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重型再生障碍性贫血:20例患者体外试验与免疫抑制临床反应的相关性

Severe aplastic anaemia: correlation of in vitro test with clinical response to immunosuppression in 20 patients.

作者信息

Bacigalupo A, Podesta' M, Van Lint M T, Vimercati R, Cerri R, Rossi E, Risso M, Carella A, Santini G, Damasio E, Giordano D, Marmont A M

出版信息

Br J Haematol. 1981 Mar;47(3):423-32. doi: 10.1111/j.1365-2141.1981.tb02810.x.

DOI:10.1111/j.1365-2141.1981.tb02810.x
PMID:6450608
Abstract

Colony formation in agar (CFU-c) was studied in 20 patients with severe aplastic anaemia by three different assays: (1) cultures of light density untreated marrow cells; (2) cultures of marrow cells manipulated in order to enhance colony formation (pretreatment with antilymphocytic globulin, ALG, or 6-methylprednisolone, 6-MPr, T cell depletion, adherent cell (AC) depletion, depletion of both AC and T cells), and (3) co-culture of putative suppressor T cells with autologous T-depleted marrow cells. By the first assay, all patients showed poor colony formation (1 +/- 1.5 colonies/10(5) cells; normal controls 46 +/- 18 colonies/10(5) cells). By the second assay, ALG and 6-MPr had no significant effect on colony formation. Removal of adherent cells proved equally without effect on colony growth. On the contrary, removal of T cells enhanced significantly (P less than 0.001) colony formation in 10 out of 20 patients. By the third assay, colony formation of marrow cells (deprived of T lymphocytes) was inhibited by the addition of autologous T cells in six patients studied. All patients were given high dose bolus 6-MPr as first treatment on admission: only patients who had detectable suppressor T cells in their marrow achieved a complete autologous haematologic reconstitution after 6-MPr or after 6-MPr and ALG. The results of this study indicate the detection of CFU-c/suppressor T cells correlates with responses to immunosuppressive regimens, and may thus help to identify patients with immune mediated aplastic anaemia.

摘要

通过三种不同的检测方法,对20例重型再生障碍性贫血患者进行了琼脂集落形成(CFU-c)研究:(1)低密度未处理骨髓细胞培养;(2)对骨髓细胞进行处理以增强集落形成(用抗淋巴细胞球蛋白、ALG或6-甲基强的松龙、6-MPr预处理,T细胞清除,贴壁细胞(AC)清除,AC和T细胞均清除),以及(3)将假定的抑制性T细胞与自体T细胞清除的骨髓细胞共培养。通过第一种检测方法,所有患者的集落形成均较差(1±1.5个集落/10⁵个细胞;正常对照为46±18个集落/10⁵个细胞)。通过第二种检测方法,ALG和6-MPr对集落形成无显著影响。事实证明,去除贴壁细胞对集落生长同样没有影响。相反,在20例患者中有10例,去除T细胞后集落形成显著增强(P<0.001)。通过第三种检测方法,在研究的6例患者中,加入自体T细胞后,(去除T淋巴细胞的)骨髓细胞集落形成受到抑制。所有患者入院时均接受大剂量冲击性6-MPr作为首次治疗:只有骨髓中可检测到抑制性T细胞的患者在接受6-MPr或6-MPr和ALG治疗后实现了完全的自体血液学重建。本研究结果表明,CFU-c/抑制性T细胞的检测与免疫抑制方案的反应相关,因此可能有助于识别免疫介导的再生障碍性贫血患者。

相似文献

1
Severe aplastic anaemia: correlation of in vitro test with clinical response to immunosuppression in 20 patients.重型再生障碍性贫血:20例患者体外试验与免疫抑制临床反应的相关性
Br J Haematol. 1981 Mar;47(3):423-32. doi: 10.1111/j.1365-2141.1981.tb02810.x.
2
Lack of in vitro colony (CFUC) formation and myelosuppressive activity in patients with severe aplastic anemia after autologous hematologic reconstitution.严重再生障碍性贫血患者自体血液重建后缺乏体外集落(CFUC)形成及骨髓抑制活性。
Exp Hematol. 1980 Jul;8(6):795-801.
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Treatment of severe aplastic anemia with high-dose methylprednisolone and antilymphocyte globulin.大剂量甲泼尼龙联合抗淋巴细胞球蛋白治疗重型再生障碍性贫血
Prog Clin Biol Res. 1984;148:271-87.
4
T cell-mediated inhibition of haematopoiesis in aplastic anaemia: serial assay of inhibitory activities of T cells to autologous CFU-E during immunosuppressive therapy.再生障碍性贫血中T细胞介导的造血抑制:免疫抑制治疗期间T细胞对自体CFU-E抑制活性的系列检测
Br J Haematol. 1986 May;63(1):69-74. doi: 10.1111/j.1365-2141.1986.tb07496.x.
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Treatment of aplastic anemia with immunosuppressive agents.使用免疫抑制剂治疗再生障碍性贫血。
Tokai J Exp Clin Med. 1986;11 Suppl:197-204.
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Inhibitory effects of peripheral blood cells on in vitro colony formation by autologous bone marrow in aplastic anaemia: relation with response to immunosuppressive therapy.再生障碍性贫血患者外周血细胞对自体骨髓体外集落形成的抑制作用:与免疫抑制治疗反应的关系
J Clin Pathol. 1982 Dec;35(12):1316-9. doi: 10.1136/jcp.35.12.1316.
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Immune suppression of hematopoiesis in aplastic anemia: activity of T-gamma lymphocytes.再生障碍性贫血中造血的免疫抑制:Tγ淋巴细胞的活性
J Immunol. 1980 Oct;125(4):1449-53.
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Effect of antilymphocyte globulin (ALG) on bone marrow T/non-T cells from aplastic anaemia patients and normal controls.
Br J Haematol. 1989 Dec;73(4):546-50. doi: 10.1111/j.1365-2141.1989.tb00295.x.
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Generation of CFU-C suppressor T cells in vitro. V. A multistep process.体外产生集落形成单位 - C 抑制性 T 细胞。V. 一个多步骤过程。
Br J Haematol. 1982 Nov;52(3):421-7. doi: 10.1111/j.1365-2141.1982.tb03911.x.
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Effect of antilymphocyte globulin on granulocyte precursors in aplastic anaemia.抗淋巴细胞球蛋白对再生障碍性贫血中粒细胞前体的作用。
Br J Haematol. 1979 Jul;42(3):371-80. doi: 10.1111/j.1365-2141.1979.tb01145.x.

引用本文的文献

1
Immunosuppressive treatment of acquired aplastic anemia and immune-mediated bone marrow failure syndromes.获得性再生障碍性贫血及免疫介导的骨髓衰竭综合征的免疫抑制治疗
Int J Hematol. 2002 Feb;75(2):129-40. doi: 10.1007/BF02982017.
2
CFU-C inhibitors in aplastic anaemia.再生障碍性贫血中的集落形成单位 - 粒细胞(CFU-C)抑制剂
Blut. 1984 Feb;48(2):61-74. doi: 10.1007/BF00320032.
3
In vitro evidence of drug action in aplastic anemia.再生障碍性贫血中药物作用的体外证据。
Blut. 1984 Jul;49(1):3-12. doi: 10.1007/BF00320378.
4
Pure red cell aplasia and thymoma associated with high levels of the suppressor/cytotoxic T lymphocyte subset.纯红细胞再生障碍性贫血与胸腺瘤伴抑制性/细胞毒性T淋巴细胞亚群水平升高相关。
Br Med J (Clin Res Ed). 1984 Nov 17;289(6455):1333-4. doi: 10.1136/bmj.289.6455.1333.
5
Bone-marrow transplantation for severe aplastic anaemia using histocompatible unrelated volunteer donors.使用组织相容性无关志愿供者进行的严重再生障碍性贫血骨髓移植
Br Med J (Clin Res Ed). 1982 Sep 25;285(6345):835-7. doi: 10.1136/bmj.285.6345.835.
6
Treatment of aplastic anemia with cyclosporin A, methylprednisolone, and antithymocyte globulin.
Klin Wochenschr. 1986 Nov 17;64(22):1165-70. doi: 10.1007/BF01728454.
7
Immunosuppressive treatment of aplastic anemia: a prospective, randomized multicenter trial evaluating antilymphocyte globulin (ALG) versus ALG and cyclosporin A.再生障碍性贫血的免疫抑制治疗:一项评估抗淋巴细胞球蛋白(ALG)与ALG加环孢素A的前瞻性、随机多中心试验。
Blut. 1988 Apr;56(4):191-2. doi: 10.1007/BF00320751.