Pilot, double-blind, randomized, placebo-controlled clinical trial of the supplement food Nyaditum resae® in adults with or without latent TB infection: Safety and immunogenicity

PLoS One. 2017 Feb 9;12(2):e0171294. doi: 10.1371/journal.pone.0171294. eCollection 2017.

Abstract

Background: Nyaditum resae® (NR) is a galenic preparation of heat-killed Mycobacterium manresensis, a new species of the fortuitum complex, that is found in drinkable water, and that has demonstrated to protect against the development of active TB in a murine experimental model that develop human-like lesions.

Methods: Double-blind, randomized, placebo-controlled Clinical Trial (51 volunteers included). Two different doses of NR and a placebo were tested, the randomization was stratified by Latent Tuberculosis Infection (LTBI)-positive (n = 21) and LTBI-negative subjects (n = 30). Each subject received 14 drinkable daily doses for 2 weeks.

Results: All patients completed the study. The 46.3% of the overall reported adverse events (AE) were considered related to the investigational treatment. None of them were severe (94% were mild and 6% moderate). No statistical differences were found when comparing the median number of AE between the placebo group and both treatment groups. The most common AE reported were gastrointestinal events, most frequently mild abdominal pain and increase in stool frequency. Regarding the immunogenic response, both LTBI-negative and LTBI-positive volunteers treated with NR experienced a global increase on the Treg response, showed both in the population of CD25+CD39-, mainly effector Treg cells, or CD25+CD39+ memory PPD-specific Treg cells.

Conclusion: This clinical trial demonstrates an excellent tolerability profile of NR linked to a significant increase in the population of specific effector and memory Tregs in the groups treated with NR in both LTBI-positive and negative subjects. NR shows a promising profile to be used to reduce the risk of active TB.

Publication types

  • Clinical Trial, Phase I
  • Randomized Controlled Trial

MeSH terms

  • Adult
  • Dietary Supplements* / adverse effects
  • Double-Blind Method
  • Female
  • Humans
  • Latent Tuberculosis / diet therapy*
  • Latent Tuberculosis / immunology
  • Male
  • Microbial Viability
  • Mycobacterium* / immunology
  • Pilot Projects
  • Placebos
  • Probiotics* / administration & dosage
  • Probiotics* / adverse effects
  • Young Adult

Substances

  • Placebos

Grants and funding

This study was funded by the Health Department of the Catalan Government; the Spanish Government through the CIBER CRP-TB project and ISCIII-Subdirección General de Evaluación and Fondo-EU de Desarrollo Regional (FEDER) through contracts CP13/00174 (CV) and IFI14/00015 (PC); and Manremyc sl. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.