The effects of daily cyclophosphamide administration on the development and extent of primary experimental interstitial nephritis in rats
Autor: | Debra Cohn, David B. Agus, Carolyn J. Kelly, L Michaud, M D Clayman, Richard Mann, Eric G. Neilson |
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Rok vydání: | 1986 |
Předmět: |
medicine.medical_specialty
Kidney Cortex Time Factors Cyclophosphamide medicine.medical_treatment Interstitial nephritis Basement Membrane 03 medical and health sciences 0302 clinical medicine Immune system Antigen Internal medicine Rats Inbred BN medicine Animals Hypersensitivity Delayed Antigens 030304 developmental biology 030203 arthritis & rheumatology 0303 health sciences Kidney biology business.industry medicine.disease 3. Good health Rats medicine.anatomical_structure Endocrinology Kidney Tubules Nephrology biology.protein Nephritis Interstitial Female Immunization Antibody business Nephritis Adjuvant medicine.drug |
Zdroj: | Kidney International. 29(3):635-640 |
ISSN: | 0085-2538 |
DOI: | 10.1038/ki.1986.46 |
Popis: | The effects of daily cyclophosphamide administration on the development and extent of primary experimental interstitial nephritis in rats. We examined the effects of daily cyclophosphamide administration on the development and extent of tubulointerstitial nephritis produced in rats injected with tubular basement membranes in adjuvant. 15 mg/kg/day of cyclophophamide completely blocked the development of interstitial lesions, while 2 mg/kg/day enhanced the degree of interstitial injury. When cyclophosphamide in the higher dose was started early in disease, 12 days after immunization, protection from progression was also observed as well as significant reductive improvement. If cyclophosphamide was administered late in disease, 21 days after immunization, no further progression was demonstrable, but substantial injury remained. In the latter two experiments, the beneficial effects of cyclophosphamide could not be explained by a reduction in anti-tubular basement membrane antibodies bound to the kidney. In groups of immunized rats that were tested, however, cyclophosphamide was able to non-specifically impair the delayed-type hypersensitivity response to tubular antigen and PPD. We conclude, therefore, that cyclophosphamide, in high but not low dosage, if given before damage is extensive and prolonged, may successfully inhibit the cellular immune response producing primary interstitial nephritis. |
Databáze: | OpenAIRE |
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