Evidence map›Paper›PMID 32879009›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2020

Plasmacytoid dendritic cells cross-prime naive CD8 T cells by transferring antigen to conventional dendritic cells through exosomes.

Chunmei Fu, Peng Peng, Jakob Loschko, Li Feng, Phuong Pham, Weiguo Cui, Kelvin P Lee, Anne B Krug, Aimin Jiang

Abstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 84 papers.

0numbers the graph read from it
0cells of the map it votes in
84citing 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

84 citing papers in PubMed.

  1. Article
  2. The DC1 conundrum: Do type I dendritic cells make or break allograft tolerance?American journal of transplantation : official journal of the American Society of Transplantation and the American Society of Transplant Surgeons · 2026
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  5. E7Science advances · 2026
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24 more citing papers are in PubMed but not listed here.

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

9 authors.

Chunmei FuCenter for Cutaneous Biology and Immunology, Department of Dermatology, Henry Ford Health System, Detroit, MI 48202.
Peng PengDepartment of Immunology, Roswell Park Comprehensive Cancer Center, Buffalo, NY 14263.ORCID 0000-0001-7022-506X
Jakob LoschkoII Medizinische Klinik, Klinikum Rechts der Isar, Technische Universität München, D-81675 Munich, Germany.
Li FengDepartment of Immunology, Roswell Park Comprehensive Cancer Center, Buffalo, NY 14263.ORCID 0000-0002-5206-6234
Phuong PhamDepartment of Immunology, Roswell Park Comprehensive Cancer Center, Buffalo, NY 14263.
Weiguo CuiBlood Research Institute, Blood Center of Wisconsin, Milwaukee, WI 53213.
Kelvin P LeeDepartment of Immunology, Roswell Park Comprehensive Cancer Center, Buffalo, NY 14263.
Anne B KrugInstitute for Immunology, Biomedical Center, Ludwig-Maximilians-University Munich, 82152 Planegg-Martinsried, Germany.
Aimin JiangCenter for Cutaneous Biology and Immunology, Department of Dermatology, Henry Ford Health System, Detroit, MI 48202; ajiang3@hfhs.org.

Funding

Two-Spirit Films in Indigenous Cancer HealthP30CA016056 · NCI · ROSWELL PARK CANCER INSTITUTE CORP · PI Dean G. Tang · 1985 to 2026
$116.6M
b-catenin in vaccine-induced anti-tumor CD8 T cell immunityR01CA198105 · NCI · ROSWELL PARK CANCER INSTITUTE CORP · PI JIANG, AIMIN · 2015 to 2019
$2.0M
NCI NIH HHS P30 CA016056NCI NIH HHS R01 CA198105
6 · The paper itself

Abstract

Although plasmacytoid dendritic cells (pDCs) have been shown to play a critical role in generating viral immunity and promoting tolerance to suppress antitumor immunity, whether and how pDCs cross-prime CD8 T cells in vivo remain controversial. Using a pDC-targeted vaccine model to deliver antigens specifically to pDCs, we have demonstrated that pDC-targeted vaccination led to strong cross-priming and durable CD8 T cell immunity. Surprisingly, cross-presenting pDCs required conventional DCs (cDCs) to achieve cross-priming in vivo by transferring antigens to cDCs. Taking advantage of an in vitro system where only pDCs had access to antigens, we further demonstrated that cross-presenting pDCs were unable to efficiently prime CD8 T cells by themselves, but conferred antigen-naive cDCs the capability of cross-priming CD8 T cells by transferring antigens to cDCs. Although both cDC1s and cDC2s exhibited similar efficiency in acquiring antigens from pDCs, cDC1s but not cDC2s were required for cross-priming upon pDC-targeted vaccination, suggesting that cDC1s played a critical role in pDC-mediated cross-priming independent of their function in antigen presentation. Antigen transfer from pDCs to cDCs was mediated by previously unreported pDC-derived exosomes (pDCexos), that were also produced by pDCs under various conditions. Importantly, all these pDCexos primed naive antigen-specific CD8 T cells only in the presence of bystander cDCs, similarly to cross-presenting pDCs, thus identifying pDCexo-mediated antigen transfer to cDCs as a mechanism for pDCs to achieve cross-priming. In summary, our data suggest that pDCs employ a unique mechanism of pDCexo-mediated antigen transfer to cDCs for cross-priming.

Indexed as

AnimalsAntigen PresentationCD8-Positive T-LymphocytesCells, CulturedCross-PrimingDendritic CellsExosomesHumansMiceMice, Inbred C57BLantigen transferconventional dendritic cellscross-primingexosomesplasmacytoid dendritic cells

Identifiers

PMID32879009
PMCPMC7519282

What OpenQuestion holds

Textmetadata
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.