Evidence map›Paper›PMID 17899077›Full record

Trial reportCancer immunology, immunotherapy : CII2008

Adoptive transfer of T(reg) depleted autologous T cells in advanced renal cell carcinoma.

Fiona C Thistlethwaite, Eyad Elkord, Richard W Griffiths, Deborah J Burt, Alaaeldin M Shablak, John D M Campbell, David E Gilham, Eric B Austin, Peter L Stern, Robert E Hawkins

Open access · bronzeAbstract readClinical Trial
In one paragraph

Trial report in Cancer immunology, immunotherapy : CII, 2008. 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
3.0field-weighted citation impact, top 8% 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

16 citing papers in PubMed, 34 citations in OpenAlex.

  1. Article
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  3. Review
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  10. Review
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  12. Review
  13. Cellular immunotherapy for ovarian cancer.Expert opinion on biological therapy · 2009
    Review
  14. Review
  15. Article
  16. Cyclophosphamide enhances the immunosuppressive action of its own active metabolites.Doklady biological sciences : proceedings of the Academy of Sciences of the USSR, Biological sciences sections
    Article
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

10 authors at 5 institutions in 3 countries.

Fiona C ThistlethwaiteCancer Research UK Department of Medical Oncology, University of Manchester and Christie Hospital NHS Foundation Trust, Manchester, UK. fthistlethwaite@PICR.man.ac.uk
Eyad Elkord
Richard W Griffiths
Deborah J Burt
Alaaeldin M Shablak
John D M Campbell
David E Gilham
Eric B Austin
Peter L Stern
Robert E Hawkins
University of Manchester · GBCancer Research UK · GBThe Christie NHS Foundation Trust · GBMiltenyi Biotec (Germany) · DENational Blood Transfusion Service · NG

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeCD4(+)CD25(+) regulatory T (T(reg)) cells are present in increased numbers in patients with advanced cancer and CD25(+) T cell depletion potentiates tumour immunity in animal models. The aim of this study was to assess the feasibility and safety of adoptive transfer of CD25(+) depleted autologous T cells in patients with advanced renal cell carcinoma and to examine resulting changes in lymphocyte subsets. PATIENTS AND

methodsSix patients with advanced renal cell carcinoma underwent leukapheresis followed by conditioning chemotherapy with cyclophosphamide and fludarabine. The autologous leukapheresis product was depleted of CD25(+) cells using CliniMACS System then re-infused into the patient.

resultsEfficient CD25(+) depletion from all leukapheresis products was achieved and 0.55-5.87 x 10(7)/kg CD3(+) cells were re-infused. Chemotherapy related haematological toxicity was observed, but blood counts recovered in all patients allowing discharge after a mean inpatient stay of 21 days. One patient subsequently developed a rapidly progressive neurological syndrome. A transient reduction in CD25(+) subset was noted in the peripheral blood of 5 out of 6 patients with evidence of increased T cell responses to PHA in 4 out of 6 patients. One patient showed increased specific proliferative responses to the tumour associated antigen h5T4 coinciding with the nadir of T(reg) cells.

conclusionsGiven the transient nature of the reduction in CD25(+) subset and the observed toxicity there is a need to explore further strategies to improve the safety and efficacy of this approach. Nevertheless, the results provide proof of concept in potentiation of tumour antigen T cell responses when T(reg) cell levels are depleted.

Indexed as

Lymphocyte DepletionT-Lymphocytes, RegulatoryAdultAgedCarcinoma, Renal CellCD3 ComplexFemaleFlow CytometryHumansImmunotherapy, AdoptiveKidney NeoplasmsLeukapheresisMaleMiddle AgedT-LymphocytesTransplantation, AutologousCD3 Complex

Identifiers

PMID17899077
PMCPMC11029890
OpenAlexW2062214336

What OpenQuestion holds

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Registered trials

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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.