Evidence map›Paper›PMID 37945636›Full record

ArticleScientific reports2023

Treatment with a Lactococcus lactis that chromosomally express E. coli cfaI mitigates salivary flow loss in a Sjögren's syndrome-like disease.

Ali Akgul, Christian Furlan Freguia, Massimo Maddaloni, Carol Hoffman, Alexandria Voigt, Cuong Q Nguyen, Neil A Fanger, Gary R Fanger, David W Pascual

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.5field-weighted citation impact, top 33% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

2 citing papers in PubMed, 3 citations in OpenAlex.

  1. Review
  2. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors at 2 institutions in 1 country.

Ali AkgulDepartment of Infectious Diseases and Immunology, University of Florida, Gainesville, FL, USA.
Christian Furlan FreguiaRise Therapeutics, Rockville, MD, USA.
Massimo MaddaloniDepartment of Infectious Diseases and Immunology, University of Florida, Gainesville, FL, USA.
Carol HoffmanDepartment of Infectious Diseases and Immunology, University of Florida, Gainesville, FL, USA.
Alexandria VoigtDepartment of Infectious Diseases and Immunology, University of Florida, Gainesville, FL, USA.
Cuong Q NguyenDepartment of Infectious Diseases and Immunology, University of Florida, Gainesville, FL, USA.
Neil A FangerVirtici, Seattle, WA, USA.
Gary R FangerRise Therapeutics, Rockville, MD, USA.
David W PascualDepartment of Infectious Diseases and Immunology, University of Florida, Gainesville, FL, USA. pascuald@ufl.edu.
University of Florida · USVirtici (United States) · US

Funding

A Novel Probiotic for the Treatment of Sjogren's SyndromeSB1DE030833 · NIDCR · RISE THERAPEUTICS, LLC · PI FANGER, GARY · 2021 to 2023
$2.9M
Mapping the T cell receptor/antigen complex and identifying the genetic-based treatment in Sjogren’s syndromeR01DE028544 · NIDCR · UNIVERSITY OF FLORIDA · PI NGUYEN, CUONG Q · 2019 to 2023
$2.6M
A Novel Probiotic for the Treatment of Sjogren's SyndromeR44DE026379 · NIDCR · RISE THERAPEUTICS, LLC · PI FANGER, GARY · 2019 to 2020
$1.9M
Regulatory Cell Therapy for Sjögren's Syndrome.R01DE026450 · NIDCR · UNIVERSITY OF FLORIDA · PI PASCUAL, DAVID W · 2017 to 2021
$1.8M
Regulatory Cell Therapy for Sjogrens SyndromeR56DE026450 · NIDCR · UNIVERSITY OF WYOMING · PI PASCUAL, DAVID W · 2023 to 2023
$351k
A Novel Probiotic for the Treatment of Sjogren's SyndromeR43DE026379 · NIDCR · VIRTICI, LLC · PI FANGER, NEIL A · 2016 to 2016
$225k
NIDCR NIH HHS R01 DE026450NIDCR NIH HHS R01 DE028544NIDCR NIH HHS R43 DE026379NIDCR NIH HHS R44 DE026379NIDCR NIH HHS R56 DE026450NIDCR NIH HHS SB1 DE030833
6 · The paper itself

Abstract

Sjögren's Syndrome (SjS) results in loss of salivary and lacrimal gland excretion due to an autoimmune attack on these secretory glands. Conventional SjS treatments address the symptoms, but not the cause of disease. Recognizing this deficit of treatments to reverse SjS disease, studies were pursued using the fimbriae from enterotoxigenic E. coli, colonization factor antigen I (CFA/I), which has anti-inflammatory properties. To determine if CFA/I fimbriae could attenuate SjS-like disease in C57BL/6.NOD-Aec1Aec2 (SjS) females, the Lactococcus lactis (LL) 301 strain was developed to chromosomally express the cfaI operon. Western blot analysis confirmed CFA/I protein expression, and this was tested in SjS females at different stages of disease. Repeated dosing with LL 301 proved effective in mitigating salivary flow loss and in reducing anti-nuclear antibodies (ANA) and inflammation in the submandibular glands (SMGs) in SjS females and in restoring salivary flow in diseased mice. LL 301 treatment reduced proinflammatory cytokine production with concomitant increases in TGF-β

Indexed as

Lactococcus lactisSjogren's SyndromeAnimalsDisease Models, AnimalEscherichia coliFemaleMiceMice, Inbred C57BLMice, Inbred NOD

Identifiers

PMID37945636
PMCPMC10636062
OpenAlexW4388540493

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.