Overview Understanding the pathogenesis of Inflammatory Bowel Diseases (IBD) represents one of the most important and unresolved challenges in both clinical and investigative digestive diseases. As a result of research advances over the past several years, including many made possible by this Center, it is now possible to formulate a central hypothesis for the pathogenesis of these disorders and to apply powerful new tools that will facilitate further advances in the next several years. The many novel aspects of our understanding of the multiple pathwavs to ulcerative colitis (UC) and Crohn's disease (CD) are based upon a comprehensive dissection of the manv complexities of mucosal biology. These advances are also based on knowledge of factors sustaining surface epithelial integrity, innate immunity, lymphocyte activation, host-microbe interaction, genetic architecture of Crohn's disease and ulcerative colitis, and functional characterization of lymphocytes and antigen presenting cell populations in the intestinal mucosa. Since the last competing application, the participating collaborating investigators in this Center for the Study of IBD (CSIBD) have made many key advances in the understanding of the processes relevant to IBD and catalyzed by CSIBD, have increased their research support. The CSIBD has achieved its original goals, primarily by expanding the infrastructural support available to a cohort of highly productive investigators, and by offering, through the awarding of pilot feasibility grants, opportunities for the initiation of new ventures in inflammatory bowel disease-related research aimed primarily at young investigators. The current proposal reflects the conviction of members of the research community at the Massachusetts General Hospital (MGH), the Beth Israel Deaconess Medical Center (BIDMC), the Massachusetts Institute of Technology (MIT), the Broad Institute of Harvard and MIT and the Tufts University Medical Center that they remain in an outstanding position to achieve integration of a broad base of investigators who study basic processes of innate and adaptive immune responses, inflammatory mediators, epithelial cell function and mucosal-microbial interaction. Specifically, Center investigators are well-positioned in the coming period to undertake novel approaches, as the CSIBD has recently initiated a collaboration with the Broad Institute that will allow CSIBD investigators access to a wide array of Broad research platforms in addition to Core services. The need for Pilot Feasibility Support (PFS) by the Boston-Cambridge IBD research communities is unabated, as evidenced by the number of applications per cycle. The Center Centers have been upgraded to offer stateof-the-art computational tools and bioinformatics support, in the coming period. Gene chip technology has now moved on from microarray to so-called deep sequencing which will be offered in the Genetics, Genomics and Molecular Biology Core both in the MGH setting and for selected projects at the Broad Institute Platform. A major focus of the next funding period will be the clinical translation of human genetics research to understand biological predisposition, to dissect biological pathways that mark disease and identify targets for drug intervention. Investigators are exploring alterations of these processes in both animal models of intestinal inflammation as well as in patients with IBD. We believe that this Center for the Study of Inflammatory Bowel Disease (CSIBD) will continue to provide a highly effective framework for promoting these interactions and a mechanism for the interface of the research community with both powerful new tools for IBD research and a large clinical investigation, patient and tissue base.

Agency
National Institute of Health (NIH)
Institute
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Type
Center Core Grants (P30)
Project #
5P30DK043351-22
Application #
8378665
Study Section
Special Emphasis Panel (ZDK1-GRB-8)
Project Start
Project End
Budget Start
2012-01-01
Budget End
2012-12-31
Support Year
22
Fiscal Year
2012
Total Cost
$769,771
Indirect Cost
$273,107
Name
Massachusetts General Hospital
Department
Type
DUNS #
073130411
City
Boston
State
MA
Country
United States
Zip Code
02199
Zhang, Sidi; Samocha, Kaitlin E; Rivas, Manuel A et al. (2018) Base-specific mutational intolerance near splice sites clarifies the role of nonessential splice nucleotides. Genome Res 28:968-974
Beaulieu, Dawn B; Ananthakrishnan, Ashwin N; Martin, Christopher et al. (2018) Use of Biologic Therapy by Pregnant Women With Inflammatory Bowel Disease Does Not Affect Infant Response to Vaccines. Clin Gastroenterol Hepatol 16:99-105
Hui, Ken Y; Fernandez-Hernandez, Heriberto; Hu, Jianzhong et al. (2018) Functional variants in the LRRK2 gene confer shared effects on risk for Crohn's disease and Parkinson's disease. Sci Transl Med 10:
Chong, Dawn Q; Banbury, Barbara L; Phipps, Amanda I et al. (2018) Association of family history and survival in patients with colorectal cancer: a pooled analysis of eight epidemiologic studies. Cancer Med 7:2192-2199
Johns, Nathan I; Gomes, Antonio L C; Yim, Sung Sun et al. (2018) Metagenomic mining of regulatory elements enables programmable species-selective gene expression. Nat Methods 15:323-329
Garber, John J; Mallick, Emily M; Scanlon, Karen M et al. (2018) Attaching-and-Effacing Pathogens Exploit Junction Regulatory Activities of N-WASP and SNX9 to Disrupt the Intestinal Barrier. Cell Mol Gastroenterol Hepatol 5:273-288
Yu, Sheng; Ma, Yumeng; Gronsbell, Jessica et al. (2018) Enabling phenotypic big data with PheNorm. J Am Med Inform Assoc 25:54-60
Bakker, Olivier B; Aguirre-Gamboa, Raul; Sanna, Serena et al. (2018) Integration of multi-omics data and deep phenotyping enables prediction of cytokine responses. Nat Immunol 19:776-786
Cox, Kimberly H; Oliveira, Luciana M B; Plummer, Lacey et al. (2018) Modeling mutant/wild-type interactions to ascertain pathogenicity of PROKR2 missense variants in patients with isolated GnRH deficiency. Hum Mol Genet 27:338-350
Ingram, Jessica R; Blomberg, Olga S; Rashidian, Mohammad et al. (2018) Anti-CTLA-4 therapy requires an Fc domain for efficacy. Proc Natl Acad Sci U S A 115:3912-3917

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