Protective Efficacy of DTaP Vaccine by Dose
The DTaP vaccine provides varying levels of protection with each dose, with a 3-dose primary series offering 79-89% efficacy against pertussis disease, while the full 5-dose series provides 88.7% overall effectiveness with protection peaking at 98.1% in the first year after the fifth dose. 1
Pertussis Protection by Dose
- A 3-dose primary series of DTaP administered at ages 2,4, and 6 months provides vaccine efficacy estimates ranging from 79% to 89% against culture-confirmed pertussis disease, with protection lasting up to 2 years after the third dose 1
- The complete 5-dose DTaP series has an estimated overall effectiveness of 88.7% (95% CI = 79.4%–93.8%) against pertussis 1
- Within the first year after receiving the fifth DTaP dose, vaccine effectiveness reaches its peak at 98.1% (95% CI = 96.1%–99.1%) 1
- Protection wanes over time, with effectiveness declining to approximately 71.2% (95% CI = 45.8%–84.8%) by ≥5 years after the fifth dose 1
- For every additional year after the last dose of DTaP, the odds of pertussis increase by 1.33 times (95% CI: 1.23-1.43) 2
- Assuming 85% vaccine efficacy initially, only about 10% of children vaccinated with DTaP would remain immune to pertussis 8.5 years after the last dose 2
Diphtheria Protection by Dose
- After receiving 3 doses of diphtheria toxoid-containing vaccines, virtually all infants develop protective diphtheria antitoxin titers >0.01 IU/mL 1
- A diphtheria antitoxin level of 0.01 to 0.09 IU/mL provides some degree of protection, whereas levels ≥0.1 IU/mL are considered fully protective 1
- Levels >1.0 IU/mL are associated with long-lasting protection against diphtheria 1
- After the primary vaccination series, protection lasts for approximately 3-5 years, requiring booster doses to maintain immunity 1
- The booster dose at age 4-6 years is crucial for maintaining protection throughout school-age years 1
Tetanus Protection by Dose
- One dose of tetanus toxoid vaccine provides little to no immunity 1
- After receiving 3 doses of tetanus toxoid-containing vaccine, virtually all infants and adults develop protective tetanus antitoxin titers >0.1 IU/mL 1
- A primary immunization series with 3 doses of tetanus toxoid induces a mean antitetanus level of 0.2 IU/mL, providing protection from tetanus for approximately 3-5 years 1
- Additional booster doses significantly heighten the immune response and prolong the duration of protective immunity 1
- Booster doses at age 4-8 years and during adolescence provide long-lasting protective immunity with protection lasting 20-30 years from the last dose 1
- Complete primary vaccination with tetanus toxoid provides protection for at least 10 years in most recipients 3
Immune Response to Individual Doses
- Immune responses following the first and second doses of DTaP have not been extensively measured in clinical studies 1
- After 4 doses of Daptacel (Sanofi Pasteur), 98.5% of children achieve diphtheria antitoxin levels of ≥1.0 IU/mL, and 100% achieve tetanus antitoxin levels of ≥1.0 IU/mL 1
- The fifth dose at age 4-6 years is expected to produce a robust immune response in children previously primed with the same vaccine 1
- Administration of DTaP at birth has been shown to be safe but results in significantly lower immune responses to diphtheria and pertussis antigens compared to the standard schedule 4
Clinical Implications and Considerations
- The waning immunity observed with DTaP vaccines may necessitate earlier booster vaccination and repeated boosting strategies to achieve necessary "herd effects" to control the spread of pertussis 2
- School-entry (ages 4-7) provides an ideal opportunity to implement DTaP booster vaccination to address the gap between waning immunity from infant/toddler vaccination and future adolescent vaccination 5
- Multiple studies support the findings of a progressive decrease in DTaP vaccine effectiveness and increased risk for pertussis over time after receipt of the fifth dose 1
- The safety profile of DTaP vaccines is well-established, with significantly fewer adverse events compared to whole-cell pertussis vaccines 1