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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.
Abstract:
No studies to date clearly define the interactions between Porphyromonas gingivalis and human peripheral blood polymorphonuclear leukocytes (PMN), nor has a protective role for antibody to P. gingivalis been defined. Using a fluorochrome phagocytosis microassay, we investigated PMN phagocytosis and killing of P. gingivalis as a function of P. gingivalis-specific antibody. Sera from a nonimmune rabbit and a healthy human subject were not opsonic for virulent P. gingivalis A7436, W83, and HG405; phagocytosis of these strains (but not 33277) required opsonization with hyperimmune antiserum (RaPg). Diluting RaPg with a constant complement source decreased proportionally the number of P. gingivalis A7436 cells phagocytosed per phagocytic PMN. Enriching for the immunoglobulin G fraction of RAPg A7436 enriched for opsonic activity toward A7436. An opsonic evaluation of 18 serum samples from adult periodontitis patients revealed that only 3 adult periodontitis sera of 17 with elevated immunoglobulin G to P. gingivalis A7436 were opsonic for A7436 and, moreover, that the serum sample with the highest enzyme-linked immunosorbent assay titer was most opsonic (patient 1). However, the opsonic activity of serum from patient 1 was qualitatively and not just quantitatively different from that of the nonopsonic human sera (but was less effective opsonin than RaPg). Strain variability was observed in resistance of P. gingivalis to phagocytosis, and opsonization was strain specific for some, but not all, strains tested. An evaluation of killing of A7436 revealed that serum killing and extracellular killing of P. gingivalis were less effective alone when compared with intracellular PMN killing alone.
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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