Evidence map›Paper›PMID 21359217›Full record

ArticlePloS one2011

Porcine sialoadhesin (CD169/Siglec-1) is an endocytic receptor that allows targeted delivery of toxins and antigens to macrophages.

Peter L Delputte, Hanne Van Gorp, Herman W Favoreel, Inge Hoebeke, Iris Delrue, Hannah Dewerchin, Frank Verdonck, Bruno Verhasselt, Eric Cox, Hans J Nauwynck

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 56 papers.

0numbers the graph read from it
0cells of the map it votes in
56citing papers in PubMed
3.0field-weighted citation impact, top 9% 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

56 citing papers in PubMed, 81 citations in OpenAlex.

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  16. Targeting of sialoadhesin-expressing macrophages through antibody-conjugated (polyethylene glycol) poly(lactic-co-glycolic acid) nanoparticles.Journal of nanoparticle research : an interdisciplinary forum for nanoscale science and technology · 2022
    Article
  17. Article
  18. Research progress on CD169-positive macrophages in tumors.American journal of translational research · 2021
    Review
  19. Article
  20. Dexamethasone enhances CD163 expression in porcine IPKM immortalized macrophages.In vitro cellular & developmental biology. Animal · 2021
    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

10 authors at 2 institutions in 2 countries.

Peter L DelputteLaboratory of Virology, Department of Virology, Parasitology, and Immunology, Faculty of Veterinary Medicine, Ghent University, Merelbeke, Belgium. Peter.Delputte@Ugent.be
Hanne Van Gorp
Herman W Favoreel
Inge Hoebeke
Iris Delrue
Hannah Dewerchin
Frank Verdonck
Bruno Verhasselt
Eric Cox
Hans J Nauwynck
Ghent University · BEDepartment of Virology · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Sialoadhesin is exclusively expressed on specific subpopulations of macrophages. Since sialoadhesin-positive macrophages are involved in inflammatory autoimmune diseases, such as multiple sclerosis, and potentially in the generation of immune responses, targeted delivery of drugs, toxins or antigens via sialoadhesin-specific immunoconjugates may prove a useful therapeutic strategy. Originally, sialoadhesin was characterized as a lymphocyte adhesion molecule, though recently its involvement in internalization of sialic acid carrying pathogens was shown, suggesting that sialoadhesin is an endocytic receptor. In this report, we show that porcine sialoadhesin-specific antibodies and F(ab')₂ fragments trigger sialoadhesin internalization, both in primary porcine macrophages and in cells expressing recombinant porcine sialoadhesin. Using chemical inhibitors, double immunofluorescence stainings and dominant-negative constructs, porcine sialoadhesin internalization was shown to be clathrin- and Eps15-dependent and to result in targeting to early endosomes but not lysosomes. Besides characterizing the sialoadhesin endocytosis mechanism, two sialoadhesin-specific immunoconjugates were evaluated. We observed that porcine sialoadhesin-specific immunotoxins efficiently kill sialoadhesin-expressing macrophages. Furthermore, porcine sialoadhesin-specific albumin immunoconjugates were shown to be internalized in macrophages and immunization with these immunoconjugates resulted in a rapid and robust induction of albumin-specific antibodies, this compared to immunization with albumin alone. Together, these data expand sialoadhesin functionality and show that it can function as an endocytic receptor, a feature that cannot only be misused by sialic acid carrying pathogens, but that may also be used for specific targeting of toxins or antigens to sialoadhesin-expressing macrophages.

Indexed as

AnimalsAntigensCarrier ProteinsCells, CulturedCell SurvivalDose-Response Relationship, DrugEndocytosisImmunotoxinsMacrophages, AlveolarMembrane GlycoproteinsProtein TransportReceptors, Cell SurfaceReceptors, ImmunologicSialic Acid Binding Ig-like Lectin 1SwineToxins, BiologicalAntigensCarrier ProteinsImmunotoxinsMembrane GlycoproteinsReceptors, Cell SurfaceReceptors, ImmunologicSialic Acid Binding Ig-like Lectin 1Toxins, Biological

Identifiers

PMID21359217
PMCPMC3040196
OpenAlexW2083337775

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.