Phagocytosis of virulent Porphyromonas gingivalis by human polymorphonuclear leukocytes requires specific

C W Cutler1, J R Kalmar, R R Arnold

  • 1Department of Oral Biology, Emory University, Atlanta, Georgia 30322.

Insights

Antibody to Porphyromonas gingivalis enhances polymorphonuclear leukocyte (PMN) phagocytosis and killing of the bacteria. Human serum antibody effectiveness varies, with some periodontitis patients showing limited opsonic activity against P. gingivalis strains.

Area of Science:

  • Microbiology and Immunology
  • Oral Health Research
  • Infectious Disease Pathogenesis

Background:

  • Limited understanding of Porphyromonas gingivalis interactions with human polymorphonuclear leukocytes (PMN).
  • The protective role of antibodies against P. gingivalis remains undefined.

Purpose of the Study:

  • To investigate PMN phagocytosis and killing of P. gingivalis.
  • To determine the role of P. gingivalis-specific antibodies in enhancing these processes.

Main Methods:

  • Utilized a fluorochrome phagocytosis microassay to quantify PMN interactions.
  • Tested opsonization with hyperimmune rabbit antiserum (RaPg) and sera from periodontitis patients.
  • Evaluated the impact of antibody concentration, complement, and immunoglobulin G (IgG) fraction.

Main Results:

  • Hyperimmune rabbit antiserum (RaPg) effectively opsonized virulent P. gingivalis strains, enhancing phagocytosis.
  • Human sera from periodontitis patients showed variable and often limited opsonic activity, even with elevated IgG.
  • Intracellular PMN killing was more effective than extracellular or serum-mediated killing of P. gingivalis.

Conclusions:

  • Antibodies, particularly hyperimmune rabbit antiserum, significantly enhance PMN phagocytosis of P. gingivalis.
  • Opsonic activity in human sera is strain-specific and not always correlated with antibody titers.
  • PMN intracellular killing is a crucial mechanism for controlling P. gingivalis infections.

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