Evidence map›Paper›PMID 39519462›Full record

ArticleNutrients2024

Immunostimulation Signaling via Toll-like Receptor 2 Activation: A Molecular Mechanism of

Hyeon-A Song, Seo-Yun Jang, Min-Ji Park, Seung Wook Kim, Choon Gil Kang, Joo Hyun Lee, Hye-Jin Kim, Jiheon Kim, Jong Kil Lee, Kyung-Sook Chung and 1 more

Abstract read
In one paragraph

Article in Nutrients, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
–field-weighted citation impact
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

6 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Article
  6. EngineeredFrontiers in immunology · 2026
    Article
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

11 authors.

Hyeon-A SongDepartment of Pharmaceutical Biochemistry, College of Pharmacy, Kyung Hee University, Seoul 02447, Republic of Korea.
Seo-Yun JangDepartment of Pharmaceutical Biochemistry, College of Pharmacy, Kyung Hee University, Seoul 02447, Republic of Korea.
Min-Ji ParkDepartment of Pharmaceutical Biochemistry, College of Pharmacy, Kyung Hee University, Seoul 02447, Republic of Korea.
Seung Wook KimOttogi Research Center, Anyang 14060, Republic of Korea.
Choon Gil KangOttogi Research Center, Anyang 14060, Republic of Korea.
Joo Hyun LeeOttogi Research Center, Anyang 14060, Republic of Korea.
Hye-Jin KimOttogi Research Center, Anyang 14060, Republic of Korea.ORCID 0009-0003-1907-4819
Jiheon KimOttogi Research Center, Anyang 14060, Republic of Korea.ORCID 0000-0003-1537-1544
Jong Kil LeeDepartment of Fundamental Pharmaceutical Science, Graduate School, Kyung Hee University, Seoul 02447, Republic of Korea.
Kyung-Sook ChungDepartment of Pharmaceutical Biochemistry, College of Pharmacy, Kyung Hee University, Seoul 02447, Republic of Korea.
Kyung-Tae LeeDepartment of Pharmaceutical Biochemistry, College of Pharmacy, Kyung Hee University, Seoul 02447, Republic of Korea.ORCID 0000-0002-3141-3727

Funding

OTTOGI Corporation OTTOGI Corporation
6 · The paper itself

Abstract

introductionThe immune system's defense against pathogens involves innate and adaptive responses, crucial in maintaining overall health. Immunosuppressed states render individuals more susceptible to potential diseases, indicating the need for effective strategies to bolster immune functions.

objectivesAlthough the immunostimulatory effects of various probiotics have been studied, the specific effects and molecular mechanisms of

methodsTo assess the macrophage activation ability and underlying mechanisms of OTG1204, RAW 264.7 cells were utilized with transfection, enzyme-linked immunosorbent assay, and quantitative real-time PCR analyses. Furthermore, to evaluate the immunostimulatory effects under immunosuppressed conditions, CTX-induced immunosuppression mice model was employed, and analyses were performed using hematoxylin and eosin staining, flow cytometry, and microbiota examination.

resultsOTG1204 activated RAW 264.7 macrophages, leading to increased production of nitric oxide, prostaglandin E2, and cytokines. This immune activation was mediated through the upregulation of toll-like receptor 2, which subsequently activated the nuclear factor-κB (NF-kB) and mitogen-activated protein kinase (MAPK)/activator protein 1 (AP-1) pathways, thereby stimulating the immune response. In CTX-treated mice, OTG1204 recovered body weight, spleen, and mesenteric lymph node indices, and natural killer cell activity. It re-established populations of innate and adaptive immune cells and activated T cells to secrete cytokines. We also examined the gut barrier integrity and microbiota composition to assess OTG1204's impact on intestinal health, as these factors play a significant role in immune enhancement. OTG1204 enhanced gut barrier integrity by upregulating mucin 2 and tight junction proteins and modulated the gut microbiota by restoring the

conclusionThese results suggest that OTG1204 may serve as an effective probiotic for immune enhancement and gut health management by targeting the NF-κB and MAPK/AP-1 pathways, with minimal side effects.

Indexed as

Lactococcus lactisProbioticsSignal TransductionToll-Like Receptor 2AnimalsCyclophosphamideCytokinesGastrointestinal MicrobiomeImmunity, InnateMacrophage ActivationMacrophagesMiceNF-kappa BRAW 264.7 CellsCyclophosphamideCytokinesNF-kappa BTlr2 protein, mouseToll-Like Receptor 2cyclophosphamidegut microbiotaimmuneLactococcus lactis OTG1204macrophagesprobiotics

Identifiers

PMID39519462
PMCPMC11547582

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LicenceCC BY
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Registered trials

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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.