Cuihua Wang, Ph.D.
Instructor in Investigation
Center for Systems Biology, Mass General Research Institute
Instructor in Radiology
Harvard Medical School
Radiology, Massachusetts General Hospital
|PhD Peking University 2006|
Neuroinflammation occurs with nearly all neurological diseases. The brain is particularly susceptible to inflammation and the resultant oxidative stress as it contains large quantities of oxidizable lipids and metals and has fewer antioxidant mechanisms than other tissues. Important to understanding what roles neuroinflammation has is to be able to track various key components of neuroinflammation in vivo without additional manipulations from ex vivo and in vitro experiments that may temper the biological processes. For example, our research in the development of activatable molecular imaging agents for neuroinflammation has developed multiple agents that can report with high sensitivity and specificity a key enzyme in inflammation, myeloperoxidase (MPO) by both MR and nuclear imaging. MPO is a potent inflammatory mediator found in many activated leukocytes and is postulated to interact with many pro-inflammatory molecules and cells that contribute to neuroinflammation. In vivo applications of these agents have led to improved understanding and the ability to evaluate novel therapies for multiple sclerosis, stroke, atherosclerosis, myocardial infarction, and heart transplant. We seek to develop novel imaging biomarkers as well as integrating existing library of inflammatory imaging sensors to decipher neuroinflammation and its relationship to pathology and disease.
Multiple sclerosis (MS) is the leading cause of non-traumatic neurological disability in young adults and MS related health costs are estimated to be more than $10 billion annually in the United States. Despite significant advances in the understanding of MS pathogenesis and high level anatomic imaging by MRI, the initial diagnosis of MS, timely diagnosis of MS relapses, and treatment of MS remain a challenge. Although the etiology of MS remains elusive to this day, there is tremendous evidence that MS is primarily an inflammatory disease and current treatment strategies are based on immune modulation of inflammation. However, there is a lack of an accurate, sensitive, and predictive biomarker to report on active inflammation and demyelination in MS. Currently, MS disease activity is diagnosed using clinical symptoms, invasive CSF analysis, and nonspecific conventional gadolinium chelate enhancement on MR imaging. Using advanced targeted multimodal molecular imaging technology and specific modulations, we study the relationship between key inflammatory enzymes, molecules, and cells to generate a roadmap of potential biomarkers to improve noninvasive diagnosis and to discover opportunities for novel, more effective therapy.