Bull R W, Lewin H A, Wu M C, Peterbaugh K, Antczak D, Bernoco D, Cwik S, Dam L, Davies C, Dawkins R L
Department of Medicine, Michigan State University, East Lansing 48824-1317.
Anim Genet. 1989;20(1):109-32. doi: 10.1111/j.1365-2052.1989.tb00849.x.
Two hundred and eighty-two alloantisera were submitted by 20 participating laboratories from 13 countries and tested against lymphocytes of 1298 cattle. The cell panel consisted of samples from 38 Bos taurus breeds, 11 Bos taurus crossbreeds, 4 Bos indicus breeds, 6 Bos taurus x Bos indicus, and a variety of other crossbred populations. Using a standardized lymphocytotoxicity test, all 17 previously identified BoLA specificities were confirmed. The workshop produced agreement on 16 new lymphocyte alloantigenic specificities. Three of the new specificities behaved as splits of previously identified BoLA specificities. Four of the new specificities behaved as alleles at the agreed BoLA-A locus. Seven new specificities are tentatively assigned to the BoLA-A locus but require further definition. Two new specificities may represent products of a second closely-linked BoLA locus.
来自13个国家的20个参与实验室提交了282份同种异体抗血清,并对1298头奶牛的淋巴细胞进行了检测。细胞样本包括来自38个黄牛品种、11个黄牛杂交品种、4个瘤牛品种、6个黄牛×瘤牛杂交品种以及各种其他杂交群体的样本。使用标准化的淋巴细胞毒性试验,确认了所有17种先前鉴定的牛白细胞抗原(BoLA)特异性。本次研讨会就16种新的淋巴细胞同种抗原特异性达成了共识。其中3种新特异性表现为先前鉴定的BoLA特异性的细分。4种新特异性表现为在已达成共识的BoLA - A位点上的等位基因。7种新特异性暂定为BoLA - A位点,但需要进一步明确。2种新特异性可能代表第二个紧密连锁的BoLA位点的产物。