Expression of Tim-3 is transiently increased before development of anterior chamber-associated immune deviation

Ocul Immunol Inflamm. 2006 Jun;14(3):151-6. doi: 10.1080/09273940600693640.

Abstract

Purpose: To assess the expression of T-cell immunoglobulin- and mucin-domain-containing molecule 3 (Tim-3) in the spleens of BALB/c mice undergoing anterior chamber-associated immune deviation (ACAID).

Methods: ACAID was generated after intracameral (i.c.) injection of ovalbumin (OVA) into BALB/c mice and evaluated by assessing the delayed-type hypersensitivity (DTH) response following a subsequent subcutaneous (s.c.) injection of OVA emulsified in complete Freund's adjuvant (CFA) on Days 0, 3, 7, 14, 21 and 28. Tim-3 mRNA levels were detected using real-time RT-PCR, and the frequency of CD4+Tim-3+ T cells in splenocytes as well as the coexpression of Tim-3 with CD25 on CD4+ T cells were assessed by flow cytometry.

Results: A significantly suppressed DTH response was observed on Days 7, 14, 21, and 28, but not on Days 0 and 3 during the development of ACAID. The levels of Tim-3 mRNA and the frequency of CD4+CD25+Tim-3+ T cells in the splenocytes reached a peak on Day 3, declined on Day 7, and returned to basal levels thereafter.

Conclusions: A transient upregulation of Tim-3 expression was observed in the early stage of ACAID, suggesting its possible involvement in the development of ACAID.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Anterior Chamber / immunology
  • Anterior Chamber / pathology*
  • Disease Models, Animal
  • Disease Progression
  • Female
  • Flow Cytometry
  • Follow-Up Studies
  • Hepatitis A Virus Cellular Receptor 2
  • Mice
  • Mice, Inbred BALB C
  • RNA, Messenger / genetics*
  • Receptors, Virus / genetics*
  • Reverse Transcriptase Polymerase Chain Reaction
  • Spleen / metabolism
  • Spleen / pathology
  • T-Lymphocytes / immunology*
  • T-Lymphocytes / pathology
  • Up-Regulation / genetics*
  • Uveitis, Anterior / immunology
  • Uveitis, Anterior / metabolism*
  • Uveitis, Anterior / pathology

Substances

  • Havcr2 protein, mouse
  • Hepatitis A Virus Cellular Receptor 2
  • RNA, Messenger
  • Receptors, Virus