Effects of immunomodulators on functional activity of innate immunity cells infected with Streptococcus pneumoniae

N G Plekhova1, N M Kondrashova, L M Somova

  • 1G. P. Somov Research Institute of Epidemiology and Microbiology, Siberian Division of the Russian Academy of Medical Sciences, Vladivostok, Russia, pl_pat@hotmail.com.

Insights

Innate immune cells infected with Streptococcus pneumoniae showed low bactericidal enzyme activity, leading to faster cell death. Maxifloxacin treatment increased enzyme activity and induced necrotic cell death, with immunomodulators improving outcomes.

Area of Science:

  • Immunology
  • Microbiology
  • Pharmacology

Background:

  • Innate immunity cells, such as phagocytes, play a crucial role in combating bacterial infections.
  • Streptococcus pneumoniae (S. pneumoniae) is a significant human pathogen that can evade or subvert host immune responses.
  • Bactericidal enzymes within immune cells are key effectors of pathogen clearance.

Purpose of the Study:

  • To investigate the impact of S. pneumoniae infection on the activity of bactericidal enzymes in innate immune cells.
  • To evaluate the effects of the antibiotic maxifloxacin on these enzymes and cell viability.
  • To assess the therapeutic potential of combining maxifloxacin with immunomodulators (tinrostim and licopid) in correcting cellular dysfunction.

Main Methods:

  • Infection models using innate immunity cells and S. pneumoniae.
  • Measurement of bactericidal enzyme activity in phagocytes.
  • Assessment of cell death pathways (necrosis).
  • Evaluation of combined therapeutic effects of maxifloxacin, tinrostim, and licopid.

Main Results:

  • S. pneumoniae infection led to decreased bactericidal enzyme activity and accelerated cell death in innate immune cells.
  • Maxifloxacin treatment enhanced bactericidal enzyme activity in phagocytes and induced necrotic cell death.
  • Combination therapy with maxifloxacin and immunomodulators (tinrostim or licopid) demonstrated a corrective effect on the functional activity of infected cells.

Conclusions:

  • S. pneumoniae infection impairs crucial innate immune cell functions, specifically bactericidal enzyme activity.
  • Maxifloxacin exhibits dual effects by boosting enzyme activity and inducing necrosis, suggesting complex interactions with immune cells.
  • Combined immunomodulator and antibiotic therapy holds promise for restoring immune cell function during S. pneumoniae infections.

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