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    • 3. 发明授权
    • Method of making non-pyrogenic lipopolysaccharide or A
    • 制备非致热性脂多糖或脂质A的方法
    • US5997881A
    • 1999-12-07
    • US802371
    • 1997-02-19
    • Robert J. PowellDavid M. Hone
    • Robert J. PowellDavid M. Hone
    • A61K48/00A61P31/04C12N15/74C12P19/04A61K39/02
    • C12R1/01A61K48/00C12N15/74C12P19/04
    • The present invention provides gram-negative bacterial strains that produce substantially pure non-pyrogenic lipopolysaccharide or lipid A. The present invention also relates to a use of said strains for the preparation of non-pyrogenic DNA and use of the same for introducing endogenous or foreign genes into animal cells or animal tissue. Further, the present invention relates to a use of said strains for the preparation of non-pyrogenic recombinant mammalian, protozoan and viral proteins. Furthermore, the present invention relates to a use of said strains for the preparation of non-pyrogenic bacterial vaccines and vaccine vectors. Yet a further use of the present invention relates to a use of said strains for the preparation of non-pyrogenic bacterial proteins and polysaccharide antigens for use as vaccines.
    • 本发明提供了产生基本上纯的非致热性脂多糖或脂质A的革兰氏阴性细菌菌株。本发明还涉及所述菌株用于制备非致热原DNA的用途,并且使用该菌株用于引入内源或外源 基因进入动物细胞或动物组织。 此外,本发明涉及所述菌株用于制备非致热性重组哺乳动物,原生动物和病毒蛋白质的用途。 此外,本发明涉及所述菌株用于制备非致热性细菌疫苗和疫苗载体的用途。 本发明的另一个用途涉及所述菌株用于制备用作疫苗的非致热性细菌蛋白质和多糖抗原的用途。
    • 5. 发明授权
    • Treatment and prevention of immunodeficiency virus infection by administration of non-pyrogenic derivatives of lipid A
    • 通过施用脂质A的非致热原衍生物来治疗和预防免疫缺陷病毒感染
    • US06596477B1
    • 2003-07-22
    • US09536668
    • 2000-03-27
    • David M. HoneRichard CrowleyGeorge Lewis
    • David M. HoneRichard CrowleyGeorge Lewis
    • C12Q170
    • A61K31/715A61K38/195A61K45/06Y02A50/473A61K2300/00
    • The present inventors have found that certain preparations containing LPS and/or lipid A variants, derivatives, and/or analogs demonstrate non-pyrogenic properties and exhibit anti-viral activities. In particular, non-pyrogenic preparations of LPS, lipid A, LPS antagonists and lipid A antagonists, and derivatives thereof induce &bgr; chemokine secretion, such as MIP-1&bgr;, but not proinflammatory cytokines, such as TNF&agr;, IL-1&bgr; and IL-6. Non-pyrogenic preparations of the invention have been demonstrated by the Applicant to suppress HIV replication in human peripheral blood monocytes, as described by way of example herein. The present invention provides preparations of LPS or lipid A variants, analogs and derivatives of decreased or absent pyrogenicity which can be used as therapeutics for the treatment or prevention of immunodeficiency virus infection and its consequences.
    • 本发明人已经发现含有LPS和/或脂质A变体,衍生物和/或类似物的某些制剂表现出非热原性质并表现出抗病毒活性。 特别地,LPS,脂质A,LPS拮抗剂和脂质A拮抗剂及其衍生物的非致热制剂诱导β趋化因子分泌,例如MIP-1β,但不引起促炎细胞因子,例如TNFα,IL-1β和IL-6 。 本发明的非热原制剂已经被申请人证实,以抑制人外周血单核细胞中的HIV复制,如本文实施例所述。 本发明提供可用作治疗或预防免疫缺陷病毒感染的治疗剂及其后果的LPS或脂质A变体,类似物和降低或不存在致热原性的衍生物的制剂。
    • 6. 发明授权
    • Non-pyrogenic bacterial strains and use of the same
    • 非热原菌菌株和使用相同
    • US06548287B1
    • 2003-04-15
    • US09339180
    • 1999-06-24
    • Robert J. PowellDavid M. Hone
    • Robert J. PowellDavid M. Hone
    • A61K3910
    • C12R1/01A61K48/00C12N15/74C12P19/04
    • The present invention provides gram-negative bacterial strains that produce substantially pure non-pyrogenic lipopolysaccharide or lipid A. The present invention also relates to a use of said strains for the preparation of non-pyrogenic DNA and use of the same for introducing endogenous or foreign genes into animal cells or animal tissue. Further, the present invention relates to a use of said strains for the preparation of non-pyrogenic recombinant mammalian, protozoan and viral proteins. Furthermore, the present invention relates to a use of said strains for the preparation of non-pyrogenic bacterial vaccines and vaccine vectors. Yet a further use of the present invention relates to a use of said strains for the preparation of non-pyrogenic bacterial proteins and polysaccharides antigens for use as vaccines.
    • 本发明提供了产生基本上纯的非致热性脂多糖或脂质A的革兰氏阴性细菌菌株。本发明还涉及所述菌株用于制备非致热原DNA的用途,并且使用该菌株用于引入内源或外源 基因进入动物细胞或动物组织。 此外,本发明涉及所述菌株用于制备非致热性重组哺乳动物,原生动物和病毒蛋白质的用途。 此外,本发明涉及所述菌株用于制备非致热性细菌疫苗和疫苗载体的用途。 本发明的进一步应用涉及所述菌株用于制备用作疫苗的非致热性细菌蛋白质和多糖抗原的用途。
    • 8. 发明授权
    • Treatment and prevention of immunodeficiency virus infection by administration of non-pyrogenic derivatives of lipid A
    • 通过施用脂质A的非致热原衍生物来治疗和预防免疫缺陷病毒感染
    • US06841345B1
    • 2005-01-11
    • US09383709
    • 1999-08-26
    • David M. HoneRichard CrowleyGeorge Lewis
    • David M. HoneRichard CrowleyGeorge Lewis
    • A61K39/02A61K45/06C12Q1/70
    • A61K31/7024A61K39/02A61K45/06Y02A50/478
    • The present inventors have found that certain preparations containing LPS and/or lipid A variants, derivatives, and/or analogs demonstrate non-pyrogenic properties and exhibit anti-viral activities. In particular, non-pyrogenic preparations of LPS, lipid A, LPS antagonists and lipid A antagonists, and derivatives thereof induce β chemokine secretion, such as MIP-1β, but not proinflammatory cytokines, such as TNFα, IL-1β and IL-6. Non-pyrogenic preparations of the invention have been demonstrated by the Applicant to suppress HIV replication in human peripheral blood monocytes, as described by way of example herein. The present invention provides preparations of LPS or lipid A variants, analogs and derivatives of decreased or absent pyrogenicity which can be used as therapeutics for the treatment or prevention of immunodeficiency virus infection and its consequences.
    • 本发明人已经发现含有LPS和/或脂质A变体,衍生物和/或类似物的某些制剂表现出非热原性质并表现出抗病毒活性。 特别地,LPS,脂质A,LPS拮抗剂和脂质A拮抗剂及其衍生物的非致热制剂诱导β趋化因子分泌,例如MIP-1β,但不引起促炎细胞因子,例如TNFα,IL-1β和IL-6 。 本发明的非热原制剂已经被申请人证实,以抑制人外周血单核细胞中的HIV复制,如本文实施例所述。 本发明提供可用作治疗或预防免疫缺陷病毒感染的治疗剂及其后果的LPS或脂质A变体,类似物和降低或不存在致热原性的衍生物的制剂。
    • 10. 发明授权
    • Non-pyrogenic derivatives of lipid A
    • 脂质A的非致热原衍生物
    • US06368604B1
    • 2002-04-09
    • US08938106
    • 1997-09-26
    • David M. HoneRichard CrowleyGeorge Lewis
    • David M. HoneRichard CrowleyGeorge Lewis
    • A61K3902
    • A61K31/7024A61K39/02A61K45/06Y02A50/478
    • The present inventors have found that certain preparations containing LPS and/or lipid A variants, derivatives, and/or analogs demonstrate non-pyrogenic properties and exhibit anti-viral activities. In particular, non-pyrogenic preparations of LPS, lipid A, LPS antagonists and lipid A antagonists, and derivatives thereof induce &bgr; chemokine secretion, such as MIP-1&bgr;, but not proinflammatory cytokines, such as TNF&agr;, IL-1&bgr; and IL-6. Non-pyrogenic preparations of the invention have been demonstrated by the Applicant to suppress HIV replication in human peripheral blood monocytes, as described by way of example herein. The present invention provides preparations of LPS or lipid A variants, analogs and derivatives of decreased or absent pyrogenicity which can be used as therapeutics for the treatment or prevention of immunodeficiency virus infection and its consequences.
    • 本发明人已经发现,含有LPS和/或脂质A变体,衍生物和/或类似物的某些制剂表现出非热原性质并表现出抗病毒活性。 特别地,LPS,脂质A,LPS拮抗剂和脂质A拮抗剂及其衍生物的非致热制剂诱导β趋化因子分泌,例如MIP-1β,但不引起促炎细胞因子,例如TNFα,IL-1β和IL-6 。 本发明的非热原制剂已经被申请人证实,以抑制人外周血单核细胞中的HIV复制,如本文实施例所述。 本发明提供可用作治疗或预防免疫缺陷病毒感染的治疗剂及其后果的LPS或脂质A变体,类似物和降低或不存在致热原性的衍生物的制剂。