Volume 13, Number 5—May 2007
Inactivated Whole Virus Influenza A (H5N1) Vaccine1
To the Editor: Avian influenza viruses of the H5N1 subtype represent a potential source of the next pandemic (1,2). Our goal was to determine the safety and immunogenicity of a newly developed vaccine in humans.
The vaccine was produced by the same method as the interpandemic influenza vaccine “FluvalAB” used in Hungary for the past 11 years (3,4). The method has been validated by meeting the requirements of the European Agency for the Evaluation of Medicinal Products (EMEA) related to interpandemic influenza vaccines each year since 1995, and by having been administered in humans in a total of >15 million cases (5).
The virus strain (NIBRG-14), a reverse genetics–derived 2:6 reassortant between A/Viet Nam/1194/2004 (H5N1) and PR8, was obtained from the National Institute for Biologic Standards and Control, London. It is one of the reference viruses indicated as suitable for use in a mock-up vaccine by the Committee for Medicinal Products for Human Use (6).
Hens’ egg–grown, formaldehyde-inactivated, whole virus vaccine, developed and produced by the Omninvest Ltd. (Budapest, Hungary), was used. The vaccine contained 6 μg hemagglutinin per dose (as determined by single radial immundiffusion test) in 0.5-mL ampules. Purity was assessed by endotoxin content (determined by chromogenic endotoxin assay, using a modified limulus amoebocyte lysate and a synthetic color-producing substrate), which was considered acceptable in concentrations <0.1 IU/mL. The amount of ovalbumin was determined by ELISA, which was considered satisfactory in concentrations <10 ng/mL. Aluminum phosphate was used as adjuvant, in the amount of 0.31 mg Al per ampule; 0.1 mg/mL merthiolate was added as preservative.
A total of 146 healthy volunteers >18 years of age (mean ± SD 42.07 ± 12.62 years). were enrolled in the study. Sixty-five male and 81 female volunteers participated. The sample size was chosen to exceed the requirement of 50 patients per group set by the European guidelines for yearly influenza vaccine trials (5). The sponsor was the National Public Health and Medical Officer Service, Budapest, Hungary.
The injection administered 0.5 mL of vaccine intramuscularly. The injection was not repeated. Serum antibody titers were measured by hemagglutination inhibition (HI) by using chicken erythrocytes, following standard procedures (7). Because the protective titer for influenza virus A (H5N1) infections is unknown, immunogenicity was assessed according to the European Medicines Agency criteria related to interpandemic influenza vaccines (Table) (5).
None of the study participants displayed measurable levels of HI antibodies before vaccination. According to EMEA requirements, both male and female groups met 2 independent criteria for immunogenicity 21 and 90 days after vaccination (Table).
In 15.7% of the participants, adverse reactions in the form of local pain at the injection site occurred within the first 48 hours; these reactions disappeared within 1 day. No other local reactions, such as injection site induration, erythema, swelling, warmth, or ecchymosis, were noted. No systemic reaction (fever, malaise, headache, shivering) was detected. No serious adverse events were observed. These results are in line with the 11-year experience using the interpandemic vaccine produced by Omninvest Ltd. by the same method, where a similar safety profile has been seen after >15 million vaccinations in humans.
This is the first study that reports that an inactivated whole virus vaccine with an aluminum phosphate adjuvant system against influenza A (H5N1) was safe and immunogenic in humans after only 1 injection. This study reports the lowest effective dose used to cause immune response. Other trials used much higher maximum doses and required 2 injections 21 or 28 days apart (8–10). Using the lowest possible amount of the antigen and fewer injections is essential for increasing the production capacity of vaccine manufacturers in a pandemic (2).
Using 1, instead of 2, injections will shorten the time needed to develop immune response by 3–4 weeks. Unlike previous studies on influenza A (H5N1) vaccines that reported only data from 21, 28, or 56 days after the final vaccination (8–10), we report data up to 90 days. The lower dose and fewer injections required to trigger an immune response can be at least partially explained by using a whole virus vaccine and an aluminum phosphate adjuvant system. The use of a different adjuvant system than ours may have influenced the results of other trials (9,10). Other investigators used a modified HI method with horse erythrocytes, which are known to be more sensitive for influenza A (H5N1) subtype than the conventionally used turkey or chicken erythrocytes (8,9). Thus, if horse erythrocytes had been used in our study, the vaccine would likely have been even more immunogenic.
This study found fewer, less frequent, and milder side effects than did other trials of influenza A (H5N1) vaccines published so far (8–10). This could possibly be explained by the smaller dose used. Also, the endotoxin content of 0.1 IU/mL in our vaccine was much smaller then the allowed amount of 100 IU/mL by standards (5).
We report an inactivated whole virus vaccine that is safe and immunogenic in healthy adults and that requires a low dose and only 1 injection to trigger an immune response. We are conducting trials in elderly persons and children.
We thank John Wood for supplying the virus strain.
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TableCite This Article
1The study design has been presented as an oral presentation at the World Health Organization Meeting on Evaluation of Pandemic Influenza Vaccines in Clinical Trials, May 4–5, 2006, Geneva, Switzerland.
Table of Contents – Volume 13, Number 5—May 2007
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Zoltan Vajo, Martonhegyi ut 6, Budapest, 1121, Hungary;