CELL-MEDIATED HYPERSENSITIVITY AND INTERSTITIAL CYSTITIS
CELL-MEDIATED HYPERSENSITIVITY AND INTERSTITIAL CYSTITIS
批准号:
3246312
负责人:
DON KREUTZER
金额:
$13.04万
依托单位国家:
美国
项目类别:
财政年份:
1992
资助国家:
美国
项目状态:
已结题
起止时间:
1992-03-01 至 1995-02-28
关键词:
B lymphocyte T lymphocyte autoimmune disorder blood chemistry cellular immunity cellular pathology clone cells colony stimulating factor cytokine receptors disease /disorder model flow cytometry human subject hypersensitivity immunocytochemistry inhibitor /antagonist interferons interleukin 1 interleukin 6 interleukin 8 interstitial cystitis laboratory mouse leukocyte activation /transformation macrophage model design /development monocyte transforming growth factors tumor necrosis factor alpha tumor necrosis factor beta urinalysis urinary bladder
中文摘要
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英文摘要
Interstitial cystitis (IC) or painful bladder syndrome is a complex
disease entity with unknown etiology and pathogenesis. The disease
effects predominantly women and encompasses a variety of symptoms
including frequent urination and pelvic pain. IC is a chronic
inflammatory disease of the bladder wall, and is characterized by edema,
fibrosis and leukocyte infiltrates and mast cells. Although the presence
of both lymphocytes as well as macrophages have been demonstrated in the
bladders of IC patients, nothing is known about the nature or contribution
of these cells nor their products (cytokine) to the pathogenesis of IC.
Thus, we have hypothesized that IC represents a disease in which bladder-
specific cell-mediated hypersensitivity participates directly in the
pathogenesis of the disease by dysfunctional regulation of T cells;
macrophages, and proinflammatory cytokines. To investigate this
hypothesis, we propose to initially define the presence of both
immunologic cells and cytokines within the blood, urine and tissue of IC
patients, and correlate their presence with clinical history and disease.
Additionally, we propose to characterize the immunologic status of
mononuclear cells isolated from IC patients using non-specific mitogens,
as well as bladder-specific antigens obtained from urine and bladder
tissue. In addition to evaluating the immune status of primary leukocyte
cultures isolated from IC patients, we also plan to isolate T cell clones
from urinary bladder tissue of patients with IC. Also we will
characterize them and evaluate their in vitro responsiveness to specific
bladder antigens, as well as bladder cells. Finally, we propose to
develop models of IC in the mouse. For these studies, we propose to
induce both cell-mediated hypersensitivity and autoimmunity in both
control and mutant mice (SCID, Steel and nude mice) using state-of-the-art
immunologic techniques. Thus using both patient and animal models, we
feel that these studies should provide important new insights into the
role of immune cells and products in cystitis in general, and IC
specifically.
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资助金额:$44.4万
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依托单位:
海外基金