Evidence map›Paper›PMID 40243284›Full record

ReviewXenotransplantation

Dendritic Cells in Xenotransplantation: Shaping the Cellular Immune Response Toward Tolerance.

Gisella L Puga Yung, Tom Wakley, Athanasios Kouklas, Jörg D Seebach

Abstract readReview
In one paragraph

Review in Xenotransplantation. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Review
  2. 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

4 authors.

Gisella L Puga YungDivision of Immunology and Allergology, Department of Medicine, University Hospitals Geneva, Geneva, Switzerland.ORCID 0000-0002-2283-7798
Tom WakleyLaboratory of Translational Immunology, Department of Medicine, University of Geneva, Geneva, Switzerland.
Athanasios KouklasLaboratory of Translational Immunology, Department of Medicine, University of Geneva, Geneva, Switzerland.ORCID 0000-0002-3282-0674
Jörg D SeebachDivision of Immunology and Allergology, Department of Medicine, University Hospitals Geneva, Geneva, Switzerland.ORCID 0000-0001-5748-4577

Funding

Private FoundationSwiss National Science Foundation CRSII5_198577
6 · The paper itself

Abstract

The molecular barriers that cause acute xenograft rejection have been identified and addressed by generating genetically modified (GM) animals, knocked out for specific xenoantigens (xenoAgs), and expressing regulatory molecules for both complement and coagulation pathways among others. The focus of xenotransplantation research now lies in delayed xenograft rejection. Dendritic cells (DC) are a specific subpopulation of professional antigen-presenting cells (APC) that play a crucial role in the context of organ transplantation. DCs, originating from both the xenograft and the recipient, have the capacity to present xenoAgs to the recipient's immune system via their respective major histocompatibility complex (MHC) molecules leading to rejection. These processes are known as direct and indirect presentation, respectively. However, under certain microenvironmental conditions, DC develops into anti-inflammatory regulatory cells that can induce immunological tolerance. The purpose of this review is to summarize current knowledge on the general characteristics and functions of DC from species relevant to xenotransplantation, specifically humans, non-human primates (NHP), and pigs. It will also cover the process of xenoAg presentation, different methods for generating DC with regulatory properties in vitro, and finally, discuss the current strategies for using regulatory DC to improve xenograft acceptance by inducing tolerance.

Indexed as

Dendritic CellsGraft RejectionHeterograftsImmune ToleranceImmunity, CellularTransplantation, HeterologousTransplantation ToleranceAnimalsHumansPrimatesSwineDCdendritic cellsspeciestolerancexenotransplantation

Identifiers

PMID40243284
PMCPMC12005074

What OpenQuestion holds

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LicenceCC BY-NC-ND
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.