How to prevent contamination with Candida albicans during the fabrication of transplantable oral mucosal epithelial cell sheets

• Published in: Regenerative therapy 2015-06, Vol.1 (C), p.1-4
• Main Authors: Takagi, Ryo, Kobayashi, Shinichiro, Yamato, Masayuki, Owaki, Toshiyuki, Kasai, Yoshiyuki, Hosoi, Takahiro, Sakai, Yusuke, Kanetaka, Kengo, Minamizato, Tokutaro, Minematsu, Asuka, Kondo, Makoto, Kanai, Nobuo, Yamaguchi, Naoyuki, Nagai, Kazuhiro, Miyazaki, Yasushi, Takeda, Naoya, Fukai, Fumio, Asahina, Izumi, Miyazaki, Taiga, Kohno, Shigeru, Yamamoto, Masakazu, Nakao, Kazuhiko, Eguchi, Susumu, Okano, Teruo
• Format: Article
• Language: English
• Subjects: Amphotericin B; Candida albicans; Oral mucosal epithelial cell; Original
• ISSN: 2352-3204; 2352-3204
• DOI: 10.1016/j.reth.2014.12.002

We have utilized patients' own oral mucosa as a cell source for the fabrication of transplantable epithelial cell sheets to treat limbal stem cell deficiency and mucosal defects after endoscopic submucosal dissection of esophageal cancer. Because there are abundant microbiotas in the human oral cavity, the oral mucosa was sterilized and 40 μg/mL gentamicin and 0.27 μg/mL amphotericin B were added to the culture medium in our protocol. Although an oral surgeon carefully checked each patient's oral cavity and although candidiasis was not observed before taking the biopsy, contamination with Candida albicans (C. albicans) was detected in the conditioned medium during cell sheet fabrication. After adding 1 μg/mL amphotericin B to the transportation medium during transport from Nagasaki University Hospital to Tokyo Women's Medical University, which are 1200 km apart, no proliferation of C. albicans was observed. These results indicated that the supplementation of transportation medium with antimycotics would be useful for preventing contamination with C. albicans derived from the oral mucosa without hampering cell proliferation. •Normal human oral mucosal epithelial cells were cultured in a clinical setting.•Contamination with Candida albicans was detected in the culture.•The culture medium included 0.27 μg/mL amphotericin B.•Contamination was prevented by 1 μg/mL amphotericin B in the medium for transportation of the oral tissue.