Evidence map›Paper›PMID 25655312›Full record

ArticleMolecular therapy : the journal of the American Society of Gene Therapy2015

T-cell subsets in peripheral blood and tumors of patients treated with oncolytic adenoviruses.

Kristian Taipale, Ilkka Liikanen, Juuso Juhila, Aila Karioja-Kallio, Minna Oksanen, Riku Turkki, Nina Linder, Johan Lundin, Ari Ristimäki, Anna Kanerva and 4 more

Erratum issuedOpen access · hybridAbstract read
In one paragraph

Article in Molecular therapy : the journal of the American Society of Gene Therapy, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.0field-weighted citation impact, top 20% 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

13 citing papers in PubMed, 15 citations in OpenAlex.

  1. Article
  2. Article
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  4. Oncolytic adenovirus decreases the proportion of TIM-3Journal for immunotherapy of cancer · 2022
    Article
  5. Article
  6. A Distinct Transcriptional Program in Human CAR T Cells Bearing the 4-1BB Signaling Domain Revealed by scRNA-Seq.Molecular therapy : the journal of the American Society of Gene Therapy · 2020
    Article
  7. Review
  8. Article
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

14 authors at 6 institutions in 1 country.

Kristian TaipaleCancer Gene Therapy Group, Department of Pathology and Transplantation laboratory, Haartman Institute, University of Helsinki, Helsinki, Finland.
Ilkka LiikanenCancer Gene Therapy Group, Department of Pathology and Transplantation laboratory, Haartman Institute, University of Helsinki, Helsinki, Finland.
Juuso JuhilaOncos Therapeutics, Ltd., Helsinki, Finland.
Aila Karioja-KallioOncos Therapeutics, Ltd., Helsinki, Finland.
Minna OksanenCancer Gene Therapy Group, Department of Pathology and Transplantation laboratory, Haartman Institute, University of Helsinki, Helsinki, Finland.
Riku TurkkiInstitute for Molecular Medicine Finland, University of Helsinki, Helsinki, Finland.
Nina LinderInstitute for Molecular Medicine Finland, University of Helsinki, Helsinki, Finland.
Johan LundinInstitute for Molecular Medicine Finland, University of Helsinki, Helsinki, Finland.
Ari RistimäkiDepartment of Pathology, HUSLAB and Haartman Institute, Helsinki University Central Hospital and Genome-Scale Biology, Research Programs Unit, University of Helsinki, Helsinki, Finland.
Anna KanervaCancer Gene Therapy Group, Department of Pathology and Transplantation laboratory, Haartman Institute, University of Helsinki, Helsinki, Finland; Department of Obstetrics and Gynecology, Helsinki University Central Hospital, Helsinki, Finland.
Anniina KoskiCancer Gene Therapy Group, Department of Pathology and Transplantation laboratory, Haartman Institute, University of Helsinki, Helsinki, Finland.
Timo JoensuuDocrates Cancer Center, Helsinki, Finland.
Markus Vähä-KoskelaCancer Gene Therapy Group, Department of Pathology and Transplantation laboratory, Haartman Institute, University of Helsinki, Helsinki, Finland.
Akseli HemminkiCancer Gene Therapy Group, Department of Pathology and Transplantation laboratory, Haartman Institute, University of Helsinki, Helsinki, Finland; TILT Biotherapeutics Ltd., Helsinki, Finland. Electronic address: akseli.hemminki@helsinki.fi.
University of Helsinki · FIOncos Therapeutics (Finland) · FIDocrates Cancer Center · FIFinland University · FIHelsinki University Hospital · FIInstitute for Molecular Medicine Finland · FI

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The quality of the antitumor immune response is decisive when developing new immunotherapies for cancer. Oncolytic adenoviruses cause a potent immunogenic stimulus and arming them with costimulatory molecules reshapes the immune response further. We evaluated peripheral blood T-cell subsets of 50 patients with refractory solid tumors undergoing treatment with oncolytic adenovirus. These data were compared to changes in antiviral and antitumor T cells, treatment efficacy, overall survival, and T-cell subsets in pre- and post-treatment tumor biopsies. Treatment caused a significant (P < 0.0001) shift in T-cell subsets in blood, characterized by a proportional increase of CD8(+) cells, and decrease of CD4(+) cells. Concomitant treatment with cyclophosphamide and temozolomide resulted in less CD4(+) decrease (P = 0.041) than cyclophosphamide only. Interestingly, we saw a correlation between T-cell changes in peripheral blood and the tumor site. This correlation was positive for CD8(+) and inverse for CD4(+) cells. These findings give insight to the interconnections between peripheral blood and tumor-infiltrating lymphocyte (TIL) populations regarding oncolytic virotherapy. In particular, our data suggest that induction of T-cell response is not sufficient for clinical response in the context of immunosuppressive tumors, and that peripheral blood T cells have a complicated and potentially misleading relationship with TILs.

Indexed as

AdenoviridaeGenetic TherapyOncolytic VirotherapyOncolytic VirusesAdolescentAdultAgedAged, 80 and overCD4-Positive T-LymphocytesCD8-Positive T-LymphocytesChildFemaleHumansLymphocyte CountLymphocytes, Tumor-InfiltratingMale

Identifiers

PMID25655312
PMCPMC4427873
OpenAlexW2035324897

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.