The development of a scientific field is often punctuated by a period when diverse observations can beunderstood in terms of a set of unifying principles. This important moment in time occurs when a critical number(and type) of observations becomes available, and the mechanistic principles often result from an amalgamationof ideas drawn from different intellectual disciplines. This period also marks the emergence of predictive models.T lymphocytes (T cells) orchestrate (and can also misregulate) the adaptive immune response. I believe that Tcell biology, especially T cell-mediated autoimmunity, is at a critical juncture where diverse data will soon beintegrated in terms of overarching principles. Modern experiments are revealing, in unprecedented detail, thefactors that are important in the emergence of T cell-mediated autoimmunity rather than tolerance to ?self?.However, general mechanistic principles necessary for predictive models have proven elusive. This is because Tcell-mediated autoimmunity is characterized by cooperative dynamic processes that occur over a spectrum oflength and time scales. Phenomena occurring on large scales (tissues) influence cooperative molecular events in asingle T cell which, in turn, influences the tissue environment. This complex hierarchical cooperativity makes itdifficult to intuit underlying mechanisms from experimental observations alone. I propose to develop theprinciples governing T cell-mediated autoimmunity by parsing the pertinent cooperative dynamics which occur ina complex space of molecular and cellular variables by integrating three great advances of the twentieth century:statistical mechanics, computational technology, and genetic, biochemical, and imaging experiments. A key tosuccess will be collaborations with experimental immunologists, and I have recently demonstrated how suchsynergies can be fruitful. If successful, the work that I envisage will provide the principles that could guide thedevelopment of therapies for diseases such as multiple sclerosis and diabetes which afflict millions of people.

Agency
National Institute of Health (NIH)
Institute
Office of The Director, National Institutes of Health (OD)
Type
NIH Director’s Pioneer Award (NDPA) (DP1)
Project #
5DP1OD001022-03
Application #
7488894
Study Section
Special Emphasis Panel (ZGM1-NDPA-G (P2))
Program Officer
Jones, Warren
Project Start
2006-09-28
Project End
2011-07-31
Budget Start
2008-08-01
Budget End
2009-07-31
Support Year
3
Fiscal Year
2008
Total Cost
$825,000
Indirect Cost
Name
Massachusetts Institute of Technology
Department
Type
DUNS #
001425594
City
Cambridge
State
MA
Country
United States
Zip Code
02139
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