Involvement of Hofbauer cells and maternal T cells in villitis of unknown aetiology

Histopathology. 2008 Mar;52(4):457-64. doi: 10.1111/j.1365-2559.2008.02964.x.

Abstract

Aims: The nature of villitis of unknown aetiology (VUE) is intriguing in terms of its aetiology, origin of inflammatory cells and immunophenotype of T cells involved. The aim was to determine the origin of macrophages and the immunophenotype of T lymphocytes in VUE associated with various complications of pregnancy.

Methods and results: Placentas with VUE (n = 45) were studied by chromogenic in-situ hybridization (CISH) for Y chromosome (DYZ1) and immunohistochemistry for CD14, CD68, Ki67 (n = 10; all from male neonates) and a panel of T-cell antigens (CD3, CD4 and CD8) (n = 35). All of the placentas from male neonates showed CISH+ signals from Y chromosomes in the majority of macrophages, but not in lymphocytes, indicating that the macrophages were of fetal origin. Many macrophages of the affected chorionic villi were Ki67+, suggesting that they are hyperplastic Hofbauer cells. Among the lymphocytes, CD8+ T cells outnumbered CD4+ T cells in all placentas with different obstetrical conditions.

Conclusions: We define primary components of VUE as maternal CD8+ T cells and hyperplastic Hofbauer cells. We propose that VUE is a unique inflammatory reaction where the leucocytes from two hosts are key partners, analogous to either allograft rejection or graft-versus-host disease.

Publication types

  • Research Support, N.I.H., Intramural

MeSH terms

  • Adult
  • CD4-Positive T-Lymphocytes / immunology
  • CD4-Positive T-Lymphocytes / metabolism
  • CD4-Positive T-Lymphocytes / pathology
  • CD8-Positive T-Lymphocytes / immunology
  • CD8-Positive T-Lymphocytes / metabolism
  • CD8-Positive T-Lymphocytes / pathology
  • Chorionic Villi / immunology
  • Chorionic Villi / pathology*
  • Chromosomes, Human, Y*
  • Female
  • Fluorescent Antibody Technique, Indirect
  • Gestational Age
  • Graft Rejection
  • Graft vs Host Disease
  • Humans
  • Immunoenzyme Techniques
  • In Situ Hybridization / methods
  • Infant, Newborn
  • Inflammation / etiology
  • Inflammation / immunology
  • Inflammation / pathology*
  • Ki-67 Antigen / metabolism
  • Macrophages / immunology
  • Macrophages / metabolism
  • Macrophages / pathology*
  • Male
  • Maternal-Fetal Exchange / genetics*
  • Placenta Diseases / etiology
  • Placenta Diseases / immunology
  • Placenta Diseases / pathology*
  • Pregnancy
  • Pregnancy Complications

Substances

  • Ki-67 Antigen