May 2008
Volume 49, Issue 13
Free
ARVO Annual Meeting Abstract  |   May 2008
Elevation of Qa-1+, F4/80+, CCR5+ Cells in the Iris and Thymus After the Intracameral Injection of Antigen
Author Affiliations & Notes
  • S. Chattopadhyay
    Immunology, Univ of Connecticut Hlth Ctr, Farmington, Connecticut
  • J. O'Rourke
    Immunology, Univ of Connecticut Hlth Ctr, Farmington, Connecticut
  • R. Sharafieh
    Immunology, Univ of Connecticut Hlth Ctr, Farmington, Connecticut
  • Y. Lemire
    Immunology, Univ of Connecticut Hlth Ctr, Farmington, Connecticut
  • R. E. Cone
    Immunology, Univ of Connecticut Hlth Ctr, Farmington, Connecticut
  • Footnotes
    Commercial Relationships  S. Chattopadhyay, None; J. O'Rourke, None; R. Sharafieh, None; Y. Lemire, None; R.E. Cone, None.
  • Footnotes
    Support  This work is supported by USPHS grants EY017289, 017537 and the Connecticut Lions Eye Research Foundation.
Investigative Ophthalmology & Visual Science May 2008, Vol.49, 2504. doi:https://doi.org/
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    • Get Citation

      S. Chattopadhyay, J. O'Rourke, R. Sharafieh, Y. Lemire, R. E. Cone; Elevation of Qa-1+, F4/80+, CCR5+ Cells in the Iris and Thymus After the Intracameral Injection of Antigen. Invest. Ophthalmol. Vis. Sci. 2008;49(13):2504. doi: https://doi.org/.

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      © ARVO (1962-2015); The Authors (2016-present)

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Abstract

Purpose: : Previously we demonstrated an increase in CCR5 and CCR2 RNA in iris cells after the intracameral injection of antigen. Here we investigated (i) the expression of Qa-1,essential to the induction of regulatory T cells in Anterior Chamber-Associated Immune Deviation (ACAID), (ii) the expression of chemokine receptor CCR5 on F4/80+ cells in the iris, thymus and spleen after the intracameral / anterior chamber (AC) injection of antigen and (iii) a role for CCR2 in the recruitment of F4/80+ peripheral blood cells (PBMC) to the iris and and transfer of the suppression of hypersensitivity.

Methods: : Ovalumin (OVA) or trinitrophenylated bovine albumin (TNP-BSA) was injected into an AC of DBA/2, BALB/c, C57BL/6 mice. FACS and confocal microscopy were used to characterize the expression of F4/80 and CCR5 by iris cells and thymocytes recovered 24 h after the intracameral injection of antigen and/or iv injection of CFSE-labeled PBMC from CCR2 -/- or +/+ mice. Delayed-type hypersensitivity (DTH) to TNP-BSA was measured in the footpads of TNP-BSA-immunized mice that received CCR2+ and CCR2- PBMC recovered from donors receiving AC, TNP-BSA.

Results: : Iris cells and thymocytes from ACAID-deficient DBA/2J mice are deficient in Qa-1b-expressing cells as compared to ACAID-competent DBA/2NCr mice. A higher frequency of F4/80+, Qa-1b+ cells was found in the irides and thymocytes of DBA/2NCr mice that received an AC injection of antigen. The number of F4/80+, CCR5+ cells increased in the irides of mice receiving an AC injection of antigen. F4/80+ PBMC from CCR2-/- mice failed to migrate to the iris, thymus or spleen after AC injection or transfer the suppression of DTH.

Keywords: ACAID • anterior chamber • immune tolerance/privilege 
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