Strategic Plan Objective Detail
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Question 2: Short-term Objective A  

$4,972,407.28
Fiscal Year: 2010

Green dot: Objective has greater than or equal to the recommended funding.2SA. Support at least four research projects to identify mechanisms of fever, metabolic and/or immune system interactions with the central nervous system that may influence ASD during prenatal-postnatal life by 2010. IACC Recommended Budget: $9,800,000 over 4 years. (Fever studies to be started by 2012.)

Download 2010 Question 2: Short-term Objective A projects (EXCEL)
Note: Initial Sort is by Principal Investigator. Sorting by other columns is available by clicking on the desired column header.
Project Title Principal Investigator Institution
Environmentally induced oxidative stress and altered local brain thyroid horomone metabolism: relevance to autism? Sajdel-Sulkowski, Elizabeth Harvard Medical School; Brigham and Women's Hospital
EFRI- BSBA: Novel microsystems for manipulation and analysis of immune cells Revzin, Alexander University of California, Davis
Early biologic markers for autism Croen, Lisa Kaiser Permanente Division of Research
Does mercury and neurotension induce mitochondrial DNA release from human mast cells and contribute to auto-immunity in ASD? Theohardies, Theoharis Tufts University
Consequences of maternal antigen exposure on offspring immunity: An animal model of vertical tolerance Rall, Glenn The Fox Chase Cancer Center
CNS toxicity of ambient air pollution: Postnatal exposure to ultrafine particles Cory-Slechta, Deborah University of Rochester
A role for immune molecules in cortical connectivity: Potential implications for autism Elmer, Bradford University of California, Davis
A primate model of gut, immune, and CNS response to childhood vaccines Sackett, Gene University of Washington
A non-human primate autism model based on maternal infection Patterson, Paul California Institute of Technology
A non-human primate autism model based on maternal immune activation Patterson, Paul University of California, Davis
An ex-vivo placental perfusion system to study materno-fetal biology Bonnin, Alexandre University of Southern California
A mitochondrial etiology of autism Wallace, Douglas Children's Hospital of Philadelphia

Objective Cumulative Funding Table

IACC Strategic Plan Objective 2008 2009 2010 2011 2012 Total
Support at least four research projects to identify mechanisms of fever, metabolic and/or immune system interactions with the central nervous system that may influence ASD during prenatal-postnatal life by 2010 (Fever studies to be started by 2012).

IACC Recommended Budget: $9,800,000 over 4 years
2.2
$3,377,568
18 projects

2.S.A
$3,584,634
30 projects

2.S.A
$4,972,407
37 projects

2.S.A
$2,013,417
25 projects

2.S.A
$3,049,827
26 projects

$16,997,853
2.S.A. Funding: The recommended budget for this objective was met.

Progress: Many projects were funded in this area (approximately 20-30 per year), but the field is still developing, and emphasis on this objective should continue in the future. Scientific advances have been made in linking maternal innate immune function and immune-system challenge to aspects of ASD. Methodological advances in the field include the development of animal models for study of the role of the immune system in ASD and PET ligands for imaging microglial activation.

Remaining Gaps, Needs and Opportunities: There is a need for a well-designed, multi-site clinical study of clinical effects of fever and to develop standard measures of fever and behavioral/cognitive outcomes. Questions about fever could be integrated into funded epidemiological studies. There is also interest in further work on metabolic and mitochondrial issues, but in order for this work to be done, there is a need for validation and standardization of measures for assessment of oxidative stress and mitochondrial function. More guidance is needed on the key questions for this field to answer – a workshop to define these methodologies may be helpful. One of the key questions is to determine whether it is the body temperature associated with fever or some consequence of immune activation and production of the febrile state that leads to amelioration of cognitive function.