Evidence map›Paper›PMID 25815811›Full record

ArticlePloS one2015

A biased competition theory of cytotoxic T lymphocyte interaction with tumor nodules.

Claire Christophe, Sabina Müller, Magda Rodrigues, Anne-Elisabeth Petit, Patrick Cattiaux, Loïc Dupré, Sébastien Gadat, Salvatore Valitutti

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.3field-weighted citation impact, top 41% 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

2 citing papers in PubMed, 10 citations in OpenAlex.

  1. Article
  2. 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

8 authors at 4 institutions in 2 countries.

Claire ChristopheInstitut de Mathématiques de Toulouse, CNRS UMR 5219, Toulouse, France; INSERM, UMR 1043, Centre de Physiopathologie de Toulouse Purpan, Section Dynamique Moléculaire des Interactions Lymphocytaires, Toulouse, France; Université Toulouse III Paul Sabatier, Toulouse, France.
Sabina MüllerINSERM, UMR 1043, Centre de Physiopathologie de Toulouse Purpan, Section Dynamique Moléculaire des Interactions Lymphocytaires, Toulouse, France; Université Toulouse III Paul Sabatier, Toulouse, France.
Magda RodriguesINSERM, UMR 1043, Centre de Physiopathologie de Toulouse Purpan, Section Dynamique Moléculaire des Interactions Lymphocytaires, Toulouse, France; Université Toulouse III Paul Sabatier, Toulouse, France.
Anne-Elisabeth PetitLudwig Institute for Cancer Research, Brussels Branch, Université de Bruxelles, Bruxelles, Belgique.
Patrick CattiauxInstitut de Mathématiques de Toulouse, CNRS UMR 5219, Toulouse, France; Université Toulouse III Paul Sabatier, Toulouse, France.
Loïc DupréINSERM, UMR 1043, Centre de Physiopathologie de Toulouse Purpan, Section Dynamique Moléculaire des Interactions Lymphocytaires, Toulouse, France; Université Toulouse III Paul Sabatier, Toulouse, France.
Sébastien GadatInstitut de Mathématiques de Toulouse, CNRS UMR 5219, Toulouse, France; Toulouse School of Economics, Université de Toulouse I Capitole, Toulouse, France.
Salvatore ValituttiINSERM, UMR 1043, Centre de Physiopathologie de Toulouse Purpan, Section Dynamique Moléculaire des Interactions Lymphocytaires, Toulouse, France; Université Toulouse III Paul Sabatier, Toulouse, France.
Centre National de la Recherche Scientifique · FRInserm · FRLudwig Cancer Research · BEUniversité Toulouse III - Paul Sabatier · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The dynamics of the interaction between Cytotoxic T Lymphocytes (CTL) and tumor cells has been addressed in depth, in particular using numerical simulations. However, stochastic mathematical models that take into account the competitive interaction between CTL and tumors undergoing immunoediting, a process of tumor cell escape from immunesurveillance, are presently missing. Here, we introduce a stochastic dynamical particle interaction model based on experimentally measured parameters that allows to describe CTL function during immunoediting. The model describes the competitive interaction between CTL and melanoma cell nodules and allows temporal and two-dimensional spatial progression. The model is designed to provide probabilistic estimates of tumor eradication through numerical simulations in which tunable parameters influencing CTL efficacy against a tumor nodule undergoing immunoediting are tested. Our model shows that the rate of CTL/tumor nodule productive collisions during the initial time of interaction determines the success of CTL in tumor eradication. It allows efficient cytotoxic function before the tumor cells acquire a substantial resistance to CTL attack, due to mutations stochastically occurring during cell division. Interestingly, a bias in CTL motility inducing a progressive attraction towards a few scout CTL, which have detected the nodule enhances early productive collisions and tumor eradication. Taken together, our results are compatible with a biased competition theory of CTL function in which CTL efficacy against a tumor nodule undergoing immunoediting is strongly dependent on guidance of CTL trajectories by scout siblings. They highlight unprecedented aspects of immune cell behavior that might inspire new CTL-based therapeutic strategies against tumors.

Indexed as

Models, ImmunologicalHumansMelanomaModels, BiologicalMonitoring, ImmunologicStochastic ProcessesT-Lymphocytes, CytotoxicTumor Cells, CulturedTumor Escape

Identifiers

PMID25815811
PMCPMC4376944
OpenAlexW2160548289

What OpenQuestion holds

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LicenceCC BY
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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.