Randomised clinical trial: faecal microbiota transplantation for recurrent Clostridum difficile infection – fresh, or frozen, or lyophilised microbiota from a small pool of healthy donors delivered by colonoscopy

• Published in: Alimentary pharmacology & therapeutics Vol. 45; no. 7; pp. 899 - 908
• Main Authors: Jiang, Z. D., Ajami, N. J., Petrosino, J. F., Jun, G., Hanis, C. L., Shah, M., Hochman, L., Ankoma‐Sey, V., DuPont, A. W., Wong, M. C., Alexander, A., Ke, S., DuPont, H. L.
• Format: Journal Article
• Language: English
• Published: England Wiley Subscription Services, Inc 01.04.2017
• Subjects: Adult; Aged; Aged, 80 and over; Antibiotics; Bacteria; Clinical trials; Clostridium difficile; Clostridium Infections - therapy; Colon; Colonoscopy; Donors; Double-Blind Method; Fecal Microbiota Transplantation; Feces - microbiology; Female; Freeze Drying; Freezing; Humans; Male; Microbiota; Microbiota - genetics; Middle Aged; Randomization; Recurrence; Recurrent infection; RNA, Ribosomal, 16S - genetics; rRNA 16S; Specimen Handling; Tissue Donors; Transplantation; Young Adult
• ISSN: 0269-2813; 1365-2036
• DOI: 10.1111/apt.13969

Summary Background Faecal microbiota transplantation (FMT) has become routine in managing recurrent C. difficile infection (CDI) refractory to antibiotics. Aim To compare clinical response and improvements in colonic microbiota diversity in subjects with recurrent CDI using different donor product. Methods Seventy‐two subjects with ≥3 bouts of CDI were randomised in a double‐blind study to receive fresh, frozen or lyophilised FMT product via colonoscopy from 50 g of stool per treatment from eight healthy donors. Recipients provided stools pre‐ and 7, 14 and 30 days post‐FMT for C. difficile toxin and, in a subset, microbiome composition by 16S rRNA gene profiling. Results Overall resolution of CDI was 87% during 2 months of follow‐up after FMT. Stool samples before FMT had significantly decreased bacterial diversity with a high proportion of Proteobacteria compared to donors. Cure rates were highest for the group receiving fresh product seen in 25/25 (100%), lowest for the lyophilised product 16/23 (78%; P = 0.022 vs. fresh and 0.255 vs. frozen) and intermediate for frozen product 20/24 (P = 0.233 vs. fresh). Microbial diversity was reconstituted by day 7 in the subjects receiving fresh or frozen product. Improvement in diversity was seen by day 7 in those randomised to lyophilised material with reconstitution by 30 days. Conclusions Comparative efficacy in faecal microbiota transplantation was observed in subjects receiving fresh or frozen faecal product from the same donors. The lyophilised product had a slightly lowered efficacy compared with fresh product, but it resembled other treatments in microbial restoration 1 month after faecal microbiota transplantation.