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Page 46

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June 10-11, 2019 | Edinburgh, Scotland

Central Nervous System and Therapeutics

2

nd

International Conference on

Journal of Neurology and Neurorehabilitation Research | Volume 4

allied

academies

Early childhood vaccines and regressive Autism: Is there a connection?

Sarah Adelaide Crawford

Southern Connecticut State University, USA

R

egressive autism may be defined as a rapid-onset loss

of previously acquired milestones in central nervous

system (CNS) development that occurs usually within

the first several years of life and may also be associated

with seizures or other abnormal CNS activity. Clinically,

this abnormal response to vaccination is termed “vaccine

encephalopathy”, in which developmentally normal infants

or children display a sudden developmental regression,

reduced developmental progression and/or seizures with

rapid onset following vaccine administration. That the

dramatic CNS changes associated with regressive autism

so rapidly follow the administration of vaccines is highly

suggestive of a causative connection which, however, has

been disputed by some reputable epidemiological studies.

The Quantitative Threshold Hypothesis (QTE) proposes that

autism results from the accumulated exposure to genetic

and environmental causes that impinge upon immunological

factors linked to CNS development to produce a critical

incidence threshold for Autism Spectrum Disorder (ASD).

The proposed connection between vaccines and regressive

autism is based on an application of this model, in which at-

risk individuals may develop regressive autism and associated

sequelae in response to vaccine administration if this causes

an individual to cross the threshold boundary for CNS

impairment. The physiological basis of the proposed vaccine/

autism connection results from the fundamental association

between vaccine-induced programming of adaptive immune

system responses and its direct dependence upon innate

immune system inflammatory responses to the vaccine. In

some at-risk individuals predisposed to neuroinflammation

due to the combined effects of genetic and environmental

immuno-stimulatory risk factors, the threshold to

immunopathology resulting in neuroinflammation and

impaired neural function may thus be induced by vaccine

administration. This paper will present risk-factor assessment

parameters that can be used preventively to identify

children for whom vaccine protocols should be adjusted to

reduce the incidence of regressive neurological impairment.

e

:

crawfords2@southernct.edu