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Characterization of intraocular immunopathology following intracameral inoculation with alloantigen.

Publication ,  Journal Article
Saban, DR; Elder, IA; Nguyen, CQ; Smith, WC; Timmers, AM; Grant, MB; Peck, AB
Published in: Mol Vis
March 26, 2008

PURPOSE: Anterior chamber-associated immune deviation (ACAID) is a form of peripheral tolerance achieved via intracameral antigen inoculation. It is well known that ACAID effectively down-regulates potentially destructive immunities such as delayed-type hypersensitivity (DTH) at extraorbital sites. However, what has not been specifically addressed is whether local intraocular tissues are negatively affected from intracamerally placed antigen. Thus, the current study was undertaken to detect and characterize potential pathological effects on intraocular tissues following intracameral inoculation with alloantigen. METHODS: ACAID induced in C57BL/6 hosts via intracameral inoculation with allogeneic (BALB/c) splenocytes was confirmed by the absence of DTH reactivity in the periphery. Injuries to the anterior segment and neuroretina following intracameral inoculation were evaluated pathologically via histological evaluation, molecularly via upregulation of glial fibrillary acidic protein (GFAP), and functionally via assessment of photoreceptor degeneration and electroretinogram (ERG) out to 24 days. In all experiments, intracamerally inoculated mice were compared to sham-operated, and controlled lens-punctured mice--a procedure that elicits intracameral inflammation for positive identification of immunopathological changes. RESULTS: Inflammation of anterior segment tissues persisted out to eight days, despite evidence that significant clearance of allogeneic cells took place within 6 h. In the neuroretina, a transient loss in ERG B-wave amplitudes was detected, but photoreceptor degeneration and GFAP upregulation were not. CONCLUSIONS: Intracameral inoculation with alloantigen leads to anterior segment inflammation and ERG dysfunction; however, this was markedly reduced and transient when compared to strong anterior segment inflammation induced by a more serious lens-puncture wound.

Duke Scholars

Published In

Mol Vis

EISSN

1090-0535

Publication Date

March 26, 2008

Volume

14

Start / End Page

615 / 624

Location

United States

Related Subject Headings

  • Wounds, Penetrating
  • Time Factors
  • Spleen
  • Retina
  • Photoreceptor Cells
  • Ophthalmology & Optometry
  • Mice, Inbred C57BL
  • Mice, Inbred BALB C
  • Mice
  • Lens, Crystalline
 

Citation

APA
Chicago
ICMJE
MLA
NLM
Saban, D. R., Elder, I. A., Nguyen, C. Q., Smith, W. C., Timmers, A. M., Grant, M. B., & Peck, A. B. (2008). Characterization of intraocular immunopathology following intracameral inoculation with alloantigen. Mol Vis, 14, 615–624.
Saban, Daniel R., Ian A. Elder, Cuong Q. Nguyen, W Clay Smith, Adrian M. Timmers, Maria B. Grant, and Ammon B. Peck. “Characterization of intraocular immunopathology following intracameral inoculation with alloantigen.Mol Vis 14 (March 26, 2008): 615–24.
Saban DR, Elder IA, Nguyen CQ, Smith WC, Timmers AM, Grant MB, et al. Characterization of intraocular immunopathology following intracameral inoculation with alloantigen. Mol Vis. 2008 Mar 26;14:615–24.
Saban, Daniel R., et al. “Characterization of intraocular immunopathology following intracameral inoculation with alloantigen.Mol Vis, vol. 14, Mar. 2008, pp. 615–24.
Saban DR, Elder IA, Nguyen CQ, Smith WC, Timmers AM, Grant MB, Peck AB. Characterization of intraocular immunopathology following intracameral inoculation with alloantigen. Mol Vis. 2008 Mar 26;14:615–624.

Published In

Mol Vis

EISSN

1090-0535

Publication Date

March 26, 2008

Volume

14

Start / End Page

615 / 624

Location

United States

Related Subject Headings

  • Wounds, Penetrating
  • Time Factors
  • Spleen
  • Retina
  • Photoreceptor Cells
  • Ophthalmology & Optometry
  • Mice, Inbred C57BL
  • Mice, Inbred BALB C
  • Mice
  • Lens, Crystalline