Evidence map›Paper›PMID 19221746›Full record

ArticleCancer immunology, immunotherapy : CII2009

Patient-derived renal cell carcinoma cells fused with allogeneic dendritic cells elicit anti-tumor activity: in vitro results and clinical responses.

Jun Zhou, Desheng Weng, Fangjian Zhou, Ke Pan, Haifeng Song, Qijing Wang, Huan Wang, Hui Wang, Yongqiang Li, Lixi Huang and 3 more

Open access · greenAbstract read
In one paragraph

Article in Cancer immunology, immunotherapy : CII, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
2.8field-weighted citation impact, top 9% 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

20 citing papers in PubMed, 43 citations in OpenAlex.

  1. Trial
  2. Trial
  3. Trial
  4. Review
  5. Dendritic Cell-Based Immunotherapy in Hot and Cold Tumors.International journal of molecular sciences · 2022
    Review
  6. Article
  7. Article
  8. Article
  9. Review
  10. Article
  11. Article
  12. Article
  13. Dendritic cell-based vaccines: barriers and opportunities.Future oncology (London, England) · 2012
    Review
  14. Article
  15. Article
  16. Review
  17. Update on vaccine development for renal cell cancer.Open access journal of urology · 2010
    Review
  18. Immunotherapy for renal cell carcinoma.Clinical & developmental immunology · 2010
    Article
  19. Regulation of tumor immunity by tumor/dendritic cell fusions.Clinical & developmental immunology · 2010
    Review
  20. Cancer vaccine by fusions of dendritic and cancer cells.Clinical & developmental immunology · 2009
    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

13 authors at 3 institutions in 1 country.

Jun ZhouState Key Laboratory of Oncology in Southern China, 510060, Guangzhou, People's Republic of China.
Desheng Weng
Fangjian Zhou
Ke Pan
Haifeng Song
Qijing Wang
Huan Wang
Hui Wang
Yongqiang Li
Lixi Huang
Huakun Zhang
Wei Huang
Jianchuan Xia
Southern Medical University · CNSun Yat-sen University · CNSun Yat-sen University Cancer Center · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Renal cell carcinoma (RCC) has been shown to be susceptible to immunotherapeutic treatment strategies. In the present study, patient-derived tumor cells were fused with allogeneic dendritic cells (DC) to elicit anti-tumor activity against RCC. DC from HLA-A2+ healthy donors were fused with primary RCC cells from ten patients. Phenotype of fusion cells were characterized by flow cytometer and confocal microscopy. In vitro, T cell proliferation, IFN-gamma secretion and cytotoxic T lymphocytes (CTL) activity elicited by allogeneic DC/RCC fusion cells were assessed. Clinically, ten patients were vaccinated with allogeneic DC/RCC fusion vaccine. The adverse effects and toxicity were observed. The clinical response was evaluated by CT scans. After fusion, the created hybrids expressed both tumor associated antigen and DC-derived molecules and could stimulate the proliferation and IFN-gamma secretion of T cells as well as elicit strong CTL activity against RCC cells in vitro. In vivo, no serious adverse effects, toxicity, or signs of autoimmune disease were observed after vaccination therapy. Percentage of T lymphocyte subsets in peripheral blood of patients was increased significantly. One of ten patients exhibited a partial response with regression of lung metastases. Six patients showed stable disease with stabilization of previously progressive disease (follow up 1.5 years). The PR and SD responses, exhibited by 7/10 patients who received the allogeneic DC/RCC fusion vaccine treatment, suggest that this approach is safe and can elicit immunological responses in a significant portion of patients with RCC.

Indexed as

Immunotherapy, AdoptiveAdultAgedCancer VaccinesCarcinoma, Renal CellCell FusionDendritic CellsFemaleFlow CytometryHLA-A2 AntigenHumansInterferon-gammaIn Vitro TechniquesKidney NeoplasmsLymphocyte ActivationMaleCancer VaccinesHLA-A2 AntigenInterferon-gamma

Identifiers

PMID19221746
PMCPMC11030900
OpenAlexW1978355683

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.