Evidence map›Paper›PMID 26098776›Full record

ArticleOncotarget2015

Lymphatic dysfunction attenuates tumor immunity through impaired antigen presentation.

Takayuki Kimura, Makoto Sugaya, Tomonori Oka, Andrew Blauvelt, Hitoshi Okochi, Shinichi Sato

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
1.7field-weighted citation impact, top 14% 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

26 citing papers in PubMed, 46 citations in OpenAlex.

  1. Article
  2. Lymphatic transport in anti-tumor immunity and metastasis.The Journal of experimental medicine · 2025
    Review
  3. Review
  4. Review
  5. Article
  6. Review
  7. Lymphatics in Tumor Progression and Immunomodulation.International journal of molecular sciences · 2022
    Review
  8. Review
  9. Article
  10. Review
  11. Review
  12. Review
  13. Lymph Node Stromal Cells: Mapmakers of T Cell Immunity.International journal of molecular sciences · 2020
    Review
  14. Review
  15. Engineering Targeting Materials for Therapeutic Cancer Vaccines.Frontiers in bioengineering and biotechnology · 2020
    Review
  16. Article
  17. Lymphatic vasculature in tumor metastasis and immunobiology.Journal of Zhejiang University. Science. B · 2019
    Review
  18. Article
  19. Review
  20. 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

6 authors at 3 institutions in 2 countries.

Takayuki KimuraDepartment of Dermatology, Faculty of Medicine, University of Tokyo, Tokyo, Japan.
Makoto SugayaDepartment of Dermatology, Faculty of Medicine, University of Tokyo, Tokyo, Japan.
Tomonori OkaDepartment of Dermatology, Faculty of Medicine, University of Tokyo, Tokyo, Japan.
Andrew BlauveltOregon Medical Research Center, Portland, OR, USA.
Hitoshi OkochiDepartment of Regenerative Medicine, Research Institute, National Center for Global Health and Medicine, Tokyo, Japan.
Shinichi SatoDepartment of Dermatology, Faculty of Medicine, University of Tokyo, Tokyo, Japan.
The University of Tokyo · JPNational Center for Global Health and Medicine · JPOregon Medical Research Center · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Tumor growth and metastasis of cancer involve autonomous tumor cell growth and host-tumor interactions. While tumor-specific immunity has been intensively studied in vitro, dynamic roles of lymphatic transport on tumor immunity in vivo have not been fully elucidated. In this study, we examined tumor growth and anti-tumor immune responses using kCYC mice, which demonstrate severe lymphatic dysfunction. Primary tumor growth was augmented in kCYC mice (compared to wild-type mice) when B16 melanoma or EL-4 lymphoma cells were subcutaneously injected. Expression of inflammatory cytokines such as IFN-γ, TNF-α, and IL-2 as well as IL-10 expression in draining lymph nodes (LNs) was significantly reduced in kCYC mice after tumor inoculation. Moreover, decreased levels of tumor-associated antigens were detected in draining LNs in kCYC mice, together with impaired antigen presentation. CD8+ T cells in draining LNs derived from kCYC mice bearing B16 melanoma also showed significantly decreased cytotoxic activity in vitro. Finally, tumor suppression activity of CD8+ T cells derived from kCYC mice bearing B16 melanoma was reduced when adoptively transferred to naive wild-type mice. In summary, these findings suggest that lymphatic transport is essential in generating optimal tumor-specific immune responses mediated by CD8+ T cells.

Indexed as

Antigen PresentationTumor EscapeAdoptive TransferAnimalsAntigens, NeoplasmCD8-Positive T-LymphocytesCyclinsCytokinesInflammation MediatorsLymph NodesLymphomaMelanoma, ExperimentalMice, TransgenicSkin NeoplasmsTime FactorsTumor BurdenAntigens, NeoplasmCyclinsCytokinesInflammation MediatorsK cyclin protein, Herpesvirus 8, HumanViral Proteinscytotoxic T cellslymphaticslymphedematumor immunity

Identifiers

PMID26098776
PMCPMC4627236
OpenAlexW1625405509

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.