Evidence map›Paper›PMID 30538706›Full record

ReviewFrontiers in immunology2018

Glycans as Key Checkpoints of T Cell Activity and Function.

Márcia S Pereira, Inês Alves, Manuel Vicente, Ana Campar, Mariana C Silva, Nuno A Padrão, Vanda Pinto, Ângela Fernandes, Ana M Dias, Salomé S Pinho

Open access · goldAbstract readReview
In one paragraph

Review in Frontiers in immunology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 91 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
91citing papers in PubMed, 1 pooled it
5.5field-weighted citation impact, top 3% 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

91 citing papers in PubMed, 1 synthesis or guideline pooled it, 159 citations in OpenAlex.

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  18. Dichotomous effects of Galectin-9 in disease modulation in murine models of inflammatory bowel disease.Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie · 2025
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31 more citing papers are in PubMed but not listed here.

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

10 authors at 2 institutions in 1 country.

Márcia S PereiraInstitute of Molecular Pathology and Immunology of the University of Porto (IPATIMUP) Porto, Portugal.
Inês AlvesInstitute of Molecular Pathology and Immunology of the University of Porto (IPATIMUP) Porto, Portugal.
Manuel VicenteInstitute of Molecular Pathology and Immunology of the University of Porto (IPATIMUP) Porto, Portugal.
Ana CamparInstitute of Molecular Pathology and Immunology of the University of Porto (IPATIMUP) Porto, Portugal.
Mariana C SilvaInstitute of Molecular Pathology and Immunology of the University of Porto (IPATIMUP) Porto, Portugal.
Nuno A PadrãoInstitute of Molecular Pathology and Immunology of the University of Porto (IPATIMUP) Porto, Portugal.
Vanda PintoInstitute of Molecular Pathology and Immunology of the University of Porto (IPATIMUP) Porto, Portugal.
Ângela FernandesInstitute of Molecular Pathology and Immunology of the University of Porto (IPATIMUP) Porto, Portugal.
Ana M DiasInstitute of Molecular Pathology and Immunology of the University of Porto (IPATIMUP) Porto, Portugal.
Salomé S PinhoInstitute of Molecular Pathology and Immunology of the University of Porto (IPATIMUP) Porto, Portugal.
Universidade do Porto · PTi3S - Instituto de Investigação e Inovação em Saúde, Universidade do Porto · PT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The immune system is highly controlled and fine-tuned by glycosylation, through the addition of a diversity of carbohydrates structures (glycans) to virtually all immune cell receptors. Despite a relative backlog in understanding the importance of glycans in the immune system, due to its inherent complexity, remarkable findings have been highlighting the essential contributions of glycosylation in the regulation of both innate and adaptive immune responses with important implications in the pathogenesis of major diseases such as autoimmunity and cancer. Glycans are implicated in fundamental cellular and molecular processes that regulate both stimulatory and inhibitory immune pathways. Besides being actively involved in pathogen recognition through interaction with glycan-binding proteins (such as C-type lectins), glycans have been also shown to regulate key pathophysiological steps within T cell biology such as T cell development and thymocyte selection; T cell activity and signaling as well as T cell differentiation and proliferation. These effects of glycans in T cells functions highlight their importance as determinants of either self-tolerance or T cell hyper-responsiveness which ultimately might be implicated in the creation of tolerogenic pathways in cancer or loss of immunological tolerance in autoimmunity. This review discusses how specific glycans (with a focus on

Indexed as

AnimalsHumansImmune ToleranceLectins, C-TypeLymphocyte ActivationNeoplasmsPolysaccharidesSelf ToleranceT-LymphocytesLectins, C-TypePolysaccharidesautoimmunityglycansimmune responseN-glycosylationself-toleranceT cells

Identifiers

PMID30538706
PMCPMC6277680
OpenAlexW2903263000

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.