Influvac Tetra: Quadrivalent Influenza Vaccine Overview
Influvac Tetra is a quadrivalent inactivated subunit influenza vaccine approved for use in individuals ≥6 months of age, demonstrating robust immunogenicity with seroprotection rates >90% for influenza A strains and 43-60% for B strains, alongside an excellent safety profile with adverse events <1%. 1, 2
Vaccine Composition and Technology
- Influvac Tetra is an egg-based, inactivated subunit vaccine containing four influenza strains (two type A and two type B) representing viruses likely to circulate in the upcoming season 1, 3
- The vaccine contains highly purified, inactivated surface antigens (hemagglutinin and neuraminidase) without whole virus particles 4, 3
- Manufacturing involves growth in embryonated hens' eggs, resulting in small amounts of residual egg protein; package inserts should be consulted for specific manufacturing details including preservatives and antibiotics used 4
Approved Patient Populations
Children (≥6 months)
- Approved for all children ≥6 months of age 1, 5
- Children <9 years who are previously unvaccinated require two doses administered at least 1 month apart for adequate immune response 4, 5
- Previously vaccinated children require only a single annual dose 4
Adults (18-60 years)
- Single dose provides adequate protection in healthy adults 2
- Vaccine effectiveness in this age group ranges from 70-90% when vaccine strains match circulating viruses 4
Elderly (>60 years)
- Single dose recommended annually 2
- While elderly patients develop lower postvaccination antibody titers than younger adults, the vaccine remains highly effective at preventing severe outcomes 4
Efficacy Data by Population
Healthy Adults and Children
- When vaccine and circulating strains are well-matched, efficacy is 70-90% in preventing laboratory-confirmed influenza illness 4, 5
- Reduces work absenteeism and healthcare resource utilization 4, 6
- Decreases influenza-associated otitis media in young children by approximately 30% 4, 6
Elderly and High-Risk Populations
- Most critically, the vaccine reduces mortality by 68-80% in elderly persons, even when efficacy against influenza illness itself is only 30-40% 4
- Prevents hospitalization for pneumonia and influenza by 30-70% in community-dwelling elderly 4
- Among nursing home residents, reduces hospitalization/pneumonia by 50-60% and death by 80% 4
- In children, vaccine effectiveness against influenza-associated death is 65% overall and 51% in those with underlying conditions 6
Immunogenicity Profile (Influvac Tetra Specific)
- Seroprotection rates >90% for influenza A strains (H1N1 and H3N2) 2
- Seroprotection rates 43-60% for influenza B strains 2
- Geometric mean fold increase ranges from 4.3-22.7 across all four strains 2
- Comparable immunogenicity in both adult (18-60 years) and elderly (>61 years) age groups 2
Chronic Medical Conditions
Priority Groups Requiring Annual Vaccination
- Chronic pulmonary disease (including asthma) 4, 6
- Chronic cardiovascular disease 4, 6
- Diabetes mellitus and other chronic metabolic diseases 4
- Renal dysfunction 4
- Hemoglobinopathies 4
- Immunosuppression (medication-induced, HIV, or transplant recipients) 4, 6
- Children/teenagers on long-term aspirin therapy (risk of Reye syndrome) 4
Special Considerations
- Patients with chronic conditions may develop lower antibody titers but still receive substantial protection against severe complications, hospitalization, and death 4
- Only inactivated vaccines (like Influvac Tetra) should be used in patients with chronic pulmonary conditions—never live attenuated nasal spray vaccines 6
Safety Profile
Common Adverse Events
- Local soreness at injection site (most frequent), typically lasting up to 2 days, mild and non-disabling 4, 7
- Systemic symptoms (fever, malaise, myalgias) beginning 6-12 hours post-vaccination, lasting 1-2 days, occurring no more frequently than placebo 4, 7
- Overall adverse events <1% in clinical trials of Influvac Tetra 2
Rare Adverse Events
- Immediate allergic reactions in patients with egg hypersensitivity (rare) 4, 7
- Guillain-Barré syndrome was associated only with the 1976 swine influenza vaccine and has NOT been associated with influenza vaccines since then 4, 7
Critical Safety Context
- The vaccine does not contain live virus and cannot cause influenza infection 4, 7
- The favorable safety profile far outweighs risks, especially given the 45-68% mortality reduction in elderly adults 7
Administration Guidelines
Dosing Schedule
- Annual vaccination required due to antigenic drift and waning immunity 4, 6
- Optimal timing: September through mid-November before influenza season 4
- Do not delay vaccination waiting for "optimal timing"—the risk of missing vaccination entirely outweighs timing concerns 6
Route and Site
- Intramuscular injection is the recommended route 4
- Adults and older children: deltoid muscle 4
- Infants and young children: anterolateral aspect of thigh 4
Healthcare Worker and Household Contact Vaccination
- Vaccination of healthcare workers is associated with decreased deaths among nursing home patients 4
- All physicians, nurses, hospital personnel, nursing home employees, and household members of high-risk patients should be vaccinated 4
Common Pitfalls to Avoid
- Do not assume prior vaccination provides multi-year protection—annual vaccination is mandatory 6
- Do not delay vaccination in high-risk patients for any reason—when multiple appropriate products exist, any licensed vaccine is acceptable 6
- Do not use expired vaccine from previous seasons—vaccine composition changes annually to match circulating strains 4
- Do not overlook racial and ethnic disparities—Black, Hispanic, and American Indian/Alaska Native children have 3-4 fold higher influenza-associated in-hospital deaths 6
- Do not withhold vaccination due to fear of side effects—the vaccine cannot cause influenza and serious adverse events are exceedingly rare 4, 7