Evidence map›Paper›PMID 34127673›Full record

ArticleNature communications2021

Structural specificities of cell surface β-glucan polysaccharides determine commensal yeast mediated immuno-modulatory activities.

Changhon Lee, Ravi Verma, Seohyun Byun, Eun-Ji Jeun, Gi-Cheon Kim, Suyoung Lee, Hye-Ji Kang, Chan Johng Kim, Garima Sharma, Abhishake Lahiri and 9 more

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 36 papers.

0numbers the graph read from it
0cells of the map it votes in
36citing papers in PubMed
11.7field-weighted citation impact, top 1% 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

36 citing papers in PubMed, 82 citations in OpenAlex.

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  14. Pharmaceuticals (Basel, Switzerland) · 2025
    Article
  15. Gut microbiota and brain-resident CD4Nature communications · 2025
    Article
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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

19 authors at 6 institutions in 4 countries.

Changhon LeeDivision of Integrative Biosciences and Biotechnology, Department of Life Sciences, Pohang University of Science and Technology (POSTECH), Pohang, Republic of Korea.
Ravi VermaDivision of Integrative Biosciences and Biotechnology, Department of Life Sciences, Pohang University of Science and Technology (POSTECH), Pohang, Republic of Korea.
Seohyun ByunDivision of Integrative Biosciences and Biotechnology, Department of Life Sciences, Pohang University of Science and Technology (POSTECH), Pohang, Republic of Korea.ORCID 0000-0001-8151-9346
Eun-Ji JeunDivision of Integrative Biosciences and Biotechnology, Department of Life Sciences, Pohang University of Science and Technology (POSTECH), Pohang, Republic of Korea.
Gi-Cheon KimDepartment of Microbiology and Immunology, Yonsei University College of Medicine, Seoul, Republic of Korea.
Suyoung LeeDivision of Integrative Biosciences and Biotechnology, Department of Life Sciences, Pohang University of Science and Technology (POSTECH), Pohang, Republic of Korea.
Hye-Ji KangAdvanced convergence, Handong Global University, Pohang, Republic of Korea.
Chan Johng KimDivision of Integrative Biosciences and Biotechnology, Department of Life Sciences, Pohang University of Science and Technology (POSTECH), Pohang, Republic of Korea.
Garima SharmaDivision of Integrative Biosciences and Biotechnology, Department of Life Sciences, Pohang University of Science and Technology (POSTECH), Pohang, Republic of Korea.
Abhishake LahiriDivision of Structural Biology and Bioinformatics, CSIR-Indian Institute of Chemical Biology, Kolkata, India.
Sandip PaulDivision of Structural Biology and Bioinformatics, CSIR-Indian Institute of Chemical Biology, Kolkata, India.ORCID 0000-0001-7406-3598
Kwang Soon KimDivision of Integrative Biosciences and Biotechnology, Department of Life Sciences, Pohang University of Science and Technology (POSTECH), Pohang, Republic of Korea.
Dong Soo HwangDivision of Integrative Biosciences and Biotechnology, Department of Life Sciences, Pohang University of Science and Technology (POSTECH), Pohang, Republic of Korea.ORCID 0000-0002-2487-2255
Yoichiro IwakuraCenter for Animal Disease Models, Research Institute for Biomedical Sciences, Tokyo University of Science, Noda-shi, Chiba, Japan.ORCID 0000-0002-9934-5775
Immacolata SpecialeDepartment of Agricultural Sciences, University of Napoli, Portici, Italy.ORCID 0000-0003-4363-7450
Antonio MolinaroTask Force on Microbiome Studies, University of Naples Federico II, Naples, Italy.ORCID 0000-0002-3456-7369
Cristina De CastroDepartment of Agricultural Sciences, University of Napoli, Portici, Italy.
Dipayan RudraDivision of Integrative Biosciences and Biotechnology, Department of Life Sciences, Pohang University of Science and Technology (POSTECH), Pohang, Republic of Korea. rudrad@postech.ac.kr.ORCID 0000-0002-9667-5891
Sin-Hyeog ImDivision of Integrative Biosciences and Biotechnology, Department of Life Sciences, Pohang University of Science and Technology (POSTECH), Pohang, Republic of Korea. iimsh@postech.ac.kr.ORCID 0000-0002-3173-1856
Pohang University of Science and Technology · KRUniversity of Naples Federico II · ITIndian Institute of Chemical Biology · INHandong Global University · KRTokyo University of Science · JPYonsei University · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Yeast is an integral part of mammalian microbiome, and like commensal bacteria, has the potential of being harnessed to influence immunity in clinical settings. However, functional specificities of yeast-derived immunoregulatory molecules remain elusive. Here we find that while under steady state, β-1,3-glucan-containing polysaccharides potentiate pro-inflammatory properties, a relatively less abundant class of cell surface polysaccharides, dubbed mannan/β-1,6-glucan-containing polysaccharides (MGCP), is capable of exerting potent anti-inflammatory effects to the immune system. MGCP, in contrast to previously identified microbial cell surface polysaccharides, through a Dectin1-Cox2 signaling axis in dendritic cells, facilitates regulatory T (Treg) cell induction from naïve T cells. Furthermore, through a TLR2-dependent mechanism, it restrains Th1 differentiation of effector T cells by suppressing IFN-γ expression. As a result, administration of MGCP display robust suppressive capacity towards experimental inflammatory disease models of colitis and experimental autoimmune encephalomyelitis (EAE) in mice, thereby highlighting its potential therapeutic utility against clinically relevant autoimmune diseases.

Indexed as

Animalsbeta-GlucansCD4-Positive T-LymphocytesCell DifferentiationColitisCyclooxygenase 2Dectin-1Dendritic CellsEncephalomyelitis, Autoimmune, ExperimentalGlucansHomeodomain ProteinsImmunityImmunomodulationLectins, C-TypeMannansMicebeta-GlucansCyclooxygenase 2Dectin-1GlucansHomeodomain ProteinsLectins, C-TypeMannansPolysaccharidesPtgs2 protein, mouseRAG-1 proteinZymosan

Identifiers

PMID34127673
PMCPMC8203763
OpenAlexW3172216030

What OpenQuestion holds

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LicenceCC BY
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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.