ArticleRoyal Society open science2017
Multiple steady states and the form of response functions to antigen in a model for the initiation of T-cell activation.
Article in Royal Society open science, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.
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Who cites it
6 citing papers in PubMed.
- A comparative mathematical modeling study of phenotypic approaches to T cell activation.Scientific reports · 2025Article
- The Enigmatic Nature of the TCR-pMHC Interaction: Implications for CAR-T and TCR-T Engineering.International journal of molecular sciences · 2022Review
- Autophosphorylation and the Dynamics of the Activation of Lck.Bulletin of mathematical biology · 2021Article
- Immunobiochemical Reconstruction of Influenza Lung Infection-Melanoma Skin Cancer Interactions.Frontiers in immunology · 2019Article
- Is TCR/pMHC Affinity a Good Estimate of the T-cell Response? An Answer Based on Predictions From 12 Phenotypic Models.Frontiers in immunology · 2019Article
- Untangling the Hairball: Fitness-Based Asymptotic Reduction of Biological Networks.Biophysical journal · 2017Article
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Authors and funding
2 authors.
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Abstract
The aim of this paper is to study the qualitative behaviour predicted by a mathematical model for the initial stage of T-cell activation. The state variables in the model are the concentrations of phosphorylation states of the T-cell receptor (TCR) complex and the phosphatase SHP-1 in the cell. It is shown that these quantities cannot approach zero and that the model possesses more than one positive steady state for certain values of the parameters. It can also exhibit damped oscillations. It is proved that the chemical concentration which represents the degree of activation of the cell, that of the maximally phosphorylated form of the TCR complex, is, in general, a non-monotone function of the activating signal. In particular, there are cases where there is a value of the dissociation constant of the ligand from the receptor which produces a maximal activation of the T cell. This suggests that mechanisms taking place in the first few minutes after activation and included in the model studied in this paper suffice to explain the optimal dissociation time seen in experiments. In this way, the results of certain simulations in the literature have been confirmed rigorously and some important features which had not previously been seen have been discovered.
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