Diphtheria Toxoid
: Characteristics,
Immunogenicity and Vaccine Efficacy with Vaccination Schedule
Characteristics
Beginning in the early 1900s, prophylaxis was attempted with
toxin–antitoxin mixtures. Toxoid was developed around 1921 but was not
widely used until the early 1930s. It was incorporated with tetanus toxoid
and pertussis vaccine and became routinely used in the 1940s.
Diphtheria toxoid is produced by growing toxigenic C. diphtheriae
in liquid medium. The filtrate is incubated with formaldehyde to convert
toxin to toxoid and is then adsorbed onto an aluminum salt.
Single-antigen diphtheria toxoid is not available. Diphtheria toxoid is
combined with tetanus toxoid as pediatric diphtheria-tetanus toxoid (DT) or
adult tetanus-diphtheria (Td), and with both tetanus toxoid and acellular
pertussis vaccine as DTaP and Tdap. Diphtheria toxoid is also available as
combined DTaP-HepB-IPV (Pediarix) and DTaP-IPV/Hib (Pentacel)—see Pertussis
chapter for more information. Pediatric formulations (DT and DTaP) contain
a similar amount of tetanus toxoid as adult Td, but contain 3 to 4 times as
much diphtheria toxoid.
Children younger than 7 years of age should receive
either DTaP or pediatric DT. Persons 7 years of age or older should receive
the adult formulation (adult Td), even if they have not completed a series
of DTaP or pediatric DT. Two brands of Tdap are available—Boostrix
(approved for persons 10 years of age or older) and Adacel (approved for
persons 10 through 64 years of age). DTaP and Tdap vaccines do not contain
thimerosal as a preservative.
Immunogenicity and Vaccine Efficacy
After a primary series of three properly spaced diphtheria toxoid doses in
adults or four doses in infants, a protective level of antitoxin (defined
as greater than 0.1 IU of antitoxin/ mL) is reached in more than 95%.
Diphtheria toxoid has been estimated to have a clinical efficacy of 97%.
Vaccination Schedule and Use
DTaP (diphtheria and tetanus toxoids and acellular pertussis vaccine) is
the vaccine of choice for children 6 weeks through 6 years of age. The
usual schedule is a primary series of 4 doses at 2, 4, 6, and 15–18 months
of age. The first, second, and third doses of DTaP should be separated by a
minimum of 4 weeks. The fourth dose should follow the third dose by no less
than 6 months, and should not be administered before 12 months of age.
If a child has a valid contraindication to pertussis vaccine, pediatric DT
should be used to complete the vaccination series. If the child was younger
than 12 months old when the first dose of DT was administered (as DTP,
DTaP, or DT), the child should receive a total of four primary DT doses. If
the child was 12 months of age or older at the time the first dose of DT
was administered, three doses (third dose 6–12 months after the second)
complete the primary DT series.
If the fourth dose of DT, DTP or DTaP is administered before the fourth
birthday, a booster (fifth) dose is recommended at 4 through 6 years of
age. The fifth dose is not required if the fourth dose was given on or
after the fourth birthday.
Vaccines containing reduced diphtheria (i.e., Td and Tdap) are indicated
for children 7 years and older and for adults. A primary series is three or
four doses, depending on whether the person has received prior doses of
diphtheria-containing vaccine, and the age these doses were administered.
The number of doses recommended for children who received one or more doses
of DTP, DTaP, or DT before age 7 years is discussed above. For unvaccinated
persons 7 years and older (including persons who cannot document prior
vaccination), the primary series is three doses. The first two doses should
be separated by at least 4 weeks, and the third dose given 6 to 12 months
after the second. ACIP recommends that one of these doses (preferably the
first) be administered as Tdap.
A booster dose of Td should be given every
10 years. Persons who have never received Tdap should be given a dose of
Tdap as one of these boosters. Refer to the pertussis chapter for more
information about Tdap.
Interruption of the recommended schedule or delay of subsequent doses does
not reduce the response to the vaccine when the series is finally
completed. There is no need to restart a series regardless of the time
elapsed between doses.
Diphtheria disease might not confer immunity. Persons recovering from
diphtheria should begin or complete active immunization with diphtheria
toxoid during convalescence.
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Diphtheria Toxoid : Characteristics, Immunogenicity and Vaccine Efficacy with Vaccination Schedule
Monday, January 7, 2019
Diphtheria Toxoid : Characteristics, Immunogenicity and Vaccine Efficacy with Vaccination Schedule
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