摘要:
An antipoliomyelitis vaccine is prepared by inactivating the poliomyelitis virus by treatment with hydroxylamine in a concentration of 0.01 to 5.0 mols/litre and (a) a pH of 4.5 to 7.0 and preferably 6.0 and temperature of 4 DEG to 40 DEG C. or (b) a pH of 6.5 to 7.0 and preferably 7.0 and a temperature of 30 DEG to 40 DEG C. and preferably 37 DEG C., allowing the hydroxylamine to act on the viruses, which may be contaminated with Simian virus 40, until the latter is free from infectious viruses, binding unreacted hydroxylamine with a carbonyl compound capable of forming an oxime therewith, and processing the inactivated virus into a vaccine in known manner. Prior to the inactivation step, the virus suspension may be concentrated. The oxime, if soluble, may be removed by dialysis and, if insoluble, it may be removed by filtration or centrifugal action. Specified carbonyl compounds are acetone, acetylacetone, acetonyl acetone, acetoacetic acid ethyl ester or acetoacetic acid methyl ester. Preferably 1-10 times the stoichiometrical amount of carbonyl compound, calculated on the hydroxylamine used, may be used for binding unreacted hydroxylamine. Conventional adjuvants for increasing antibody formation, e.g. aluminium hydroxide or phosphate, may be present.
摘要:
The present invention concerns a method for inactivating a virus for use in e.g. a vaccine, by treating the virus with an ethyleneimine at a pH of less than 7.0, and methods of treatment with the inactivated virus.
摘要:
The present invention is directed to improved methods of Enterovirus inactivation by formaldehyde in presence of tromethamine buffer resulting in maximum recovery of D-antigen. Subsequent adsorption of said sIPV on aluminium hydroxide provides significantly dose reduced sIPV compositions.
摘要:
The present invention provides a method for inactivating viruses, by contacting the viruses with a haloperoxidase, hydrogen peroxide, chloride ions, bromide ions, and ammonium ions.
摘要:
Method for inactivating non-enveloped viruses using a viricide-potentiating agent. In a preferred embodiment, the method may be used to inactivate non-enveloped viruses present within a sample of whole blood or a blood product and comprises (a) adding to the blood sample a photoactivatable viricide, such as a psoralen, hypericin, methylene blue, toluidine blue or the like, which, when activated, is effective in inactivating enveloped viruses; (b) adding to the blood sample a viricide-potentiating chemical agent that increases the sensitivity of non-enveloped viruses to the activated viricide; and (c) activating the photoactivatable viricide. Preferably, the viricide-potentiating chemical agent includes a first moiety which possesses an affinity for a component of the non-enveloped virus and a second moiety which includes a lipid tail, the first and second moieties being structurally interrelated so that, when the first moiety becomes associated with a component of the non-enveloped virus, the second moiety penetrates or at least partially surrounds the viral capsid of the non-enveloped virus. Examples of the chemical agent include cationic lipopolyamines, such as dioctadecylamidoglycylspermine.
摘要:
The present disclosure provides methods of inhibiting viral activity in a cell, the methods generally involving contacting the cell with a soluble CD137 polypeptide or a FAM3C polypeptide. The present disclosure provides methods for treating a virus infection in an individual, the methods generally involving administering to the individual an effective amount of a soluble CD137 polypeptide or a FAM3C polypeptide.