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结节病中的免疫功能。关于迟发型超敏反应、B淋巴细胞和T淋巴细胞、血清免疫球蛋白及血清补体成分的研究。

Immune function in sarcoidosis. Studies on delayed hypersensitivity, B and T lymphocytes, serum immunoglobulins and serum complement components.

作者信息

Tannenbaum H, Rocklin R E, Schur P H, Sheffer A L

出版信息

Clin Exp Immunol. 1976 Dec;26(3):511-9.

Abstract

An assessment of immune function was performed in twenty-four patients with recently diagnosed active sarcoidosis. Four patients manifested skin anergy to four antigens. All subjects except one were capable of generating a positive skin response to a croton oil patch test. The incorporation of [3H]thymidine by lymphocytes in vitro in response to the nonspecific mitogens--phytohaemagglutinin, pokeweed mitogen and Con A did not differ between anergic and non-anergic thymidine incorporation in vitro when stimulated by the specific antigens, streptokinase/streptodornase or Candida albicans. Lymphocytes obtained from nine of eleven patients having positive delayed hypersensitivity skin reactions demonstrated MIF production in vitro upon specific antigen challenge. Quantities of circulating B and T lymphocytes did not differ between anergic and absolute numbers of circulating B and T lymphocytes, as well as hypercomplementaemia and hypergammaglobulinaemia when compared to the control group.

摘要

对24例近期诊断为活动性结节病的患者进行了免疫功能评估。4例患者对4种抗原表现出皮肤无反应性。除1例受试者外,所有受试者对巴豆油斑贴试验均能产生阳性皮肤反应。在体外,淋巴细胞对非特异性有丝分裂原(植物血凝素、商陆有丝分裂原和刀豆球蛋白A)的[3H]胸腺嘧啶核苷掺入量,在无反应性和非无反应性受试者之间并无差异,在受到特异性抗原(链激酶/链道酶或白色念珠菌)刺激时,体外[3H]胸腺嘧啶核苷掺入情况也是如此。从11例具有阳性迟发型超敏反应皮肤反应的患者中,有9例患者的淋巴细胞在受到特异性抗原攻击后,在体外表现出巨噬细胞移动抑制因子的产生。与对照组相比,无反应性和有反应性受试者的循环B淋巴细胞和T淋巴细胞的数量、循环B淋巴细胞和T淋巴细胞的绝对数量,以及补体血症和高球蛋白血症均无差异。

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本文引用的文献

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Precise standardization of reagents for complement fixation.补体结合反应试剂的精确标准化
Am J Trop Med Hyg. 1963 Jan;12:103-16. doi: 10.4269/ajtmh.1963.12.103.
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Studies on the mechanism of lymphocyte transformation inhibition in sarcoidosis.
Br J Dermatol. 1969 Nov;81(11):829-34. doi: 10.1111/j.1365-2133.1969.tb15952.x.
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Monocyte receptor activity in normal individuals and patients with sarcoidosis.
Immunol Commun. 1972;1(1):25-38. doi: 10.3109/08820137209022890.

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