Study of acellular pertussis vaccine and its effect on whooping cough colonization in healthy adults using controlled human infection
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Poliovirus type 1 (inactivated) is one of three inactivated poliovirus strains used in inactivated poliovirus vaccines (IPV). The other two strains are poliovirus type 2 (inactivated) and poliovirus type 3 (inactivated).[2] Together, these three strains make up the IPV vaccine, which is a sterile suspension of highly purified, inactivated poliovirus with enhanced potency.[2] The type 1 strain is the Mahoney strain, grown in vero cells, a continuous line of monkey kidney cells cultivated on microcarriers.[2] In the UK dm+d browser, the ingredient is listed under the name "Human poliovirus type 1 inactivated".[3] The vaccine is classified as a vaccine and is used to stimulate active immunity to poliovirus.[4] In the EU clinical trials registry, the substance appears as part of the fixed-combination vaccine REVAXIS, which contains diphtheria toxoid, tetanus toxoid, and all three inactivated poliovirus types, and is authorised as a medicine in the Netherlands.[1]
Poliovirus type 1 (inactivated) works by stimulating the body's immune system to produce antibodies against poliovirus type 1. Because the virus is inactivated, it cannot cause polio, but it still triggers active immunity.[4] The IPV vaccine contains all three poliovirus types so that immunity is developed against each one.[4] The inactivation and purification process produces a vaccine that is more potent and consistent than earlier inactivated polio vaccines available in the US before 1988.[2] Comprehensive inactivated polio vaccine can also help prevent rare persistent cases of vaccine-derived poliovirus infection from seeding new outbreaks.[5]
Poliovirus type 1 (inactivated) is given as a suspension for injection.[1] In the EU registry, the product REVAXIS is a suspension for injection in a pre-filled syringe, with a 0.5 ml dose given by injection.[1] In the UK, the ingredient is available in several fixed-combination vaccines, including diphtheria, tetanus, and poliomyelitis (inactivated) vaccine as a suspension for injection in 0.5 ml pre-filled syringes.[3] In the US, IPV is available as a standalone vaccine and in fixed-combination vaccines containing diphtheria, tetanus, pertussis, and poliovirus antigens, among others.[4]
One completed phase 3 trial, the KIM-study, included poliovirus type 1 (inactivated) as part of the comparator vaccine. The trial enrolled 99 healthy adults and investigated whether booster vaccination with Tdap-IPV reduces Bordetella pertussis colonisation after intranasal challenge compared to a Td-IPV control group.[1] The primary outcome measured was the Bordetella pertussis colonisation rate in the vaccination groups, defined as any positive culture from nasal wash samples taken between day 3 and day 28 after challenge.[1] The role of the polio-containing vaccine in this trial was as a comparator, meaning it was used for comparison rather than being the main substance under investigation.[1]
The provided sources do not list specific side effects for poliovirus type 1 (inactivated) in the text available. The WHO report notes that vaccine-associated poliovirus infection is on a downswing, and that comprehensive inactivated polio vaccine can prevent rare persistent cases from seeding outbreaks.[5] The DailyMed label for IPOL describes the vaccine as a sterile suspension of highly purified, inactivated poliovirus, but the provided excerpt does not include a side effects section.[2]
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