Myers L K, Ball E J, Nunez G, Fink C W, Stastny P
Arthritis Rheum. 1987 Jul;30(7):744-51. doi: 10.1002/art.1780300704.
The HLA-D region antigens DR5 (w11,w12), DRw6 (w13,w14), DRw8, DRw52, and DQw1 have previously been shown to be increased in frequency in subsets of patients with juvenile arthritis. Since the HLA-D region is complex (composed of at least 3 subregions encoding multiple molecules, each in turn presenting multiple alloantigenic epitopes), we sought to clarify whether one strongly associated factor might explain the previous findings. To search for the pertinent HLA-D region stimulatory epitopes, alloreactive T cells were primed against DR5 and DRw6 haplotypes and cloned by limiting dilution. Three T cell clones and 1 alloantiserum met the criteria for significant association with juvenile arthritis on patient testing, including DR5, DRw6, and DRw8 haplotypes. Monoclonal antibody blocking revealed that all 4 recognized epitopes on DR subregion products. For 2 of the clones, the relative risks for JA (10.5 and 9.4) were higher than the risks with any other previously described typing reagents.
先前已证明,HLA - D区域抗原DR5(w11、w12)、DRw6(w13、w14)、DRw8、DRw52和DQw1在青少年关节炎患者亚组中的出现频率增加。由于HLA - D区域很复杂(由至少3个编码多种分子的亚区域组成,每个亚区域又呈现多种同种异体抗原表位),我们试图阐明是否有一个强相关因素可以解释先前的发现。为了寻找相关的HLA - D区域刺激表位,用DR5和DRw6单倍型刺激同种反应性T细胞并通过有限稀释法进行克隆。在对患者进行检测时,3个T细胞克隆和1种同种抗血清符合与青少年关节炎显著相关的标准,包括DR5、DRw6和DRw8单倍型。单克隆抗体阻断显示,所有4种都识别DR亚区域产物上的表位。对于其中2个克隆,青少年关节炎的相对风险(分别为10.5和9.4)高于任何其他先前描述的分型试剂的风险。