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. 2004 Apr;72(4):2408–2411. doi: 10.1128/IAI.72.4.2408-2411.2004

TABLE 2.

Assessment of the interaction of P. gingivalis with murine inflammatory cells in murine chamber fluids by fluorescent microscopya

Group Data for day 1
Data for day 3
P. gingivalis/ PMNb % Phagocytosisc P. gingivalis/ PMN % Phagocytosis
1 NDd ND ND ND
2 4.81 ± 4.35 55.39 ± 42.29 3.90 ± 3.68 42.41 ± 20.45
3 0.24 ± 0.19 4.33 ± 4.91 5.62 ± 7.81 37.35 ± 27.93
4 8.08 ± 7.95 59.15 ± 30.45 2.82 ± 1.91 44.34 ± 17.41
5 7.12 ± 7.27 53.65 ± 39.66 5.66 ± 4.20 52.32 ± 14.85
6 14.81 ± 4.5 40.79 ± 44.08 1.53 ± 1.32 30.92 ± 21.94
a

Groups of mice (n = 8 animals per group) were challenged subcutaneously with P. gingivalis, and chamber fluid samples were harvested at 1 and 3 days after challenge. Group 1 received vehicle only, group 2 was challenged with P. gingivalis, group 3 received P. gingivalis-specific IgG injection into the chamber 24 h prior to challenge, group 4 received IRR-IgG injection prior to challenge, group 5 was challenged with P. gingivalis opsonized with P. gingivalis-specific IgG, and group 6 was challenged with IRR-IgG-opsonized P. gingivalis.

b

P. gingivalis/PMN was determined as the total number of live and dead bacteria present within at least 100 live PMNs.

c

% Phagocytosis was determined as the number of viable PMNs that have at least one associated bacterium divided by the total number of PMNs counted, all multiplied by 100.

d

ND, not determined.