TY - JOUR
T1 - Molecular confocal laser endomicroscopy
T2 - A novel technique for in vivo cellular characterization of gastrointestinal lesions
AU - Karstensen, John Gásdal
AU - Klausen, Pia Helene
AU - Saftoiu, Adrian
AU - Vilmann, Peter
PY - 2014/6/28
Y1 - 2014/6/28
N2 - While flexible endoscopy is essential for macroscopic evaluation, confocal laser endomicroscopy (CLE) has recently emerged as an endoscopic method enabling visualization at a cellular level. Two systems are currently available, one based on miniprobes that can be inserted via a conventional endoscope or via a needle guided by endoscopic ultrasound. The second system has a confocal microscope integrated into the distal part of an endoscope. By adding molecular probes like fluorescein conjugated antibodies or fluorescent peptides to this procedure (either topically or systemically administered during on-going endoscopy), a novel world of molecular evaluation opens up. The method of molecular CLE could potentially be used for estimating the expression of important receptors in carcinomas, subsequently resulting in immediate individualization of treatment regimens, but also for improving the diagnostic accuracy of endoscopic procedures by identifying otherwise invisible mucosal lesions. Furthermore, studies have shown that fluorescein labelled drugs can be used to estimate the affinity of the drug to a target organ, which probably can be correlated to the efficacy of the drug. However, several of the studies in this research field have been conducted in animal facilities or in vitro, while only a limited number of trials have actually been carried out in vivo. Therefore, safety issues still needs further evaluations. This review will present an overview of the implications and pitfalls, as well as future challenges of molecular CLE in gastrointestinal diseases.
AB - While flexible endoscopy is essential for macroscopic evaluation, confocal laser endomicroscopy (CLE) has recently emerged as an endoscopic method enabling visualization at a cellular level. Two systems are currently available, one based on miniprobes that can be inserted via a conventional endoscope or via a needle guided by endoscopic ultrasound. The second system has a confocal microscope integrated into the distal part of an endoscope. By adding molecular probes like fluorescein conjugated antibodies or fluorescent peptides to this procedure (either topically or systemically administered during on-going endoscopy), a novel world of molecular evaluation opens up. The method of molecular CLE could potentially be used for estimating the expression of important receptors in carcinomas, subsequently resulting in immediate individualization of treatment regimens, but also for improving the diagnostic accuracy of endoscopic procedures by identifying otherwise invisible mucosal lesions. Furthermore, studies have shown that fluorescein labelled drugs can be used to estimate the affinity of the drug to a target organ, which probably can be correlated to the efficacy of the drug. However, several of the studies in this research field have been conducted in animal facilities or in vitro, while only a limited number of trials have actually been carried out in vivo. Therefore, safety issues still needs further evaluations. This review will present an overview of the implications and pitfalls, as well as future challenges of molecular CLE in gastrointestinal diseases.
KW - Biological Markers
KW - Endoscopes, Gastrointestinal
KW - Endoscopy, Gastrointestinal
KW - Gastrointestinal Diseases
KW - Gastrointestinal Tract
KW - Humans
KW - Individualized Medicine
KW - Microscopy, Confocal
KW - Molecular Imaging
KW - Patient Selection
KW - Predictive Value of Tests
KW - Prognosis
U2 - 10.3748/wjg.v20.i24.7794
DO - 10.3748/wjg.v20.i24.7794
M3 - Journal article
C2 - 24976717
SN - 1007-9327
VL - 20
SP - 7794
EP - 7800
JO - World Journal of Gastroenterology
JF - World Journal of Gastroenterology
IS - 24
ER -