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DTP VACCINE
DTwP is a trivalent vaccine containing diphtheria toxoid,
pertussis vaccine (Whole Cell Pertussis), and tetanus toxoid. It is also
referred to as triple antigen. This vaccine is aimed at inducing active
immunity in children against diphtheria, tetanus and whooping cough
(pertussis).
It consists of toxoids of diphtheria and
tetanus along with killed whole cell suspension of Bordetella
pertussis. Each of the components can be given separately, but
administering them in combination minimizes the number of injections and
improves the immune response against toxoids because the pertussis
bacilli act as an adjuvant.
Vaccine preparation and composition:
Each 0.5-mL dose is formulated to contain 6.7-12.5 Lf units of
diphtheria toxoid, 5 Lf units of tetanus toxoid, and less than or equal
to 16 opacity units of pertussis vaccine. The cells of Bordetella
pertussis in DTP vaccine are inactivated either with formalin or
treatment with 0.2% merthiolate at
4oC for several months. Toxins are toxoided either by heating
or treatment with formaldehyde.
Course of vaccine:
Primary course of DPT immunization consists of three
intramuscular injections at intervals of 4-6 weeks initiated before the
age of six months. The first dose is usually started by 2 months of age.
The primary dose is followed by a booster dose at the end of first year
of life. Subsequent booster doses are given at five years of age and 10
years of age. DTwP is not recommended in children aged 7 years and
older due to increased risk of side effects. Even though the infant
receives maternal antibodies against tetanus, the immunization is
started by 2 months because there is very little maternal immunity
against pertussis. Diphtheria and pertussis are uncommon after the age
of 5 years but tetanus can occur at any age. Therefore a booster dose of
tetanus toxoid is administered at school entry.
Side effects of vaccine:
The side effects, whenever seen are usually because of pertussis
component in the vaccine. About 20% of the children, who receive the
whole cell vaccine experience mild side effects such as local
inflammation and fever. About 0.1% of infants experience convulsions
soon after receiving the vaccine and in a very small number of cases (1
in 150,000) severe or irreversible brain damage may occur. Because of
possibility of provocative poliomyelitis, it is advisable not to carry
out routine immunization if poliomyelitis is active in the
area.
Alternatives:
Beginning in 1996 several new acellular pertussis vaccines have
been developed from purified components of
B.pertussis. These multicomponent vaccines contain combinations
of pertussis toxoid, filamentous hemagglutinin, pertactin, and the two
types of fimbriae. The diphtheria-tetanus-pertussis vaccine using
acellular pertussis is known as DTaP. It is possible to combine the DTaP
vaccine with the vaccine against Haemophilus influenzae type b
(Hib). This vaccine is called DTaP/Hib.
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