## Abstract Lymphocytes from 16 stage 1, 6 stage II and 31 stage III melanoma patients (MP) and 51 healthy donors (HD) were tested as far as possible in parallel on a melanoma cell line (NK1‐4), a bladder carcinoma cell line (T 24) and 18 different short‐term melanoma cultures. Lymphocytes from MP
Cytotoxic lymphocytes in melanoma patients
✍ Scribed by Jan E. De Vries; Philip Rümke; Jean L. Bernheim
- Publisher
- John Wiley and Sons
- Year
- 1972
- Tongue
- French
- Weight
- 670 KB
- Volume
- 9
- Category
- Article
- ISSN
- 0020-7136
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
Peripheral blood lymphocytes from 61 melanoma patients were tested by a microcytotoxicity test for cell‐mediated immunity against melanoma cells. Lymphocytes from 13/25 patients were cytotoxic for autologous tumour cells, while lymphocytes from 31/56 patients were cytotoxic in the allogeneic situation. In the cases tested no cytotoxic reaction was found against autologous or allogeneic normal skin fibroblasts. Normal control lymphocytes were cytotoxic in 2/50 individuals tested. Lymphocytes from patients with other neoplastic diseases showed a positive cytotoxic effect in 1/18 patients tested. In seven cases lymphocytes from melanoma patients, which were cytotoxic for melanoma cells, did not show any cytotoxic effect on plated choriocarcinoma cells. There was no correlation between the presence of specifically immune lymphocytes and the clinical staging of the disease. In the serum of patients with distant metastases, preliminary results indicated the presence of factors which could block the cytotoxic effect of specifically immune lymphocytes.
The data suggest that most malignant melanomas contain a common antigen which is immunogenic in patients with this neoplasm. However, individual‐ or subgroupspecific melanoma antigens may exist. Evidence is found that lymphocytes can lose their capacity to kill melanoma cells in the course of the disease. Change of antigenic expression or sensitivity to the killing effect of lymphocytes during culturing of the melanoma cells may explain the irregularity of some results.
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## Abstract Lymphocytes from 25 healthy donors were separated into T‐ and non‐T‐fractions by means of E and EAC rosette‐formation. The unfractionated lymphocyte population was tested simultaneously with E and non‐EAC rosette‐forming cells (T‐cells) and EAC and non‐E rosette‐forming cells (non‐T cel