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骨髓移植后的淋巴细胞嵌合现象。供体和受体淋巴细胞亚群的表面标志物及体外功能。

Lymphocyte chimerism after bone marrow transplantation. Surface markers and in vitro function of donor and recipient lymphocyte subpopulations.

作者信息

Hansen G S, Dupont B, Faber V, Jakobsen B K, Juhl F, Nielsen L S, Svejgaard A, Thomsen M, Wiik A

出版信息

Scand J Immunol. 1977;6(4):299-303. doi: 10.1111/j.1365-3083.1977.tb00397.x.

DOI:10.1111/j.1365-3083.1977.tb00397.x
PMID:323963
Abstract

Specific HLA antibodies were used to eliminate donor and recipient cells, respectively, from lymphocyte suspensions prepared from the blood of a child who had been transplanted with bone marrow from an HLA-A- and HLA-B-incompatible, HLA-D-compatible donor. About 70% of the lymphocytes were of donor HLA type, the remaining of recipient type. The phytohemagglutinin-responsive lymphocytes were exclusively limited to the lymphocyte population carrying donor-type HLA antigens. Membrane immunofluorescence investigations of the donor and recipient populations showed a low percentage of IgM-positive lymphocytes in the donor population and an extremely high proportion of IgM-positive lymphocytes in the recipient population. About 90% of the donor lymphocytes were T cells, as judged by their capacity to form rosettes between sheep erythrocytes and T lymphocytes; no cells in the recipient cell population expressed this ability.

摘要

使用特异性HLA抗体分别从一名接受了来自HLA - A和HLA - B不相容但HLA - D相容供体骨髓移植的儿童血液制备的淋巴细胞悬液中去除供体和受体细胞。约70%的淋巴细胞为供体HLA类型,其余为受体类型。对植物血凝素产生反应的淋巴细胞仅局限于携带供体型HLA抗原的淋巴细胞群体。对供体和受体群体进行的膜免疫荧光研究显示,供体群体中IgM阳性淋巴细胞的比例较低,而受体群体中IgM阳性淋巴细胞的比例极高。根据绵羊红细胞与T淋巴细胞形成花环的能力判断,约90%的供体淋巴细胞为T细胞;受体细胞群体中没有细胞表现出这种能力。

相似文献

1
Lymphocyte chimerism after bone marrow transplantation. Surface markers and in vitro function of donor and recipient lymphocyte subpopulations.骨髓移植后的淋巴细胞嵌合现象。供体和受体淋巴细胞亚群的表面标志物及体外功能。
Scand J Immunol. 1977;6(4):299-303. doi: 10.1111/j.1365-3083.1977.tb00397.x.
2
Bone marrow transplanation for severe combined immunodeficiency with the HL-A-incompatible but MLC-identical mother as a donor.以HL - A不相容但混合淋巴细胞培养相同的母亲作为供体,为重症联合免疫缺陷患者进行骨髓移植。
Transplant Proc. 1976 Dec;8(4):623-8.
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Evidence for engraftment of donor-type multipotent CD34+ cells in a patient with selective T-lymphocyte reconstitution after bone marrow transplantation for B-SCID.骨髓移植治疗重症联合免疫缺陷病(B-SCID)后选择性T淋巴细胞重建患者中供体来源多能CD34+细胞植入的证据。
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Lymphoid chimerism after allogeneic bone marrow transplantation. Y-chromatin staining of peripheral T and B lymphocytes and allotyping of serum immunoglobulins.异基因骨髓移植后的淋巴细胞嵌合体。外周T和B淋巴细胞的Y染色体染色及血清免疫球蛋白的同种异型分型。
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Poor immune reconstitution after four or five major HLA antigens mismatched T cell-depleted allogeneic and autologous stem cell transplantation.在四或五个主要人类白细胞抗原(HLA)抗原不匹配且去除T细胞的异基因和自体干细胞移植后免疫重建不良。
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Reconstitution after transplantation with T-lymphocyte-depleted HLA haplotype-mismatched bone marrow for severe combined immunodeficiency.采用去除T淋巴细胞的HLA单倍型不相合骨髓移植治疗重症联合免疫缺陷后的重建。
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Evaluation of pretransplant donor anti-recipient cytotoxic and helper T lymphocyte responses as correlates of acute graft-vs.-host disease and survival after unrelated marrow transplantation.移植前供体抗受体细胞毒性和辅助性T淋巴细胞反应作为无关骨髓移植后急性移植物抗宿主病和生存相关性的评估。
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Modified responses to recipient and donor B cells by genetically donor T cells from human haploidentical bone marrow chimeras.来自人类单倍体相合骨髓嵌合体的基因改造供体T细胞对受体和供体B细胞的反应改变
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Minor histocompatibility antigen-specific cytotoxic T cell lines, capable of lysing human hematopoietic progenitor cells, can be generated in vitro by stimulation with HLA-identical bone marrow cells.通过与 HLA 相同的骨髓细胞刺激,能够在体外产生可裂解人类造血祖细胞的次要组织相容性抗原特异性细胞毒性 T 细胞系。
J Exp Med. 1991 Jan 1;173(1):101-9. doi: 10.1084/jem.173.1.101.

引用本文的文献

1
Proceedings of the Annual Meeting of the European Foundation for Bone Marrow Transplantation, Sils Maria (Engadine), Switzerland, April 13-16, 1980.欧洲骨髓移植基金会年度会议论文集,瑞士锡尔斯玛利亚(恩加丁),1980年4月13日至16日。
Blut. 1980 Sep;41(3):151-245. doi: 10.1007/BF02464145.
2
Bone marrow transplantation for severe combined immunodeficiency disease. Reported from 1968 to 1977.1968年至1977年报告的严重联合免疫缺陷病的骨髓移植。
Eur J Pediatr. 1979 Jun 28;131(3):155-77. doi: 10.1007/BF00538940.