Evidence map›Paper›PMID 40791842›Full record

ArticleJournal of immunology research2025

Intradermally Administered Retinoic Acid or Vitamin D3-Loaded Liposomes Induce Tolerogenic Skin Dendritic Cells.

Noémi Anna Nagy, Sanne G Celant, Toni M M van Capel, Rinske Sparrius, Fernando Lozano Vigario, Ronald van Ree, Bram Slütter, Teunis B H Geijtenbeek, Sander W Tas, Esther C de Jong

Abstract read
In one paragraph

Article in Journal of immunology research, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
–field-weighted citation impact
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

4 citing papers in PubMed.

  1. Review
  2. Article
  3. Review
  4. 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

10 authors.

Noémi Anna NagyDepartment of Experimental Immunology, Amsterdam University Medical Centers, Amsterdam Institute for Infection and Immunity, Amsterdam, Netherlands.ORCID https://orcid.org/0009-0006-8719-3336
Sanne G CelantDepartment of Experimental Immunology, Amsterdam University Medical Centers, Amsterdam Institute for Infection and Immunity, Amsterdam, Netherlands.ORCID https://orcid.org/0009-0009-1598-7446
Toni M M van CapelDepartment of Experimental Immunology, Amsterdam University Medical Centers, Amsterdam Institute for Infection and Immunity, Amsterdam, Netherlands.ORCID https://orcid.org/0009-0005-9403-9866
Rinske SparriusDepartment of Experimental Immunology, Amsterdam University Medical Centers, Amsterdam Institute for Infection and Immunity, Amsterdam, Netherlands.ORCID https://orcid.org/0009-0008-0753-372X
Fernando Lozano VigarioDivision of BioTherapeutics, Leiden Academic Center for Drug Research, Leiden University, Leiden, Netherlands.ORCID https://orcid.org/0000-0003-0994-8773
Ronald van ReeDepartment of Experimental Immunology, Amsterdam University Medical Centers, Amsterdam Institute for Infection and Immunity, Amsterdam, Netherlands.ORCID https://orcid.org/0000-0003-0767-0894
Bram SlütterDivision of BioTherapeutics, Leiden Academic Center for Drug Research, Leiden University, Leiden, Netherlands.ORCID https://orcid.org/0000-0003-3996-0503
Teunis B H GeijtenbeekDepartment of Experimental Immunology, Amsterdam University Medical Centers, Amsterdam Institute for Infection and Immunity, Amsterdam, Netherlands.ORCID https://orcid.org/0000-0002-5710-2839
Sander W TasDepartment of Experimental Immunology, Amsterdam University Medical Centers, Amsterdam Institute for Infection and Immunity, Amsterdam, Netherlands.ORCID https://orcid.org/0000-0002-8940-1788
Esther C de JongDepartment of Experimental Immunology, Amsterdam University Medical Centers, Amsterdam Institute for Infection and Immunity, Amsterdam, Netherlands.ORCID https://orcid.org/0000-0003-0410-3018

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In vivo targeting of dendritic cells (DCs) with nanocarriers containing tolerogenic adjuvants is an attractive strategy to dampen inflammation. Here, we used ex vivo skin vaccination to examine the effect of intradermal injection of liposomes loaded with the tolerogenic adjuvants all-trans retinoic acid (RA) and vitamin D3 (VD3). We investigated the effect of intradermal liposome injection on skin DCs and the skin DC-induced T cell response. Our study shows that intradermal injection of RA or VD3-loaded anionic phospholipid 1,2-distearoyl-sn-glycero-3-phosphoglycerol (DSPG) liposomes selectively induces CD14+ dermal DC (DDC) migration while reducing migration of CD1a dim DDCs. Migrated CD14+ DDCs displayed a partially immature phenotype. RA or VD3 liposome-treated CD1a dim DDCs exhibited reduced expression of maturation markers and induced expression of coinhibitory immunoglobulin-like transcript 3 (ILT3). VD3 liposome-treated CD14+ DDCs, as well as, CD1a dim DDCs, exhibited reduced expression of maturation markers, induction of coinhibitory molecules ILT3, and programmed death-ligand 1 (PD-L1). Migrated DCs from RA or VD3 liposome-injected skin differentiated naïve CD4+ T cells into FoxP3+ CD127 low and ICOS+ Tregs, expressing functional regulatory markers. Thus, our findings provide further substantiation for in vivo DC-modulating vaccines with tolerogenic liposomes as a putative clinical therapy for autoimmune diseases and allergies.

Indexed as

CholecalciferolDendritic CellsLangerhans CellsLiposomesSkinTretinoinAdjuvants, ImmunologicAnimalsAntigens, CD1Cell DifferentiationCell MovementCells, CulturedFemaleHumansImmune ToleranceInjections, IntradermalAdjuvants, ImmunologicAntigens, CD1CholecalciferolLipopolysaccharide ReceptorsLiposomesTretinoin

Identifiers

PMID40791842
PMCPMC12339165

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Registered trials

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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.