INFECTIOUS DNA VACCINES AGAINST CHIKUNGUNYA VIRUS
    5.
    发明申请
    INFECTIOUS DNA VACCINES AGAINST CHIKUNGUNYA VIRUS 审中-公开
    感染性DNA疫苗对CHIKUNGUNYA病毒

    公开(公告)号:WO2011082388A2

    公开(公告)日:2011-07-07

    申请号:PCT/US2011000001

    申请日:2011-01-03

    Abstract: Described herein are i-DNATM vectors and vaccines and methods for using the same. The i-DNATM generates live attenuated vaccines in eukaryotic cells in vitro or in vivo for pathogenic RNA viruses, particularly chikungunya virus (CHIKV). When iDNA is injected into the vaccine recipient, RNA of live attenuated virus is generated by in vivo transcription in the recipient's tissues. This initiates production of progeny attenuated viruses in the tissues of the vaccine recipient, as well as elicitation of an effective immune response protecting against wild-type, non-attenuated virus.

    Abstract translation: 本文描述了i-DNATM载体和疫苗以及使用它们的方法。 i-DNATM在体外或体内真核细胞中产生致病RNA病毒特别是基孔肯雅病毒(CHIKV)的减毒活疫苗。 当iDNA被注射到疫苗接受者体内时,活的减毒病毒的RNA通过在受体组织中的体内转录产生。 这启动了疫苗接受者组织中子代减毒病毒的产生,以及引发针对野生型非减毒病毒的有效免疫应答。

    EXPRESSION VECTOR ENCODING ALPHAVIRUS REPLICASE AND THE USE THEREOF AS IMMUNOLOGICAL ADJUVANT
    6.
    发明申请
    EXPRESSION VECTOR ENCODING ALPHAVIRUS REPLICASE AND THE USE THEREOF AS IMMUNOLOGICAL ADJUVANT 审中-公开
    表达载体编码ALPHAVIRUS REPLICASE及其作为免疫调节剂的用途

    公开(公告)号:WO2009141434A4

    公开(公告)日:2010-01-14

    申请号:PCT/EP2009056240

    申请日:2009-05-22

    Abstract: The present invention relates to an alphaviral replicase, especially Semliki Forest Virus replicase, or an expression vector encoding an alphaviral replicase, said alphaviral replicase comprising RNA dependent RNA polymerase activity, for use as an immune system modulating adjuvant. The alphaviral replicase may be used in the combination with a vaccine providing an adjuvant function therein, which when present therein will generate an additional boost to the immune response in the subject to whom this combination is administered as compared to when the vaccine alone is administered to a subject in need thereof. The aim of the present invention is to provide an efficient and easy to administer, species-independent adjuvant which will provide advantages to the adjuvants used together with vaccines today.

    Abstract translation: 本发明涉及甲病毒复制酶,特别是塞米利奇森林病毒复制酶,或编码甲病毒复制酶的表达载体,所述甲病毒复制酶包含RNA依赖性RNA聚合酶活性,用作免疫系统调节佐剂。 甲病毒复制酶可以与提供其中的佐剂功能的疫苗组合使用,当其中存在时,其将在给予该组合的受试者中产生额外的促进作用,与将单独的疫苗施用于 有需要的科目。 本发明的目的是提供一种有效和易于施用的与物种无关的佐剂,其将为今天与疫苗一起使用的佐剂提供优点。

    A VACCINE FOR CHIKUNGUNYA VIRUS INFECTION
    7.
    发明申请
    A VACCINE FOR CHIKUNGUNYA VIRUS INFECTION 审中-公开
    针对CHIKUNGUNYA病毒感染的疫苗

    公开(公告)号:WO2008026225A3

    公开(公告)日:2008-09-25

    申请号:PCT/IN2007000383

    申请日:2007-08-31

    Abstract: The present invention relates to vaccine formulation capable of eliciting protective immune response against Chikungunya virus infection in humans and other mammalian hosts. The immunogenic formulation comprises purified inactivated Chikungunya virus in a stable formulation. Methods of propagation and purification of the virus are discussed. The inactivated virus formulation is non-infectious, immunogenic and elicits protective immune response in mammalian host. The immunogenic composition is formulated for in vivo administration to humans. The invention also discusses the strategy of developing a subunit vaccine using the recombinant viral proteins as antigens for immunization. The recombinant virus antigens that are potentially immunogenic can be used in diagnosing for the presence of the virus.

    Abstract translation: 本发明涉及能够在人和其他哺乳动物宿主中引发针对基孔肯雅病毒感染的保护性免疫应答的疫苗制剂。 免疫原性制剂包含稳定制剂中的纯化的灭活基孔肯雅病毒。 讨论了病毒繁殖和纯化的方法。 灭活的病毒制剂是非感染性的,免疫原性的并在哺乳动物宿主中引起保护性免疫应答。 配制免疫原性组合物用于体内施用给人。 本发明还讨论了使用重组病毒蛋白作为免疫抗原开发亚单位疫苗的策略。 具有潜在免疫原性的重组病毒抗原可用于诊断病毒的存在。

    DEFECTIVE SINDBIS VIRAL VECTORS
    8.
    发明申请
    DEFECTIVE SINDBIS VIRAL VECTORS 审中-公开
    有缺陷的SINDBIS VIRAL VECTORS

    公开(公告)号:WO2006105279A2

    公开(公告)日:2006-10-05

    申请号:PCT/US2006011617

    申请日:2006-03-29

    Abstract: Disclosed herein are new defective Sindbis viral vectors made from wild type Ar-339 Sindbis virus, with differences in replicase and envelope proteins between JT vectors and consensus Sindbis virus sequences, and also between JT and Ar-339 vectors. Also disclosed are plasmids used for the production of the vectors, methods for producing the vectors, methods for treating mammals suffering from tumors and pharmaceutical formulations for use in the treatment methods.

    Abstract translation: 本文公开了由野生型Ar-339辛德毕斯病毒制备的新的有缺陷的辛德比斯病毒载体,其在JT载体和共有的辛德比斯病毒序列之间以及JT和Ar-339载体之间具有复制酶和包膜蛋白的差异。 还公开了用于生产载体的质粒,用于生产载体的方法,用于治疗患有肿瘤的哺乳动物的方法和用于治疗方法的药物制剂。

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