Revisiting the NIH Taskforce on the Research needs of Eosinophil-Associated Diseases (RE-TREAD)

被引:30
作者
Khoury, Paneez [1 ]
Akuthota, Praveen [2 ]
Ackerman, Steven J. [3 ]
Arron, Joseph R. [4 ]
Bochner, Bruce S. [5 ]
Collins, Margaret H. [6 ]
Kahn, Jean-Emmanuel [7 ]
Fulkerson, Patricia C. [8 ]
Gleich, Gerald J. [9 ,10 ]
Gopal-Srivastava, Rashmi [11 ]
Jacobsen, Elizabeth A. [12 ]
Leiferman, Kristen M. [9 ]
Francesca, Levi-Schaffer [13 ]
Mathur, Sameer K. [14 ]
Minnicozzi, Michael [15 ]
Prussin, Calman [16 ]
Rothenberg, Marc E. [8 ]
Roufosse, Florence [17 ]
Sable, Kathleen [18 ]
Simon, Dagmar [19 ]
Simon, Hans-Uwe [20 ]
Spencer, Lisa A. [21 ]
Steinfeld, Jonathan [22 ]
Wardlaw, Andrew J. [23 ]
Wechsler, Michael E. [24 ]
Weller, Peter F. [21 ]
Klion, Amy D. [1 ]
机构
[1] NIAID, Lab Parasit Dis, NIH, 9000 Rockville Pike, Bethesda, MD 20892 USA
[2] Univ Calif San Diego, Div Pulm Crit Care & Sleep Med, La Jolla, CA 92093 USA
[3] Univ Illinois, Dept Biochem & Mol Genet, Chicago, IL USA
[4] Genentech Inc, Immunol Discovery, San Francisco, CA 94080 USA
[5] Northwestern Univ, Feinberg Sch Med, Div Allergy & Immunol, Dept Med, Chicago, IL 60611 USA
[6] Univ Cincinnati, Cincinnati Childrens Hosp Med Ctr, Div Pathol & Lab Med, Cincinnati, OH USA
[7] Hop Foch, Dept Internal Med, Suresnes, France
[8] Univ Cincinnati, Cincinnati Childrens Hosp Med Ctr, Div Allergy & Immunol, Dept Pediat,Coll Med, Cincinnati, OH USA
[9] Univ Utah Hlth, Dept Dermatol, Salt Lake City, UT USA
[10] Univ Utah Hlth, Dept Med, Salt Lake City, UT USA
[11] NIH, Natl Ctr Adv Translat Sci, Bldg 10, Bethesda, MD 20892 USA
[12] Mayo Clin Arizona, Scottsdale, AZ USA
[13] Hebrew Univ Jerusalem, Inst Drug Res, Sch Pharm, Pharmacol & Expt Therapeut Unit,Fac Med, Jerusalem, Israel
[14] Univ Wisconsin, Sch Med & Publ Hlth, Madison, WI USA
[15] NIAID, Div Allergy Immunol & Transplantat, NIH, 9000 Rockville Pike, Bethesda, MD 20892 USA
[16] Knopp Biosci, Pittsburgh, PA USA
[17] Univ Libre Bruxelles, Hop Erasme, Brussels, Belgium
[18] Amer Partnership Eosinophil Disorders, Atlanta, GA USA
[19] Univ Bern, Bern Univ Hosp, Dept Dermatol, Bern, Switzerland
[20] Univ Bern, Inst Pharmacol, Bern, Switzerland
[21] Harvard Med Sch, Beth Israel Deaconess Med Ctr, Boston, MA USA
[22] GlaxoSmithKline, Philadelphia, PA USA
[23] Univ Leicester, Inst Lung Hlth, Leicester, Leics, England
[24] Natl Jewish Hlth, Denver, CO USA
基金
以色列科学基金会;
关键词
biomarkers; eosinophil-related disorders; eosinophilia; hypereosinophilic syndromes; murine models; translational research; QUALITY-OF-LIFE; MAST-CELLS; TC-99M-LABELED EOSINOPHILS; HYPEREOSINOPHILIC SYNDROME; CLINICAL-FEATURES; TRANSGENIC MICE; DOUBLE-BLIND; MOUSE MODEL; INFLAMMATION; EXPRESSION;
D O I
10.1002/JLB.5MR0118-028R
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
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. Review on eosinophil biology and eosinophil-related disorders (2012-2017) with a focus on continued unmet needs in eosinophil-associated diseases.
引用
收藏
页码:69 / 83
页数:15
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