Modelling the dynamics of LCMV infection in mice. II: Compartmental structure and immunopathology (Q2177125): Difference between revisions

From MaRDI portal
Created claim: Wikidata QID (P12): Q48029521, #quickstatements; #temporary_batch_1711094041063
ReferenceBot (talk | contribs)
Changed an Item
 
Property / cites work
 
Property / cites work: Q4749635 / rank
 
Normal rank
Property / cites work
 
Property / cites work: Q4114633 / rank
 
Normal rank
Property / cites work
 
Property / cites work: Numerical treatment of the parameter identification problem for delay- differential systems arising in immune response modelling / rank
 
Normal rank
Property / cites work
 
Property / cites work: Distribution of recirculating lymphocytes: A stochastic model foundation / rank
 
Normal rank
Property / cites work
 
Property / cites work: Qualitative Theory of Compartmental Systems / rank
 
Normal rank
Property / cites work
 
Property / cites work: Drug concentration heterogeneity facilitates the evolution of drug resistance / rank
 
Normal rank
Property / cites work
 
Property / cites work: Low level viral persistence after infection with LCMV: A quantitative insight through numerical bifurcation analysis / rank
 
Normal rank
Property / cites work
 
Property / cites work: Q4337615 / rank
 
Normal rank
Property / cites work
 
Property / cites work: Q4449282 / rank
 
Normal rank
Property / cites work
 
Property / cites work: Mathematical Analysis of HIV-1 Dynamics in Vivo / rank
 
Normal rank

Latest revision as of 15:13, 22 July 2024

scientific article
Language Label Description Also known as
English
Modelling the dynamics of LCMV infection in mice. II: Compartmental structure and immunopathology
scientific article

    Statements

    Modelling the dynamics of LCMV infection in mice. II: Compartmental structure and immunopathology (English)
    0 references
    0 references
    0 references
    0 references
    6 May 2020
    0 references
    The authors develop an immunopathology of lymphocytic choriomeningitis virus infection model in mice and analyze the dynamics of the LCMV infection model. The modelling analysis suggests that quantitative demands to CTL memory for maximal protection against a wide range of doses of infection with a primarilyperipher al site of virus replication without the risk of favoring immunopathology. It specifies objectives for CTL vaccination to ensure virus elimination with minimal immunopathology vs. vaccination for disease.
    0 references
    0 references
    0 references
    LCMV Infection model
    0 references
    vaccination
    0 references
    mice
    0 references
    0 references
    0 references