January 1989
Volume 30, Issue 1
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Articles  |   January 1989
Changes in aqueous immunoglobulin and albumin levels following penetrating keratoplasty.
Author Affiliations
  • D E Lopatin
    Department of Oral Biology, School of Dentistry, University of Michigan, Ann Arbor 48109-0402.
  • N Van Poperin
    Department of Oral Biology, School of Dentistry, University of Michigan, Ann Arbor 48109-0402.
  • D K MacCallum
    Department of Oral Biology, School of Dentistry, University of Michigan, Ann Arbor 48109-0402.
  • R F Meyer
    Department of Oral Biology, School of Dentistry, University of Michigan, Ann Arbor 48109-0402.
  • J H Lillie
    Department of Oral Biology, School of Dentistry, University of Michigan, Ann Arbor 48109-0402.
Investigative Ophthalmology & Visual Science January 1989, Vol.30, 122-131. doi:
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    • Get Citation

      D E Lopatin, N Van Poperin, D K MacCallum, R F Meyer, J H Lillie; Changes in aqueous immunoglobulin and albumin levels following penetrating keratoplasty.. Invest. Ophthalmol. Vis. Sci. 1989;30(1):122-131.

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

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Abstract

The feline model of induced rejection of corneal allografts was employed to define the changes in the concentrations of immunoglobulins and albumin in the anterior chamber prior to, and concomitant with the rejection of the transplanted cornea. Fourteen animals received unilateral exchange corneal allografts. Aqueous humor obtained by anterior chamber paracentesis at regular intervals prior to and following the performance of the penetrating keratoplasties was analyzed for IgG, IgM and albumin concentrations using the micro enzyme-linked immunosorbant assay (ELISA). Two patterns of anterior chamber protein modulation were observed. Eight of the animals demonstrated a biphasic pattern in which both immunoglobulin and albumin concentrations were elevated two- to five-fold above presurgical values 14 days postkeratoplasty, returning to preoperative values by day 42. Three to 5 weeks after corneal rejection was induced increases in protein concentrations were observed that correlated with the appearance of clinical signs of rejection. A second, monophasic pattern of anterior chamber protein modulation following keratoplasty was observed in four of the animals. It was distinguishable from the biphasic pattern in that levels did not return to baseline values after the initial rise following keratoplasty until the rejection process was completed. The monophasic response was found to be characteristic of more rapid and vigorous corneal rejection. Examination of albumin to immunoglobulin ratios suggested that all changes in protein levels following keratoplasty were a result of increased influx of serum proteins into the anterior chamber, rather than due to local immunoglobulin synthesis.

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