Statistical mechanics of clonal expansion in lymphocyte networks modelled with slow and fast variables
Alexander Mozeika, Anthony CC Coolen

TL;DR
This paper applies statistical mechanics to model the adaptive immune system, analyzing how B and T cell populations evolve on different timescales and predicting clone size distributions using a theoretical framework that aligns with experimental data.
Contribution
It introduces a novel statistical mechanics approach to model lymphocyte interactions with different timescales, deriving clone size distributions independently of network topology.
Findings
Derived stationary distributions for B and T cell populations.
Predicted B clone size distributions consistent with experimental observations.
Developed a Bethe-Peierls based framework for random network topologies.
Abstract
We study the Langevin dynamics of the adaptive immune system, modelled by a lymphocyte network in which the B cells are interacting with the T cells and antigen. We assume that B clones and T clones are evolving in different thermal noise environments and on different timescales. We derive stationary distributions and use statistical mechanics to study clonal expansion of B clones in this model when the B and T clone sizes are assumed to be the slow and fast variables respectively and vice versa. We derive distributions of B clone sizes and use general properties of ferromagnetic systems to predict characteristics of these distributions, such as the average B cell concentration, in some regimes where T cells can be modelled as binary variables. This analysis is independent of network topologies and its results are qualitatively consistent with experimental observations. In order to…
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