Related Experiment Video
Updated: Aug 12, 2026

Isolation of Brain-infiltrating Leukocytes
Published on: June 13, 2011
Complement (C5)-derived chemotactic activity accounts for accumulation of polymorphonuclear leukocytes in
Abstract:
Experiments were performed to identify the chemoattractant for polymorphonuclear leukocytes that appears in the cerebrospinal fluid of rabbits with experimental pneumococcal meningitis. Meningitis was induced in anesthetized New Zealand white rabbits by injecting 10(4) cells of stationary-phase Streptococcus pneumoniae type III intracisternally. Before bacteria were injected, cerebrospinal fluid contained neither polymorphonuclear leukocytes nor chemotactic activity. Significant chemotactic activity for rabbit polymorphonuclear leukocytes was detected 12 h after inoculation with bacteria and was maximal after 18 to 20 h. Chemotactic activity appeared in cerebrospinal fluid while concentrations of pneumococci and total protein were increasing but before there was any accumulation of polymorphonuclear leukocytes. The chemotactic activity in cerebrospinal fluid was heat stable (56 degrees C for 30 min), eluted from Sephadex G-75 with a profile identical to that of the chemotactic activity in zymosan-activated rabbit serum, and was inhibited by treatment with antibodies to native human C5. In addition, preincubation of polymorphonuclear leukocytes with partially purified rabbit C5a selectively inhibited their subsequent chemotactic responses to cerebrospinal fluid. These data indicate that complement (C5)-derived chemotactic activity appears in cerebrospinal fluid during the course of experimental pneumococcal meningitis in rabbits and suggest that this activity accounts for the accumulation of polymorphonuclear leukocytes observed in this infection.
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.
Related Concept Videos
Differentiation of Common Myeloid Progenitor Cells
Complement System
Bacterial Meningitis
Bacterial Meningitis II: Pathophysiology

