Abstract
This study was undertaken to determine the effect of cyclophosphamide, methotrexate, hydrocortisone, and cyclosporin A on a model of granulomatous infiltration in the terminal ileum and draining lymph nodes of the guinea pig. Treatment groups of six animals were used and compared to untreated groups of 12. Epithelioid cell granulomas and primary macrophage granulomas were induced by the inoculation of BCG (Pasteur) and irradiated Mycobacterium leprae respectively into the terminal ileum of the guinea pig. The response to purified protein derivative of tuberculin was reduced in both groups of animals receiving any of these agents. Cyclophosphamide and methotrexate treated animals inoculated with BCG or M leprae showed a significant reduction of granulomatous infiltration at the inoculation site (p less than 0.05 and p less than 0.001 respectively). BCG inoculated animals treated with either hydrocortisone or cyclosporin A showed no reduction in granulomatous infiltration at either the inoculation site or the draining lymph nodes. By contrast M leprae inoculated animals receiving either of these agents showed a significant reduction of granulomatous infiltration at both the inoculation site (p less than 0.001) and in the primary draining lymph node (p less than 0.001). Ziehl Neelsen staining showed an increased proportion of animals with detectable acid fast bacilli (AFB) at the inoculation site in the groups receiving hydrocortisone (50%) and methotrexate (67%) compared to untreated controls (8%). No AFB were observed in any of the animals inoculated with M leprae. In conclusion, this model may be helpful in elucidating the mechanism of T lymphocyte response in Crohn's disease and the variable clinical response seen with the use of immunosuppressive agents in this condition.
Full text
PDF




Selected References
These references are in PubMed. This may not be the complete list of references from this article.
- Alberti S., Boraschi D., Luini W., Tagliabue A. Effects of in vivo treatments with cyclosporin-A on mouse cell-mediated immune responses. Int J Immunopharmacol. 1981;3(4):357–364. doi: 10.1016/0192-0561(81)90031-x. [DOI] [PubMed] [Google Scholar]
- Allison M. C., Pounder R. E. Cyclosporin for Crohn's disease. Aliment Pharmacol Ther. 1987 Feb;1(1):39–43. doi: 10.1111/j.1365-2036.1987.tb00604.x. [DOI] [PubMed] [Google Scholar]
- Balow J. E., Hurley D. L., Fauci A. S. Immunosuppressive effects of glucocorticosteroids: differential effects of acute vs chronic administration on cell-mediated immunity. J Immunol. 1975 Mar;114(3):1072–1076. [PubMed] [Google Scholar]
- Balow J. E., Rosenthal A. S. Glucocorticoid suppression of macrophage migration inhibitory factor. J Exp Med. 1973 Apr 1;137(4):1031–1041. doi: 10.1084/jem.137.4.1031. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Bunjes D., Hardt C., Röllinghoff M., Wagner H. Cyclosporin A mediates immunosuppression of primary cytotoxic T cell responses by impairing the release of interleukin 1 and interleukin 2. Eur J Immunol. 1981 Aug;11(8):657–661. doi: 10.1002/eji.1830110812. [DOI] [PubMed] [Google Scholar]
- Gupta S. K., Curtis J., Turk J. L. The effect of hydrocortisone and cyclosporin A on bacillus Calmette-Guérin epitheloid cell granulomas. Cell Immunol. 1985 Jun;93(1):189–198. doi: 10.1016/0008-8749(85)90399-5. [DOI] [PubMed] [Google Scholar]
- HART P. D., REES R. J. Effect of macrocyclon in acute and chronic pulmonary tuberculous infection in mice as shown by viable and total bacterial counts. Br J Exp Pathol. 1960 Aug;41:414–421. [PMC free article] [PubMed] [Google Scholar]
- Hawkey C. J., Truelove S. C. Effect of prednisolone on prostaglandin synthesis by rectal mucosa in ulcerative colitis: investigation by laminar flow bioassay and radioimmunoassay. Gut. 1981 Mar;22(3):190–193. doi: 10.1136/gut.22.3.190. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Kupiec-Weglinski J. W., Filho M. A., Strom T. B., Tilney N. L. Sparing of suppressor cells: a critical action of cyclosporine. Transplantation. 1984 Aug;38(2):97–101. doi: 10.1097/00007890-198408000-00001. [DOI] [PubMed] [Google Scholar]
- Lauritsen K., Laursen L. S., Bukhave K., Rask-Madsen J. Effects of topical 5-aminosalicylic acid and prednisolone on prostaglandin E2 and leukotriene B4 levels determined by equilibrium in vivo dialysis of rectum in relapsing ulcerative colitis. Gastroenterology. 1986 Oct;91(4):837–844. doi: 10.1016/0016-5085(86)90684-0. [DOI] [PubMed] [Google Scholar]
- Lauritsen K., Laursen L. S., Bukhave K., Rask-Madsen J. In vivo effects of orally administered prednisolone on prostaglandin and leucotriene production in ulcerative colitis. Gut. 1987 Sep;28(9):1095–1099. doi: 10.1136/gut.28.9.1095. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Mathew R. C., Katayama I., Gupta S. K., Curtis J., Turk J. L. Analysis of cells of the mononuclear phagocyte series in experimental mycobacterial granulomas by monoclonal antibodies. Infect Immun. 1983 Jan;39(1):344–352. doi: 10.1128/iai.39.1.344-352.1983. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Mitchell I. C., Turk J. L. An experimental animal model of granulomatous bowel disease. Gut. 1989 Oct;30(10):1371–1378. doi: 10.1136/gut.30.10.1371. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Munro C. S., Campbell D. A., Collings L. A., Poulter L. W. Monoclonal antibodies distinguish macrophages and epithelioid cells in sarcoidosis and leprosy. Clin Exp Immunol. 1987 May;68(2):282–287. [PMC free article] [PubMed] [Google Scholar]
- Narayanan R. B., Badenoch-Jones P., Curtis J., Turk J. L. Comparison of mycobacterial granulomas in guinea-pig lymph nodes. J Pathol. 1982 Nov;138(3):219–233. doi: 10.1002/path.1711380304. [DOI] [PubMed] [Google Scholar]
- Parrott N. R., Taylor R. M., Venables C. W., Record C. O. Treatment of Crohn's disease in relapse with cyclosporin A. Br J Surg. 1988 Dec;75(12):1185–1188. doi: 10.1002/bjs.1800751213. [DOI] [PubMed] [Google Scholar]
- Schmidt M. E., Douglas S. D., Rubin A. D. Human monocyte activation by supernatants from concanavalin A (con A) stimulated lymphocytes. Cell Immunol. 1973 Oct;9(1):45–59. doi: 10.1016/0008-8749(73)90166-4. [DOI] [PubMed] [Google Scholar]
- Summers R. W., Switz D. M., Sessions J. T., Jr, Becktel J. M., Best W. R., Kern F., Jr, Singleton J. W. National Cooperative Crohn's Disease Study: results of drug treatment. Gastroenterology. 1979 Oct;77(4 Pt 2):847–869. [PubMed] [Google Scholar]
- Suya H., Fujioka A., Pincelli C., Fukuyama K., Epstein W. L. Skin granuloma formation in mice immunosuppressed by cyclosporine. J Invest Dermatol. 1988 Apr;90(4):430–433. doi: 10.1111/1523-1747.ep12460866. [DOI] [PubMed] [Google Scholar]
- TURK J. L. STUDIES ON THE MECHANISM OF ACTION OF METHOTREXATE AND CYCLOPHOSPHAMIDE ON CONTACT SENSITIVITY IN THE GUINEA PIG. Int Arch Allergy Appl Immunol. 1964;24:191–200. doi: 10.1159/000229459. [DOI] [PubMed] [Google Scholar]
- Thomson A. W., Moon D. K., Geczy C. L., Nelson D. S. Cyclosporin A inhibits lymphokine production but not the responses of macrophages to lymphokines. Immunology. 1983 Feb;48(2):291–299. [PMC free article] [PubMed] [Google Scholar]
- Wang B. S., Heacock E. H., Collins K. H., Hutchinson I. F., Tilney N. L., Mannick J. A. Suppressive effects of cyclosporin A on the induction of alloreactivity in vitro and in vivo. J Immunol. 1981 Jul;127(1):89–93. [PubMed] [Google Scholar]
- Weston W. L., Claman H. N., Krueger G. G. Site of action of cortisol in cellular immunity. J Immunol. 1973 Mar;110(3):880–883. [PubMed] [Google Scholar]
