Evidence map›Paper›PMID 30906773›Full record

ArticleBioMed research international2019

Oxaliplatin Treatment Alters Systemic Immune Responses.

Vanesa Stojanovska, Monica Prakash, Rachel McQuade, Sarah Fraser, Vasso Apostolopoulos, Samy Sakkal, Kulmira Nurgali

Open access · hybridAbstract read
In one paragraph

Article in BioMed research international, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 34 papers.

0numbers the graph read from it
0cells of the map it votes in
34citing papers in PubMed
4.6field-weighted citation impact, top 5% 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

34 citing papers in PubMed, 48 citations in OpenAlex.

  1. Review
  2. Improved Systemic Immunochemotherapy Employing an Oxaliplatin-TLR7/8 Agonist Prodrug Strategy.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026
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  11. Observational
  12. Platinum(IV) Derivatives of [Pt(1Journal of medicinal chemistry · 2023
    Article
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  14. Review
  15. Review
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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

7 authors at 2 institutions in 1 country.

Vanesa StojanovskaInstitute for Health and Sport, Victoria University, Melbourne, VIC 8001, Australia.
Monica PrakashInstitute for Health and Sport, Victoria University, Melbourne, VIC 8001, Australia.
Rachel McQuadeInstitute for Health and Sport, Victoria University, Melbourne, VIC 8001, Australia.
Sarah FraserInstitute for Health and Sport, Victoria University, Melbourne, VIC 8001, Australia.
Vasso ApostolopoulosInstitute for Health and Sport, Victoria University, Melbourne, VIC 8001, Australia.ORCID 0000-0001-6788-2771
Samy SakkalInstitute for Health and Sport, Victoria University, Melbourne, VIC 8001, Australia.
Kulmira NurgaliInstitute for Health and Sport, Victoria University, Melbourne, VIC 8001, Australia.ORCID 0000-0002-2597-6929
Victoria University · AUThe University of Melbourne · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeOxaliplatin is a platinum-based chemotherapeutic agent demonstrating significant antitumor efficacy. Unlike conventional anticancer agents which are immunosuppressive, oxaliplatin has the capacity to stimulate immunological effects in response to the presentation of damage associated molecular patterns (DAMPs) elicited upon cell death. However, the effects of oxaliplatin treatment on systemic immune responses remain largely unknown. Aims of this study were to investigate the effects of oxaliplatin treatment on the proportions of (1) splenic T cells, B cells, macrophages, pro-/anti-inflammatory cytokines, gene expression of splenic cytokines, chemokines, and mediators; (2) double-positive and single-positive CD4

methodsMale BALB/c mice received intraperitoneal injections of oxaliplatin (3mg/kg/d) or sterile water tri-weekly for 2 weeks. Leukocyte populations within the spleen, thymus, and bone-marrow were assessed using flow cytometry. RT-PCR was performed to characterise changes in splenic inflammation-associated genes.

resultsOxaliplatin treatment reduced spleen size and cellularity (CD45

conclusionOxaliplatin does not cause systemic immunosuppression and, instead, has the capacity to induce beneficial antitumor immune responses.

Indexed as

AnimalsBone Marrow CellsCD4-Positive T-LymphocytesCD8-Positive T-LymphocytesChemokinesCytokinesGene ExpressionHematopoietic Stem CellsHumansImmune ToleranceImmunity, CellularMaleMice, Inbred BALB CNeoplasmsOxaliplatinSpleenChemokinesCytokinesOxaliplatin

Identifiers

PMID30906773
PMCPMC6398049
OpenAlexW2912766931

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.