Evidence map›Paper›PMID 35741093›Full record

ArticleCells2022

Proteomic and Metabolomic Profiles of T Cell-Derived Exosomes Isolated from Human Plasma.

Aneta Zebrowska, Karol Jelonek, Sujan Mondal, Marta Gawin, Katarzyna Mrowiec, Piotr Widłak, Theresa Whiteside, Monika Pietrowska

Abstract read
In one paragraph

Article in Cells, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing 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

16 citing papers in PubMed.

  1. Review
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  5. Review
  6. Article
  7. Review
  8. Signature Proteins in Small Extracellular Vesicles of Granulocytes and CD4International journal of molecular sciences · 2024
    Article
  9. Tumor-derived Exosomes and Antitumor Immunity.Journal of immunology (Baltimore, Md. : 1950) · 2024
    Review
  10. Review
  11. Review
  12. Article
  13. Exosomal cargos-mediated metabolic reprogramming in tumor microenvironment.Journal of experimental & clinical cancer research : CR · 2023
    Review
  14. Article
  15. Review
  16. 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

8 authors.

Aneta ZebrowskaMaria Sklodowska-Curie National Research Institute of Oncology, 44-102 Gliwice, Poland.
Karol JelonekMaria Sklodowska-Curie National Research Institute of Oncology, 44-102 Gliwice, Poland.ORCID 0000-0002-7233-7695
Sujan MondalUPMC Hillman Cancer Center, University of Pittsburgh Cancer Institute, Pittsburgh, PA 15232, USA.
Marta GawinMaria Sklodowska-Curie National Research Institute of Oncology, 44-102 Gliwice, Poland.ORCID 0000-0002-2834-5129
Katarzyna MrowiecMaria Sklodowska-Curie National Research Institute of Oncology, 44-102 Gliwice, Poland.
Piotr WidłakClinical Research Support Centre, Medical University of Gdańsk, 80-210 Gdańsk, Poland.
Theresa WhitesideUPMC Hillman Cancer Center, University of Pittsburgh Cancer Institute, Pittsburgh, PA 15232, USA.ORCID 0000-0001-7316-6181
Monika PietrowskaMaria Sklodowska-Curie National Research Institute of Oncology, 44-102 Gliwice, Poland.ORCID 0000-0001-9317-7822

Funding

Depleting exosomes to improve responses to immune therapy in HNSCCU01DE029759 · NIDCR · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI WHITESIDE, THERESA L. · 2020 to 2024
$3.5M
Small extracellular vesicles as biomarkers of prognosis and response to therapy in head and neck cancerR01DE031299 · NIDCR · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI Brenda B. Diergaarde, Theresa L. Whiteside · 2023 to 2026
$2.9M
The Adenosinergic Pathway in Tumor-derived ExosomesR01CA256068 · NCI · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI JACKSON, EDWIN KERRY, WHITESIDE, THERESA L. · 2021 to 2025
$2.5M
Restoring anti-tumor immunity in the microenvironment of head and neck cancerR01CA168628 · NCI · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI WHITESIDE, THERESA L. · 2013 to 2017
$1.7M
NCI NIH HHS R01 CA168628NCI NIH HHS R01 CA256068NIDCR NIH HHS R01 DE031299NIDCR NIH HHS U01 DE029759
6 · The paper itself

Abstract

Exosomes that are released by T cells are key messengers involved in immune regulation. However, the molecular profiling of these vesicles, which is necessary for understanding their functions, requires their isolation from a very heterogeneous mixture of extracellular vesicles that are present in the human plasma. It has been shown that exosomes that are produced by T cells could be isolated from plasma by immune capture using antibodies that target the CD3 antigen, which is a key component of the TCR complex that is present in all T lymphocytes. Here, we demonstrate that CD3(+) exosomes that are isolated from plasma can be used for high-throughput molecular profiling using proteomics and metabolomics tools. This profiling allowed for the identification of proteins and metabolites that differentiated the CD3(+) from the CD3(-) exosome fractions that were present in the plasma of healthy donors. Importantly, the proteins and metabolites that accumulated in the CD3(+) vesicles reflected the known molecular features of T lymphocytes. Hence, CD3(+) exosomes that are isolated from human plasma by immune capture could serve as a "T cell biopsy".

Indexed as

ExosomesCD3 ComplexHumansMetabolomicsProteinsProteomicsT-LymphocytesCD3 ComplexProteinsCD3 antigenexosomesimmune capturemetabolomicsproteomicssmall extracellular vesiclesT lymphocytes

Identifiers

PMID35741093
PMCPMC9222142

What OpenQuestion holds

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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.