Figure 5. The role of individual inflammation history in the case of slow inflammation resolution (IR <<1).

(a–c) ASM population size dynamics (c-cells, red; p-cells, blue; total population s, black) and (d–f) the corresponding inflammatory status evolution (μ, solid black; inflammatory thresholds μ₁ and μ₂, dashed), characterized by the same inflammation resolution rate, magnitude and average stimulus frequency (λ_d/λ_p  = 0.08, a/μ₁  = 0.5, ω/λ_p  = 0.25). (d) Regular series of inflammatory events; (e–f) two realisations of a series of inflammatory events at random times for the same mean frequency (about once a fortnight) as in (d). (g) Distribution of fold-increase in ASM mass after 300 days for a random sequence of inflammatory events with the same characteristics as in panels (b, c); arrows indicate the fold-increase corresponding to (a–c). (h) The distribution of outcomes with an increase of 25% in the inflammation resolution rate (λ_d/λ_p  = 0.1). (The outcome histograms (g,h) are computed for N = 1000 instances).