Evidence map›Paper›PMID 12147373›Full record

ArticleLancet (London, England)2002

Malignant effusions and immunogenic tumour-derived exosomes.

Fabrice Andre, Noel E C Schartz, Mojgan Movassagh, Caroline Flament, Patricia Pautier, Philippe Morice, Christophe Pomel, Catherine Lhomme, Bernard Escudier, Thierry Le Chevalier and 5 more

Abstract read
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In one paragraph

Article in Lancet (London, England), 2002. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 462 papers.

0numbers the graph read from it
0cells of the map it votes in
462citing papers in PubMed
6.2field-weighted citation impact, top 3% 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

462 citing papers in PubMed, 938 citations in OpenAlex.

  1. Trial
  2. Towards liquid biopsy-based analysis of antitumour immunity.Nature reviews. Clinical oncology · 2026
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  18. A zinc transporter drives glioblastoma progression via extracellular vesicles-reprogrammed microglial plasticity.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
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  20. Article

402 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

15 authors at 3 institutions in 1 country.

Fabrice AndreDepartments of Clinical Biology, Immunology Unit, Institut Gustave Roussy, Villejuif, France.
Noel E C Schartz
Mojgan Movassagh
Caroline Flament
Patricia Pautier
Philippe Morice
Christophe Pomel
Catherine Lhomme
Bernard Escudier
Thierry Le Chevalier
Thomas Tursz
Sebastian Amigorena
Graca Raposo
Eric Angevin
Laurence Zitvogel
Institut Gustave Roussy · FRCentre National de la Recherche Scientifique · FRInserm · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundExosomes derived from tumours are small vesicles released in vitro by tumour cell lines in culture supernatants. To assess the role of these exosomes in vivo, we examined malignant effusions for their presence. We also investigated whether these exosomes could induce production of tumour-specific T cells when pulsed with dendritic cells.

methodsWe isolated exosomes by ultracentrifugation on sucrose and D(2)O gradients of 11 malignant effusions. We characterised exosomes with Western blot analyses, immunoelectron microscopy, and in-vitro stimulations of autologous T lymphocytes.

findingsMalignant effusions accumulate high numbers of membrane vesicles that have a mean diameter of 80 nm (SD 30). These vesicles have antigen-presenting molecules (MHC class-I heat-shock proteins), tetraspanins (CD81), and tumour antigens (Her2/Neu, Mart1, TRP, gp100). These criteria, including their morphological characteristics, indicate the similarities between these vesicles and exosomes. Exosomes from patients with melanoma deliver Mart1 tumour antigens to dendritic cells derived from monocytes (MD-DCs) for cross presentation to clones of cytotoxic T lymphocytes specific to Mart1. In seven of nine patients with cancer, lymphocytes specific to the tumour could be efficiently expanded from peripheral blood cells by pulsing autologous MD-DCs with autologous ascitis exosomes. In one patient tested, we successfully expanded a restricted T-cell repertoire, which could not be recovered carcinomatosis nodules.

interpretationExosomes derived from tumours accumulate in ascites from patients with cancer. Ascitis exosomes are a natural and new source of tumour-rejection antigens, opening up new avenues for immunisation against cancers.

Indexed as

AdenocarcinomaAdultAgedAged, 80 and overAntigens, NeoplasmCarcinomaCytoplasmic VesiclesDendritic CellsFemaleHumansMaleMART-1 AntigenMiddle AgedNeoplasm ProteinsPleural Effusion, MalignantTumor Cells, CulturedAntigens, NeoplasmMART-1 AntigenMLANA protein, humanNeoplasm Proteins

Identifiers

PMID12147373
OpenAlexW2141003137

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.