Ziegler Andreas, Loll Bernhard, Misselwitz Rolf, Uchanska-Ziegler Barbara
Institut für Immungenetik, Charité-Universitätsmedizin Berlin, Freie Universität Berlin, Berlin, Germany.
Adv Exp Med Biol. 2009;649:177-95. doi: 10.1007/978-1-4419-0298-6_13.
Structural and thermodynamic properties of HLA-B27 molecules provide the basis for their function within the immune system and are probably also central for the understanding of the pathology of HLA-B27-associated diseases such as ankolysing spondylitis (AS). Several HLA-B27 alleles are AS-associated, whereas some are not, although the protein encoded by the former may differ in only a single amino acid exchange from those specified by the latter. This indicates that subtype-specific polymorphic residues play a key role in determining whether an HLA-B27 subtype is AS-associated or not and open the possibility to correlate structural, thermodynamic and functional characteristics ofa given subtype with the disease association. Our studies involved X-ray crystallography and various other biophysical techniques to examine how several different peptides are accommodated within the binding groove of the molecules. The HLA-B2705 and HLA-B2709 subtypes, whose products differ in only a single amino acid residue of their heavy chains from each other, were primarily chosen for these analyses, but our studies have recently also been extended to the closely related subtypes HLA-B2703, HLA-B2704 and HLA-B2706. The analyses reveal that structural and thermodynamic differences between HLA-B27 complexes may exist, depending on the peptide that is displayed. Furthermore, aviralpeptide and two self-peptides were found that exhibit HLA-B27 subtype-dependent molecular mimicry, thereby providing a molecular basis to account for the subtype-dependent presence of autoreactive T-cells. Although these results do not exclude other theories for the pathogenesis of AS, they support the arthritogenic peptide hypothesis which envisages molecular mimicry between HLA-B27-presented foreign and self-peptides to explain the cross-reactivity of autoreactive T-cells that are found in HLA-B2705-positive individuals, in particular when they suffer from AS.
HLA - B27分子的结构和热力学性质为其在免疫系统中的功能提供了基础,对于理解诸如强直性脊柱炎(AS)等HLA - B27相关疾病的病理学可能也至关重要。几种HLA - B27等位基因与AS相关,而有些则不然,尽管前者编码的蛋白质与后者指定的蛋白质可能仅在单个氨基酸交换上有所不同。这表明亚型特异性多态性残基在决定HLA - B27亚型是否与AS相关方面起着关键作用,并为将给定亚型的结构、热力学和功能特征与疾病关联起来提供了可能性。我们的研究涉及X射线晶体学和各种其他生物物理技术,以研究几种不同的肽如何容纳在分子的结合槽中。HLA - B2705和HLA - B2709亚型,其产物的重链彼此仅在单个氨基酸残基上有所不同,主要被选用于这些分析,但我们的研究最近也扩展到了密切相关的亚型HLA - B2703、HLA - B2704和HLA - B2706。分析表明,根据所展示的肽,HLA - B27复合物之间可能存在结构和热力学差异。此外,发现一种病毒肽和两种自身肽表现出HLA - B27亚型依赖性分子模拟,从而为自身反应性T细胞的亚型依赖性存在提供了分子基础。尽管这些结果不排除AS发病机制的其他理论,但它们支持致关节炎肽假说,该假说设想HLA - B27呈递的外来肽和自身肽之间的分子模拟来解释在HLA - B2705阳性个体中发现的自身反应性T细胞的交叉反应性,特别是当他们患有AS时。