Abstract

Measles virus (MV) is a highly contagious respiratory morbillivirus that results in many disabilities and deaths. A crucial challenge in studying MV infection is to understand the so-called ‘measles paradox’—the progression of the infection to severe immunosuppression before clearance of acute viremia, which is also observed in canine distemper virus (CDV) infection. However, a lack of models that match in vivo data has restricted our understanding of this complex and counter-intuitive phenomenon. Recently, progress was made in the development of a model that fits data from acute measles infection in rhesus macaques. This progress motivates our investigations to gain additional insights from this model into the control mechanisms underlying the paradox. In this paper, we investigated analytical conditions determining the control and robustness of viral clearance for MV and CDV, to untangle complex feedback mechanisms underlying the dynamics of acute infections in their natural hosts. We applied control theory to this model to help resolve the measles paradox. We showed that immunosuppression is important to control and clear the virus. We also showed under which conditions T-cell killing becomes the primary mechanism for immunosuppression and viral clearance. Furthermore, we characterized robustness properties of T-cell immunity to explain similarities and differences in the control of MV and CDV. Together, our results are consistent with experimental data, advance understanding of control mechanisms of viral clearance across morbilliviruses, and will help inform the development of effective treatments. Further the analysis methods and results have the potential to advance understanding of immune system responses to a range of viral infections such as COVID-19.

Highlights

  • Measles virus (MV) is one of the most transmissible viruses affecting humans and results in many disabilities and deaths [1,2,3]

  • The killing of infected lymphocytes remains lower than the production of infected lymphocytes during acute canine distemper virus (CDV) infection, see figure 2B4. These results support previous findings which suggest that the depletion of lymphocytes by CDV enforces the clearance of acute CDV infection [13,14,15,16]. These results indicate that the balance between the production and killing of infected lymphocytes determines the control of acute viremia by virus-induced lymphocyte death or by T-cell immunity

  • The control analysis of MV and CDV infections contributes to the resolution of the measles paradox

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Summary

Introduction

Measles virus (MV) is one of the most transmissible viruses affecting humans and results in many disabilities and deaths [1,2,3]. Since the virus mainly replicates in lymphoid tissues, virus-induced lymphocyte death seems to be the major cause of immunosuppression and extensive target-cell depletion could lead to viral clearance [8,9,14,16]. The simulations in [16] provide quantitative evidence suggesting that the clearance of acute viremia is dominated by T-cell immunity during measles infection, but dominated by target-cell depletion when viral fitness is increased to simulate CDV infection. This model has yet to be mathematically analysed beyond simulations and we still lack insight into the underlying causes of this paradox. Our results advance understanding of virus–host interactions leading to the control of acute viremia and immunosuppression during morbillivirus infections

Background
Experimental data
Mathematical model
A infected lymphocytes feedback control
Immunosuppression enforces viral clearance
B1: CDV infected lymphocytes
B3: CDV specific T cells cells m1–1 magnitude
T-cell immunity ensures the robustness of measles viral clearance
Discussion
Analysis to determine the control of viral clearance
Analysing the robustness of viral clearance
Full Text
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