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本文引用的文献

1
Immunologic precursors of autoimmune hematologic disorders. Autoimmune hematologic disorders. Autoimmune hemolytic anemia and thrombocytopenic purpura.自身免疫性血液系统疾病的免疫学前体。自身免疫性血液系统疾病。自身免疫性溶血性贫血和血小板减少性紫癜。
Johns Hopkins Med J. 1981 Sep;149(3):101-9.
2
Graves' disease and idiopathic thrombocytopenic purpura.格雷夫斯病和特发性血小板减少性紫癜。
Arch Intern Med. 1980 Sep;140(9):1252-3.
3
Systemic lupus erythematosus: presence in human serum of an unusual acid-labile leukocyte interferon.系统性红斑狼疮:人血清中存在一种异常的酸不稳定白细胞干扰素。
Science. 1982 Apr 23;216(4544):429-31. doi: 10.1126/science.6176024.
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Purification of human fibroblast interferon prepared from modified fibroblasts.
Methods Enzymol. 1981;78(Pt A):422-30. doi: 10.1016/0076-6879(81)78152-7.
5
Cyclic thrombocytopenia associated with multiple autoantibodies.与多种自身抗体相关的周期性血小板减少症。
Br Med J. 1969 Aug 16;3(5667):397-8. doi: 10.1136/bmj.3.5667.397.
6
Semi-micro, dye-binding assay for rabbit interferon.兔干扰素的半微量染料结合测定法。
Appl Microbiol. 1971 Apr;21(4):723-5. doi: 10.1128/am.21.4.723-725.1971.
7
Immunodeficiency and grouping with thyrogastric autoimmune disease in patients with chronic idiopathic thrombocytopenic purpura.慢性特发性血小板减少性紫癜患者的免疫缺陷及与甲状腺胃自身免疫性疾病的分组
Aust N Z J Med. 1974 Jun;4(3):243-6. doi: 10.1111/j.1445-5994.1974.tb03182.x.
8
Interferon.
Annu Rev Microbiol. 1975;29:131-61. doi: 10.1146/annurev.mi.29.100175.001023.
9
Autoimmune hematologic diseases associated with infraclinical systemic lupus erythematosus in four patients. A human equivalent of the NZB mice.4例与亚临床系统性红斑狼疮相关的自身免疫性血液病。人类中的新西兰黑小鼠。
Am J Med. 1979 Jan;66(1):91-95. doi: 10.1016/0002-9343(79)90487-x.
10
Chronic idiopathic thrombocytopenic purpura. A familial immunodeficiency syndrome?慢性特发性血小板减少性紫癜。一种家族性免疫缺陷综合征?
JAMA. 1978 Mar 6;239(10):939-42.

特发性血小板减少性紫癜患者脾淋巴细胞在体外自发产生人γ干扰素。

Spontaneous production of human gamma interferon in vitro by splenic lymphocytes of patients with idiopathic thrombocytopenic purpura.

作者信息

Hu Y W, Xue G X, Tan Y H

出版信息

Clin Exp Immunol. 1984 May;56(2):459-63.

PMID:6428786
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1536219/
Abstract

Lymphocytes derived from spleens of traffic trauma victims do not appear to produce human interferon (IFN) activity, spontaneously, in vitro. However, lymphocytes derived from spleens of four ITP patients were found to produce significant amounts of human IFN activity. The IFN activity produced by the splenic lymphocytes of ITP patients was neutralized by anti-gamma-IFN antisera but not anti-alpha or anti-beta antisera. The IFN activity was found to be unstable at pH 2.0 and at 56 degrees C. Thus the human IFN activity of splenic lymphocytes is characterized as human gamma-IFN. No human IFN activity was detectable in the serum of the ITP patients and it is not known whether the splenic lymphocytes of ITP patients also produce human gamma-IFN in vivo. The observations suggest that conditions prevail in the ITP state that predispose the splenic lymphocytes to produce human gamma-IFN without stimulation by exogenously added inducer.

摘要

交通创伤受害者脾脏来源的淋巴细胞在体外似乎不会自发产生人干扰素(IFN)活性。然而,发现来自4例免疫性血小板减少性紫癜(ITP)患者脾脏的淋巴细胞能产生大量人IFN活性。ITP患者脾脏淋巴细胞产生的IFN活性可被抗γ-IFN抗血清中和,但不能被抗α或抗β抗血清中和。发现该IFN活性在pH 2.0和56℃时不稳定。因此,脾脏淋巴细胞的人IFN活性被鉴定为人γ-IFN。在ITP患者血清中未检测到任何人类IFN活性,并且尚不清楚ITP患者的脾脏淋巴细胞在体内是否也产生人γ-IFN。这些观察结果表明,在ITP状态下存在一些条件,使脾脏淋巴细胞在没有外源性添加诱导剂刺激的情况下易于产生人γ-IFN。