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免疫缺陷疾病中对B淋巴细胞系的体外反应。

In vitro responses to a B-lymphoblastoid cell line in immunodeficiency diseases.

作者信息

Sullivan J L, Ochs H D, Wedgwood R J

出版信息

J Clin Immunol. 1982 Apr;2(2):150-5. doi: 10.1007/BF00916899.

DOI:10.1007/BF00916899
PMID:6461669
Abstract

The use of a B-lymphoblastoid cell line (B-L-CL) as a stimulator cell in the mixed leukocyte reaction (MLR) was investigated in patients with immunodeficiency disorders. The kinetics of the MLR stimulated by B-L-CL are similar to those stimulated by normal allogeneic leukocytes, however, B-L-CL stimulate a greater quantitative response. Comparison of a LCL-stimulated and normal allogeneic lymphocyte-stimulated MLR in 32 patients and normal controls demonstrated that variation in the MLR was reduced when B-LCL were used as stimulator cells. The decrease in variability allowed for more sensitivity in the determination of abnormal responses; 9 of 32 patients had abnormal B-LCL-stimulated MLC responses, compared with 5 of 32 patients with abnormal responses to normal allogeneic leukocytes. Dose-response studies showed that vigorous responses could be obtained with low doses of B-LCL stimulator cells which served to better define deficient patient responses. Several patients demonstrated dissociation between the B-LCL-stimulated MLR and mitogen responses. The use of a B-LCL as a stimulator in the MLR is a valuable tool for the assessment of the immune status of patients with a variety of immunodeficiency disorders.

摘要

在免疫缺陷疾病患者中,研究了使用B淋巴细胞系(B-L-CL)作为混合淋巴细胞反应(MLR)中的刺激细胞。B-L-CL刺激的MLR动力学与正常同种异体白细胞刺激的相似,然而,B-L-CL刺激产生的定量反应更大。在32例患者和正常对照中比较LCL刺激的MLR和正常同种异体淋巴细胞刺激的MLR表明,当使用B-LCL作为刺激细胞时,MLR的变异性降低。变异性的降低使得在确定异常反应时更具敏感性;32例患者中有9例对B-LCL刺激的MLC反应异常,而对正常同种异体白细胞反应异常的32例患者中有5例。剂量反应研究表明,低剂量的B-LCL刺激细胞即可产生强烈反应,这有助于更好地界定免疫缺陷患者的反应。一些患者表现出B-LCL刺激的MLR与有丝分裂原反应之间的分离。在MLR中使用B-LCL作为刺激物是评估各种免疫缺陷疾病患者免疫状态的一种有价值的工具。

相似文献

1
In vitro responses to a B-lymphoblastoid cell line in immunodeficiency diseases.免疫缺陷疾病中对B淋巴细胞系的体外反应。
J Clin Immunol. 1982 Apr;2(2):150-5. doi: 10.1007/BF00916899.
2
Lymphocyte markers for B- and T-cells in primary immunodeficiency diseases.原发性免疫缺陷病中B细胞和T细胞的淋巴细胞标志物
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Relative increase of T cells expressing the gamma/delta rather than the alpha/beta receptor in ataxia-telangiectasia.共济失调毛细血管扩张症中表达γ/δ而非α/β受体的T细胞相对增加。
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Interactions in immunodeficiency.免疫缺陷中的相互作用。
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T and B markers in immunodeficiencies.免疫缺陷中的T和B细胞标志物。
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The Epstein-Barr virus (EBV)-transformed lymphoblastoid cell lines (LCL) as stimulating cells in mixed lymphocyte culture (MLC).爱泼斯坦-巴尔病毒(EBV)转化的淋巴母细胞系(LCL)作为混合淋巴细胞培养(MLC)中的刺激细胞。
Arch Immunol Ther Exp (Warsz). 1983;31(6):879-85.

引用本文的文献

1
X-linked lymphoproliferative syndrome. Natural history of the immunodeficiency.X连锁淋巴增殖综合征。免疫缺陷的自然史。
J Clin Invest. 1983 Jun;71(6):1765-78. doi: 10.1172/jci110932.

本文引用的文献

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Immunodeficiency associated with loss of T4+ inducer T-cell function.与T4 +诱导性T细胞功能丧失相关的免疫缺陷。
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