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HLA-DR2单倍型的T细胞克隆分析。

T-cell clonal analysis of HLA-DR2 haplotypes.

作者信息

Reinsmoen N L, Bach F H

机构信息

Immunobiology Research Center, University of Minnesota Hospital and Clinic, Minneapolis 55455.

出版信息

Hum Immunol. 1987 Sep;20(1):13-31. doi: 10.1016/0198-8859(87)90003-6.

DOI:10.1016/0198-8859(87)90003-6
PMID:3316134
Abstract

Individuals carrying the serologically-defined DR2 haplotypes can be further subdivided by utilizing T cell response to define several HLA-Dw/LD clusters: Dw2, Dw12, LD-5a, and a related group composed of FJO, AZH, and MN2. We have used cytotoxic T cell clones generated against these DR2 haplotypes to define the DR and DQ associated Dw/LD polymorphisms. Clones were categorized as DR, DQ, DP, or class I-directed based on monoclonal antibody (MoAb) inhibition studies. We analyzed the distribution of the determinants detected by these clones based on analysis with panels of cells. Some DR-directed clones only lysed cells positive for the Dw subtype of the sensitizing cell. A few DR-directed clones lysed most DR2 positive cells. Other DR-directed clones detected determinants shared by cells of different subtypes: determinants shared by Dw2 and Dw12 positive cells and determinants shared by MN2, FJO, AZH, and LD-5a positive cells. The majority of the DQ-directed clones only lysed cells positive for the sensitizing HLA-Dw subtype. A group of clones primed against an LD-5a HTC, whose cytolytic activity was not blocked by any monoclonal antibodies tested, lysed some, but not all, DR2 positive cells as well as Dw1 and Dw10 positive cells. The results suggest the detection of determinants on these molecules which may be shared by cells of specific Dw subgroups and determinants shared by most cells of the sensitizing serological specificity. The basis of this observed polymorphism and influence on the allogeneic response are discussed.

摘要

携带血清学定义的DR2单倍型的个体可通过利用T细胞反应进一步细分,以定义几个HLA-Dw/LD簇:Dw2、Dw12、LD-5a以及由FJO、AZH和MN2组成的相关组。我们使用针对这些DR2单倍型产生的细胞毒性T细胞克隆来定义与DR和DQ相关的Dw/LD多态性。根据单克隆抗体(MoAb)抑制研究,克隆被分类为DR、DQ、DP或I类定向。我们基于细胞系分析了这些克隆检测到的决定簇的分布。一些DR定向克隆仅裂解对致敏细胞的Dw亚型呈阳性的细胞。少数DR定向克隆裂解大多数DR2阳性细胞。其他DR定向克隆检测到不同亚型细胞共有的决定簇:Dw2和Dw12阳性细胞共有的决定簇以及MN2、FJO、AZH和LD-5a阳性细胞共有的决定簇。大多数DQ定向克隆仅裂解对致敏HLA-Dw亚型呈阳性的细胞。一组针对LD-5a HTC致敏的克隆,其细胞溶解活性未被任何测试的单克隆抗体阻断,裂解了一些但不是所有的DR2阳性细胞以及Dw1和Dw10阳性细胞。结果表明在这些分子上检测到了可能由特定Dw亚组的细胞共有的决定簇以及由致敏血清学特异性的大多数细胞共有的决定簇。讨论了这种观察到的多态性的基础及其对同种异体反应的影响。

相似文献

1
T-cell clonal analysis of HLA-DR2 haplotypes.HLA-DR2单倍型的T细胞克隆分析。
Hum Immunol. 1987 Sep;20(1):13-31. doi: 10.1016/0198-8859(87)90003-6.
2
Clonal analysis of HLA-DR and -DQ associated determinants: their contribution to Dw specificities.HLA-DR和-DQ相关决定簇的克隆分析:它们对Dw特异性的贡献。
Hum Immunol. 1986 Aug;16(4):329-46. doi: 10.1016/0198-8859(86)90060-1.
3
Protein analysis of HLA-DR2.3 haplotype.HLA-DR2.3单倍型的蛋白质分析。
Hum Immunol. 1987 Jun;19(2):127-37. doi: 10.1016/0198-8859(87)90100-5.
4
Molecular studies of a rare DR2/LD-5a/DQw3 HLA class II haplotype. Multiple genetic mechanisms in the generation of polymorphic HLA class II genes.一种罕见的DR2/LD-5a/DQw3 HLA II类单倍型的分子研究。多态性HLA II类基因产生中的多种遗传机制。
J Immunol. 1988 May 15;140(10):3631-9.
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Dw subtypes of serologically defined DR-DQ specificities restrict recognition of cytomegalovirus.血清学定义的DR-DQ特异性的Dw亚型限制了对巨细胞病毒的识别。
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Functional definition of HLA-DR and -DQ epitopes specific for DR2-short, DwFJO haplotype.针对DR2-短、DwFJO单倍型的HLA-DR和-DQ表位的功能定义。
Immunogenetics. 1986;23(6):385-92. doi: 10.1007/BF00372671.
8
Alloreactive cytolytic T cell clones with dual recognition of HLA-B27 and HLA-DR2 antigens. Selective involvement of CD8 in their class I--directed cytotoxicity.对HLA - B27和HLA - DR2抗原具有双重识别能力的同种反应性细胞溶解性T细胞克隆。CD8在其针对I类抗原的细胞毒性中具有选择性参与作用。
J Exp Med. 1987 Feb 1;165(2):428-43. doi: 10.1084/jem.165.2.428.
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A new HTC, a PLT and a PLT clone define a split of HLA-DR2 in the Austrian population.一种新的HTC、一种PLT和一种PLT克隆体定义了奥地利人群中HLA-DR2的一种分型。
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HLA-DR2-associated Dw subtypes correlate with RFLP clusters: most DR2 IDDM patients belong to one of these clusters.与HLA - DR2相关的Dw亚型与限制性片段长度多态性(RFLP)簇相关:大多数DR2型胰岛素依赖型糖尿病(IDDM)患者属于这些簇中的一种。
Immunogenetics. 1986;23(2):84-9. doi: 10.1007/BF00377966.