Dr. Jean Dodd's Vaccine Recommendations
Article courtesy of ItsFortheAnimals.com
2009 CANINE VACCINATION PROTOCOL
MINIMAL VACCINE USE
W. Jean Dodds, DVM
HEMOPET
938 Stanford Street
Santa Monica, CA 90403
310-828-4804; Fax 310-828-8251
e-mail
Note: The following vaccine protocol is offered for those dogs where minimal vaccinations are advisable or desirable.The schedule is one I recommend and follow and should not interpreted to mean that other protocols recommended by a veterinarian would be less satisfactory. It's a matter of professional judgment and choice.
Age of Pups | Vaccine Type |
9 - 10 weeks 14 weeks 20 weeks or older, if allowable by law 1 year 1 year |
Distemper virus + Parvovirus, MLV Same as above Rabies Distemper virus + Parvovirus, MLV (0ptional) Rabies, killed 3-year product (give 3-4 weeks apart from any other vaccine) |
Perform vaccine antibody titers for distemper and parvovirus every three years thereafter, or more often, if desired. Vaccinate for rabies virus according to the law, except where circumstances indicate that a written waiver needs to be obtained from the primary care veterinarian. In that case, a rabies antibody titer can also be performed to accompany the waiver request. See Rabies Challenge Fund.org
REASONS FOR VACCINE TITER TESTING *
- To determine that animal is protected (suggested by a positive test result)
- To identify a susceptible animal (suggested by a negative test result)
- To determine whether an individual animal has responded to a vaccine
- To determine whether an individual vaccine is effectively immunizing animals
* from: Schultz, Ford, Olsen, Scott. Vet Med, 97: 1-13,2002 (insert)
AVAILABLE VACCINE TITERS FOR DOGS
- Distemper Virus
- Parvovirus
- Adenovirus 2 (hepatitis)
- Bordetella
- Panleukopenia
- Corona Virus [not recommended]
Table 1. Core Vaccines * | |
Dog | Cat |
Distemper | Feline Parvovirus |
Adenovirus | Herpesvirus |
Parvovirus | Calicivirus |
Rabies | Rabies |
_______________________________________ * Vaccines that every dog and cat should have |
|
Table 2. Adverse Reaction Risks for
Vaccines *
?There is less risk associated with taking a blood sample
_______________________________________________
|
|
Table 3. Titer Testing and Vaccination * While difficult to prove, risks
associated with overvaccination
_____________________________________________________
|
|
Table 4. Vaccine Titer Testing * Research shows that once an
animal's titer stabilizes,
_____________________________________________ |
This thought-provoking article by Dr.. Jean Dodds, provides valuable information regarding making informed decisions about vaccinating your animal companion and is reprinted here with her kind permission.
CHANGING VACCINE PROTOCOLS
W. Jean Dodds, DVM
The challenge to produce effective and safe vaccines for the prevalent infectious diseases of humans and animals has become increasingly difficult. In veterinary medicine, evidence implicating vaccines in triggering immune-mediated and other chronic disorders (vaccinosis) is compelling, While some of these problems have been traced to contaminated or poorly attenuated batches of vaccine that revert to virulence, others apparently reflect the hosts genetic predisposition to react adversely upon receiving the single (monovalent) or multiple antigen ?combo? (polyvalent) products given routinely to animals. Animals of certain susceptible breeds or families appear to be at increased risk for severe and lingering adverse reactions to vaccines.
The onset of adverse reactions to conventional vaccinations (or other inciting drugs, chemicals, or infectious agents) can be an immediate hypersensitivity or anaphylactic reaction, or can occur acutely (24-48 hours afterwards), or later on (10-45 days) in a delayed type immune response often caused by immune-complex formation. Typical signs of adverse immune reactions include fever, stiffness, sore joints and abdominal tenderness, susceptibility to infections, central and peripheral nervous system disorders or inflammation, collapse with autoagglutinated red blood cells and jaundice, or generalized pinpoint hemorrhages or bruises. Liver enzymes may be markedly elevated, and liver or kidney failure may accompany bone marrow suppression. Furthermore, recent vaccination of genetically susceptible breeds has been associated with transient seizures in puppies and adult dogs, as well as a variety of autoimmune diseases including those affecting the blood, endocrine organs, joints, skin and mucosa, central nervous system, eyes, muscles, liver, kidneys, and bowel. It is postulated that an underlying genetic predisposition to these conditions places other littermates and close relatives at increased risk. Vaccination of pet and research dogs with polyvalent vaccines containing rabies virus or rabies vaccine alone was recently shown to induce production of antithyroglobulin autoantibodies, a provocative and important finding with implications for the subsequent development of hypothyroidism (Scott-Moncrieff et al, 2002).
Vaccination also can overwhelm the immunocompromised or even healthy
host that is repeatedly challenged with other environmental stimuli and
is genetically predisposed to react adversely upon viral exposure. The
recently weaned young puppy or kitten entering a new environment is at
greater risk here, as its relatively immature immune system can be
temporarily or more permanently harmed. Consequences in later life may
be the increased susceptibility to chronic debilitating diseases.
As combination vaccines contain antigens other than those of the
clinically important infectious disease agents, some may be unnecessary;
and their use may increase the risk of adverse reactions. With the
exception of a recently introduced mutivalent Leptospira spp. vaccine,
the other leptospirosis vaccines afford little protection against the
clinically important fields strains of leptospirosis, and the antibodies
they elicit typically last only a few months. Other vaccines, such as
for Lyme disease, may not be needed, because the disease is limited to
certain geographical areas. Annual revaccination for rabies is required
by some states even though there are USDA licensed rabies vaccine with a
3-year duration. Thus, the overall risk-benefit ratio of using certain
vaccines or multiple antigen vaccines given simultaneously and
repeatedly should be reexamined. It must be recognized, however, that we
have the luxury of asking such questions today only because the risk of
disease has been effectively reduced by the widespread use of
vaccination programs.
Given this troublesome situation, what are the experts saying about
these issues? In 1995, a landmark review commentary focused the
attention of the veterinary profession on the advisability of current
vaccine practices. Are we overvaccinating companion animals, and if so,
what is the appropriate periodicity of booster vaccines ?
Discussion of this provocative topic has generally lead to other
questions about the duration of immunity conferred by the currently
licensed vaccine components.
Inresponse to questions posed in the first part of this article,
veterinary vaccinologists have recommended new protocols for dogs and
cats. These include: 1) giving the puppy or kitten vaccine series
followed by a booster at one year of age; 2) administering further
boosters in a combination vaccine every three years or as split
components alternating every other year until; 3) the pet reaches
geriatric age, at which time booster vaccination is likely to be
unnecessary and may be unadvisable for those with aging or immunologic
disorders. In the intervening years between booster vaccinations, and
in the case of geriatric pets, circulating humoral immunity can be
evaluated by measuring serum vaccine antibody titers as an indication of
the presence of immune memory. Titers do not distinguish between
immunity generated by vaccination and/or exposure to the disease,
although the magnitude of immunity produced just by vaccination is
usually lower.
Except where vaccination is required by law, all
animals, but especially those dogs or close relatives that previously
experienced an adverse reaction to vaccination can have serum antibody
titers measured annually instead of revaccination. If adequate titers are
found, the animal should not need revaccination until some future date.
Rechecking antibody titers can be performed annually, thereafter, or can
be offered as an alternative to pet owners who prefer not to follow the
conventional practice of annual boosters. Reliable serologic vaccine
titering is available from several university and commercial laboratories
and the cost is reasonable (Twark and Dodds, 2000; Lappin et al, 2002;
Paul et al, 2003; Moore and Glickman, 2004).
Relatively little has been published about the duration
of immunity following vaccination, although new data are beginning to
appear for both dogs and cats.
Our recent study (Twark and Dodds, 2000), evaluated 1441 dogs for CPV antibody titer and 1379 dogs for CDV antibody titer. Of these, 95.1 % were judged to have adequate CPV titers, and nearly all (97.6 %) had adequate CDV titers. Vaccine histories were available for 444 dogs (CPV) and 433 dogs (CDV). Only 43 dogs had been vaccinated within the previous year, with the majority of dogs (268 or 60%) having received a booster vaccination 1-2 years beforehand. On the basis of our data, we concluded that annual revaccination is unnecessary. Similar findings and conclusions have been published recently for dogs in New Zealand (Kyle et al, 2002), and cats (Scott and Geissinger, 1999; Lappin et al, 2002). Comprehensive studies of the duration of serologic response to five viral vaccine antigens in dogs and three viral vaccine antigens in cats were recently published by researchers at Pfizer Animal Health ( Mouzin et al, 2004).
When an adequate immune memory has already been established, there is little reason to introduce unnecessary antigen, adjuvant, and preservatives by administering booster vaccines. By titering annually, one can assess whether a given animal humoral immune response has fallen below levels of adequate immune memory. In that event, an appropriate vaccine booster can be administered.
References
- Dodds WJ. More bumps on the vaccine road. Adv Vet Med 41:715-732, 1999.
- Dodds WJ. Vaccination protocols for dogs predisposed to vaccine reactions. J Am An Hosp Assoc 38: 1-4, 2001.
- Hogenesch H, Azcona-Olivera J, Scott-Moncreiff C, et al. Vaccine-induced autoimmunity in the dog. Adv Vet Med 41: 733-744, 1999.
- Hustead DR, Carpenter T, Sawyer DC, et al. Vaccination issues of concern to practitioners. J Am Vet Med Assoc 214: 1000-1002, 1999.
- Kyle AHM, Squires RA,Davies PR. Serologic status and response to vaccination against canine distemper (CDV) and canine parvovirus (CPV) of dogs vaccinated at different intervals. J Sm An Pract, June 2002.
- Lappin MR, Andrews J, Simpson D, et al. Use of serologic tests to predict resistance to feline herpesvirus 1, feline calicivirus, and feline parvovirus infection in cats. J Am Vet Med Assoc 220: 38-42, 2002.
- McGaw DL, Thompson M, Tate, D, et al. Serum distemper virus and parvovirus antibody titers among dogs brought to a veterinary hospital for revaccination. J Am Vet Med Assoc 213: 72-75, 1998.
- Moore GE, Glickman LT. A perspective on vaccine guidelines and titer tests for dogs. J Am Vet Med Assoc 224: 200-203. 2004.
- Mouzin DE, Lorenzen M J, Haworth, et al. Duration of serologic response to five viral antigens in dogs. J Am Vet Med Assoc 224: 55-60, 2004.
- Mouzin DE, Lorenzen M J, Haworth, et al. Duration of serologic response to three viral antigens in cats. J Am Vet Med Assoc 224: 61-66, 2004.
- Paul MA.Credibility in the face of controversy. Am An Hosp Assoc Trends MagazineXIV(2):19-21,1998.
- Paul MA (chair) et al. Report of the AAHA Canine Vaccine Task Force: 2003 canine vaccine guidelines, recommendations, and supporting literature. AAHA, April 2003, 28 pp.
- Schultz RD. Current and future canine and feline vaccination programs. Vet Med 93:233-254, 1998.
- Schultz RD, Ford RB, Olsen J, Scott F. Titer testing and vaccination: a new look at traditional practices. Vet Med, 97: 1-13, 2002 (insert).
- Scott FW, Geissinger CM. Long-term immunity in cats vaccinated with an inactivated trivalent vaccine. Am J Vet Res 60: 652-658, 1999.
- Scott-Moncrieff JC, Azcona-Olivera J, Glickman NW, et al. Evaluation of antithyroglobulin antibodies after routine vaccination in pet and research dogs. J Am Vet Med Assoc 221: 515-521, 2002.
- Smith CA. Are we vaccinating too much? J Am Vet Med Assoc 207:421-425, 1995.
- Tizard I, Ni Y. Use of serologic testing to assess immune status of companion animals. J Am Vet Med Assoc 213: 54-60, 1998.
- Twark L, Dodds WJ. Clinical application of serum parvovirus and distemper virus antibody titers for determining revaccination strategies in healthy dogs. J Am Vet Med Assoc 217:1021-1024, 2000.
- Vascellari M, Melchiotti E, Bozza MA et al. Fibrosarcomas at presumed sites of injection in dogs: characteristics and comparison with non-vaccination site fibrosarcomas and feline post-vaccinal firosarcomas. J Vet Med 50 (6): 286-291, 2003.
W. Jean Dodds, DVM
HEMOPET
938 Stanford Street
Santa Monica, CA 90403
310/ 828-4804
fax: 310/ 828-8251
Note: This schedule is the one I recommend and should not be interpreted to mean that other protocols recommended by a veterinarian would be less satisfactory. It's a matter of professional judgment and choice. For breeds or families of dogs susceptible to or affected with immune dysfunction, immune-mediated disease, immune-reactions associated with vaccinations, or autoimmune endocrine disease (e.g., thyroiditis, Addison's or Cushing's disease, diabetes, etc.) the above protocol is recommended.
After 1 year, annually measure serum antibody titers against specific canine infectious agents such as distemper and parvovirus. This is especially recommended for animals previously experiencing adverse vaccine reactions or breeds at higher risk for such reactions (e.g., Weimaraner, Akita, American Eskimo, Great Dane).
W. Jean Dodds, DVM Printable Titers Forms and
Instructions for Testing: http://www.itsfortheanimals.com/HEMOPET.HTM
HEMOPET