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
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....
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description | 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.
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.
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.
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. |
doi_str_mv | 10.1371/journal.pone.0171294 |
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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.
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.
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.</description><identifier>ISSN: 1932-6203</identifier><identifier>EISSN: 1932-6203</identifier><identifier>DOI: 10.1371/journal.pone.0171294</identifier><identifier>PMID: 28182700</identifier><language>eng</language><publisher>United States: Public Library of Science</publisher><subject>Adult ; Adults ; Biology and Life Sciences ; CD25 antigen ; Clinical trials ; Control methods ; Dietary Supplements - adverse effects ; Double-Blind Method ; Double-blind studies ; Drinking water ; Effector cells ; Female ; Hospitals ; Humans ; Immunogenicity ; Infections ; Infectious diseases ; Latent Tuberculosis - diet therapy ; Latent Tuberculosis - immunology ; Lesions ; Lymphocytes ; Lymphocytes T ; Male ; Medicine and Health Sciences ; Microbial Viability ; Mycobacterium ; Mycobacterium - immunology ; Mycobacterium tuberculosis ; New species ; Pain ; Pathogens ; Pharmacology ; Pilot Projects ; Placebos ; Population (statistical) ; Probiotics - administration & dosage ; Probiotics - adverse effects ; Randomization ; Research and Analysis Methods ; Risk reduction ; Toxicology ; Tuberculosis ; Young Adult</subject><ispartof>PloS one, 2017-02, Vol.12 (2), p.e0171294</ispartof><rights>2017 Montané et al. This is an open access article distributed under the terms of the Creative Commons Attribution License: http://creativecommons.org/licenses/by/4.0/ (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>2017 Montané et al 2017 Montané et al</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c456t-b608602106a73749aba138aced393ead6babce5a419c56f4ba44ce452621c1473</citedby><cites>FETCH-LOGICAL-c456t-b608602106a73749aba138aced393ead6babce5a419c56f4ba44ce452621c1473</cites><orcidid>0000-0001-5623-7873</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC5300153/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC5300153/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,860,881,2096,2915,23845,27901,27902,53766,53768,79343,79344</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/28182700$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Montané, Eva</creatorcontrib><creatorcontrib>Barriocanal, Ana Maria</creatorcontrib><creatorcontrib>Arellano, Ana Lucía</creatorcontrib><creatorcontrib>Valderrama, Angelica</creatorcontrib><creatorcontrib>Sanz, Yolanda</creatorcontrib><creatorcontrib>Perez-Alvarez, Nuria</creatorcontrib><creatorcontrib>Cardona, Paula</creatorcontrib><creatorcontrib>Vilaplana, Cristina</creatorcontrib><creatorcontrib>Cardona, Pere-Joan</creatorcontrib><title>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</title><title>PloS one</title><addtitle>PLoS One</addtitle><description>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.
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.
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.
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.</description><subject>Adult</subject><subject>Adults</subject><subject>Biology and Life Sciences</subject><subject>CD25 antigen</subject><subject>Clinical trials</subject><subject>Control methods</subject><subject>Dietary Supplements - adverse effects</subject><subject>Double-Blind Method</subject><subject>Double-blind studies</subject><subject>Drinking water</subject><subject>Effector cells</subject><subject>Female</subject><subject>Hospitals</subject><subject>Humans</subject><subject>Immunogenicity</subject><subject>Infections</subject><subject>Infectious diseases</subject><subject>Latent Tuberculosis - diet therapy</subject><subject>Latent Tuberculosis - immunology</subject><subject>Lesions</subject><subject>Lymphocytes</subject><subject>Lymphocytes T</subject><subject>Male</subject><subject>Medicine and Health Sciences</subject><subject>Microbial Viability</subject><subject>Mycobacterium</subject><subject>Mycobacterium - 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adverse effects</topic><topic>Double-Blind Method</topic><topic>Double-blind studies</topic><topic>Drinking water</topic><topic>Effector cells</topic><topic>Female</topic><topic>Hospitals</topic><topic>Humans</topic><topic>Immunogenicity</topic><topic>Infections</topic><topic>Infectious diseases</topic><topic>Latent Tuberculosis - diet therapy</topic><topic>Latent Tuberculosis - immunology</topic><topic>Lesions</topic><topic>Lymphocytes</topic><topic>Lymphocytes T</topic><topic>Male</topic><topic>Medicine and Health Sciences</topic><topic>Microbial Viability</topic><topic>Mycobacterium</topic><topic>Mycobacterium - immunology</topic><topic>Mycobacterium tuberculosis</topic><topic>New species</topic><topic>Pain</topic><topic>Pathogens</topic><topic>Pharmacology</topic><topic>Pilot Projects</topic><topic>Placebos</topic><topic>Population (statistical)</topic><topic>Probiotics - administration & dosage</topic><topic>Probiotics - adverse effects</topic><topic>Randomization</topic><topic>Research and Analysis Methods</topic><topic>Risk reduction</topic><topic>Toxicology</topic><topic>Tuberculosis</topic><topic>Young Adult</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Montané, Eva</creatorcontrib><creatorcontrib>Barriocanal, Ana Maria</creatorcontrib><creatorcontrib>Arellano, Ana Lucía</creatorcontrib><creatorcontrib>Valderrama, Angelica</creatorcontrib><creatorcontrib>Sanz, Yolanda</creatorcontrib><creatorcontrib>Perez-Alvarez, Nuria</creatorcontrib><creatorcontrib>Cardona, Paula</creatorcontrib><creatorcontrib>Vilaplana, Cristina</creatorcontrib><creatorcontrib>Cardona, Pere-Joan</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Animal Behavior Abstracts</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Biotechnology Research Abstracts</collection><collection>Nursing & Allied Health Database</collection><collection>Ecology Abstracts</collection><collection>Entomology Abstracts (Full archive)</collection><collection>Immunology Abstracts</collection><collection>Meteorological & Geoastrophysical Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Agricultural Science Collection</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Public Health Database</collection><collection>Technology Research Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Technology Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>Materials Science & Engineering Collection</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest One Sustainability</collection><collection>ProQuest Central UK/Ireland</collection><collection>Advanced Technologies & Aerospace Collection</collection><collection>Agricultural & Environmental Science Collection</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Technology Collection</collection><collection>Natural Science Collection</collection><collection>Environmental Sciences and Pollution Management</collection><collection>ProQuest One Community College</collection><collection>ProQuest Materials Science Collection</collection><collection>ProQuest Central Korea</collection><collection>Engineering Research Database</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Materials Science Database</collection><collection>Nursing & Allied Health Database (Alumni Edition)</collection><collection>Meteorological & Geoastrophysical Abstracts - 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Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>PloS one</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Montané, Eva</au><au>Barriocanal, Ana Maria</au><au>Arellano, Ana Lucía</au><au>Valderrama, Angelica</au><au>Sanz, Yolanda</au><au>Perez-Alvarez, Nuria</au><au>Cardona, Paula</au><au>Vilaplana, Cristina</au><au>Cardona, Pere-Joan</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>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</atitle><jtitle>PloS one</jtitle><addtitle>PLoS One</addtitle><date>2017-02-09</date><risdate>2017</risdate><volume>12</volume><issue>2</issue><spage>e0171294</spage><pages>e0171294-</pages><issn>1932-6203</issn><eissn>1932-6203</eissn><abstract>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.
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.
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.
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.</abstract><cop>United States</cop><pub>Public Library of Science</pub><pmid>28182700</pmid><doi>10.1371/journal.pone.0171294</doi><orcidid>https://orcid.org/0000-0001-5623-7873</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Adult Adults Biology and Life Sciences CD25 antigen Clinical trials Control methods Dietary Supplements - adverse effects Double-Blind Method Double-blind studies Drinking water Effector cells Female Hospitals Humans Immunogenicity Infections Infectious diseases Latent Tuberculosis - diet therapy Latent Tuberculosis - immunology Lesions Lymphocytes Lymphocytes T Male Medicine and Health Sciences Microbial Viability Mycobacterium Mycobacterium - immunology Mycobacterium tuberculosis New species Pain Pathogens Pharmacology Pilot Projects Placebos Population (statistical) Probiotics - administration & dosage Probiotics - adverse effects Randomization Research and Analysis Methods Risk reduction Toxicology Tuberculosis Young Adult |
title | 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 |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-04T00%3A49%3A14IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_plos_&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Pilot,%20double-blind,%20randomized,%20placebo-controlled%20clinical%20trial%20of%20the%20supplement%20food%20Nyaditum%20resae%C2%AE%20in%20adults%20with%20or%20without%20latent%20TB%20infection:%20Safety%20and%20immunogenicity&rft.jtitle=PloS%20one&rft.au=Montan%C3%A9,%20Eva&rft.date=2017-02-09&rft.volume=12&rft.issue=2&rft.spage=e0171294&rft.pages=e0171294-&rft.issn=1932-6203&rft.eissn=1932-6203&rft_id=info:doi/10.1371/journal.pone.0171294&rft_dat=%3Cproquest_plos_%3E1867543397%3C/proquest_plos_%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=1866630530&rft_id=info:pmid/28182700&rft_doaj_id=oai_doaj_org_article_3c74d87573364b8f8678a875936e1be7&rfr_iscdi=true |