还原酶抑制剂如羟基脲(HU)等;DNA多聚酶抑制剂如阿糖胞苷(Ara-C)和健择(Gemz)等;(3)作用于核酸转录的药物:选择性作用于DNA模板,抑制DNA依赖RNA聚合酶,从而抑制RNA合成的药物如:放线菌素D、柔红霉素、阿霉素、表阿霉素、阿克拉霉素、光辉霉素等;(4)主要作用于微管蛋白合成的药物:紫杉醇、泰索帝、长春花碱、长春瑞滨、鬼臼硷类、高三尖杉酯碱;(5)其他细胞毒药:门冬酰胺酶主要抑制蛋白质的合成;2、激素类抗雌激素:三苯氧胺、屈洛昔芬、依西美坦等;芳香化酶抑制剂:氨鲁米特、兰特隆、来曲唑、瑞宁德等;抗雄激素:氟它氨RH-LH激动剂/拮抗剂:诺雷德、依那通等;3、生物反应调节剂:主要通过机体免疫功能抑制肿瘤干扰素;白细胞介素-2;胸腺肽类;4、单克隆抗体:美罗华(MabThera);Cetuximab(C225);赫赛汀(Trastuzumab);Bevacizumab(Avastin);Yervoy(Ipilimumab);5、其他括一些目前机制不明和有待进一步研究的药物;细胞分化诱导剂如维甲类;细胞凋亡诱导剂。
根据本发明的另一个方面,具体建立了上述EGFR/PD-L1双靶向抗体的制备方法。
在本发明的双靶向抗体制备方法中,可以使用任何合适的载体,可选自pDR1、pcDNA3.1(+)、pcDNA3.1/ZEO(+)、pDHFR之一,表达载体中包括连接有合适的转录和翻译调节序列的融合DNA序列。
真核/原核宿主细胞均可用于本发明的双功能融合蛋白(EGFR/PD-1双靶向抗体)的表达,真核宿主细胞优选哺乳动物或昆虫宿主细胞培养系统,优选COS、CHO、NS0、sf9及sf21等细胞均;原核宿主细胞优选为DH5a、BL21(DE3)、TG1之一。
可在表达条件下,培养上述的宿主细胞,从而表达双功能融合蛋白,分离或纯化所述的双功能融合蛋白。
可以利用亲和层析的方法对本发明公开的双功能融合蛋白进行分离纯化,根据所利用的亲和柱的特性,可以使用常规的方法例如高盐缓冲液、改变PH等方法洗脱结合在亲和柱上的双功能融合蛋白。
利用上述方法,可以将双功能融合蛋白纯化为基本均一的物质,例如在SDS-PAGE电泳上为单一条带。
根据本发明的一个优选实施例,一类EGFR/PD-L1双靶向抗体包含Cetuximab和RG7446的抗原结合区。
所述制备方法具体包括以下步骤:
1)分别克隆Cetuximab抗体和RG7446抗体可变区基因;
2)将RG7446抗体重链可变区基因与抗体轻链恒定区进行融合,构建RG7446HV-CL融合片段;
3)将RG7446抗体轻链可变区基因与抗体重链恒定区CH1进行融合,构建RG7446LV-CH1融合片段;
4)分别对抗体Fc区域构建knob突变体:T366W,S354C;hole突变体:T366S,L368A,Y407V和Y394C;
5)分别将Cetuximab重链可变区与knob突变体融合,RG7446HV-CL与hole突变体融合,装入表达载体;
6)将上述表达载体与Cetuximab抗体轻链进行共转表达,通过分离纯化得到双靶向抗体;其中所述表达载体为pcDNA3.1(+)(Invitrogen公司产品),用脂质体法转染或电转CHO-K1细胞(ATCC),并用含600μg/ml G418的选择培养基筛选稳定表达双功能融合蛋白的细胞克隆,利用Protein A层析柱,通过亲和层析从细胞培养物的上清中纯化得到双靶向抗体。
附图说明
图1.Cetu-RG7446CrossMab双靶向抗体结构示意图;
图2.Cetuximab重链knob突变体结构图;
图3.RG7446重链hole突变体RG7446HV-CL-Hinge-CH2-CH3结构图;
图4.Cetu-RG7446CrossMab双靶向抗体结合活性;
图5.Cetu-RG7446CrossMab双靶向抗体的小鼠体内抗肿瘤活性。
具体实施方式
以下结合具体实施方式对本发明进行进一步阐述,但不对本发明权利要求构成限制。
本发明所使用的试剂均为市售,Cetuximab抗体购买自默克公司,RG7446购买自罗氏公司。
实施例1.【Cetuximab和RG7446抗体可变区基因的克隆】
参照专利(PCT/US96/09847和US 12/633,339),分别合成Cetuximab和RG7446重链可变区基因和轻链可变区基因,分别命名为Cetuximab HV、Cetuximab LV、RG7446HV及RG7446LV。抗体信号肽氨基酸序列MGWSCIILFLVATATGVHS。SEQ ID NO:2显示Cetuximab重链可变区的氨基酸序列,其核苷酸序列为SEQ ID NO:1;SEQ ID NO:3为RG7446重链可变区的核苷酸序列,其氨基酸序列为SEQ ID NO:4;SEQ ID NO:6显示RG7446轻链可变区的氨基酸序列,其核苷酸序列为SEQ ID NO:5;SEQ ID NO:24为Cetuximab轻链可变区的氨基酸序列,其核苷酸序列为SEQ ID NO:23。
实施例2.【人源抗体CL、重链CH1、Fc区的克隆】
用淋巴细胞分离液(鼎国生物技术发展公司产品)分离健康人淋巴细胞,用Trizol试剂(Life公司产品)提取总RNA,根据文献(Cloned human and mouse kappaimmunoglobulin constant and J region genes conserve homology in functionalsegments.Hieter PA,Max EE,Seidman JG,Maizel JV Jr,Leder P.Cell.Cell.1980Nov;22(1Pt 1):197-207.)和文献(The nucleotide sequence of a human immunoglobulin Cgamma1gene.Ellison JW,Berson BJ,Hood LE.Nucleic Acids Res.1982Jul 10;10(13):4071-9.)。采用RT-PCR反应扩增抗体轻链恒定区,重链恒定区CH1以及Fc区基因。PCR产物经琼脂糖凝胶电泳纯化回收并克隆到pGEM-T载体中,测序验证后确认获得了正确的克隆。SEQID NO:8显示CL氨基酸序列,其核苷酸序列为SEQ ID NO:7;SEQ ID NO:10显示Fc氨基酸序列,其核苷酸序列为SEQ ID NO:9;SEQ ID NO:12显示CH1氨基酸序列,其核苷酸序列为SEQID NO:11。
实施例3.【抗体Fc区knob突变体的构建】
将实施例2中获得的抗体Fc区,采用overlap PCR的方法引入突变点:T366W、S354C。PCR产物经琼脂糖凝胶电泳纯化回收并克隆到pGEM-T载体中,测序验证后确认获得了正确的克隆。SEQ ID NO:14显示Fc-knob氨基酸序列,其核苷酸序列为SEQ ID NO:13。
实施例4.【抗体Fc区hole突变体的构建】
将实施例3中获得的抗体Fc区,采用PCR的方法将Fc区的部分hinge及CH2、CH3区克隆到pGEM-T载体,测序验证后。采用overlap PCR的方法引入突变点:T366S、L368A、Y407V、Y394C。PCR产物经琼脂糖凝胶电泳纯化回收并克隆到pGEM-T载体中,测序验证后确认获得了正确的克隆。SEQ ID NO:16显示Fc-hole氨基酸序列,其核苷酸序列为SEQ ID NO:15。
实施例5.【Cetuximab重链突变体的构建】
以实施例1获得的Cetuximab重链可变区和实施例3获得的Fc区knob突变体为模板,采用overlap PCR的方法将Cetuximab重链可变区与Fc区knob突变体进行融合,构建Cetuximab重链knob突变体(图2)。SEQ ID NO:18显示Cetuximab重链knob突变体氨基酸序列,其核苷酸序列为SEQ ID NO:17。
实施例6.【RG7446重链突变体的构建】
以实施例1获得的RG7446重链可变区,实施例2获得的CL以及实施例4获得的Fc区hole突变体为模板,采用overlap PCR的方法将RG7446重链可变区与CL及Fc区hole进行片段融合,然后装入表达载体,构建RG7446HV-CL-Hinge-CH2-CH3(图3)。SEQ ID NO:20显示RG7446HV-CL-Hinge-CH2-CH3氨基酸序列,其核苷酸序列为SEQ ID NO:19。
实施例7.【RG7446轻链突变体的构建】
以实施例1获得的RG7446轻链可变区,实施例2获得的CH1为模板,采用overlapPCR的方法将RG7446轻链可变区与CH1进行片段融合,然后装入表达载体,构建RG7446LV-CH1。SEQ ID NO:22显示RG7446LV-CH1的氨基酸序列,其核苷酸序列为SEQ ID NO:21。
实施例8.【Cetuximab轻链的构建】
以实施例1获得的Cetuximab轻链可变区,实施例2获得的CL为模板,采用overlapPCR的方法将Cetuximab轻链可变区与CL进行片段融合,然后装入表达载体,构建Cetuximab轻链。SEQ ID NO:26显示Cetuximab轻链的氨基酸序列,其核苷酸序列为SEQ ID NO:25。
实施例9.【Cetu-RG7446CrossMab的表达与纯化】
于3.5cm组织培养皿中接种3×105CHO-K1细胞(ATCC CRL-9618),细胞培养至90%-95%融合时进行转染:取质粒10μg Cetuximab重链knob突变体(SEQ ID NO:17),RG7446重链hole突变体(SEQ ID NO:19)以及4μg Cetuximab轻链(SEQ ID NO:25)及RG7446轻链突变体(SEQ ID NO:21)和20μl Lipofectamine2000Reagent(Invitrogen公司产品)分别溶于500μl无血清DMEM培养基,室温静置5分钟,将以上2种液体混合,室温孵育20分钟以使DNA-脂质体复合物形成,其间用3ml无血清的DMEM培养基替换培养皿中的含血清培养基,然后将形成的DNA-脂质体复合物加入到板中,CO2孵箱培养4小时后补加2ml含10%血清的DMEM完全培养基,置于CO2孵箱中继续培养。转染进行24h后细胞换含600μg/ml G418选择培养基筛选抗性克隆。取细胞培养上清用ELISA检测筛选高表达克隆:羊抗人IgG(Fc)包被于ELISA板,4℃过夜,用2%BSA-PBS于37℃封闭2h,加入待测的抗性克隆培养上清或标准品(Human myeloma IgG1,κ),37℃温育2h,加入HRP-羊抗人IgG(κ)进行结合反应,37℃温育1h,加入TMB于37℃作用5min,最后用H2SO4终止反应,测A450值。将筛选得到的高表达克隆用无血清培养基扩大培养,用Protein A亲和柱(GE公司产品)分离纯化双靶向抗体。将纯化抗体用PBS进行透析,最后以紫外吸收法定量确定纯化后抗体的浓度。
实施例10.【双靶向抗体结合活性检测】
参照"Development of a Two-part Strategy to Identify a TherapeuticHuman Bispecific Antibody That Inhibits IgE Receptor Signaling".J BiolChem.2010Jul 2;285(27):20850–20859.将EGFR-ECD包被ELISA板上并封闭后,与纯化后不同浓度的抗体与包被在ELISA板上的EGFR-ECD蛋白37度孵育1小时。PBST洗板三次后,将生物素标记的PD-L1-ECD加入进行37度孵育1小时。PBST洗板三次后,将亲和素标记的HRP加入进行37度孵育1小时。洗板后,进行DAB显色。如图4所示,只有双靶向抗体Cetu-RG7446CrossMab能够同时靶向两个不同的抗原,而Cetuximab及RG7446抗体由于不能够同时结合两种不同抗原,因此未表现出结合活性。
实施例11.【Cetu-RG7446CrossMab双靶向抗体的肿瘤活性检测】
选取雌性C57BL小鼠(购自北京维通利华实验动物技术有限公司),皮下接种稳定表达人EGFR蛋白的3LL小鼠肺癌细胞(3LL-huEGFR)。其中3LL小鼠肺癌细胞系购自ATCC(CRL-1642),将装载人EGFR基因的pcDNA3.1,用lipofectamin2000(购自Thermo Fisher公司)参照该试剂转染使用说明书,转染3LL细胞。后续采用G418筛选出能稳定表达人EGFR蛋白的3LL细胞。
当肿瘤体积达到100mm3后将荷瘤小鼠采用随机分组法进行分组后,每周接种三次,分别接种PBS、Cetu-RG7446CrossMab、Cetuximab、RG7446或者Cetuximab+RG7446抗体(100μg),连续接种四周。通过测量肿瘤体积大小变化评价双靶向抗体的小鼠体内抗肿瘤活性。如图5所示,Cetu-RG7446CrossMab双靶向抗体表现出比单药亲本抗体Cetuximab、RG7446以及Cetuximab与RG7446联合用药更强的小鼠体内杀伤肿瘤的能力。
SEQUENCE LISTING
<110> 胡, 毅
<120> 一种EGFR/PD-L1双靶向抗体、其制备方法及用途
<130> BJ1929-17P121570
<160> 26
<170> PatentIn version 3.3
<210> 1
<211> 357
<212> DNA
<213> Artificial
<220>
<223> Cetuximab重链可变区核苷酸序列
<400> 1
caggtgcagc tgaagcagtc aggacctggc ctagtgcagc cctcacagag cctgtccatc 60
acctgcacag tctctggttt ctcattaact aactatggtg tacactgggt tcgccagtct 120
ccaggaaagg gtctggagtg gctgggagtg atatggagtg gtggaaacac agactataat 180
acacctttca catccagact gagcatcaac aaggacaatt ccaagagcca agttttcttt 240
aaaatgaaca gtctgcaatc taatgacaca gccatatatt actgtgccag agccctcacc 300
tactatgatt acgagtttgc ttactggggc caagggactc tggtcactgt ctctgca 357
<210> 2
<211> 119
<212> PRT
<213> Artificial
<220>
<223> Cetuximab重链可变区氨基酸序列
<400> 2
Gln Val Gln Leu Lys Gln Ser Gly Pro Gly Leu Val Gln Pro Ser Gln
1 5 10 15
Ser Leu Ser Ile Thr Cys Thr Val Ser Gly Phe Ser Leu Thr Asn Tyr
20 25 30
Gly Val His Trp Val Arg Gln Ser Pro Gly Lys Gly Leu Glu Trp Leu
35 40 45
Gly Val Ile Trp Ser Gly Gly Asn Thr Asp Tyr Asn Thr Pro Phe Thr
50 55 60
Ser Arg Leu Ser Ile Asn Lys Asp Asn Ser Lys Ser Gln Val Phe Phe
65 70 75 80
Lys Met Asn Ser Leu Gln Ser Asn Asp Thr Ala Ile Tyr Tyr Cys Ala
85 90 95
Arg Ala Leu Thr Tyr Tyr Asp Tyr Glu Phe Ala Tyr Trp Gly Gln Gly
100 105 110
Thr Leu Val Thr Val Ser Ala
115
<210> 3
<211> 354
<212> DNA
<213> Artificial
<220>
<223> RG7446重链可变区的核苷酸序列
<400> 3
gaagttcaat tagtcgagtc tggtggcgga ttggtacagc ctgggggttc ccttcgtctc 60
tcatgtgctg cctcgggctt tactttcagt gatagctgga ttcattgggt gcgccaagca 120
cccggaaaag ggctagaatg ggttgcgtgg atctctccat atggtggctc cacctactat 180
gctgactcag tcaagggacg atttacaata tcggccgata cgagtaaaaa tactgcatac 240
ctgcagatga acagcttacg ggcggaggac accgctgtat attactgcgc cagaaggcac 300
tggccggggg gtttcgatta ttggggccaa ggaacattgg tgacggtttc tgca 354
<210> 4
<211> 118
<212> PRT
<213> Artificial
<220>
<223> RG7446重链可变区的氨基酸序列
<400> 4
Glu Val Gln Leu Val Glu Ser Gly Gly Gly Leu Val Gln Pro Gly Gly
1 5 10 15
Ser Leu Arg Leu Ser Cys Ala Ala Ser Gly Phe Thr Phe Ser Asp Ser
20 25 30
Trp Ile His Trp Val Arg Gln Ala Pro Gly Lys Gly Leu Glu Trp Val
35 40 45
Ala Trp Ile Ser Pro Tyr Gly Gly Ser Thr Tyr Tyr Ala Asp Ser Val
50 55 60
Lys Gly Arg Phe Thr Ile Ser Ala Asp Thr Ser Lys Asn Thr Ala Tyr
65 70 75 80
Leu Gln Met Asn Ser Leu Arg Ala Glu Asp Thr Ala Val Tyr Tyr Cys
85 90 95
Ala Arg Arg His Trp Pro Gly Gly Phe Asp Tyr Trp Gly Gln Gly Thr
100 105 110
Leu Val Thr Val Ser Ala
115
<210> 5
<211> 321
<212> DNA
<213> Artificial
<220>
<223> RG7446轻链可变区的核苷酸序列
<400> 5
gatattcaaa tgactcagtc tccttcctca ttatcggcta gtgttggtga ccgtgtcacc 60
atcacatgtc gcgccagcca agatgtatct acggcagtgg cgtggtatca gcaaaaaccc 120
ggcaaggctc caaaattgct tatatactcc gcctcatttc tctattcggg agttccgagt 180
cgattcagcg ggtctggttc cggcactgac tttaccctaa caatttcatc gctgcagcct 240
gaagatttcg caacgtacta ttgccaacag tacttatatc atcccgcgac ttttggacaa 300
gggaccaagg tcgagatcaa a 321
<210> 6
<211> 107
<212> PRT
<213> Artificial
<220>
<223> RG7446轻链可变区的氨基酸序列
<400> 6
Asp Ile Gln Met Thr Gln Ser Pro Ser Ser Leu Ser Ala Ser Val Gly
1 5 10 15
Asp Arg Val Thr Ile Thr Cys Arg Ala Ser Gln Asp Val Ser Thr Ala
20 25 30
Val Ala Trp Tyr Gln Gln Lys Pro Gly Lys Ala Pro Lys Leu Leu Ile
35 40 45
Tyr Ser Ala Ser Phe Leu Tyr Ser Gly Val Pro Ser Arg Phe Ser Gly
50 55 60
Ser Gly Ser Gly Thr Asp Phe Thr Leu Thr Ile Ser Ser Leu Gln Pro
65 70 75 80
Glu Asp Phe Ala Thr Tyr Tyr Cys Gln Gln Tyr Leu Tyr His Pro Ala
85 90 95
Thr Phe Gly Gln Gly Thr Lys Val Glu Ile Lys
100 105
<210> 7
<211> 315
<212> DNA
<213> Artificial
<220>
<223> CL核苷酸序列
<400> 7
gtggctgcac catctgtctt catcttcccg ccatctgatg agcagttgaa atctggaact 60
gcctctgttg tgtgcctgct gaataacttc taccccagag aagccaaagt gcagtggaag 120
gtggacaacg ccctgcagag cggaaacagc caggaaagcg tgacagagca ggattccaag 180
gattccacat acagcctgag cagcacactg acactgtcca aggccgacta cgagaagcac 240
aaggtgtacg cctgcgaagt gacacaccag ggactgtcct cccctgtgac aaagagcttc 300
aacagaggag aatgc 315
<210> 8
<211> 105
<212> PRT
<213> Artificial
<220>
<223> CL氨基酸序列
<400> 8
Val Ala Ala Pro Ser Val Phe Ile Phe Pro Pro Ser Asp Glu Gln Leu
1 5 10 15
Lys Ser Gly Thr Ala Ser Val Val Cys Leu Leu Asn Asn Phe Tyr Pro
20 25 30
Arg Glu Ala Lys Val Gln Trp Lys Val Asp Asn Ala Leu Gln Ser Gly
35 40 45
Asn Ser Gln Glu Ser Val Thr Glu Gln Asp Ser Lys Asp Ser Thr Tyr
50 55 60
Ser Leu Ser Ser Thr Leu Thr Leu Ser Lys Ala Asp Tyr Glu Lys His
65 70 75 80
Lys Val Tyr Ala Cys Glu Val Thr His Gln Gly Leu Ser Ser Pro Val
85 90 95
Thr Lys Ser Phe Asn Arg Gly Glu Cys
100 105
<210> 9
<211> 990
<212> DNA
<213> Artificial
<220>
<223> Fc核苷酸序列
<400> 9
gctagcacca agggcccatc ggtcttcccc ctggcaccct cctccaagag cacctctggg 60
ggcacagcgg ccctgggctg cctggtcaag gactacttcc ccgaacctgt gacggtgtcg 120
tggaactcag gcgccctgac cagcggcgtg cacaccttcc cggctgtcct acagtcctca 180
ggactctact ccctcagcag cgtggtgacc gtgccctcca gcagcttggg cacccagacc 240
tacatctgca acgtgaatca caagcccagc aacaccaagg tggacaagaa agttgagccc 300
aaatcttgtg acaaaactca cacatgccca ccgtgcccag cacctgaact cctgggggga 360
ccgtcagtct tcctcttccc cccaaaaccc aaggacaccc tcatgatctc ccggacccct 420
gaggtcacat gcgtggtggt ggacgtgagc cacgaagacc ctgaggtcaa gttcaactgg 480
tacgtggacg gcgtggaggt gcataatgcc aagacaaagc cgcgggagga gcagtacaac 540
agcacgtacc gtgtggtcag cgtcctcacc gtcctgcacc aggactggct gaatggcaag 600
gagtacaagt gcaaggtctc caacaaagcc ctcccagccc ccatcgagaa aaccatctcc 660
aaagccaaag ggcagccccg agaaccacag gtgtacaccc tgcccccatc ccgggatgag 720
ctgaccaaga accaggtcag cctgacctgc ctggtcaaag gcttctatcc cagcgacatc 780
gccgtggagt gggagagcaa tgggcagccg gagaacaact acaagaccac gcctcccgtg 840
ctggactccg acggctcctt cttcctctac agcaagctca ccgtggacaa gagcaggtgg 900
cagcagggga acgtcttctc atgctccgtg atgcatgagg ctctgcacaa ccactacacg 960
cagaagagcc tctccctgtc tccgggtaaa 990
<210> 10
<211> 330
<212> PRT
<213> Artificial
<220>
<223> Fc氨基酸序列
<400> 10
Ala Ser Thr Lys Gly Pro Ser Val Phe Pro Leu Ala Pro Ser Ser Lys
1 5 10 15
Ser Thr Ser Gly Gly Thr Ala Ala Leu Gly Cys Leu Val Lys Asp Tyr
20 25 30
Phe Pro Glu Pro Val Thr Val Ser Trp Asn Ser Gly Ala Leu Thr Ser
35 40 45
Gly Val His Thr Phe Pro Ala Val Leu Gln Ser Ser Gly Leu Tyr Ser
50 55 60
Leu Ser Ser Val Val Thr Val Pro Ser Ser Ser Leu Gly Thr Gln Thr
65 70 75 80
Tyr Ile Cys Asn Val Asn His Lys Pro Ser Asn Thr Lys Val Asp Lys
85 90 95
Lys Val Glu Pro Lys Ser Cys Asp Lys Thr His Thr Cys Pro Pro Cys
100 105 110
Pro Ala Pro Glu Leu Leu Gly Gly Pro Ser Val Phe Leu Phe Pro Pro
115 120 125
Lys Pro Lys Asp Thr Leu Met Ile Ser Arg Thr Pro Glu Val Thr Cys
130 135 140
Val Val Val Asp Val Ser His Glu Asp Pro Glu Val Lys Phe Asn Trp
145 150 155 160
Tyr Val Asp Gly Val Glu Val His Asn Ala Lys Thr Lys Pro Arg Glu
165 170 175
Glu Gln Tyr Asn Ser Thr Tyr Arg Val Val Ser Val Leu Thr Val Leu
180 185 190
His Gln Asp Trp Leu Asn Gly Lys Glu Tyr Lys Cys Lys Val Ser Asn
195 200 205
Lys Ala Leu Pro Ala Pro Ile Glu Lys Thr Ile Ser Lys Ala Lys Gly
210 215 220
Gln Pro Arg Glu Pro Gln Val Tyr Thr Leu Pro Pro Ser Arg Asp Glu
225 230 235 240
Leu Thr Lys Asn Gln Val Ser Leu Thr Cys Leu Val Lys Gly Phe Tyr
245 250 255
Pro Ser Asp Ile Ala Val Glu Trp Glu Ser Asn Gly Gln Pro Glu Asn
260 265 270
Asn Tyr Lys Thr Thr Pro Pro Val Leu Asp Ser Asp Gly Ser Phe Phe
275 280 285
Leu Tyr Ser Lys Leu Thr Val Asp Lys Ser Arg Trp Gln Gln Gly Asn
290 295 300
Val Phe Ser Cys Ser Val Met His Glu Ala Leu His Asn His Tyr Thr
305 310 315 320
Gln Lys Ser Leu Ser Leu Ser Pro Gly Lys
325 330
<210> 11
<211> 309
<212> DNA
<213> Artificial
<220>
<223> CH1核苷酸序列
<400> 11
cgtacgacca agggcccatc ggtcttcccc ctggcaccct cctccaagag cacctctggg 60
ggcacagcgg ccctgggctg cctggtcaag gactacttcc ccgaacctgt gacggtgtcg 120
tggaactcag gcgccctgac cagcggcgtg cacaccttcc cggctgtcct acagtcctca 180
ggactctact ccctcagcag cgtggtgacc gtgccctcca gcagcttggg cacccagacc 240
tacatctgca acgtgaatca caagcccagc aacaccaagg tggacaagaa agttgagccc 300
aaatcttgt 309
<210> 12
<211> 103
<212> PRT
<213> Artificial
<220>
<223> CH1氨基酸序列
<400> 12
Arg Thr Thr Lys Gly Pro Ser Val Phe Pro Leu Ala Pro Ser Ser Lys
1 5 10 15
Ser Thr Ser Gly Gly Thr Ala Ala Leu Gly Cys Leu Val Lys Asp Tyr
20 25 30
Phe Pro Glu Pro Val Thr Val Ser Trp Asn Ser Gly Ala Leu Thr Ser
35 40 45
Gly Val His Thr Phe Pro Ala Val Leu Gln Ser Ser Gly Leu Tyr Ser
50 55 60
Leu Ser Ser Val Val Thr Val Pro Ser Ser Ser Leu Gly Thr Gln Thr
65 70 75 80
Tyr Ile Cys Asn Val Asn His Lys Pro Ser Asn Thr Lys Val Asp Lys
85 90 95
Lys Val Glu Pro Lys Ser Cys
100
<210> 13
<211> 990
<212> DNA
<213> Artificial
<220>
<223> Fc-knob核苷酸序列
<400> 13
gctagcacca agggcccatc ggtcttcccc ctggcaccct cctccaagag cacctctggg 60
ggcacagcgg ccctgggctg cctggtcaag gactacttcc ccgagccagt gacggtgtcg 120
tggaactcag gcgccctgac cagcggcgtg cacaccttcc cggctgtcct acagtcctca 180
ggactctact ccctcagcag cgtggtgacc gtgccctcca gcagcttggg cacccagacc 240
tacatctgca acgtgaatca caagcccagc aacaccaagg tggacaagaa agttgagccc 300
aaatcttgtg acaaaactca cacatgccca ccgtgcccag cacctgaact cctgggggga 360
ccgtcagtct tcctcttccc cccaaaaccc aaggacaccc tcatgatctc ccggacccct 420
gaggtcacat gcgtggtggt ggacgtgagc cacgaagacc ctgaggtcaa gttcaactgg 480
tacgtggacg gcgtggaggt gcataatgcc aagacaaagc cgcgggagga gcagtacaac 540
agcacgtacc gtgtggtcag cgtcctcacc gtcctgcacc aggactggct gaatggcaag 600
gagtacaagt gcaaggtctc caacaaagcc ctcccagccc ccatcgagaa aaccatctcc 660
aaagccaaag ggcagccccg agaaccacag gtgtacaccc tgcccccatg ccgggatgag 720
ctgaccaaga accaggtcag cctgtggtgc ctggtcaaag gcttctatcc cagcgacatc 780
gccgtggagt gggagagcaa tgggcagccg gagaacaact acaagaccac gcctcccgtg 840
ctggactccg acggctcctt cttcctctac agcaagctca ccgtggacaa gagcaggtgg 900
cagcagggga acgtcttctc atgctccgtg atgcatgagg ctctgcacaa ccactacacg 960
cagaagagcc tctccctgtc tccgggtaaa 990
<210> 14
<211> 330
<212> PRT
<213> Artificial
<220>
<223> Fc-knob氨基酸序列
<400> 14
Ala Ser Thr Lys Gly Pro Ser Val Phe Pro Leu Ala Pro Ser Ser Lys
1 5 10 15
Ser Thr Ser Gly Gly Thr Ala Ala Leu Gly Cys Leu Val Lys Asp Tyr
20 25 30
Phe Pro Glu Pro Val Thr Val Ser Trp Asn Ser Gly Ala Leu Thr Ser
35 40 45
Gly Val His Thr Phe Pro Ala Val Leu Gln Ser Ser Gly Leu Tyr Ser
50 55 60
Leu Ser Ser Val Val Thr Val Pro Ser Ser Ser Leu Gly Thr Gln Thr
65 70 75 80
Tyr Ile Cys Asn Val Asn His Lys Pro Ser Asn Thr Lys Val Asp Lys
85 90 95
Lys Val Glu Pro Lys Ser Cys Asp Lys Thr His Thr Cys Pro Pro Cys
100 105 110
Pro Ala Pro Glu Leu Leu Gly Gly Pro Ser Val Phe Leu Phe Pro Pro
115 120 125
Lys Pro Lys Asp Thr Leu Met Ile Ser Arg Thr Pro Glu Val Thr Cys
130 135 140
Val Val Val Asp Val Ser His Glu Asp Pro Glu Val Lys Phe Asn Trp
145 150 155 160
Tyr Val Asp Gly Val Glu Val His Asn Ala Lys Thr Lys Pro Arg Glu
165 170 175
Glu Gln Tyr Asn Ser Thr Tyr Arg Val Val Ser Val Leu Thr Val Leu
180 185 190
His Gln Asp Trp Leu Asn Gly Lys Glu Tyr Lys Cys Lys Val Ser Asn
195 200 205
Lys Ala Leu Pro Ala Pro Ile Glu Lys Thr Ile Ser Lys Ala Lys Gly
210 215 220
Gln Pro Arg Glu Pro Gln Val Tyr Thr Leu Pro Pro Cys Arg Asp Glu
225 230 235 240
Leu Thr Lys Asn Gln Val Ser Leu Trp Cys Leu Val Lys Gly Phe Tyr
245 250 255
Pro Ser Asp Ile Ala Val Glu Trp Glu Ser Asn Gly Gln Pro Glu Asn
260 265 270
Asn Tyr Lys Thr Thr Pro Pro Val Leu Asp Ser Asp Gly Ser Phe Phe
275 280 285
Leu Tyr Ser Lys Leu Thr Val Asp Lys Ser Arg Trp Gln Gln Gly Asn
290 295 300
Val Phe Ser Cys Ser Val Met His Glu Ala Leu His Asn His Tyr Thr
305 310 315 320
Gln Lys Ser Leu Ser Leu Ser Pro Gly Lys
325 330
<210> 15
<211> 681
<212> DNA
<213> Artificial
<220>
<223> Fc-hole核苷酸序列
<400> 15
gacaaaactc acacatgccc accgtgccca gcacctgaac tcctgggggg accgtcagtc 60
ttcctcttcc ccccaaaacc caaggacacc ctcatgatct cccggacccc tgaggtcaca 120
tgcgtggtgg tggacgtgag ccacgaagac cctgaggtca agttcaactg gtacgtggac 180
ggcgtggagg tgcataatgc caagacaaag ccgcgggagg agcagtacaa cagcacgtac 240
cgtgtggtca gcgtcctcac cgtcctgcac caggactggc tgaatggcaa ggagtacaag 300
tgcaaggtct ccaacaaagc cctcccagcc cccatcgaga aaaccatctc caaagccaaa 360
gggcagcccc gagaaccaca ggtgtgcacc ctgcccccat cccgggatga gctgaccaag 420
aaccaggtca gcctgtcctg cgcggtcaaa ggcttctatc ccagcgacat cgccgtggag 480
tgggagagca atgggcagcc ggagaacaac tacaagacca cgcctcccgt gctggactcc 540
gacggctcct tcttcctcgt gagcaagctc accgtggaca agagcaggtg gcagcagggg 600
aacgtcttct catgctccgt gatgcatgag gctctgcaca accactacac gcagaagagc 660
ctctccctgt ctccgggtaa a 681
<210> 16
<211> 227
<212> PRT
<213> Artificial
<220>
<223> Fc-hole氨基酸序列
<400> 16
Asp Lys Thr His Thr Cys Pro Pro Cys Pro Ala Pro Glu Leu Leu Gly
1 5 10 15
Gly Pro Ser Val Phe Leu Phe Pro Pro Lys Pro Lys Asp Thr Leu Met
20 25 30
Ile Ser Arg Thr Pro Glu Val Thr Cys Val Val Val Asp Val Ser His
35 40 45
Glu Asp Pro Glu Val Lys Phe Asn Trp Tyr Val Asp Gly Val Glu Val
50 55 60
His Asn Ala Lys Thr Lys Pro Arg Glu Glu Gln Tyr Asn Ser Thr Tyr
65 70 75 80
Arg Val Val Ser Val Leu Thr Val Leu His Gln Asp Trp Leu Asn Gly
85 90 95
Lys Glu Tyr Lys Cys Lys Val Ser Asn Lys Ala Leu Pro Ala Pro Ile
100 105 110
Glu Lys Thr Ile Ser Lys Ala Lys Gly Gln Pro Arg Glu Pro Gln Val
115 120 125
Cys Thr Leu Pro Pro Ser Arg Asp Glu Leu Thr Lys Asn Gln Val Ser
130 135 140
Leu Ser Cys Ala Val Lys Gly Phe Tyr Pro Ser Asp Ile Ala Val Glu
145 150 155 160
Trp Glu Ser Asn Gly Gln Pro Glu Asn Asn Tyr Lys Thr Thr Pro Pro
165 170 175
Val Leu Asp Ser Asp Gly Ser Phe Phe Leu Val Ser Lys Leu Thr Val
180 185 190
Asp Lys Ser Arg Trp Gln Gln Gly Asn Val Phe Ser Cys Ser Val Met
195 200 205
His Glu Ala Leu His Asn His Tyr Thr Gln Lys Ser Leu Ser Leu Ser
210 215 220
Pro Gly Lys
225
<210> 17
<211> 1347
<212> DNA
<213> Artificial
<220>
<223> Cetuximab重链knob突变体核苷酸序列
<400> 17
caggtgcagc tgaagcagtc aggacctggc ctagtgcagc cctcacagag cctgtccatc 60
acctgcacag tctctggttt ctcattaact aactatggtg tacactgggt tcgccagtct 120
ccaggaaagg gtctggagtg gctgggagtg atatggagtg gtggaaacac agactataat 180
acacctttca catccagact gagcatcaac aaggacaatt ccaagagcca agttttcttt 240
aaaatgaaca gtctgcaatc taatgacaca gccatatatt actgtgccag agccctcacc 300
tactatgatt acgagtttgc ttactggggc caagggactc tggtcactgt ctctgcagct 360
agcaccaagg gcccatcggt cttccccctg gcaccctcct ccaagagcac ctctgggggc 420
acagcggccc tgggctgcct ggtcaaggac tacttccccg agccagtgac ggtgtcgtgg 480
aactcaggcg ccctgaccag cggcgtgcac accttcccgg ctgtcctaca gtcctcagga 540
ctctactccc tcagcagcgt ggtgaccgtg ccctccagca gcttgggcac ccagacctac 600
atctgcaacg tgaatcacaa gcccagcaac accaaggtgg acaagaaagt tgagcccaaa 660
tcttgtgaca aaactcacac atgcccaccg tgcccagcac ctgaactcct ggggggaccg 720
tcagtcttcc tcttcccccc aaaacccaag gacaccctca tgatctcccg gacccctgag 780
gtcacatgcg tggtggtgga cgtgagccac gaagaccctg aggtcaagtt caactggtac 840
gtggacggcg tggaggtgca taatgccaag acaaagccgc gggaggagca gtacaacagc 900
acgtaccgtg tggtcagcgt cctcaccgtc ctgcaccagg actggctgaa tggcaaggag 960
tacaagtgca aggtctccaa caaagccctc ccagccccca tcgagaaaac catctccaaa 1020
gccaaagggc agccccgaga accacaggtg tacaccctgc ccccatgccg ggatgagctg 1080
accaagaacc aggtcagcct gtggtgcctg gtcaaaggct tctatcccag cgacatcgcc 1140
gtggagtggg agagcaatgg gcagccggag aacaactaca agaccacgcc tcccgtgctg 1200
gactccgacg gctccttctt cctctacagc aagctcaccg tggacaagag caggtggcag 1260
caggggaacg tcttctcatg ctccgtgatg catgaggctc tgcacaacca ctacacgcag 1320
aagagcctct ccctgtctcc gggtaaa 1347
<210> 18
<211> 449
<212> PRT
<213> Artificial
<220>
<223> Cetuximab重链knob突变体氨基酸序列
<400> 18
Gln Val Gln Leu Lys Gln Ser Gly Pro Gly Leu Val Gln Pro Ser Gln
1 5 10 15
Ser Leu Ser Ile Thr Cys Thr Val Ser Gly Phe Ser Leu Thr Asn Tyr
20 25 30
Gly Val His Trp Val Arg Gln Ser Pro Gly Lys Gly Leu Glu Trp Leu
35 40 45
Gly Val Ile Trp Ser Gly Gly Asn Thr Asp Tyr Asn Thr Pro Phe Thr
50 55 60
Ser Arg Leu Ser Ile Asn Lys Asp Asn Ser Lys Ser Gln Val Phe Phe
65 70 75 80
Lys Met Asn Ser Leu Gln Ser Asn Asp Thr Ala Ile Tyr Tyr Cys Ala
85 90 95
Arg Ala Leu Thr Tyr Tyr Asp Tyr Glu Phe Ala Tyr Trp Gly Gln Gly
100 105 110
Thr Leu Val Thr Val Ser Ala Ala Ser Thr Lys Gly Pro Ser Val Phe
115 120 125
Pro Leu Ala Pro Ser Ser Lys Ser Thr Ser Gly Gly Thr Ala Ala Leu
130 135 140
Gly Cys Leu Val Lys Asp Tyr Phe Pro Glu Pro Val Thr Val Ser Trp
145 150 155 160
Asn Ser Gly Ala Leu Thr Ser Gly Val His Thr Phe Pro Ala Val Leu
165 170 175
Gln Ser Ser Gly Leu Tyr Ser Leu Ser Ser Val Val Thr Val Pro Ser
180 185 190
Ser Ser Leu Gly Thr Gln Thr Tyr Ile Cys Asn Val Asn His Lys Pro
195 200 205
Ser Asn Thr Lys Val Asp Lys Lys Val Glu Pro Lys Ser Cys Asp Lys
210 215 220
Thr His Thr Cys Pro Pro Cys Pro Ala Pro Glu Leu Leu Gly Gly Pro
225 230 235 240
Ser Val Phe Leu Phe Pro Pro Lys Pro Lys Asp Thr Leu Met Ile Ser
245 250 255
Arg Thr Pro Glu Val Thr Cys Val Val Val Asp Val Ser His Glu Asp
260 265 270
Pro Glu Val Lys Phe Asn Trp Tyr Val Asp Gly Val Glu Val His Asn
275 280 285
Ala Lys Thr Lys Pro Arg Glu Glu Gln Tyr Asn Ser Thr Tyr Arg Val
290 295 300
Val Ser Val Leu Thr Val Leu His Gln Asp Trp Leu Asn Gly Lys Glu
305 310 315 320
Tyr Lys Cys Lys Val Ser Asn Lys Ala Leu Pro Ala Pro Ile Glu Lys
325 330 335
Thr Ile Ser Lys Ala Lys Gly Gln Pro Arg Glu Pro Gln Val Tyr Thr
340 345 350
Leu Pro Pro Cys Arg Asp Glu Leu Thr Lys Asn Gln Val Ser Leu Trp
355 360 365
Cys Leu Val Lys Gly Phe Tyr Pro Ser Asp Ile Ala Val Glu Trp Glu
370 375 380
Ser Asn Gly Gln Pro Glu Asn Asn Tyr Lys Thr Thr Pro Pro Val Leu
385 390 395 400
Asp Ser Asp Gly Ser Phe Phe Leu Tyr Ser Lys Leu Thr Val Asp Lys
405 410 415
Ser Arg Trp Gln Gln Gly Asn Val Phe Ser Cys Ser Val Met His Glu
420 425 430
Ala Leu His Asn His Tyr Thr Gln Lys Ser Leu Ser Leu Ser Pro Gly
435 440 445
Lys
<210> 19
<211> 1350
<212> DNA
<213> Artificial
<220>
<223> RG7446HV-CL-Hinge-CH2-CH3核苷酸序列
<400> 19
gaagttcaat tagtcgagtc tggtggcgga ttggtacagc ctgggggttc ccttcgtctc 60
tcatgtgctg cctcgggctt tactttcagt gatagctgga ttcattgggt gcgccaagca 120
cccggaaaag ggctagaatg ggttgcgtgg atctctccat atggtggctc cacctactat 180
gctgactcag tcaagggacg atttacaata tcggccgata cgagtaaaaa tactgcatac 240
ctgcagatga acagcttacg ggcggaggac accgctgtat attactgcgc cagaaggcac 300
tggccggggg gtttcgatta ttggggccaa ggaacattgg tgacggtttc tgcagtggct 360
gcaccatctg tcttcatctt cccgccatct gatgagcagt tgaaatctgg aactgcctct 420
gttgtgtgcc tgctgaataa cttctacccc agagaagcca aagtgcagtg gaaggtggac 480
aacgccctgc agagcggaaa cagccaggaa agcgtgacag agcaggattc caaggattcc 540
acatacagcc tgagcagcac actgacactg tccaaggccg actacgagaa gcacaaggtg 600
tacgcctgcg aagtgacaca ccagggactg tcctcccctg tgacaaagag cttcaacaga 660
ggagaatgcg acaaaactca cacatgccca ccgtgcccag cacctgaact cctgggggga 720
ccgtcagtct tcctcttccc cccaaaaccc aaggacaccc tcatgatctc ccggacccct 780
gaggtcacat gcgtggtggt ggacgtgagc cacgaagacc ctgaggtcaa gttcaactgg 840
tacgtggacg gcgtggaggt gcataatgcc aagacaaagc cgcgggagga gcagtacaac 900
agcacgtacc gtgtggtcag cgtcctcacc gtcctgcacc aggactggct gaatggcaag 960
gagtacaagt gcaaggtctc caacaaagcc ctcccagccc ccatcgagaa aaccatctcc 1020
aaagccaaag ggcagccccg agaaccacag gtgtgcaccc tgcccccatc ccgggatgag 1080
ctgaccaaga accaggtcag cctgtcctgc gcggtcaaag gcttctatcc cagcgacatc 1140
gccgtggagt gggagagcaa tgggcagccg gagaacaact acaagaccac gcctcccgtg 1200
ctggactccg acggctcctt cttcctcgtg agcaagctca ccgtggacaa gagcaggtgg 1260
cagcagggga acgtcttctc atgctccgtg atgcatgagg ctctgcacaa ccactacacg 1320
cagaagagcc tctccctgtc tccgggtaaa 1350
<210> 20
<211> 450
<212> PRT
<213> Artificial
<220>
<223> RG7446HV-CL-Hinge-CH2-CH3氨基酸序列
<400> 20
Glu Val Gln Leu Val Glu Ser Gly Gly Gly Leu Val Gln Pro Gly Gly
1 5 10 15
Ser Leu Arg Leu Ser Cys Ala Ala Ser Gly Phe Thr Phe Ser Asp Ser
20 25 30
Trp Ile His Trp Val Arg Gln Ala Pro Gly Lys Gly Leu Glu Trp Val
35 40 45
Ala Trp Ile Ser Pro Tyr Gly Gly Ser Thr Tyr Tyr Ala Asp Ser Val
50 55 60
Lys Gly Arg Phe Thr Ile Ser Ala Asp Thr Ser Lys Asn Thr Ala Tyr
65 70 75 80
Leu Gln Met Asn Ser Leu Arg Ala Glu Asp Thr Ala Val Tyr Tyr Cys
85 90 95
Ala Arg Arg His Trp Pro Gly Gly Phe Asp Tyr Trp Gly Gln Gly Thr
100 105 110
Leu Val Thr Val Ser Ala Val Ala Ala Pro Ser Val Phe Ile Phe Pro
115 120 125
Pro Ser Asp Glu Gln Leu Lys Ser Gly Thr Ala Ser Val Val Cys Leu
130 135 140
Leu Asn Asn Phe Tyr Pro Arg Glu Ala Lys Val Gln Trp Lys Val Asp
145 150 155 160
Asn Ala Leu Gln Ser Gly Asn Ser Gln Glu Ser Val Thr Glu Gln Asp
165 170 175
Ser Lys Asp Ser Thr Tyr Ser Leu Ser Ser Thr Leu Thr Leu Ser Lys
180 185 190
Ala Asp Tyr Glu Lys His Lys Val Tyr Ala Cys Glu Val Thr His Gln
195 200 205
Gly Leu Ser Ser Pro Val Thr Lys Ser Phe Asn Arg Gly Glu Cys Asp
210 215 220
Lys Thr His Thr Cys Pro Pro Cys Pro Ala Pro Glu Leu Leu Gly Gly
225 230 235 240
Pro Ser Val Phe Leu Phe Pro Pro Lys Pro Lys Asp Thr Leu Met Ile
245 250 255
Ser Arg Thr Pro Glu Val Thr Cys Val Val Val Asp Val Ser His Glu
260 265 270
Asp Pro Glu Val Lys Phe Asn Trp Tyr Val Asp Gly Val Glu Val His
275 280 285
Asn Ala Lys Thr Lys Pro Arg Glu Glu Gln Tyr Asn Ser Thr Tyr Arg
290 295 300
Val Val Ser Val Leu Thr Val Leu His Gln Asp Trp Leu Asn Gly Lys
305 310 315 320
Glu Tyr Lys Cys Lys Val Ser Asn Lys Ala Leu Pro Ala Pro Ile Glu
325 330 335
Lys Thr Ile Ser Lys Ala Lys Gly Gln Pro Arg Glu Pro Gln Val Cys
340 345 350
Thr Leu Pro Pro Ser Arg Asp Glu Leu Thr Lys Asn Gln Val Ser Leu
355 360 365
Ser Cys Ala Val Lys Gly Phe Tyr Pro Ser Asp Ile Ala Val Glu Trp
370 375 380
Glu Ser Asn Gly Gln Pro Glu Asn Asn Tyr Lys Thr Thr Pro Pro Val
385 390 395 400
Leu Asp Ser Asp Gly Ser Phe Phe Leu Val Ser Lys Leu Thr Val Asp
405 410 415
Lys Ser Arg Trp Gln Gln Gly Asn Val Phe Ser Cys Ser Val Met His
420 425 430
Glu Ala Leu His Asn His Tyr Thr Gln Lys Ser Leu Ser Leu Ser Pro
435 440 445
Gly Lys
450
<210> 21
<211> 630
<212> DNA
<213> Artificial
<220>
<223> RG7446LV-CH1的核苷酸序列
<400> 21
gatattcaaa tgactcagtc tccttcctca ttatcggcta gtgttggtga ccgtgtcacc 60
atcacatgtc gcgccagcca agatgtatct acggcagtgg cgtggtatca gcaaaaaccc 120
ggcaaggctc caaaattgct tatatactcc gcctcatttc tctattcggg agttccgagt 180
cgattcagcg ggtctggttc cggcactgac tttaccctaa caatttcatc gctgcagcct 240
gaagatttcg caacgtacta ttgccaacag tacttatatc atcccgcgac ttttggacaa 300
gggaccaagg tcgagatcaa acgtacgacc aagggcccat cggtcttccc cctggcaccc 360
tcctccaaga gcacctctgg gggcacagcg gccctgggct gcctggtcaa ggactacttc 420
cccgaacctg tgacggtgtc gtggaactca ggcgccctga ccagcggcgt gcacaccttc 480
ccggctgtcc tacagtcctc aggactctac tccctcagca gcgtggtgac cgtgccctcc 540
agcagcttgg gcacccagac ctacatctgc aacgtgaatc acaagcccag caacaccaag 600
gtggacaaga aagttgagcc caaatcttgt 630
<210> 22
<211> 210
<212> PRT
<213> Artificial
<220>
<223> RG7446LV-CH1的氨基酸序列
<400> 22
Asp Ile Gln Met Thr Gln Ser Pro Ser Ser Leu Ser Ala Ser Val Gly
1 5 10 15
Asp Arg Val Thr Ile Thr Cys Arg Ala Ser Gln Asp Val Ser Thr Ala
20 25 30
Val Ala Trp Tyr Gln Gln Lys Pro Gly Lys Ala Pro Lys Leu Leu Ile
35 40 45
Tyr Ser Ala Ser Phe Leu Tyr Ser Gly Val Pro Ser Arg Phe Ser Gly
50 55 60
Ser Gly Ser Gly Thr Asp Phe Thr Leu Thr Ile Ser Ser Leu Gln Pro
65 70 75 80
Glu Asp Phe Ala Thr Tyr Tyr Cys Gln Gln Tyr Leu Tyr His Pro Ala
85 90 95
Thr Phe Gly Gln Gly Thr Lys Val Glu Ile Lys Arg Thr Thr Lys Gly
100 105 110
Pro Ser Val Phe Pro Leu Ala Pro Ser Ser Lys Ser Thr Ser Gly Gly
115 120 125
Thr Ala Ala Leu Gly Cys Leu Val Lys Asp Tyr Phe Pro Glu Pro Val
130 135 140
Thr Val Ser Trp Asn Ser Gly Ala Leu Thr Ser Gly Val His Thr Phe
145 150 155 160
Pro Ala Val Leu Gln Ser Ser Gly Leu Tyr Ser Leu Ser Ser Val Val
165 170 175
Thr Val Pro Ser Ser Ser Leu Gly Thr Gln Thr Tyr Ile Cys Asn Val
180 185 190
Asn His Lys Pro Ser Asn Thr Lys Val Asp Lys Lys Val Glu Pro Lys
195 200 205
Ser Cys
210
<210> 23
<211> 321
<212> DNA
<213> Artificial
<220>
<223> Cetuximab轻链可变区的核苷酸序列
<400> 23
gacatcttgc tgactcagtc tccagtcatc ctgtctgtga gtccaggaga aagagtcagt 60
ttctcctgca gggccagtca gagtattggc acaaacatac actggtatca gcaaagaaca 120
aatggttctc caaggcttct cataaagtat gcttctgagt ctatctctgg gatcccttcc 180
aggtttagtg gcagtggatc agggacagat tttactctta gcatcaacag tgtggagtct 240
gaagatattg cagattatta ctgtcaacaa aataataact ggccaaccac gttcggtgct 300
gggaccaagc tggagctgaa a 321
<210> 24
<211> 107
<212> PRT
<213> Artificial
<220>
<223> Cetuximab轻链可变区的氨基酸序列
<400> 24
Asp Ile Leu Leu Thr Gln Ser Pro Val Ile Leu Ser Val Ser Pro Gly
1 5 10 15
Glu Arg Val Ser Phe Ser Cys Arg Ala Ser Gln Ser Ile Gly Thr Asn
20 25 30
Ile His Trp Tyr Gln Gln Arg Thr Asn Gly Ser Pro Arg Leu Leu Ile
35 40 45
Lys Tyr Ala Ser Glu Ser Ile Ser Gly Ile Pro Ser Arg Phe Ser Gly
50 55 60
Ser Gly Ser Gly Thr Asp Phe Thr Leu Ser Ile Asn Ser Val Glu Ser
65 70 75 80
Glu Asp Ile Ala Asp Tyr Tyr Cys Gln Gln Asn Asn Asn Trp Pro Thr
85 90 95
Thr Phe Gly Ala Gly Thr Lys Leu Glu Leu Lys
100 105
<210> 25
<211> 642
<212> DNA
<213> Artificial
<220>
<223> Cetuximab轻链的核苷酸序列
<400> 25
gacatcttgc tgactcagtc tccagtcatc ctgtctgtga gtccaggaga aagagtcagt 60
ttctcctgca gggccagtca gagtattggc acaaacatac actggtatca gcaaagaaca 120
aatggttctc caaggcttct cataaagtat gcttctgagt ctatctctgg gatcccttcc 180
aggtttagtg gcagtggatc agggacagat tttactctta gcatcaacag tgtggagtct 240
gaagatattg cagattatta ctgtcaacaa aataataact ggccaaccac gttcggtgct 300
gggaccaagc tggagctgaa acgtacggtg gctgcaccat ctgtcttcat cttcccgcca 360
tctgatgagc agttgaaatc tggaactgcc tctgttgtgt gcctgctgaa taacttctac 420
cccagagaag ccaaagtgca gtggaaggtg gacaacgccc tgcagagcgg aaacagccag 480
gaaagcgtga cagagcagga ttccaaggat tccacataca gcctgagcag cacactgaca 540
ctgtccaagg ccgactacga gaagcacaag gtgtacgcct gcgaagtgac acaccaggga 600
ctgtcctccc ctgtgacaaa gagcttcaac agaggagaat gc 642
<210> 26
<211> 214
<212> PRT
<213> Artificial
<220>
<223> Cetuximab轻链的氨基酸序列
<400> 26
Asp Ile Leu Leu Thr Gln Ser Pro Val Ile Leu Ser Val Ser Pro Gly
1 5 10 15
Glu Arg Val Ser Phe Ser Cys Arg Ala Ser Gln Ser Ile Gly Thr Asn
20 25 30
Ile His Trp Tyr Gln Gln Arg Thr Asn Gly Ser Pro Arg Leu Leu Ile
35 40 45
Lys Tyr Ala Ser Glu Ser Ile Ser Gly Ile Pro Ser Arg Phe Ser Gly
50 55 60
Ser Gly Ser Gly Thr Asp Phe Thr Leu Ser Ile Asn Ser Val Glu Ser
65 70 75 80
Glu Asp Ile Ala Asp Tyr Tyr Cys Gln Gln Asn Asn Asn Trp Pro Thr
85 90 95
Thr Phe Gly Ala Gly Thr Lys Leu Glu Leu Lys Arg Thr Val Ala Ala
100 105 110
Pro Ser Val Phe Ile Phe Pro Pro Ser Asp Glu Gln Leu Lys Ser Gly
115 120 125
Thr Ala Ser Val Val Cys Leu Leu Asn Asn Phe Tyr Pro Arg Glu Ala
130 135 140
Lys Val Gln Trp Lys Val Asp Asn Ala Leu Gln Ser Gly Asn Ser Gln
145 150 155 160
Glu Ser Val Thr Glu Gln Asp Ser Lys Asp Ser Thr Tyr Ser Leu Ser
165 170 175
Ser Thr Leu Thr Leu Ser Lys Ala Asp Tyr Glu Lys His Lys Val Tyr
180 185 190
Ala Cys Glu Val Thr His Gln Gly Leu Ser Ser Pro Val Thr Lys Ser
195 200 205
Phe Asn Arg Gly Glu Cys
210

Claims (7)

1.一种EGFR/PD-L1双靶向抗体,其特征在于所述抗体由下述氨基酸序列的四条肽链组成,分别为如SEQ ID NO : 20所示的RG7446HV-CL-Hinge-CH2-CH3、如SEQ ID NO : 22所示的RG7446LV-CH1、如SEQ ID NO :18所示的Cetuximab重链knob突变体和如SEQ ID NO :26所示的Cetuximab轻链。
2.一种分离的多核苷酸,其编码权利要求1所述的抗体,包括如下述核苷酸序列所示的多核苷酸:编码RG7446HV-CL-Hinge-CH2-CH3的如SEQ ID NO:19所示的多核苷酸,编码RG7446LV-CH1的如SEQ ID NO:21所示的多核苷酸,编码Cetuximab重链knob突变体的如SEQID NO :17所示的多核苷酸,和编码Cetuximab轻链的如SEQ ID NO:25所示的多核苷酸。
3.一种表达载体,其特征在于含有权利要求2所述的多核苷酸。
4.一种宿主细胞,其特征在于含有权利要求3所述的表达载体。
5.一种权利要求1所述的EGFR/PD- L1双靶向抗体的制备方法,包括:
1)分别克隆EGFR抗体Cetuximab可变区与PD-L1抗体RG7446可变区;
2)在抗体Fc区域分别构建knob突变体,以及hole突变体;
3)将PD-L1抗体RG7446轻链可变区与抗体重链CH1区融合构建RG7446LV-CH1融合片段;
4)将PD-L1抗体RG7446重链可变区与抗体轻链恒定区融合构建RG7446HV-CL融合片段;
5)将Cetuximab重链可变区与knob突变体融合,将RG7446HV-CL与hole突变体融合,装入表达载体;
6)将构建好的三个表达载体与装有Cetuximab轻链基因的表达载体共同转染进行表达,分离纯化;
所述抗体Fc区域knob突变体的突变方式为,第366位的Thr突变为Trp,第354位的Ser突变为Cys;所述抗体Fc区域hole突变体的突变方式为,第366位的Thr突变为Ser,第368位的Leu突变为Ala,第407位的Tyr突变为Val,第394位的Tyr突变为Cys。
6.一种药物组合物,含有权利要求1所述的EGFR/PD- L1双靶向抗体。
7.权利要求1所述双靶向抗体在制备治疗肺癌药物中的用途。
CN201710369198.4A 2017-05-23 2017-05-23 一种抗egfr/pd-l1双靶向抗体、其制备方法及用途 Active CN108948195B (zh)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN201710369198.4A CN108948195B (zh) 2017-05-23 2017-05-23 一种抗egfr/pd-l1双靶向抗体、其制备方法及用途

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN201710369198.4A CN108948195B (zh) 2017-05-23 2017-05-23 一种抗egfr/pd-l1双靶向抗体、其制备方法及用途

Publications (2)

Publication Number Publication Date
CN108948195A CN108948195A (zh) 2018-12-07
CN108948195B true CN108948195B (zh) 2022-05-31

Family

ID=64493663

Family Applications (1)

Application Number Title Priority Date Filing Date
CN201710369198.4A Active CN108948195B (zh) 2017-05-23 2017-05-23 一种抗egfr/pd-l1双靶向抗体、其制备方法及用途

Country Status (1)

Country Link
CN (1) CN108948195B (zh)

Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2014108854A1 (en) * 2013-01-09 2014-07-17 Fusimab Ltd. Monospecific anti-hgf and anti-ang2 antibodies and bispecific anti-hgf/anti-ang2 antibodies
CN104203981A (zh) * 2011-12-19 2014-12-10 合成免疫股份有限公司 双特异性抗体分子
CN104403004A (zh) * 2014-11-24 2015-03-11 苏州丁孚靶点生物技术有限公司 抗体-干扰素异二聚体的制备和用途
CN106659779A (zh) * 2014-12-22 2017-05-10 西雅图免疫公司 双特异性四价抗体及其制造和使用方法

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DK3186283T3 (da) * 2014-08-29 2020-03-02 Hoffmann La Roche Kombinationsbehandling med tumormålrettede IL-2- immuncytokinervarianter og antistoffer mod humant PD-L1

Patent Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN104203981A (zh) * 2011-12-19 2014-12-10 合成免疫股份有限公司 双特异性抗体分子
WO2014108854A1 (en) * 2013-01-09 2014-07-17 Fusimab Ltd. Monospecific anti-hgf and anti-ang2 antibodies and bispecific anti-hgf/anti-ang2 antibodies
CN104403004A (zh) * 2014-11-24 2015-03-11 苏州丁孚靶点生物技术有限公司 抗体-干扰素异二聚体的制备和用途
CN106659779A (zh) * 2014-12-22 2017-05-10 西雅图免疫公司 双特异性四价抗体及其制造和使用方法

Also Published As

Publication number Publication date
CN108948195A (zh) 2018-12-07

Similar Documents

Publication Publication Date Title
RU2744866C2 (ru) Антитело против lag-3
CN109715671B (zh) 双特异性抗her2抗体
KR102363008B1 (ko) 표적화된 TGFβ 억제
KR102182485B1 (ko) 단백질 약물의 불활성화를 위한 항체 로커
CN101312989B (zh) 用于治疗癌症的针对密蛋白-18的单克隆抗体
CN101628939B (zh) 治疗性人抗-il-1r1单克隆抗体
CN108503713A (zh) 新的免疫缀合物
CN111448323B (zh) 精确制导的多功能治疗抗体
CN101687929A (zh) 用于治疗癌症的抗密蛋白-18的单克隆抗体
CN110869392A (zh) 用抗gitr激动性抗体治疗癌症
CN111303293B (zh) 一种融合蛋白及其用途
KR20060126659A (ko) 키메라 항 cd44 항체 및 그 급성 골수성 백혈병 치료용용도
CN113493506A (zh) 新型冠状病毒抗体及其应用
KR20200109339A (ko) Tim3에 대한 항체를 사용하여 암을 치료하는 방법
CN113583137B (zh) 一种新型冠状病毒南非突变株的重组亚单位疫苗及其应用
CN109536476A (zh) 具备透明质酸酶活性的靶向融合蛋白、制备方法及用途
CN104447993A (zh) 一种高活性全人源抗her2单克隆抗体、其制备方法及用途
CN108948206B (zh) 一种抗egfr/pd-1双靶向抗体、其制备方法及用途
CN104558194B (zh) 一类抗CD20-Flex双功能融合蛋白、其制备方法及用途
CN108948195B (zh) 一种抗egfr/pd-l1双靶向抗体、其制备方法及用途
CN108752478B (zh) 全人源抗人EGFR和Notch2/3多特异性抗体、其制备方法及用途
CN104610453A (zh) 一类抗her2双靶向抗体、其制备方法及用途
CN112118858A (zh) 用于未经治疗对象中癌症治疗的靶向tgf-β抑制的给药方案
CN109280085B (zh) 一种异二聚体蛋白及其制备方法
CN104418952B (zh) 一种用于治疗乳腺癌的抗ErbB2双特异性抗体

Legal Events

Date Code Title Description
PB01 Publication
PB01 Publication
SE01 Entry into force of request for substantive examination
SE01 Entry into force of request for substantive examination
GR01 Patent grant
GR01 Patent grant
TR01 Transfer of patent right

Effective date of registration: 20220616

Address after: 100853 Fuxing Road 28, Beijing, Haidian District

Patentee after: CHINESE PLA GENERAL Hospital

Address before: No. 28 Fuxing Road, Haidian District, Beijing 100000

Patentee before: Hu Yi

TR01 Transfer of patent right