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Description: VANGUARD®
Plus 5/CV is a freeze-dried preparation of attenuated strains of CD virus,
CAV-2, CPI virus, and CPV, plus a liquid preparation of inactivated CCV with an
adjuvant. The CPV fraction is high titer (>107.0 TCID50/dose)
and was attenuated by low passage (35 passes from the canine isolate with a
maximum of 2 additional passes allowed for production) on the canine cell line
which gives it the immunogenic properties capable of overriding maternal
antibody interference at the levels indicated in Table 2. Some puppies in the
field may have higher levels of maternal antibodies than those evaluated in our
pivotal efficacy study. All viruses were propagated on established cell lines.
The liquid component is used to rehydrate the freeze-dried component, which is
packaged with inert gas in place of vacuum.
Contains penicillin
and streptomycin as preservatives.
Indications: VANGUARD®
Plus 5/CV is for vaccination of healthy dogs 6 weeks of age or older as an aid
in preventing canine distemper caused by canine distemper (CD) virus, infectious
canine hepatitis (ICH) caused by canine adenovirus type 1 (CAV-1), respiratory
disease caused by canine adenovirus type 2 (CAV-2), canine parainfluenza caused
by canine parainfluenza (CPI) virus, and enteritis caused by canine coronavirus
(CCV) and canine parvovirus (CPV).
Directions:
1. General Directions:
Vaccination of healthy dogs is recommended. Aseptically rehydrate the
freeze-dried vaccine (Vanguard® Plus 5) with the accompanying vial
of liquid vaccine (FirstDose® CV), shake well, and administer 1 mL
subcutaneously or intramuscularly.
2. Primary
Vaccination: Healthy dogs 6 weeks of age or older should receive 3 doses, each
administered 3 weeks apart.
3. Revaccination:
Annual revaccination with a single dose is recommended.
Precaution(s):
Store at 2°-7°C. Prolonged exposure to higher temperatures and/or direct
sunlight may adversely affect potency. Do not freeze.
Use entire contents
when first opened.
Sterilized syringes
and needles should be used to administer this vaccine. Do not sterilize with
chemicals because traces of disinfectant may inactivate the vaccine.
Burn containers and
all unused contents.
Caution(s): Vaccination
of pregnant bitches should be avoided.
As with many vaccines,
anaphylaxis may occur after use. Initial antidote of epinephrine is recommended
and should be followed with appropriate supportive therapy.
This product has been
shown to be efficacious in healthy animals. A protective immune response may not
be elicited if animals are incubating an infectious disease, are malnourished or
parasitized, are stressed due to shipment or environmental conditions, are
otherwise immunocompromised, or the vaccine is not administered in accordance
with label directions.
Warning(s): For
use in dogs only.
For veterinary use
only.
Discussion:
Disease Description: CD is a universal, high-mortality viral disease with
variable manifestations. Approximately 50% of nonvaccinated, nonimmune dogs
infected with CD virus develop clinical signs, and approximately 90% of those
dogs die.1 ICH, caused by CAV-1, is a universal, sometimes fatal,
viral disease of dogs characterized by hepatic and generalized endothelial
lesions. CAV-2 causes respiratory disease which in severe cases may include
pneumonia and bronchopneumonia. CPI is a common viral upper respiratory disease.
Uncomplicated CPI may be mild or subclinical, with signs becoming more severe if
concurrent infection with other respiratory pathogens exists. CPV infection
results in enteric disease characterized by sudden onset of vomiting and
diarrhea, often hemorrhagic. Leukopenia commonly accompanies clinical signs.
Susceptible dogs of any age can be affected, but mortality is greatest in
puppies. In puppies 4-12 weeks of age CPV may occasionally cause myocarditis
that can result in acute heart failure after a brief and inconspicuous illness.
Following infection many dogs are refractory to the disease for a year or more.
Similarly, seropositive bitches may transfer to their puppies CPV antibodies
which can interfere with active immunization of the puppies through 16 weeks of
age. CCV also causes enteric disease in susceptible dogs of all ages worldwide.2
Highly contagious, the virus is transmitted primarily through direct contact
with infectious feces, and may cause clinical enteritis within 1-4 days after
exposure. Severity of disease may be exacerbated by concurrent infection with
other agents.3 Primary signs of CCV infection include anorexia,
vomiting, and diarrhea. Frequency of vomiting usually diminishes within a day or
2 after onset of diarrhea, but diarrhea may linger through the course of
infection, and stools occasionally may contain streaks of blood. With CCV
infection most dogs remain afebrile and leukopenia is not observed in
uncomplicated cases.2-4
Trial Data:
Safety and Efficacy: Laboratory evaluation demonstrated that VANGUARD®
Plus 5/CV immunized dogs against CD, ICH, CAV-2 and CPI respiratory disease, and
enteritis caused by CCV and CPV infection, and that no immunologic interference
existed among the vaccine fractions. Extensive field safety trials conducted by
Pfizer Animal Health showed it to be safe and essentially reaction-free in dogs
as young as 6 weeks of age under normal usage conditions.
It has been
demonstrated that CAV-2 vaccine cross-protects against ICH caused by CAV-1. The
CAV-2 fraction in Vanguard® vaccines is used as a replacement for
CAV-1 because it has significant advantages. Some CAV-1 vaccines may produce
undesirable reactions, including persistent kidney infections, uveitis, and
corneal opacity (“blue eye”), which have not been reported after vaccination
with CAV-2.5 In addition, the CAV-2 strain used in Vanguard®
vaccines has been specially selected for freedom from oncogenic properties
characteristic of adenoviruses.
Studies conducted at
Pfizer demonstrated that CAV-2 not only protects against ICH, but against CAV-2
respiratory disease as well.6 Although conventional CAV-1 (ICH)
vaccines cross-protect against CAV-2, they may not prevent subclinical infection
and spread of the CAV-2 agent. Canine adenovirus type 2 challenge virus was not
recovered from CAV-2-vaccinated dogs in tests conducted at Pfizer.
The CPV fraction in
VANGUARD® Plus 5/CV was subjected to comprehensive safety and
efficacy testing at Pfizer. It was shown safe and essentially reaction-free in
laboratory tests and in clinical trials under field conditions. Product safety
was further demonstrated by a backpassage study which included oral
administration of multiple doses of the vaccine strain to susceptible dogs, all
of whom remained normal. The CPV virus in VANGUARD® Plus 5/CV shares
a characteristic with other live CPV vaccine strains in that the vaccine virus
may be present in the feces following administration. Although this CPV vaccine
virus was found occasionally and in low titers in the feces of vaccinated dogs,
testing demonstrated that the vaccine master seed did not revert to virulence
following 6 consecutive backpassages in susceptible dogs.
Research at Pfizer
demonstrated that 3 doses of the vaccine with increased CPV virus titer can
overcome serum neutralization (SN) titers associated with maternal antibody.
Serum neutralization titers as low as 1:4 have been shown by others to interfere
with active immunization using conventional modified live vaccines.7,8
A clinical trial was conducted with fifty 6-week-old puppies [25 vaccinates (SN
titer range <2-256) and 25 nonvaccinated controls (SN titer range 4-1024)]
(Table 1). The group of vaccinates received 3 doses, with vaccinations
administered 3 weeks apart beginning at 6 weeks of age. After 1 vaccination,
13/25 puppies exhibited a 4-fold or greater increase in CPV SN titer (seroconversion)
(Table 2). Twelve of these 13 puppies had maternal SN titers £1:16
at the time of the first vaccination with the remaining puppy having an SN titer
of 1:64. Another 9 puppies with initial SN titers between 1:16 and 1:256
seroconverted after the second vaccination. Their maternal antibody SN titers
had declined to £1:64
at the time of the second vaccination. Similarly, the last 3 vaccinates, with
initial SN titers of 1:128, seroconverted after the third vaccination, after
their maternal antibody CPV titer dropped £1:64.
Therefore, in this study, when 3 doses of vaccine were given beginning at 6
weeks of age, all 25 vaccinates, even those with the highest maternal antibody
levels, became actively immunized (GM = 1:1176; range of SN titers 128-4096).
All 50 dogs were challenged 3 weeks after the third vaccination with a
heterologous CPV challenge virus. Fourteen of 25 nonvaccinated control dogs died
or showed illness severe enough to warrant euthanasia, while all 25 vaccinates
remained essentially healthy. The high-titer, low-passage vaccine virus in
VANGUARD® Plus 5/CV is therefore highly immunogenic and capable of
stimulating active immunity in the presence of maternal antibodies.
Table 1. Initial Serum
Neutralization (SN) Titers of Vaccinates and Controls
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SN Titers
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# Vaccinates
Included
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# Controls
Included
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<1:2
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3
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0
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|
1:4
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4
|
3
|
|
1:8
|
1
|
3
|
|
1:16
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4
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1
|
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1:32
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2
|
5
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1:64
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3
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1
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1:128
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6
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3
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1:256
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2
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3
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1:512
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0
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5
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1:1024
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0
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1
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Table 2.
Postvaccination Serum Neutralization (SN) Titers Geometric Mean (Range)a
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Groups
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N
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Pre-vaccination
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Postvaccination
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1
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2
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3b
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All Vaccinated
Dogs
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25
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1:24
(<2-256)
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1:108
(8-1024)
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1:605
(8-4096)
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1:1176
(128->4096)
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Responders
Post 1st Vaccination
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13
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1:6
(<2-64)
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1:460
(64-1024)
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1:1745
(256-4096)
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1:1410
(256-4096)
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Responders
Post 2nd Vaccination
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9
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1:87
(16-256)
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1:20
(8-64)
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1:376
(256-1024)
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1:1625
(256-4096)
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Responders
Post 3rd Vaccination
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3
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1:128
(128)
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1:32
(16-64)
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1:25
(8-64)
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1:203
(128-256)
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Nonvaccinated
Control Dogs
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25
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1:64
(4-1024)
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1:9
(<2-64)
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1:3
(<2-64)
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<1:2
(<2-4)
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aDogs
were vaccinated at 6, 9, and 12 weeks of age.
bPre-challenge
SN titers
The efficacy of the
CCV fraction of VANGUARD® Plus 5/CV was demonstrated in an extensive
vaccination challenge study. Sixteen 7- to 8-week-old puppies were vaccinated
with Vanguard® Plus 5/CV-L (vaccinates) and 17 with Vanguard®
Plus 5 (controls). All puppies received three 1-mL doses at 3-week intervals.
Three weeks following the third vaccination, puppies were challenged with a
virulent strain of CCV (CV-6). Clinical observations, temperatures, weights, and
blood parameters were monitored for 21 days following infection. CCV vaccinates
demonstrated a reduction in the occurrence of diarrhea and amount of virulent
CCV shed when compared to controls. At 21 days postchallenge, fluorescent
antibody staining for virulent CCV of small intestinal sections demonstrated a
significant reduction (P<0.05) in detectable CCV antigen between CCV
vaccinates and controls (Table 3).
Table 3. Fluorescent
Antibody Staining of Small Intestinal Sections 21 Days Following Challenge
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Gut Section
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% Dogs
Fluorescent Antibody Positive
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Vaccinates
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Controls
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Duodenum
Jejunum
Ileum
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1
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0
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89
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2
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0
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100
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|
3
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0
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100
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|
4
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0
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89
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|
5
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0
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100
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6
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12.5
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56
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7
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0
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78
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8
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12.5
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78
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9
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0
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67
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10
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12.5
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56
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Product Information Provided by
Pfizer Animal Health©
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