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. 1992 Feb;60(2):401–405. doi: 10.1128/iai.60.2.401-405.1992

Circulating and localized immune complexes in experimental mycoplasma-induced arthritis-associated ocular inflammation.

C E Thirkill 1, N K Tyler 1, A M Roth 1
PMCID: PMC257642  PMID: 1730469

Abstract

Ocular deposits of immune complexes are believed to contribute to the anterior segment inflammations observed in association with the human arthritides. Arthritis-related ocular inflammations may be reproduced in animals by infection with certain species of mycoplasma. To evaluate the role of immune complexes in the production of ocular lesions, we studied their involvement in the rodent model of experimental arthritis-associated ocular inflammation induced by Mycoplasma arthritidis. Sprague-Dawley rats were infected with viable concentrates of M. arthritidis and monitored for the production of related circulating and intraocular immune complexes. Circulating immune complexes were monitored by antigen capture systems, and localized intraocular complexes were identified by indirect immunohistochemistry. Polyacrylamide gel immunoblot analysis of captured complexes confirmed the antigen(s) involved as proteins derived from M. arthritidis. Indirect immunofluorescence revealed localized complexes containing mycoplasma antigens within the ciliary-iris vasculature. Concentrations of the generated complexes diminished rapidly over a 30-day period. While complex deposits within ocular tissues could represent a contributing cause to the localized anterior segment inflammation reported in this rodent model, secondary challenge with viable M. arthritidis, which reproduced high concentrations of intraocular and circulating immune complexes, failed to elicit any ocular response.

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  1. Atkin C. L., Cole B. C., Sullivan G. J., Washburn L. R., Wiley B. B. Stimulation of mouse lymphocytes by a mitogen derived from Mycoplasma arthritidis. V. A small basic protein from culture supernatants is a potent T cell mitogen. J Immunol. 1986 Sep 1;137(5):1581–1589. [PubMed] [Google Scholar]
  2. Bekoff M. C., Cole B. C., Grey H. M. Studies on the mechanism of stimulation of T cells by the Mycoplasma arthritidis-derived mitogen. Role of class II IE molecules. J Immunol. 1987 Nov 15;139(10):3189–3194. [PubMed] [Google Scholar]
  3. Brinkman K., Termaat R., Berden J. H., Smeenk R. J. Anti-DNA antibodies and lupus nephritis: the complexity of crossreactivity. Immunol Today. 1990 Jul;11(7):232–234. doi: 10.1016/0167-5699(90)90095-q. [DOI] [PubMed] [Google Scholar]
  4. Buchvarova Y. a., Vesselinova A. Arthritis in calves caused by mycoplasmas. Arch Exp Veterinarmed. 1986 Jan;40(1):41–43. [PubMed] [Google Scholar]
  5. Char D. H., Stein P., Masi R., Christensen M. Immune complexes in uveitis. Am J Ophthalmol. 1979 May;87(5):678–681. doi: 10.1016/0002-9394(79)90303-9. [DOI] [PubMed] [Google Scholar]
  6. Cole B. C., Araneo B. A., Sullivan G. J. Stimulation of mouse lymphocytes by a mitogen derived from Mycoplasma arthritidis. IV. Murine T hybridoma cells exhibit differential accessory cell requirements for activation by M. arthritidis T cell mitogen, concanavalin A, or hen egg-white lysozyme. J Immunol. 1986 May 15;136(10):3572–3578. [PubMed] [Google Scholar]
  7. Cole B. C., Kartchner D. R., Wells D. J. Stimulation of mouse lymphocytes by a mitogen derived from Mycoplasma arthritidis (MAM). VIII. Selective activation of T cells expressing distinct V beta T cell receptors from various strains of mice by the "superantigen" MAM. J Immunol. 1990 Jan 15;144(2):425–431. [PubMed] [Google Scholar]
  8. Cole B. C., Kartchner D. R., Wells D. J. Stimulation of mouse lymphocytes by a mitogen derived from Mycoplasma arthritidis. VII. Responsiveness is associated with expression of a product(s) of the V beta 8 gene family present on the T cell receptor alpha/beta for antigen. J Immunol. 1989 Jun 15;142(12):4131–4137. [PubMed] [Google Scholar]
  9. Cole B. C., Tuller J. W., Sullivan G. J. Stimulation of mouse lymphocytes by a mitogen derived from Mycoplasma arthritidis. VI. Detection of a non-MHC gene(s) in the E alpha-bearing RIIIS mouse strain that is associated with a specific lack of T cell responses to the M. arthritidis soluble mitogen. J Immunol. 1987 Aug 1;139(3):927–935. [PubMed] [Google Scholar]
  10. Cole B. C., Wells D. J. Immunosuppressive properties of the Mycoplasma arthritidis T-cell mitogen in vivo: inhibition of proliferative responses to T-cell mitogens. Infect Immun. 1990 Jan;58(1):228–236. doi: 10.1128/iai.58.1.228-236.1990. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. Dumonde D. C., Kasp-Grochowska E., Graham E., Sanders M. D., Faure J. P., de Kozak Y., van Tuyen V. Anti-retinal autoimmunity and circulating immune complexes in patients with retinal vasculitis. Lancet. 1982 Oct 9;2(8302):787–792. doi: 10.1016/s0140-6736(82)92679-4. [DOI] [PubMed] [Google Scholar]
  12. Gershoni J. M., Palade G. E. Protein blotting: principles and applications. Anal Biochem. 1983 May;131(1):1–15. doi: 10.1016/0003-2697(83)90128-8. [DOI] [PubMed] [Google Scholar]
  13. Hermanns W., Schulz L. C., Kirchhoff H., Heitmann J. Studies of polyarthritis caused by mycoplasma arthritidis in rats. III. Histopathological findings. Zentralbl Bakteriol Mikrobiol Hyg A. 1983 May;254(3):423–434. [PubMed] [Google Scholar]
  14. Howes E. L., Jr, McKay D. G. Circulating immune complexes. Effects on ocular vascular permeability in the rabbit. Arch Ophthalmol. 1975 May;93(5):365–370. doi: 10.1001/archopht.1975.01010020377013. [DOI] [PubMed] [Google Scholar]
  15. Hylkema H. A., Rathman W. M., Kijlstra A. Deposition of immune complexes in the mouse eye. Exp Eye Res. 1983 Sep;37(3):257–265. doi: 10.1016/0014-4835(83)90160-4. [DOI] [PubMed] [Google Scholar]
  16. Jansson E., Backman A., Hakkarainen K., Miettinen A., Seniusová B. Mycoplasmas and arthritis. Z Rheumatol. 1983 Nov-Dec;42(6):315–319. [PubMed] [Google Scholar]
  17. Key S. N., 3rd, Kimura S. J. Iridocyclitis associated with juvenile rheumatoid arthritis. Am J Ophthalmol. 1975 Sep;80(3 Pt 1):425–429. doi: 10.1016/0002-9394(75)90529-2. [DOI] [PubMed] [Google Scholar]
  18. Kirchhoff H., Binder A., Runge M., Meier B., Jacobs R., Busche K. Pathogenetic mechanisms in the Mycoplasma arthritidis polyarthritis of rats. Rheumatol Int. 1989;9(3-5):193–196. doi: 10.1007/BF00271879. [DOI] [PubMed] [Google Scholar]
  19. Lowder C. Y., Char D. H. Immune complexes in ocular disease. Int Ophthalmol Clin. 1985 Summer;25(2):143–151. doi: 10.1097/00004397-198502520-00016. [DOI] [PubMed] [Google Scholar]
  20. Matsuo T., Nakayama T., Matsuo N., Koide N. Immunological studies of uveitis. 1. Immune complex containing herpes virus antigens in four patients with acute retinal necrosis syndrome. Jpn J Ophthalmol. 1986;30(4):472–479. [PubMed] [Google Scholar]
  21. Matsuo T., Nakayama T., Tsuji T., Koyama T., Matsuo N., Koide N. Immunological studies of uveitis. 2. Immune complex containing retinal S antigen in patient with chronic intractable uveitis. Jpn J Ophthalmol. 1986;30(4):480–486. [PubMed] [Google Scholar]
  22. Moore T. L., Sheridan P. W., Traycoff R. B., Zuckner J., Dorner R. W. Immune complexes in juvenile rheumatoid arthritis: a comparison of four methods. J Rheumatol. 1982 May-Jun;9(3):395–401. [PubMed] [Google Scholar]
  23. Peress N. S. Immune complex deposition in the ciliary process of rabbits with acute and chronic serum sickness. Exp Eye Res. 1980 Apr;30(4):371–378. doi: 10.1016/0014-4835(80)90052-4. [DOI] [PubMed] [Google Scholar]
  24. Petty R. E., Hunt D. W. Immunity to ocular and collagen antigens in childhood arthritis and uveitis. Int Arch Allergy Appl Immunol. 1989;89(1):31–37. doi: 10.1159/000234919. [DOI] [PubMed] [Google Scholar]
  25. Surelia P., Boxall E. H. Hepatitis B virus infection: detection of circulating HBsAg/IgM antibody immune complexes. Med Lab Sci. 1990 Jul;47(3):204–209. [PubMed] [Google Scholar]
  26. Swenson P. D., Kaplan M. H. Rapid detection of respiratory syncytial virus in nasopharyngeal aspirates by a commercial enzyme immunoassay. J Clin Microbiol. 1986 Mar;23(3):485–488. doi: 10.1128/jcm.23.3.485-488.1986. [DOI] [PMC free article] [PubMed] [Google Scholar]
  27. Thirkill C. E., Gregerson D. S. Diphtheroid-like properties of Mycoplasma arthritidis. Med Lab Sci. 1986 Jan;43(1):9–13. [PubMed] [Google Scholar]
  28. Thirkill C. E., Gregerson D. S. Mycoplasma arthritidis-induced ocular inflammatory disease. Infect Immun. 1982 May;36(2):775–781. doi: 10.1128/iai.36.2.775-781.1982. [DOI] [PMC free article] [PubMed] [Google Scholar]
  29. Thirkill C. E., Muchmore H. G., Hyde R. M., Scott L. V. Immunologic reactions of rabbit anti-Mycoplasma arthritidis serum with in vitro cultivated rat synovial cells. In Vitro. 1981 May;17(5):405–411. doi: 10.1007/BF02626740. [DOI] [PubMed] [Google Scholar]
  30. Thirkill C. E., Roth A. M., Munn R. J., Lee P., Tyler N. K. Interactions of cultured rat synovial and ocular ciliary body cells with two strains of Mycoplasma arthritidis. In Vitro Cell Dev Biol. 1990 Feb;26(2):140–146. doi: 10.1007/BF02624104. [DOI] [PubMed] [Google Scholar]
  31. Thirkill C. E., Song D. Y., Gregerson D. S. Application of monoclonal antibodies to detect intraocular mycoplasma antigens in Mycoplasma arthritidis-infected Sprague-Dawley rats. Infect Immun. 1983 Apr;40(1):389–397. doi: 10.1128/iai.40.1.389-397.1983. [DOI] [PMC free article] [PubMed] [Google Scholar]
  32. Towbin H., Staehelin T., Gordon J. Electrophoretic transfer of proteins from polyacrylamide gels to nitrocellulose sheets: procedure and some applications. Proc Natl Acad Sci U S A. 1979 Sep;76(9):4350–4354. doi: 10.1073/pnas.76.9.4350. [DOI] [PMC free article] [PubMed] [Google Scholar]
  33. Vinayak V. K., Purnima, Singh K., Venkatwswarlu K., Nain C. K., Mehta S. K. Specific circulating immune complexes in amoebic liver abscess. J Clin Microbiol. 1986 Jun;23(6):1088–1090. doi: 10.1128/jcm.23.6.1088-1090.1986. [DOI] [PMC free article] [PubMed] [Google Scholar]
  34. Washburn L. R., Cole B. C., Ward J. R. Expression of metabolism-inhibition antibodies against Mycoplasma arthritidis in rats. Am J Vet Res. 1988 Jan;49(1):52–57. [PubMed] [Google Scholar]
  35. Washburn L. R., Ramsay J. R. Experimental induction of arthritis in LEW rats and antibody response to four Mycoplasma arthritidis strains. Vet Microbiol. 1989 Nov;21(1):41–55. doi: 10.1016/0378-1135(89)90017-5. [DOI] [PubMed] [Google Scholar]
  36. Washburn L. R. The Derrick Edward award lecture. Immunologic aspects of Mycoplasma arthritidis-induced arthritis. Isr J Med Sci. 1987 May;23(5):326–333. [PubMed] [Google Scholar]

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