Photofrin is a potent sensitizer which localizes, among other sites in
membranes of malignant cells. To evaluate the effect of photodymanic
therapy (PDT) on specific antitumoral immunological response, we used
a chromium release assay to compare the specific cytolytic activity (C
LA) of primed mouse spleen T lymphocytes sensitized against syngeneic
mastocytoma P511 cells. P511 cells or lymphocytes or both were treated
or not with Photofrin and/or light (514 nm). Photofrin alone (1 mu g/
ml, 2 h) reduced CLA by 59% when P511 cells were treated although this
decrease was not drug dose dependent. Photofrin (1 mu g/ml, 2 h) foll
owed by light (25 J/cm(2)) reduced CLA by 35% in a drug dose dependent
manner. Longer incubation times led to reduced CLA inhibition (10% fo
r 3 h incubation) after Photofrin followed by light. The light dose (2
5, 37, 50 J/cm(2)) did not influence CLA for a given Photofrin concent
ration. Photofrin alone (0.5 mu g/ml, followed by light (25 J/cm(2) fo
r 2 h) reduced CLA respectively by 8 and 45% only when lymphocytes wer
e treated. When lymphocytes and P511 cells were treated with Photofrin
alone or followed by light (25 J/cm(2)), CLA was also reduced (by 19
and 41% respectively). This type of damage can be evaluated in terms o
f antigen expression on the target cells, on the lymphocyte T receptor
, on H-2 (histocompatibility major complex), or on lymphocyte activity
after PDT. (C) 1997 International Society for Immunopharmacology.