Development of a ligand-directed approach to study the pathogenesis of invasive apergillosis

被引:12
|
作者
Lionakis, MS
Lahdenranta, J
Sun, J
Liu, WI
Lewis, RE
Albert, ND
Pasqualini, R
Arap, W
Kontoyiannis, DP
机构
[1] Univ Texas, MD Anderson Canc Ctr, Dept Infect Dis Infect Control & Employee Hlth, Unit 402, Houston, TX 77030 USA
[2] Univ Texas, MD Anderson Canc Ctr, Dept Genitourinary Med Oncol, Houston, TX USA
[3] Univ Texas, MD Anderson Canc Ctr, Dept Canc Biol, Houston, TX USA
[4] Univ Houston, Coll Pharm, Houston, TX 77030 USA
关键词
D O I
10.1128/IAI.73.11.7747-7758.2005
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Invasive aspergillosis is a leading cause of infectious death in immunosuppressed patients. Here, we adapted a phage display library-based selection to screen and identify binding peptides to the surface of Aspergillus fumigatus conidia and hyphae. We identified a peptide (sequence CGGRLGPFC) that reliably binds to the surface of Aspergillus fumigatus hyphae. Binding was not Aspergillus strain specific, as it was also observed in hyphae of other Aspergillus clinical isolates. Furthermore, CGGRLGPFC-displaying phage targets Aspergillus fumigatus hyphae on formal in-fixed paraffin-embedded histopathology sections of lung tissue recovered from mice with invasive pulmonary aspergillosis. This approach may yield reagents such as peptidomimetics for novel diagnostic and therapeutic interventions in invasive aspergillosis.
引用
收藏
页码:7747 / 7758
页数:12
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