Repertoire and clonality of T-cell receptor beta variable genes expressed in endometrium and blood T cells of patients with recurrent spontaneous abortion

Am J Reprod Immunol. 2008 Aug;60(2):160-71. doi: 10.1111/j.1600-0897.2008.00608.x.

Abstract

Problem: Recurrent spontaneous abortion (RSA) is a relatively common disorder, the underlying causes of which are thought to be immunological in most cases.

Method of study: Expression profile and clonality pattern of T-cell receptor beta variable (TCRBV) genes in endometrium and blood of patients with RSA were investigated by semi-quantitative reverse transcriptase polymerase chain reaction (RT-PCR) using BV gene-specific primers. Relative expression of each BV family was determined and clonal expansion of the over-expressed genes was assessed by analysis of CDR3 length polymorphism.

Results: Compared to blood, relative expression of four TCRBV genes was significantly higher in the endometrium of RSA group. Over-expressed genes, except for TCRBV3, all had restricted and oligoclonal patterns of expression in the endometrium.

Conclusion: Endometrial T cells have a skewed TCRBV repertoire with restricted transcript heterogeneity, which is shared by both groups and minor variations observed in this pattern in RSA patients may reflect more recent and/or repeated exposure to nominal antigens or superantigens.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Abortion, Habitual / genetics
  • Abortion, Habitual / immunology*
  • Abortion, Habitual / metabolism
  • Adult
  • Case-Control Studies
  • Complementarity Determining Regions / genetics
  • Endometrium / immunology*
  • Endometrium / metabolism
  • Female
  • Gene Expression
  • Genes, T-Cell Receptor beta*
  • Humans
  • Polymorphism, Genetic
  • Pregnancy
  • Receptors, Antigen, T-Cell, alpha-beta / genetics
  • Receptors, Antigen, T-Cell, alpha-beta / immunology
  • Receptors, Antigen, T-Cell, alpha-beta / metabolism*
  • T-Lymphocytes / immunology*
  • T-Lymphocytes / metabolism

Substances

  • Complementarity Determining Regions
  • Receptors, Antigen, T-Cell, alpha-beta