Evidence map›Paper›PMID 32164343›Full record

ArticlePharmaceutics2020

MHC Class I Stability is Modulated by Cell Surface Sialylation in Human Dendritic Cells.

Zélia Silva, Tiago Ferro, Danielle Almeida, Helena Soares, José Alexandre Ferreira, Fanny M Deschepper, Paul J Hensbergen, Martina Pirro, Sandra J van Vliet, Sebastian Springer and 1 more

Open access · goldAbstract read
In one paragraph

Article in Pharmaceutics, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
1.5field-weighted citation impact, top 18% 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

17 citing papers in PubMed, 31 citations in OpenAlex.

  1. Article
  2. Review
  3. Frontiers in immunology · 2025
    Article
  4. Article
  5. Review
  6. Review
  7. Review
  8. Review
  9. Article
  10. Article
  11. Article
  12. Sialic acid blockade in dendritic cells enhances CD8Cellular and molecular life sciences : CMLS · 2022
    Article
  13. Article
  14. Neoantigen Controversies.Annual review of biomedical data science · 2021
    Review
  15. Article
  16. Article
  17. 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

11 authors at 5 institutions in 3 countries.

Zélia SilvaUCIBIO, Departamento Ciências da Vida, Faculdade de Ciências e Tecnologia, Universidade Nova de Lisboa, 2829-516 Caparica,Portugal.
Tiago FerroUCIBIO, Departamento Ciências da Vida, Faculdade de Ciências e Tecnologia, Universidade Nova de Lisboa, 2829-516 Caparica,Portugal.
Danielle AlmeidaUCIBIO, Departamento Ciências da Vida, Faculdade de Ciências e Tecnologia, Universidade Nova de Lisboa, 2829-516 Caparica,Portugal.
Helena SoaresHuman Immunobiology and Pathogenesis, CEDOC-Chronic Diseases Research Centre, NOVA Medical School, Faculdade de Ciências Médicas, Universidade Nova de Lisboa, 1150-082 Lisbon, Portugal.
José Alexandre FerreiraExperimental Pathology and Therapeutics Group, Portuguese Institute of Oncology, 4200-162 Porto, Portugal.ORCID 0000-0002-0097-6148
Fanny M DeschepperUCIBIO, Departamento Ciências da Vida, Faculdade de Ciências e Tecnologia, Universidade Nova de Lisboa, 2829-516 Caparica,Portugal.
Paul J HensbergenCenter for Proteomics and Metabolomics, Leiden University Medical Center, 2300 RC Leiden, The Netherlands.
Martina PirroCenter for Proteomics and Metabolomics, Leiden University Medical Center, 2300 RC Leiden, The Netherlands.ORCID 0000-0001-9562-2395
Sandra J van VlietAmsterdam UMC, Vrije Universiteit Amsterdam, Department of Molecular Cell Biology and Immunology, Cancer Center Amsterdam, Amsterdam Infection and Immunity Institute, De Boelelaan 1117, 1081 HzAmsterdam, The Netherlands.
Sebastian SpringerDepartment of Life Sciences and Chemistry, Jacobs University, 28759 Bremen, Germany.
Paula A VideiraUCIBIO, Departamento Ciências da Vida, Faculdade de Ciências e Tecnologia, Universidade Nova de Lisboa, 2829-516 Caparica,Portugal.ORCID 0000-0001-5987-2485
Universidade Nova de Lisboa · PTLeiden University Medical Center · NLAmsterdam University Medical Centers · NLConstructor University · DEInstituto Português de Oncologia Francisco Gentil · PT

Funding

FCT/MCTES (UID/Multi/04378/2013) POCI-01-0145-FEDER-007728Horizon 2020 GlyCoCan programme; grant agreement number 676421Ministério da Ciência, Tecnologia e Ensino Superior CEECIND/03186/2017Ministério da Ciência, Tecnologia e Ensino Superior PD/BD/52472/2014;
6 · The paper itself

Abstract

Maturation of human Dendritic Cells (DCs) is characterized by increased expression of antigen presentation molecules, and overall decreased levels of sialic acid at cell surface. Here, we aimed to identify sialylated proteins at DC surface and comprehend their role and modulation. Mass spectrometry analysis of DC's proteins, pulled down by a sialic acid binding lectin, identified molecules of the major human histocompatibility complex class I (MHC-I), known as human leucocyte antigen (HLA). After desialylation, DCs showed significantly higher reactivity with antibodies specific for properly folded MHC-I-β2-microglobulin complex and for β2-microglobulin but showed significant lower reactivity with an antibody specific for free MHC-I heavy chain. Similar results for antibody reactivities were observed for TAP2-deficient lymphoblastoid T2 cells, which express HLA-A*02:01. Using fluorescent peptide specifically fitting the groove of HLA-A*02:01, instead of antibody staining, also showed higher peptide binding on desialylated cells, confirming higher surface expression of MHC-I complex. A decay assay showed that desialylation doubled the half-life of MHC-I molecules at cell surface in both DCs and T2 cells. The biological impact of DC´s desialylation was evaluated in co-cultures with autologous T cells, showing higher number and earlier immunological synapses, and consequent significantly increased production of IFN-γ by T cells. In summary, sialic acid content modulates the expression and stability of complex MHC-I, which may account for the improved DC-T synapses.

Indexed as

cancer-vaccinesdendritic-cells, antigen-presentation, MHC-I, immunogenicity, T-cell response

Identifiers

PMID32164343
PMCPMC7150992
OpenAlexW3011543036

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.