Topical ALA–PDT modifies neutrophils’ chemiluminescence, lymphocytes’ interleukin-1beta secretion and serum level of transforming growth factor beta1 in patients with nonmelanoma skin malignancies:
A clinical study
Summary
Background:
Photodynamic therapy (PDT) has been recognized as a noninvasive therapeutic approach for the effective treatment of tumors. It has been shown in studies conducted on malignant cell lines and various animal tumor models, that the interaction of photosensitizing substances with light leads to the release of cytotoxic substances and stimulates the immune response.
Purpose:
The aim of our study was to analyze the immune system response in patients undergoing photodynamic therapy due to basal cell carcinoma (BCC).
Methods:
Patients with skin malignancies have been treated by 10% delta-aminolevulinic acid (ALA) (Medac GmbH, Wedel, Germany) topically and light from a diode laser. Blood samples were obtained from each patient twice in the same day: before and 4
h after photodynamic treatment procedure. In patients’ serum the concentration of transforming growth factor beta1 (TGF-β1) was determined. Additionally the study has been conducted on lymphocytes and granulocytes from peripheral blood. In cell culture supernatants the concentration of interleukin 1beta (IL-1β), interleukin 2 (IL-2), interleukin 6 (IL-6), tumor necrosis factor alpha (TNFα), the percentile composition of patients’ lymphocytes and the chemiluminescence of neutrophils have been measured.
Results:
We have observed a significant increase (p
=
0.015) in the intensity of the neutrophil chemiluminescence and significant diminution (p
=
0.006) of IL-1β concentration in supernatants. Similarly the serum level of TGF-β1 has been significantly decreased (p
<
0.001).
Conclusion:
It is very likely that human immune system activity is modified by topical ALA–PDT and may potentially contribute to its final outcome.
Abbreviations: PDT, photodynamic therapy, BCC, basal cell carcinoma, ALA, delta-aminolevulinic acid, DMSO, dimethyl sulphoxide, PpIX, Protoporphyrin IX, PHA, phytohaemaglutinin, Con A, concanavalin-A, LPS, lypopolisacharide, PMA, Phorbol Myristate Acetate, GM-CSF, granulocyte-macrophage colony-stimulating factor
Keywords: Photodynamic therapy (PDT), Basal cell carcinoma (BCC), Immunomodulation
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PII: S1572-1000(05)00004-9
doi:10.1016/S1572-1000(05)00004-9
© 2005 Elsevier B.V. All rights reserved.
