Abstract |
A variety of immunologic mechanisms may theoretically give rise to disease in the salivary glands. Among them are abnormal antibody production, hyper-reactive T-lymphocytes, and mono- or oligoclonal expansions of B-lymphocytes. While it is not clear which, if any, of these mechanisms are of prime importance in the immunopathology of salivary gland disease, they provide a framework within which to discuss theoretical approaches to the treatment of auto-immune salivary gland disease. Among the techniques used to decrease antibody-induced damage are non-steroidal anti-inflammatory agents, plasmapheresis, and corticosteroids. Cyclosporin, monoclonal antibodies, and biologic response-modifiers may be used to modulate T-cell function, and anti-idiotype antibodies or immunosuppressive agents may be used to treat malignant expansions of B-cells. Although the generally benign nature of auto-immune salivary gland disease precludes the use of many of the potentially toxic treatment regimens discussed here, the appreciation of these approaches to immunomodulation provides a basis upon which to develop new and innovative therapeutic strategies.
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Authors | H C Lane, A S Fauci |
Journal | Journal of dental research
(J Dent Res)
Vol. 66 Spec No
Pg. 703-8
(Feb 1987)
ISSN: 0022-0345 [Print] United States |
PMID | 3497965
(Publication Type: Journal Article)
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Chemical References |
- Adrenal Cortex Hormones
- Antibodies, Anti-Idiotypic
- Antibodies, Monoclonal
- Antigen-Antibody Complex
- Cyclosporins
- Immunoglobulin Idiotypes
- Interleukin-2
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Topics |
- Adrenal Cortex Hormones
(therapeutic use)
- Antibodies, Anti-Idiotypic
(administration & dosage)
- Antibodies, Monoclonal
(therapeutic use)
- Antibody Formation
- Antigen-Antibody Complex
- Autoimmune Diseases
(therapy)
- B-Lymphocytes
(immunology)
- Cyclosporins
(therapeutic use)
- Humans
- Immunoglobulin Idiotypes
(immunology)
- Interleukin-2
(therapeutic use)
- Lymphocyte Activation
(drug effects)
- Plasmapheresis
- Salivary Gland Diseases
(immunology, therapy)
- T-Lymphocytes
(immunology)
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