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第五届马淋巴细胞同种抗原国际研讨会联合报告,路易斯安那州巴吞鲁日,1987年10月31日至11月1日。

Joint Report of the Fifth International Workshop on Lymphocyte Alloantigens of the Horse, Baton Rouge, Louisiana, 31 October-1 November 1987.

作者信息

Lazary S, Antczak D F, Bailey E, Bell T K, Bernoco D, Byrns G, McClure J J

机构信息

Division of Immunogenetics, School of Veterinary Medicine, University of Berne, Switzerland.

出版信息

Anim Genet. 1988;19(4):447-56. doi: 10.1111/j.1365-2052.1988.tb00836.x.

Abstract

Six laboratories participated in the Fifth International Workshop on Lymphocyte Alloantigens of the Horse, testing 132 alloantisera against lymphocytes of 880 horses chosen to represent different families and breeds. Most of the alloantisera were produced by lymphocyte immunization between horses matched at the ELA-A locus. All horses were also tested with antisera contributed to the workshop by participating laboratories which identified ELA specificities A1-A10 and W12-W21. Previously identified workshop specificities ELA-W14, W15 and W19 were accepted as products of the ELA-A locus based on family and population studies by the workshop. Their designations were changed to ELA-A14, ELA-A15 and ELA-A19, respectively. Two new specificities were identified, namely ELA-W22 (W22) and ELA-W23 (W23). Population and family studies indicated that W22 and W23 as well as W13 are products of an ELA locus other than ELA-A. The presence of these specificities was correlated with the presence of certain ELA-A locus specificities, e.g. W13 with A3, W22 with A2 and W23 with A5. However, the association was not complete and W13, W22 and W23 also segregated with other ELA-A specificities in some families. Evidence for recombination was found between the ELA-A locus and the locus or loci encoding these specificities resulting in seven recombinant haplotypes found among the data presented in this workshop. Further studies are required for definitive assignment of the specificities to a class I or class II locus.

摘要

六个实验室参与了第五届马淋巴细胞同种异体抗原国际研讨会,用132种同种抗血清检测了880匹选自不同家族和品种的马的淋巴细胞。大多数同种抗血清是通过在ELA-A位点匹配的马之间进行淋巴细胞免疫产生的。所有马匹还用参与研讨会的实验室提供的抗血清进行了检测,这些抗血清鉴定出了ELA特异性A1-A10和W12-W21。根据研讨会的家族和群体研究,先前确定的研讨会特异性ELA-W14、W15和W19被认为是ELA-A位点的产物。它们的名称分别改为ELA-A14、ELA-A15和ELA-A19。确定了两种新的特异性,即ELA-W22(W22)和ELA-W23(W23)。群体和家族研究表明,W22和W23以及W13是ELA-A位点以外的ELA位点的产物。这些特异性的存在与某些ELA-A位点特异性的存在相关,例如W13与A3相关,W22与A2相关,W23与A5相关。然而,这种关联并不完全,在一些家族中,W13、W22和W23也与其他ELA-A特异性分离。在ELA-A位点与编码这些特异性的一个或多个位点之间发现了重组证据,在本次研讨会提供的数据中发现了七种重组单倍型。需要进一步研究以明确将这些特异性指定到I类或II类位点。

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