Abstract
The blastogenic response to a crude cell extract of ovarian cancer cells has been studied in 48 patients with ovarian cancer (9, autologous, 39 allogeneic), in 26 female controls matched for age and in 18 female patients with other types of cancer in remission from disease. The responses in ovarian cancer patients in remission and relapse were considered separately. The blastogenic responses to cell extracts of foetal ovary, foetal lung, foetal liver and normal adult ovary were also assessed in a proportion of all 3 groups. The blastogenic responses to ovarian cancer and foetal ovary cell extracts were found to be significantly greater in the ovarian cancer patients in remission than in the controls, but the responses to ovarian cancer extract were not greater in the relapse group or in patients with other cancers. As a blastogenic response to normal ovarian extract was also present in some of these patients, the data so far do not support the hypothesis of a tumour specific antigen. This tumour associated response may be occurring to determinants in foetal or adult ovarian tissue to which the patient becomes sensitized in malignant disease. The response is complex and the nature of the antigen requires further analysis.
Highlights
The blastogenic responses to ovarian cancer and foetal ovary cell extracts were found to be significantly greater in the ovarian cancer patients in remission than in the controls, but the responses to ovarian cancer extract were not greater in the relapse group or in patients with other cancers
We have determined whether the lymphocytes from patients with ovarian cancer will transform when challenged with ovarian cancer cell extracts and whether there is any correlation between the extent of disease and the ability of the lymphocytes to transform in vitro
Dose response assays for ovarian cancer cell extract (CE)
Summary
The blastogenic responses to ovarian cancer and foetal ovary cell extracts were found to be significantly greater in the ovarian cancer patients in remission than in the controls, but the responses to ovarian cancer extract were not greater in the relapse group or in patients with other cancers. As a blastogenic response to normal ovarian extract was present in some of these patients, the data so far do not support the hypothesis of a tumour specific antigen. This tumour associated response may be occurring to determinants in foetal or adult ovarian tissue to which the patient becomes sensitized in malignant disease. AN IMMUNE response which appears to be directed towards tumour antigens has been demonstrated in vitro for several human tissues (Hellstrom et al, 1971). Attention in recent years has been centred on the cell mediated immune response to tumours and this response appears to be instrumental in facilitating tumour rejection (Burnet, 1968). We have looked at the blastogenic response to a cell extract of foetal ovary to see whether an oncofoetal antigen might be at least partly responsible for this blastogenic response
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