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结节病:迟发型超敏反应、混合淋巴细胞培养反应及淋巴细胞毒性与疾病活动度的相关性

Sarcoidosis: correlation of delayed hypersensitivity, MLC reactivity and lymphocytotoxicity with disease activity.

作者信息

Broom B C, MacLaurin B P

出版信息

Clin Exp Immunol. 1973 Nov;15(3):355-64.

Abstract

Delayed skin reactivity to a battery of antigens was assessed for a series of sarcoidosis patients and closely matched controls. It was compared with the proliferative and cytotoxic capacity of corresponding blood lymphocyte preparations after challenge in mixed lymphocyte culture with an allogeneic lymphoma cell line. Skin anergy to all antigens tested was found only within the patient group having definitely active disease. These patients also showed depression of lymphocyte proliferative response in the test system as compared to matched controls and to patients with apparently inactive disease. Both of these differences were statistically significant. Skin reactivity to tuberculin was significantly depressed for the whole sarcoidosis group (both active and inactive) as compared to the control group and significant impairment of capacity to develop cytotoxicity was also found in comparison of these same groups. The results obtained confirm the association of impaired delayed skin hypersensitivity in sarcoidosis with diminished lymphocyte reactivity , especially when the disease is active. The reduced cytotoxic capacity of sarcoid lymphocytes may reflect a comparable impairment and partly explain the depressed skin tests and also contribute to the protracted nature of the disease because of failure to eradicate the postulated `sarcoid agent'.

摘要

对一系列结节病患者和与之密切匹配的对照组,评估了其对一组抗原的迟发性皮肤反应性。将其与相应血液淋巴细胞制剂在用同种异体淋巴瘤细胞系进行混合淋巴细胞培养激发后的增殖能力和细胞毒性能力进行了比较。仅在患有明确活动性疾病的患者组中发现对所有测试抗原的皮肤无反应性。与匹配的对照组以及明显无活动性疾病的患者相比,这些患者在测试系统中还表现出淋巴细胞增殖反应降低。这两种差异均具有统计学意义。与对照组相比,整个结节病组(包括活动性和非活动性)对结核菌素的皮肤反应性均显著降低,并且在比较这些相同组时还发现细胞毒性发展能力有显著损害。获得的结果证实了结节病中迟发性皮肤超敏反应受损与淋巴细胞反应性降低之间的关联,尤其是在疾病活动时。结节病淋巴细胞细胞毒性能力的降低可能反映了类似的损害,部分解释了皮肤试验的降低,并且由于未能根除假定的“结节病病原体”,也导致了疾病的迁延不愈。

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本文引用的文献

4
Skin tests in sarcoidosis.
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Klin Wochenschr. 1968 Sep 15;46(18):1010-1. doi: 10.1007/BF01745597.
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Pneumonologie. 1971;144(4):281-7. doi: 10.1007/BF02102457.

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