February 1987
Volume 28, Issue 2
Free
Articles  |   February 1987
Experimental autoimmune dacryoadenitis. II. Harderian gland disease in the rat.
Author Affiliations
  • S H Liu
    Wilmer Ophthalmological Institute, Johns Hopkins University School of Medicine, Baltimore, MD 21205, USA.
  • F Sakai
    Wilmer Ophthalmological Institute, Johns Hopkins University School of Medicine, Baltimore, MD 21205, USA.
  • R A Prendergast
    Wilmer Ophthalmological Institute, Johns Hopkins University School of Medicine, Baltimore, MD 21205, USA.
  • A M Silverstein
    Wilmer Ophthalmological Institute, Johns Hopkins University School of Medicine, Baltimore, MD 21205, USA.
Investigative Ophthalmology & Visual Science February 1987, Vol.28, 276-280. doi:
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      S H Liu, F Sakai, R A Prendergast, A M Silverstein; Experimental autoimmune dacryoadenitis. II. Harderian gland disease in the rat.. Invest. Ophthalmol. Vis. Sci. 1987;28(2):276-280.

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Abstract

Experimental autoimmune dacryoadenitis was induced in 100% of Lewis rats by immunization with a KCl extract of Harderian gland in complete Freund's adjuvant (CFA), providing that the animals had received simultaneously i.v. injection of killed Bordetella pertussis. No significant pathological changes in the Harderian gland were observed in control animals immunized with KCl extracts of lacrimal or salivary glands. Gel filtration of the KCl extract on Sephacryl S-300 column yielded three protein fractions. Fraction II (MW = 50-100K) induced severe Harderian gland disease following a single injection of 2.0 mg protein in CFA plus pertussis. The initial lesions consisted of multiple focal infiltrates of mononuclear cells. Later, the inflammatory process assumed a more granulomatous form, with significant contribution by epithelioid and giant cells. In contrast, Lewis rats immunized with Harderian gland fractions I or III proteins, or with extracts of lacrimal or salivary gland, showed little or no inflammatory lesions. These data suggest that Harderian gland contains unique tissue-specific autoantigen(s) capable of inducing autoimmune granulomatous dacryoadenitis in the rat.

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