Non-live trivalent influenza vaccine for one-dose intradermal delivery
The invention relates to the use of a trivalent, non-live influenza antigen preparation, particularly a split influenza preparation, in the manufacture of a one-dose influenza vaccine for intradermal delivery. In particular, the invention relates to the use of split influenza preparations wherein the vaccine comprises at least one non-ionic surfactant selected from the group consisting of the octyl-or nonylphenoxy polyoxyethanols (for example the commercially available Triton™ series), polyoxyethylene sorbitan esters (Tween™ series) and polyoxyethylene ethers or esters of general formula (I): HO(CH 2 CH 2 O) n -A-R, wherein n is 1-50, A is a bond or —C(O)—, R is C 1-50 alkyl or phenyl C 1-50 alkyl; and combinations of two or more of these.
1. A method for inducing a protective immune response in a human population of at least 18 years old comprising administering intradermally a single dose of a trivalent, split or subunit influenza vaccine antigen preparation using a short needle device, wherein the single dose results in said protective immune response meeting at least one criterion chosen from the group of: (1) a protection rate of >70% in adults of 18-60 years old or of >60% in elderly people of above 60 years old; (2) a seroconversion rate of >40% in adults of 18-60 years old or of >30% in elderly people of above 60 years old; and (3) a conversion factor of >2.5 HI titres in adults of 18-60 years old or of >2.0 HI titres in elderly people of above 60 years old, for each influenza strain.
2. The method according to claim 1 , wherein the influenza antigen is egg-derived.
3. The method according to claim 1 , wherein the vaccine comprises at least one non-ionic surfactant selected from the group consisting of an octyl-or nonylphenoxy polyoxyethanol, polyoxyethylene sorbitan ester and a polyoxyethylene ether or ester of general formula (I): HO(CH 2 CH 2 O) n -A-R (I) wherein n is 1-50, A is a bond or —C(O)—, R is C 1-50 alkyl or phenyl C 1-50 alkyl.
4. The method according to claim 3 , wherein the vaccine comprises a combination of polyoxyethylene sorbitan monooleate (Tween 80) and t-octylphenoxy polyethoxyethanol (Triton X-100).
5. The method according to claim 1 , wherein the vaccine further comprises a bile acid or cholic acid, or derivative thereof.
6. The method according to claim 1 , wherein the vaccine is provided in a dose volume of between about 0.1 and about 0.2 ml.
7. The method according claim 1 , wherein the vaccine further comprises an adjuvant comprising a combination of cholesterol, a saponin and an LPS derivative.
8. The method according to claim 1 , wherein said influenza vaccine antigen preparation is obtained by a process comprising: (i) harvesting virus-containing material from a culture; (ii) clarifying the harvested material to remove non-virus material; (iii) concentrating the harvested virus; (iv) separating whole virus from non-virus material; (v) splitting the whole virus using a suitable splitting agent in a density gradient centrifugation step; and (vi) filtering the product of step (v) to remove undesired materials.
9. A method for inducing a protective immune response in a human population of at least 18 years old comprising administering intradermally a single dose of a trivalent, split or subunit influenza vaccine antigen preparation using a short needle device, wherein said protective immune response meets at least two criteria chosen from the group of: (1) a protection rate of >70% in adults of 18-60 years old or of >60% in elderly people of above 60 years old; (2) a seroconversion rate of >40% in adults of 18-60 years old or of >30% in elderly people of above 60 years old; and (3) a conversion factor of >2.5 HI titres in adults of 18-60 years old or of >2.0 HI titres in elderly people of above 60 years old, for each influenza strain.
10. A method for inducing a protective immune response in a human population of at least 18 years old comprising administering intradermally a single dose of a trivalent, split or subunit influenza vaccine antigen preparation using a short needle device, wherein said protective immune response meets all criteria chosen from the group: (1) a protection rate of >70% in adults of 18-60 years old or of >60% in elderly people of above 60 years old; (2) a seroconversion rate of >40% in adults of 18-60 years old or of >30% in elderly people of above 60 years old; and (3) a conversion factor of >2.5 HI titres in adults of 18-60 years old or of >2.0 HI titres in elderly people of above 60 years old, for each influenza strain.
11. The method according to claim 5 , wherein the cholic acid derivative is sodium deoxycholate.
12. The method according to claim 1 , wherein the influenza vaccine antigen preparation comprises two A strains and one B strain.