Recombinant interleukin-2 corrects in vitro the immunological defect of endometriosis

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Recombinant interleukin-2 restored the diminished cytotoxic activity of T-cells against autologous endometrial cells in peripheral blood lymphocytes from endometriosis patients.

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Abstract

PROBLEM: It has been shown recently that women with endometriosis have several immunological defects. In particular, these patients have a defect in peripheral blood natural killer cell activity and have lost their capacity of recognizing and lysing autologous endometrial cells. METHOD: We evaluated the effect of recombinant interleukin-2 (rIL-2) on peripheral blood lymphocytes obtained from both healthy donors and endometriosis patients. The generation of a strong cytolytic activity against autologous endometrial cells was obtained from both normal donors and endometriosis patients. RESULTS: Interestingly, these cytolytic cells belong to the T-cell lineage and do not recognize both autologous keratinocytes and allogeneic endometrial cells, thus suggesting a mechanism of specific recognition of autologous cells. CONCLUSION: The capability of restoring cytolytic activity using rIL-2 suggests a new immunotherapeutic approach for the treatment of severe endometriosis.

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Condition tags

endometriosis

MeSH descriptors

Endometriosis Endometriosis Interleukin-2 Antigens, Differentiation, T-Lymphocyte Antigens, Differentiation, T-Lymphocyte Antigens, Differentiation, T-Lymphocyte Autoimmunity Autoimmunity CD4-Positive T-Lymphocytes CD4-Positive T-Lymphocytes CD4-Positive T-Lymphocytes CD8 Antigens CD8 Antigens CD8 Antigens Cells, Cultured Cells, Cultured Cytotoxicity, Immunologic Cytotoxicity, Immunologic Endometriosis Endometriosis

Citation neighborhood (2-hop)

Papers in the corpus that this work cites (lower rings, blue) and that cite this one (upper rings, green). Dot size scales with the paper's in-corpus citation count — bigger dot = more influential within the endo/adeno field. Click a dot to open that paper. Outer rings show 2-hop neighbours — papers reached through the immediate citers/citees. [ collapse to 1-hop ]

References (30)

Cited by (38)

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