|
AS A PEDIATRICIAN, vaccine researcher
and the father of an autistic child, I have great concerns regarding the
debate about the safety of our infant and childhood vaccines. The unfounded
association that has been proposed by some between vaccines and autism is at
best misleading and at worst a serious undermining of children's health.
The vaccine/autism question stems from two separate theories that are
unscientific and have been determined to be invalid by the qualified experts
in vaccine science. The first claims autism is the result of the
combination measles, mumps, rubella (MMR) vaccine. The second claims
thimerosal is the autism culprit. Thimerosal is a mercury-based compound
that was used in many vaccines since the 1930s, but MMR vaccine does not,
and has never, contained thimerosal.
Let's begin with the MMR question. Numerous large-scale studies have shown
no increase in autism for children who received the MMR vaccine. The most
recent study, published in The New England Journal of Medicine and funded by
the National Alliance for Autism Research, examined more than 500,000 Danish
children. The study found there was no greater incidence of autism among
children who received the MMR vaccine than those who did not.
Scientific organizations including the Centers for Disease Control, the
Institute of Medicine and the American Academy of Pediatrics have all said
that the scientific evidence does not support a causal link between MMR and
autism. Ironically, the only known cause of autism is rubella, which the
MMR vaccine prevents.
The second vaccine/autism theory is based on the idea that autism is the
result of mercury poisoning from the thimerosal in vaccines. In 1999, public
health officials decided that thimerosal should be removed from vaccines as
a precautionary measure.
A study on thimerosal conducted by the University of Rochester was
published last fall in the British medical journal The Lancet. The study
showed that ethyl mercury - which is what thimerosal becomes as it is
metabolized - is excreted from the body within seven days and does not
appear to build up from one vaccination to the next. Even when it is still
in the body following immunization, the levels of this mercury do not exceed
the government standard, which is based on a more potentially harmful form
of mercury known as methyl mercury - the type found in some types of fish.
When the report was released, researchers wrote that children would likely
be exposed to more mercury by eating a tuna fish sandwich than by vaccines.
More research into thimerosal is under way, though if thimerosal were the
cause of what some believe is a dramatic increase in the incidence of
autism, one would expect the incidence to drop dramatically since the
removal of thimerosal from vaccines in 1999. But it hasn't. As the father
of a child with autism, I know the need for parents to understand the root
of this heartbreaking disorder and find something to blame. However, as a
medical doctor, I believe a more constructive focus is on advancing
treatment options, extending reimbursement policies and finding a cure.
By focusing on unproved theories, we not only risk wasting our precious
resources and not finding the real cause of autism, but we also risk parents
losing confidence in vaccines, resulting in fewer children being immunized.
This would leave our youngest vulnerable to diseases that we have only read
about in history books, reversing one of the world's most successful public
health programs.
A proposed link between autism and vaccines is a distraction that focuses
attention away from the real needs of parents of autistic children, namely
finding respite care, searching for a child psychiatrist who accepts health
insurance, and getting quality special education through public school
systems. Ireland and parts of the United Kingdom are a case study of what
happens when the fear spreads through the media; fears of the "MMR jab" have
led to a significant drop in the immunization rate, resulting in a dramatic
increase in the number of measles and mumps cases. We often forget that
measles is still the single leading killer of children in the world. With
today's ease of travel, these diseases can quickly be imported into the
United States, putting children who are unprotected at great risk of
contracting the disease.
Every parent has to decide: Is it worth protecting my child from a
real, deadly threat or protecting him from a hypothetical, scientifically
unproven leap of logic? I chose the former, and I am confident I made the
right decision.
PETER HOTEZ is chairman of the Department of Microbiology and Tropical
Medicine at George Washington University. He also is a senior fellow and
chairman of the Sabin Vaccine Institute's Scientific Advisory Council.
KNIGHT RIDDER/TRIBUNE


CBER Research Projects
(This is the FDA) Looks like they are doing a study
on this subject. The date is APR 2002

Project Title
Vaccine Safety: Pathogenesis of Virus Vaccine
Neurotoxicity
Principal Investigator
K. M. Carbone
Laboratory
Laboratory of Pediatric and Respiratory Viral
Diseases; Division of Viral Products; Office of Vaccines Research and
Review
Project Summary
Since the developing nervous system is uniquely
sensitive to damage following virus infection, postnatal CNS development
during the first several years of life provides for continued
susceptibility of the infant CNS to damage by viral infection after
birth. Administering insufficiently attenuated vaccines to infants may
place the child's CNS at increased risk for injury. Thus, it is
imperative to develop methods of pre-clinical neurovirulence testing
with which to predict which vaccines might have significant
neurovirulence potential for human CNS.
Thus, it is important to develop valid molecular
biological, in vitro and in vivo models to evaluate the pathogenesis of
the neurotoxic effects of vaccine viruses. Development of these models
will lead to improved safety of childhood vaccines, cost saving and
improved predictability of neurovirulence testing, and information
obtained in these studies will be useful in testing potentially
neurovirulent vaccines (e.g., measles, mumps, HIV, parainfluenza,
Japanese encephalitis).
Progress: 2001 CBER Outstanding Regulatory Research
Project
-
Molecular Markers of Neurotoxicity: We have
identified vaccine virus-related perturbations in CNS gene expression
by standard semiquantitative RT-PCR and by differential display
techniques, including endogenous immune mediators of the CNS. We have
recovered un-characterized gene products from new genes that are
altered by virus infection of the brain. We have initiated RPA to
compare changes in endogenous immune mediators in the CNS in animals
infected with low and high neurovirulence strains of mumps virus.
-
Animal Models of CNS Diseases Following Childhood
Virus Infection: Autism. Viruses are known etiologic agents of
autism (e.g., rubella). Therefore, concerns are raised
regarding a possible relationship between childhood vaccines and
autism. Because no valid animal models existed to study the
pathogenesis of the neuroanatomical and behavioral signs of autism, we
developed a rat model of autism using neonatal infection with
neurotropic viruses. We have characterized autistic-like changes in
neuroanatomy, neurochemistry, neurological disease and behavior in
these rats. In addition, we have identified regional and developmental
changes in neurotransmitters, including serotonin and norepinephrine.
A developmental study of damage to developing brain (e.g., cerebellum)
in virus infected rats was performed demonstrating anatomical,
behavioral and neurological consequences.
Publications
 |
J Virol 1998 Oct;72(10):8037-42
Comparison of the neurovirulence of a vaccine and a wild-type mumps
virus strain in the developing rat brain.
Rubin SA, Pletnikov M, Carbone KM
Pub Med
|
 |
J Vet Diagn Invest 1998 Oct;10(4):338-43
Clinical, serologic, and histopathologic characterization of
experimental Borna disease in ponies.
Katz JB, Alstad D, Jenny AL, Carbone KM, Rubin SA, Waltrip RW 2nd
Pub Med
|
 |
Behav Brain Res 1999 Apr;100(1-2):43-50
Developmental brain injury associated with abnormal play behavior in
neonatally Borna disease virus-infected Lewis rats: a model of autism.
Pletnikov MV, Rubin SA, Vasudevan K, Moran TH, Carbone KM
Pub Med
|
 |
Brain Res Bull 1999 Jan 1;48(1):23-30
Borna disease virus-induced hippocampal dentate gyrus damage is
associated with spatial learning and memory deficits.
Rubin SA, Sylves P, Vogel M, Pletnikov M, Moran TH, Schwartz GJ,
Carbone KM
Pub Med
|
 |
J Infect Dis 1999 Aug;180(2):521-525
The Mumps Virus Neurovirulence Safety Test in Rhesus Monkeys:A
Comparison of Mumps Virus Strains.
Rubin SA, Snoy PJ, Wright KE, Brown EG, Reeve P, Beeler JA, Carbone KM
Pub Med
|
 |
Physiol Behav 1999 Jul;66(5):823-31
Persistent neonatal Borna disease virus (BDV) infection of the brain
causes chronic emotional abnormalities in adult rats.
Pletnikov MV, Rubin SA, Schwartz GJ, Moran TH, Sobotka TJ, Carbone KM
Pub Med
|
 |
J Virol 2000 Jun 1;74(11):5382-5384
Evaluation of a Neonatal Rat Model for Prediction of Mumps Virus
Neurovirulence in Humans.
Rubin SA, Pletnikov M, Taffs R, Snoy PJ, Kobasa D, Brown EG, Wright KE,
Carbone KM
Pub Med
|
 |
Dev Brain Res 2000 Feb 7;119(2):179-85
Effects of neonatal rat Borna disease virus (BDV) infection on the
postnatal development of the brain monoaminergic systems.
Pletnikov MV, Rubin SA, Schwartz GJ, Carbone KM, Moran TH
Pub Med
|
 |
Ann N Y Acad Sci 2001 Jun;939:318-9
Rat model of autism spectrum disorders. Genetic background effects on
Borna disease virus-induced developmental brain damage.
Pletnikov MV, Jones ML, Rubin SA, Moran TH, Carbone KM
Pub Med
|
 |
Clin Microbiol Rev 2001 Jul;14(3):513-27
Borna disease virus and human disease.
Carbone KM
Pub Med
|
 |
Mol Psychiatr 2000 Nov;5(6):577
Borna again, starting from the beginning.
Carbone KM, Pletnikov M
Pub Med
|
 |
Ann Clin Biochem 2001 Jul;38(Pt 4):348-55
Synthetic peptide-based electrochemiluminescence immunoassay for anti-Borna
disease virus p40 and p24 antibodies in rat and horse serum.
Yamaguchi K, Sawada T, Yamane S, Haga S, Ikeda K, Igata-Yi R, Yoshiki
K, Matsuoka M, Okabe H, Horii Y, Nawa Y, Waltrip RW 2nd, Carbone KM
Pub Med
|
 |
Brain Res Dev Brain Res 2001 Jan 31;126(1):1-12
Neonatal Borna disease virus infection (BDV)-induced damage to the
cerebellum is associated with sensorimotor deficits in developing
Lewis rats.
Pletnikov MV, Rubin SA, Carbone KM, Moran TH, Schwartz GJ
Pub Med
|
 |
Curr Opin Microbiol 2001 Aug;4(4):467-75
Borna disease: virus-induced neurobehavioral disease pathogenesis.
Carbone KM, Rubin SA, Nishino Y, Pletnikov MV
Pub Med |
|
Back to page
|
|