COMBINED MUCOSAL AND PARENTERAL IMMUNIZATION AGAINST HIV
    86.
    发明申请
    COMBINED MUCOSAL AND PARENTERAL IMMUNIZATION AGAINST HIV 审中-公开
    组合肌肉和抗艾滋病毒的家属免疫

    公开(公告)号:US20100285062A1

    公开(公告)日:2010-11-11

    申请号:US12225653

    申请日:2007-03-29

    IPC分类号: A61K39/21 A61P31/18

    摘要: HIV antigens are mucosally administered in one or more priming immunization(s), and then HIV antigens are parenterally administered in one or more boosting immunization(s). Thus the invention provides a method for raising an immune response in a patient, comprising: (i) administering a HIV antigen to the patient via a mucosal route; and then (ii) administering a HIV antigen to the patient via a parenteral route. The antigens will typically be adjuvanted. Preferred mucosal immunizations are via the intranasal route using a detoxified mutant of E. coli heat labile toxin as the adjuvant. Preferred parenteral immunizations are via the intramuscular route using an oil-in-water emulsion adjuvant.

    摘要翻译: HIV抗原在一次或多次引发免疫中粘膜施用,然后HIV抗原在一次或多次加强免疫中肠胃外给药。 因此,本发明提供了一种提高患者免疫应答的方法,包括:(i)通过粘膜途径向患者施用HIV抗原; 然后(ii)通过胃肠外途径向患者施用HIV抗原。 抗原通常将被佐剂化。 优选的粘膜免疫是通过使用大肠杆菌热不稳定毒素的解毒突变体作为佐剂的鼻内途径。 优选的肠胃外免疫是通过肌内途径使用水包油乳剂佐剂。

    BLOCKING INTERACTION BETWEEN PATHOGEN FACTORS AND FACTOR H TO INHIBIT HEMORRHAGIC SYNDROMES
    87.
    发明申请
    BLOCKING INTERACTION BETWEEN PATHOGEN FACTORS AND FACTOR H TO INHIBIT HEMORRHAGIC SYNDROMES 审中-公开
    致病因素与因子H之间的阻断相互作用以抑制HEMORRHAGIC综合征

    公开(公告)号:US20100150912A1

    公开(公告)日:2010-06-17

    申请号:US12450697

    申请日:2008-04-11

    申请人: Rino Rappuoli

    发明人: Rino Rappuoli

    摘要: If pathogen factors such as meningococcal NMB 1870 or flaviviral NS1 are able to sequester factor H in the blood then its inhibitory effect on complement may be disturbed, thereby permitting C3 to initiate a dramatic attack on host endothelial tissue. In combination with a strong inflammatory response, this attack can result in sever damage to the endothelium, with resulting hemorrhagic syndrome. Blocking the interaction between pathogen factors and factor H may thus be used to treat and/or prevent these pathogen-induced hemorrhagic syndromes. The interaction may, for instance, be blocked by antibodies, either delivered endogenously (passive immunisation) or produced by a patient's immune system (active immunisation).

    摘要翻译: 如果病原体因子如脑膜炎球菌NMB1870或黄病毒NS1能够在血液中螯合因子H,则其对补体的抑制作用可能受到干扰,从而允许C3引发对宿主内皮组织的剧烈攻击。 结合强烈的炎症反应,这种攻击可能导致对内皮的严重损伤,导致出血综合征。 因此,阻断病原体因子和因子H之间的相互作用因此可用于治疗和/或预防这些病原体诱导的出血综合征。 例如,相互作用可被抗体阻断,内源性递送(被动免疫)或由患者的免疫系统产生(主动免疫)。

    85kDa neisserial antigen
    90.
    发明授权
    85kDa neisserial antigen 失效
    85kDa neisserial抗原

    公开(公告)号:US07700119B2

    公开(公告)日:2010-04-20

    申请号:US11264676

    申请日:2005-11-01

    摘要: An 85 kDa antigen from Neisseria meningitidis and Neisseria gonorrhoeae has been cloned, sequenced and expressed. The antigen is common to diverse strains, serogroups and serotypes of N. meningitidis, and also to N. gonorrhoeae, N. polysaccharia and N. lactamica. The protein sequences of N. meningitidis (serogroups A and B) and N. gonorrhoeae are highly homologous.

    摘要翻译: 来自脑膜炎奈瑟氏球菌和淋病奈瑟氏球菌的85kDa抗原已被克隆,测序和表达。 该抗原对于脑膜炎奈瑟氏球菌的不同菌株,血清型和血清型以及淋病奈瑟氏球菌,多糖和内酰胺酶是常见的。 脑膜炎奈瑟氏球菌(血清群A和B)和淋病奈瑟氏球菌的蛋白质序列高度同源。