Humoral immunity in normal and complicated pregnancy

• Published in: European journal of obstetrics & gynecology and reproductive biology Vol. 19; no. 4; p. 205
• Main Authors: Houwert-de Jong, M H, Claas, F H, Gmelig-Meyling, F H, Kalsbeek, G L, Valentijn, R M, te Velde, E R, Schuurman, H J
• Format: Journal Article
• Language: English
• Published: Ireland 01-04-1985
• Subjects: Adult; Antibody Formation; Antigen-Antibody Complex - immunology; Complement Activating Enzymes - immunology; Complement C1q; Complement C3 - immunology; Complement C4 - immunology; Complement System Proteins - immunology; Female; Fetal Growth Retardation - immunology; Humans; Immunoglobulin G - immunology; Immunoglobulins - immunology; Isoantibodies - immunology; Lymphocytes - immunology; Phagocytosis; Postpartum Period; Pre-Eclampsia - immunology; Pregnancy; Pregnancy Trimester, Third; Skin - immunology
• ISSN: 0301-2115
• DOI: 10.1016/0028-2243(85)90031-0

To evaluate the role of some immunological phenomena involved in the pathogenesis of preeclamptic toxaemia, we studied the humoral immune reactivity in patients with preeclamptic toxaemia during the third trimester of pregnancy, and three days and six weeks after delivery. The results were compared with those of patients with intrauterine growth retardation and with uneventful pregnancy. During the third trimester, patients with complicated preeclamptic toxaemia had significantly lower IgG, CH50, C4 and C3 levels than normal pregnants. Post-partum levels of IgM were significantly higher than in all other groups of patients. Circulating immune complexes were not detectable by a C1q binding assay in patients and controls. However, with a conglutinin binding assay and a granulocyte phagocytosis test complexes were demonstrable in patients with complicated preeclampsia (incidence 44% and 33%, respectively). In addition, 66% of these patients showed deposits of immunoglobulins and complement components in superficial blood vessels of the skin biopsy, suggestive of the presence of tissue deposits of immune complexes. This was found in about 30% of the other patient groups and in none of control pregnants. Allo-antibodies to lymphocytes were present in 63% of complicated preeclamptic toxaemia patients and 22% of normal pregnants. Our data show several changes in humoral immune reactivity in preeclamptic toxaemia which may contribute to the pathogenesis of this disorder.