Aberrant Tolerance Induction with Cationic Antigens
Autor: | A. E. M. Van Den Hoek, L. B. A. Van De Putte, W.B. van den Berg, M. J. M. Jacobs |
---|---|
Rok vydání: | 1993 |
Předmět: |
medicine.medical_specialty
Cellular immunity Ovalbumin Immunology Administration Oral Immune tolerance Mice Antigen Cations Internal medicine Immune Tolerance medicine Animals Potency Hypersensitivity Delayed Antigens Bovine serum albumin biology Serum Albumin Bovine General Medicine Mice Inbred C57BL Tolerance induction Endocrinology Delayed hypersensitivity Injections Intravenous biology.protein Female Immunization |
Zdroj: | Scandinavian Journal of Immunology. 37:97-103 |
ISSN: | 1365-3083 0300-9475 |
DOI: | 10.1111/j.1365-3083.1993.tb01670.x |
Popis: | We studied the induction of tolerance in female C57B1/6 mice by oral and intravenous (i.v.) administration of protein antigens before immunization. Native proteins [chicken egg albumin (OVA), bovine serum albumin (BSA)] and their cationic derivatives [amidated (a)OVA, aBSA, methylated (m)BSA] were compared in their capacity to suppress cell-mediated immunity (CMI), as measured by a delayed type hypersensitivity test (DTH). Oral feeding of 0.5 mg negative proteins gave a clear suppression. By contrast, cationic derivatives (50 micrograms to 50 mg) did not suppress CMI. Data from cross-experiments, where aOVA was fed in OVA-immune mice, showed no suppression at all. When OVA was fed in aOVA-immune mice, only a partial suppression was achieved. The potency to induce tolerance differed also when the antigens were administered i.v.: 25 micrograms OVA was sufficient to induce a clear suppression, whereas a much higher amount of aOVA (500 micrograms) caused marginal suppression in OVA- and aOVA-immune mice, respectively. Nevertheless, when concentrations of aOVA up to 2.5 mg were tested in a chronic model of arthritis, a significant suppression was achieved. The differences in inducing a CMI suppression may have implications for the feasibility of immunointervention. Successful modulation of human arthritis may be highly dependent on the nature of the antigen involved. |
Databáze: | OpenAIRE |
Externí odkaz: |