Molecular imaging of lymphoid organs and immune activation by positron emission tomography with a new [18F]-labeled 2′-deoxycytidine analog

被引:0
|
作者
Caius G Radu
Chengyi J Shu
Evan Nair-Gill
Stephanie M Shelly
Jorge R Barrio
Nagichettiar Satyamurthy
Michael E Phelps
Owen N Witte
机构
[1] 23-120 Center for Health Sciences,Department of Molecular and Medical Pharmacology
[2] Crump Institute for Molecular Imaging,Department of Microbiology
[3] 700 Westwood Boulevard,undefined
[4] Immunology and Molecular Genetics,undefined
[5] David Geffen School of Medicine,undefined
[6] University of California at Los Angeles,undefined
[7] 1602 MSB,undefined
[8] Howard Hughes Medical Institute at the University of California at Los Angeles (UCLA),undefined
来源
Nature Medicine | 2008年 / 14卷
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摘要
Noninvasively monitoring immune function by positron emission tomography could affect the diagnosis and treatment evaluation of immunological disorders. Progress, however, has been hampered by the lack of probes with distinct biodistribution patterns. Radu et al. exploit the fact that many immune cells utilize a salvage pathway for nucleotide generation during DNA synthesis to develop [18F]FAC (1-(2′-deoxy-2′[18F]fluoroarabinofuranosyl) cytosine), a new probe with increased accumulation in proliferating T cells. Studies in mice show it has advantages over commonly used probes and may be clinically useful.
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页码:783 / 788
页数:5
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