Table 1.

Effect of photodynamic cell purging process on antigen-specific interferon-γ secretion measured by enzyme-linked immunospot assay

GroupsResponder onlyAgainst BALB/cAgainst C3H/HeJ
SPOTSSPOTSSISPOTSSI
Naı̈ve C57BL/6 22 ± 11 96 ± 11 4.4 ± 0.5 63 ± 7 2.9 ± 0.3 
Untreated primed cells 64 ± 64 2672 ± 68 36.6 ± 1.0 181 ± 103 2.5 ± 1.4 
PDP-treated primed cells 73 ± 12 650 ± 42*, 10.2 ± 0.7*, 144 ± 11 2.3 ± 0.2 
GroupsResponder onlyAgainst BALB/cAgainst C3H/HeJ
SPOTSSPOTSSISPOTSSI
Naı̈ve C57BL/6 22 ± 11 96 ± 11 4.4 ± 0.5 63 ± 7 2.9 ± 0.3 
Untreated primed cells 64 ± 64 2672 ± 68 36.6 ± 1.0 181 ± 103 2.5 ± 1.4 
PDP-treated primed cells 73 ± 12 650 ± 42*, 10.2 ± 0.7*, 144 ± 11 2.3 ± 0.2 

Spleen cells from C57BL/6 mice were first primed with BALB/c spleen cells in a 5-day mixed lymphocyte culture. The primed cells were then treated with photodynamic cell therapy. After treatment, the cells were incubated with a variety of irradiated stimulators for 42 hours. Frequencies of antigen-specific IFNγ-secreting cells were determined by enzyme-linked immunospot (ELISPOT) assay. The values represent mean ± SD of triplicates per 106 spleen cells. The experiments were repeated twice. SI indicates stimulation index; PDP, photodynamic cell purging process.

*

P < .001, compared with untreated primed cells.

P < .05, compared with naı̈ve C57BL/6.

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