Presence of Aberrant Tumor-Reactive Immunoglobulins in the Circulation of Patients with Ovarian Cancer

• Published in: Gynecologic oncology Vol. 81; no. 1; pp. 71 - 76
• Main Authors: Gerçel-Taylor, Çiçek, Bazzett, Lisa B., Taylor, Douglas D.
• Format: Journal Article
• Language: English
• Published: San Diego, CA Elsevier Inc 01.04.2001; Elsevier
• Subjects: Antibodies, Neoplasm - blood; Antibodies, Neoplasm - immunology; Antigens, Neoplasm - immunology; Biological and medical sciences; Chromatography, Affinity; Concanavalin A - immunology; Concanavalin A - metabolism; Female; Female genital diseases; Gynecology. Andrology. Obstetrics; Humans; IgG glycosylation; Immunoglobulin G - blood; Immunoglobulin G - immunology; Immunoglobulin G - isolation & purification; Medical sciences; Middle Aged; Neoplastic Cells, Circulating - immunology; Oligosaccharides - immunology; Oligosaccharides - metabolism; ovarian cancer; Ovarian Neoplasms - blood; Ovarian Neoplasms - immunology; Ovarian Neoplasms - pathology; Pilot Projects; Receptors, Concanavalin A - immunology; Receptors, Concanavalin A - metabolism; tumor-reactive antibodies; Tumors; ovarian cancer; IgG glycosylation; tumor-reactive antibodies; Human; Immunoglobulins; Carcinoma; Prognosis; Tumor associated antigen; Antibody; IgG; Glycosylation; Malignant tumor; Female genital diseases; Ovarian diseases; Ovary; Female; Advanced stage
• ISSN: 0090-8258; 1095-6859
• DOI: 10.1006/gyno.2000.6102

Objectives. Cancer patients generally exhibit circulating tumor-reactive immunoglobulins; however, these antibodies fail to eradicate tumors or prevent their progression. This study identifies and characterizes an aberrant tumor-reactive IgG population present in women with ovarian cancer. Methods. In this pilot study, IgG was isolated from the sera of women with advanced-stage ovarian cancer (stages III and IV, n = 62) and age-matched female volunteers (n = 50) by affinity chromatography. These IgGs were characterized on the basis on their aberrant binding to concanavalin A affinity columns. Subsequently, the concanavalin A-binding moiety was localized following IgG fragmentation, analyzed by sodium dodecyl sulfate–polyacrylamide gel electrophoresis, and characterized by oligosaccharide profiling. Results. The level of concanavalin A-binding IgG in our control population was 8.9 ± 2.9%, whereas in ovarian cancer patients, the level of concanavalin A-binding IgG was 38.8 ± 7.4%. In the patients with ovarian cancer, 87.5 ± 5.7% of the tumor-reactive IgG was demonstrated to be concanavalin A-binding. Based on oligosaccharide profiling of the fragmented concanavalin A-binding IgG, the aberrant lectin binding appeared to be the consequence of altered glycosylation of one of the two Fc chains. Conclusions. While our previous studies have identified the presence of circulating IgG reactive with specific tumor-associated antigens and its association with poor prognosis, this report demonstrated the presence of an aberrantly glycosylated IgG population in cancer patients. This altered IgG appeared to be the primary class of tumor-reactive antibodies in these women.