Revisiting the NIH Taskforce on the Research needs of Eosinophil-Associated Diseases (RE-TREAD)
journal contribution
posted on 2019-04-11, 09:15authored byP Khoury, P Akuthota, SJ Ackerman, JR Arron, BS Bochner, MH Collins, J-E Kahn, PC Fulkerson, GJ Gleich, R Gopal-Srivastava, EA Jacobsen, KM Leiferman, L-S Francesca, SK Mathur, M Minnicozzi, C Prussin, ME Rothenberg, F Roufosse, K Sable, D Simon, H-U Simon, LA Spencer, J Steinfeld, AJ Wardlaw, ME Wechsler, PF Weller, AD Klion
Eosinophil-associated diseases (EADs) are rare, heterogeneous disorders characterized by the presence of eosinophils in tissues and/or peripheral blood resulting in immunopathology. The heterogeneity of tissue involvement, lack of sufficient animal models, technical challenges in working with eosinophils, and lack of standardized histopathologic approaches have hampered progress in basic research. Additionally, clinical trials and drug development for rare EADs are limited by the lack of primary and surrogate endpoints, biomarkers, and validated patient-reported outcomes. Researchers with expertise in eosinophil biology and eosinophil-related diseases reviewed the state of current eosinophil research, resources, progress, and unmet needs in the field since the 2012 meeting of the NIH Taskforce on the Research of Eosinophil-Associated Diseases (TREAD). RE-TREAD focused on gaps in basic science, translational, and clinical research on eosinophils and eosinophil-related pathogenesis. Improved recapitulation of human eosinophil biology and pathogenesis in murine models was felt to be of importance. Characterization of eosinophil phenotypes, the role of eosinophil subsets in tissues, identification of biomarkers of eosinophil activation and tissue load, and a better understanding of the role of eosinophils in human disease were prioritized. Finally, an unmet need for tools for use in clinical trials was emphasized. Histopathologic scoring, patient- and clinician-reported outcomes, and appropriate coding were deemed of paramount importance for research collaborations, drug development, and approval by regulatory agencies. Further exploration of the eosinophil genome, epigenome, and proteome was also encouraged. Although progress has been made since 2012, unmet needs in eosinophil research remain a priority.
Funding
NIH. Grant Numbers: K08 HL116429, UG1 HL139117
FDA. Grant Number: R01FD004086
APFED. Grant Numbers: R01 AI072265, P01 HL107151, R01 AI105839
Campaign Urging Research for Eosinophilic Disease
Buckeye Foundation
Sunshine Charitable Foundation
Rare Disease Clinical Research Network
National Fund for Scientific Research. Grant Number: F 5/4/150/4
Israel Science Foundation. Grant Number: ISF 472/15
National Institute for Health Research
NIAID. Grant Number: R37020241
History
Citation
J Leukoc Biol, 2018, 104 (1), pp. 69-83
Author affiliation
/Organisation/COLLEGE OF LIFE SCIENCES/School of Medicine/Department of Infection, Immunity and Inflammation
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