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引用次数: 11

摘要

以前用于治疗免疫系统介导疾病(如慢性过敏性哮喘和类风湿关节炎)的免疫抑制剂包括嘌呤拮抗剂、甲氨蝶呤和金盐。这些治疗方式在许多个体中显示出有限的治疗效果或产生不良的副作用。环孢素A是一种有效的免疫抑制剂,似乎可以阻止T淋巴细胞的分裂并抑制肥大细胞释放介质。然而,像其他免疫抑制剂一样,环孢素A也可能产生许多潜在的严重副作用;其中之一就是不可逆肾损害的可能性。肾毒性可以减轻,因为肾脏病理改变似乎是高累积剂量相关的。如果环孢素A的全血水平维持在200 - 500纳克/毫升之间,严重的肾毒性是不常见的。环孢素A在患有严重的长期皮质类固醇依赖性慢性哮喘的个体中的研究已经证明了该药物的有效性,导致肺功能的临床显着改善。因此,可以假设T淋巴细胞可能在特应性变应性炎症的细胞介导的超敏反应中起效应细胞的作用。
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Immunosuppressive agents in chronic severe asthma.

Previous immunosuppressive agents utilized as therapies for immune system mediated diseases such as chronic allergic asthma, and rheumatoid arthritis include purine antagonists, methotrexate, and gold salts. These treatment modalities have been shown to elicit either limited treatment efficacy or to produce undesirable side effects in many individuals. Cyclosporin A is a potent immunosuppressive agent which appears to arrest division of T lymphocytes and inhibit mediator release from mast cells. However, like other immunosuppressive agents, cyclosporin A may also produce many potentially serious side effects; among these is the possibility of irreversible renal damage. Nephrotoxicity can be attenuated, because renal pathological changes seem to be high cumulative dose-related. If whole blood levels of cyclosporin A are maintained between 200 and 500 ng/mL, serious renal toxicity is unusual. Investigation of cyclosporin A in individuals who have severe long-term corticosteroid-dependent chronic asthma has demonstrated the efficacy of this agent, resulting in clinically significant improvement in pulmonary function. Therefore, it can be hypothesized that T lymphocytes may act as effector cells in cell-mediated hypersensitivity reactions in atopic allergic inflammation.

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The School of Salernum, regimen Sanitatis Salernitanum. Update on urticaria and angioedema (hives). Adverse reactions associated with skin testing and immunotherapy. Implications of practice parameters (guidelines). The role of immunotherapy in allergic rhinitis/allergic asthma.
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