Abstract | BACKGROUND: METHODS: Two patients with MHE responded well to intralesional injections of recombinant IL-2 (rIL-2) without major side effects. The purpose of this study was to characterize cells infiltrating the regressing tumor following rIL-2 treatment. Immunohistochemical studies were performed on biopsy specimens taken from rIL-2-injected lesional skin. RESULTS: It was shown that CD8+ lymphocytes and CD56+ natural killer (NK) cells infiltrated at the rIL-2-injection sites, suggesting that these cells contributed to the tumor regression. In addition, MHE cells bore intercellular adhesion molecule-1 (ICAM-1) whose expression was augmented by rIL-2 injections. CONCLUSIONS: These findings suggested, that rIL-2 not only induces lymphokine-activated killer (LAK) cells and NK cells, but also facilitates these cytotoxic cells to adhere to MHE cells by enhancing ICAM-1 expression of tumor cells.
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Authors | H Ihda, Y Tokura, M Fushimi, R Yokote, H Hashizume, S Shirahama, K Iwatsuki, K Murakami, M Takigawa |
Journal | International journal of dermatology
(Int J Dermatol)
Vol. 34
Issue 11
Pg. 811-6
(Nov 1995)
ISSN: 0011-9059 [Print] England |
PMID | 8543420
(Publication Type: Case Reports, Journal Article)
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Chemical References |
- Interleukin-2
- Recombinant Proteins
- Intercellular Adhesion Molecule-1
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Topics |
- Aged
- CD8-Positive T-Lymphocytes
(pathology)
- Female
- Hemangiosarcoma
(immunology, pathology, therapy)
- Humans
- Immunohistochemistry
- Intercellular Adhesion Molecule-1
(analysis)
- Interleukin-2
(therapeutic use)
- Killer Cells, Natural
(immunology, pathology)
- Male
- Middle Aged
- Recombinant Proteins
- Skin Neoplasms
(immunology, pathology, therapy)
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