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温抗体型自身免疫性溶血性贫血(AIHA)患者淋巴细胞的功能和表面特征

Functional and surface characterisitics of lymphocytes from patients with warm-antibody type autoimmunhemolytic anemia (AIHA).

作者信息

Krüger J, Desaga F J

出版信息

Blut. 1978 Jun 20;36(6):315-23. doi: 10.1007/BF01000587.

DOI:10.1007/BF01000587
PMID:306850
Abstract

As part of an overall assessment of immunological function, several aspects of cellular immunity and circulating lymphocyte subpopulations were evaluated in a group of 10 patients with idiopathic autoimmunhemolytic anemia (AIHA). The absolute numbers of circulating T and B cells were reduced in the patient group compared to normals. A shift from "corticosteroid-sensitive" to "corticosteroid-resistent" and activated cells in the cytogram of clustered Fe-(III)-hydroxide-glucane saccharose labeled T lymphocytes was apparent. In vitro studies of cellular reactivity, as evaluated by PHA, ConA, PWM, antigens and allogeneic cell induced proliferation showed a blend of general or selective depression and sometimes a normal or increased activity with no definite correlation with both the number of circulating T cells and the extent of the hemolytic activity by the disease. The possible significance of the findings is discussed.

摘要

作为免疫功能全面评估的一部分,对一组10例特发性自身免疫性溶血性贫血(AIHA)患者的细胞免疫和循环淋巴细胞亚群的几个方面进行了评估。与正常人相比,患者组循环T细胞和B细胞的绝对数量减少。在聚集的氢氧化铁(III)-葡聚糖蔗糖标记的T淋巴细胞的细胞图中,从“皮质类固醇敏感”细胞向“皮质类固醇抵抗”和活化细胞的转变很明显。通过PHA、ConA、PWM、抗原和同种异体细胞诱导的增殖评估的细胞反应性的体外研究显示,存在普遍或选择性抑制,有时活性正常或增加,与循环T细胞数量和疾病溶血活性程度均无明确相关性。讨论了这些发现的可能意义。

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引用本文的文献

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本文引用的文献

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The ultrastructural basis of capillary permeability studied with peroxidase as a tracer.以过氧化物酶为示踪剂研究毛细血管通透性的超微结构基础。
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Response of NZB and NZB-NZW spleen cells to mitogenic agents.新西兰黑鼠(NZB)和新西兰黑鼠-新西兰白鼠(NZB-NZW)脾细胞对促有丝分裂剂的反应。
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Clin Exp Immunol. 1971 Mar;8(3):479-90.
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B-cell suppression of delayed hypersensitivity reactions.B细胞对迟发型超敏反应的抑制作用。
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Lymphocyte subpopulations in NZB mice: deficit of thymus-dependent lymphocytes.NZB小鼠的淋巴细胞亚群:胸腺依赖性淋巴细胞缺乏
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Decline in suppressor T cell function with age in female NZB mice.雌性新西兰黑小鼠随着年龄增长抑制性T细胞功能下降。
J Immunol. 1974 Jan;112(1):9-16.