Evidence map›Paper›PMID 35309936›Full record

ArticleFrontiers in cell and developmental biology2022

Siglec Receptors Modulate Dendritic Cell Activation and Antigen Presentation to T Cells in Cancer.

Jinyu Wang, Michela Manni, Anne Bärenwaldt, Ronja Wieboldt, Nicole Kirchhammer, Robert Ivanek, Michal Stanczak, Alfred Zippelius, David König, Natalia Rodrigues Manutano and 1 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in cell and developmental biology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed
4.1field-weighted citation impact, top 5% 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

31 citing papers in PubMed, 48 citations in OpenAlex.

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  9. Bisecting GlcNAc enhances CD8Experimental hematology & oncology · 2025
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  13. Frontiers in immunology · 2025
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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

11 authors at 2 institutions in 1 country.

Jinyu WangDepartment of Biomedicine, University Hospital and University of Basel, Basel, Switzerland.
Michela ManniDepartment of Biomedicine, University Hospital and University of Basel, Basel, Switzerland.
Anne BärenwaldtDepartment of Biomedicine, University Hospital and University of Basel, Basel, Switzerland.
Ronja WieboldtDepartment of Biomedicine, University Hospital and University of Basel, Basel, Switzerland.
Nicole KirchhammerDepartment of Biomedicine, University Hospital and University of Basel, Basel, Switzerland.
Robert IvanekDepartment of Biomedicine, University Hospital and University of Basel, Basel, Switzerland.
Michal StanczakDepartment of Biomedicine, University Hospital and University of Basel, Basel, Switzerland.
Alfred ZippeliusDepartment of Biomedicine, University Hospital and University of Basel, Basel, Switzerland.
David KönigDepartment of Biomedicine, University Hospital and University of Basel, Basel, Switzerland.
Natalia Rodrigues ManutanoDepartment of Biomedicine, University Hospital and University of Basel, Basel, Switzerland.
Heinz LäubliDepartment of Biomedicine, University Hospital and University of Basel, Basel, Switzerland.
University of Basel · CHUniversity Hospital of Basel · CH

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Interactions between sialylated glycans and sialic acid-binding immunoglobulin-like lectin (Siglec) receptors have been recently described as potential new immune checkpoint that can be targeted to improve anticancer immunity. Myeloid cells have been reported to express a wide range of different Siglecs; however, their expression and functions on cancer-associated dendritic cells (DCs) were not fully characterized. We found that classical conventional DCs (cDCs) from cancer patient samples have a high expression of several inhibitory Siglecs including Siglec-7, Siglec-9, and Siglec-10. In subcutaneous murine tumor models, we also found an upregulation of the inhibitory Siglec-E receptor on cancer-associated cDCs. DC lines and bone marrow-derived DCs (BMDCs) with expression of these inhibitory Siglecs showed impaired maturation states on transcriptome and protein level. Furthermore, ablation of these inhibitory Siglecs from DCs enhanced their capability to prime antigen-specific T cells and induce proliferation. Our work provides a deeper understanding of the influence of inhibitory Siglecs on DCs and reveals a potential new target to improve cancer immunotherapy.

Indexed as

antigenantigen processingglyco-immune checkpointsialic acidtumor immunology

Identifiers

PMID35309936
PMCPMC8927547
OpenAlexW4214885668

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.