The Host Response Core (Core C) will assist the research base and pilot project investigators by providing support to assess various endpoints and processes of inflammation, leukocyte activation, metabolism and the host response to bacteria relevant to cystic fibrosis (CF). This primary goal of the Host Response Core will be met by conducting a variety of routine and specialized procedures and assays and providing access to and training with sophisticated analytical and imaging equipment. To accomplish this goal the Host Response Core was incorporated into the existing, fully equipped Histology and Imaging Core, which is part of the Comparative Pathology Program in the Department of Comparative Medicine at the University of Washington. The primary services of Core C will be to conduct a variety of routine and specialized procedures and assays including histology, immunohistochemistry and imaging; provide access to automated immunohistochemistry and image analysis to assist CF investigators obtain quantitative histologic and immunohistochemical data; provide access to and expertise and training with sophisticated analytical and imaging equipment: provide access to comparative pathologists to assist and consult with basic research and preclinical studies; and promote increased interdisciplinary interactions to provide access to flow cytometry, metabolic profiling and training. The scientific focus of the Host Response Core is to obtain information on relevant parameters of the host response to bacteria or changes in the microbiome by processing biological samples from animal studies and human patients with CF. By providing diverse, yet complimentary tools and endpoints, the Host Response Core will greatly enhance the depth and accuracy of investigation. Finally, by providing support for preclinical studies and through interactions with the Clinical Core the HRC furthers translational research with the goal to better understand and correct the common sequela caused by mutations of CFTR through development of novel therapeutics for CF patients.

Agency
National Institute of Health (NIH)
Institute
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Type
Center Core Grants (P30)
Project #
5P30DK089507-10
Application #
9989218
Study Section
Special Emphasis Panel (ZDK1)
Program Officer
Eggerman, Thomas L
Project Start
Project End
Budget Start
2019-06-01
Budget End
2020-05-31
Support Year
10
Fiscal Year
2019
Total Cost
Indirect Cost
Name
Seattle Children's Hospital
Department
Type
DUNS #
048682157
City
Seattle
State
WA
Country
United States
Zip Code
98105
Matamouros, Susana; Hayden, Hillary S; Hager, Kyle R et al. (2018) Adaptation of commensal proliferating Escherichia coli to the intestinal tract of young children with cystic fibrosis. Proc Natl Acad Sci U S A 115:1605-1610
Heltshe, Sonya L; Taylor-Cousar, Jennifer L (2018) Let's talk about sex: Behaviors, experience and health care utilization in young women with CF. J Cyst Fibros 17:5-6
Ding, Fengming; Oinuma, Ken-Ichi; Smalley, Nicole E et al. (2018) The Pseudomonas aeruginosa Orphan Quorum Sensing Signal Receptor QscR Regulates Global Quorum Sensing Gene Expression by Activating a Single Linked Operon. MBio 9:
Gelfond, Daniel; Heltshe, Sonya L; Skalland, Michelle et al. (2018) Pancreatic Enzyme Replacement Therapy Use in Infants With Cystic Fibrosis Diagnosed by Newborn Screening. J Pediatr Gastroenterol Nutr 66:657-663
Hobler, Mara R; Engelberg, Ruth A; Curtis, J Randall et al. (2018) Exploring Opportunities for Primary Outpatient Palliative Care for Adults with Cystic Fibrosis: A Mixed-Methods Study of Patients' Needs. J Palliat Med 21:513-521
Hull, Rebecca L; Gibson, Ronald L; McNamara, Sharon et al. (2018) Islet Interleukin-1? Immunoreactivity Is an Early Feature of Cystic Fibrosis That May Contribute to ?-Cell Failure. Diabetes Care 41:823-830
Heltshe, S L; Khan, U; Beckett, V et al. (2018) Longitudinal development of initial, chronic and mucoid Pseudomonas aeruginosa infection in young children with cystic fibrosis. J Cyst Fibros 17:341-347
Irons, Jessica; Hodge-Hanson, Kelsey M; Downs, Diana M (2018) PA5339, a RidA Homolog, Is Required for Full Growth in Pseudomonas aeruginosa. J Bacteriol 200:
Klose, Alexander D; Paragas, Neal (2018) Automated quantification of bioluminescence images. Nat Commun 9:4262
Roch, Melanie; Varela, Maria Celeste; Taglialegna, Agustina et al. (2018) Activity of Telavancin against Staphylococcus aureus Isolates, Including Those with Decreased Susceptibility to Ceftaroline, from Cystic Fibrosis Patients. Antimicrob Agents Chemother 62:

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