Published online Jun 28, 2014. doi: 10.3748/wjg.v20.i24.7794
Revised: January 14, 2014
Accepted: March 19, 2014
Published online: June 28, 2014
Processing time: 241 Days and 12.5 Hours
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.
Core tip: Confocal laser endomicroscopy (CLE) enables cellular visualization during on-going endoscopy. Lately, the method has been further refined by using fluorescent labelled molecular probes for estimation of receptors in carcinomas, illumination of subtle lesions and assessment of the affinity of drugs to specific lesions. This article presents the method of molecular CLE and gives a review of the current applications and drawbacks.