Evidence map›Paper›PMID 27350044›Full record

ArticleJournal of mathematical biology2017

Stochastic descriptors to study the fate and potential of naive T cell clonotypes in the periphery.

J R Artalejo, A Gómez-Corral, M López-García, C Molina-París

Abstract read
In one paragraph

Article in Journal of mathematical biology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
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

3 citing papers in PubMed.

  1. Article
  2. Fate of a Naive T Cell: A Stochastic Journey.Frontiers in immunology · 2019
    Review
  3. 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

4 authors.

J R ArtalejoDepartment of Statistics and Operations Research, Faculty of Mathematics, Complutense University of Madrid, 28040, Madrid, Spain.
A Gómez-CorralDepartment of Statistics and Operations Research, Faculty of Mathematics, Complutense University of Madrid, 28040, Madrid, Spain.
M López-GarcíaDepartment of Applied Mathematics, School of Mathematics, University of Leeds, Leeds, LS2 9JT, UK.
C Molina-ParísDepartment of Applied Mathematics, School of Mathematics, University of Leeds, Leeds, LS2 9JT, UK. carmen@maths.leeds.ac.uk.

Funding

Biotechnology and Biological Sciences Research Council BB/G023395/1
6 · The paper itself

Abstract

The population of naive T cells in the periphery is best described by determining both its T cell receptor diversity, or number of clonotypes, and the sizes of its clonal subsets. In this paper, we make use of a previously introduced mathematical model of naive T cell homeostasis, to study the fate and potential of naive T cell clonotypes in the periphery. This is achieved by the introduction of several new stochastic descriptors for a given naive T cell clonotype, such as its maximum clonal size, the time to reach this maximum, the number of proliferation events required to reach this maximum, the rate of contraction of the clonotype during its way to extinction, as well as the time to a given number of proliferation events. Our results show that two fates can be identified for the dynamics of the clonotype: extinction in the short-term if the clonotype experiences too hostile a peripheral environment, or establishment in the periphery in the long-term. In this second case the probability mass function for the maximum clonal size is bimodal, with one mode near one and the other mode far away from it. Our model also indicates that the fate of a recent thymic emigrant (RTE) during its journey in the periphery has a clear stochastic component, where the probability of extinction cannot be neglected, even in a friendly but competitive environment. On the other hand, a greater deterministic behaviour can be expected in the potential size of the clonotype seeded by the RTE in the long-term, once it escapes extinction.

Indexed as

Models, BiologicalClone CellsHomeostasisReceptors, Antigen, T-CellT-LymphocytesReceptors, Antigen, T-CellCompetitionCross-reactivityExtinctionStochastic descriptorStochastic univariate birth and death processT cell homeostasisTCR diversity

Identifiers

PMID27350044
PMCPMC5258823

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.