Complement (C5)-derived chemotactic activity accounts for accumulation of polymorphonuclear leukocytes in

Infection and Immunity
|October 1, 1984
PubMed

Insights

In rabbit meningitis, complement C5-derived factors attract polymorphonuclear leukocytes to cerebrospinal fluid. This chemoattractant activity drives leukocyte accumulation during infection.

Area of Science:

  • Immunology
  • Neuroscience
  • Microbiology

Background:

  • Polymorphonuclear leukocytes (PMNs) are crucial for combating bacterial infections.
  • Cerebrospinal fluid (CSF) analysis is vital for diagnosing meningitis.
  • The specific chemoattractants driving PMN infiltration in pneumococcal meningitis are not fully understood.

Purpose of the Study:

  • To identify the chemoattractant responsible for polymorphonuclear leukocyte (PMN) accumulation in the cerebrospinal fluid (CSF) during experimental pneumococcal meningitis.
  • To elucidate the role of complement system activation in this process.

Main Methods:

  • Induction of Streptococcus pneumoniae meningitis in New Zealand white rabbits.
  • Measurement of chemotactic activity in CSF using rabbit PMNs.
  • Characterization of chemoattractant properties (heat stability, size exclusion chromatography).
  • Inhibition studies using antibodies to human C5 and purified rabbit C5a.

Main Results:

  • Chemotactic activity for PMNs significantly increased in CSF 12 hours post-infection, peaking at 18-20 hours.
  • The chemotactic activity was heat-stable and co-eluted with complement-derived factors.
  • Activity was inhibited by anti-C5 antibodies and selective blockade with C5a.

Conclusions:

  • Complement (C5)-derived chemoattractant activity appears in CSF during experimental pneumococcal meningitis.
  • This C5-derived activity is a primary driver for the accumulation of polymorphonuclear leukocytes in the infected CSF.
  • Findings highlight the role of the complement system in the inflammatory response to bacterial meningitis.

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