Uniformed Services University of the Health Sciences, Bethesda, MD.
Independent Consultant, Cambridge, MA.
Blood Adv. 2023 Sep 12;7(17):4983-4998. doi: 10.1182/bloodadvances.2021004909.
The most common complication in hemophilia A (HA) treatment, affecting 25% to 30% of patients with severe HA, is the development of alloimmune inhibitors that foreclose the ability of infused factor VIII (FVIII) to participate in coagulation. Inhibitors confer significant pathology on affected individuals and present major complexities in their management. Inhibitors are more common in African American patients, and it has been hypothesized that this is a consequence of haplotype (H)-treatment product mismatch. F8 haplotypes H1 to H5 are defined by nonsynonymous single-nucleotide polymorphisms encoding sequence variations at FVIII residues 1241, 2238, and 484. Haplotypes H2 to H5 are more prevalent in individuals with Black African ancestry, whereas 80% to 90% of the White population has the H1 haplotype. This study used an established multiplex fluorescence immunoassay to determine anti-FVIII antibody titers in plasma from 394 individuals with HA (188 Black, 206 White), measuring their binding to recombinant full-length H1 and H2 and B-domain-deleted (BDD) H1/H2, H3/H5, and H4 FVIII proteins. Inhibitor titers were determined using a chromogenic assay and linear B-cell epitopes characterized using peptide microarrays. FVIII-reactive antibodies were readily detected in most individuals with HA, with higher titers in those with a current inhibitor, as expected. Neither total nor inhibitory antibody titers correlated with F8 haplotype mismatches, and peptides with D1241E and M2238V polymorphisms did not comprise linear B-cell epitopes. Interestingly, compared with the full-length FVIII products, the BDD-FVIII proteins were markedly more reactive with plasma antibodies. The stronger immunoreactivity of BDD-FVIII suggests that B-domain removal might expose novel B-cell epitopes, perhaps through conformational rearrangements of FVIII domains.
最常见的血友病 A (HA) 治疗并发症,影响 25%至 30%的重度 HA 患者,是产生同种免疫抑制剂,从而使输注的因子 VIII (FVIII) 丧失参与凝血的能力。抑制剂会对受影响的个体造成重大病理影响,并在其管理方面带来重大复杂性。抑制剂在非裔美国人患者中更为常见,有人假设这是单倍型 (H)-治疗产品不匹配的结果。FVIII 单倍型 H1 至 H5 通过编码 FVIII 残基 1241、2238 和 484 处序列变异的非同义单核苷酸多态性来定义。单倍型 H2 至 H5 在具有黑非洲血统的个体中更为常见,而 80%至 90%的白人人群具有 H1 单倍型。本研究使用已建立的多重荧光免疫测定法来确定 394 名 HA 患者(188 名黑人,206 名白人)血浆中的抗 FVIII 抗体滴度,测量其与重组全长 H1 和 H2 以及 B 结构域缺失 (BDD) H1/H2、H3/H5 和 H4 FVIII 蛋白的结合。使用显色测定法确定抑制剂滴度,并使用肽微阵列表征线性 B 细胞表位。FVIII 反应性抗体在大多数 HA 患者中很容易检测到,预期具有当前抑制剂的患者的滴度更高。总抗体和抑制性抗体滴度均与 F8 单倍型不匹配无关,并且具有 D1241E 和 M2238V 多态性的肽不构成线性 B 细胞表位。有趣的是,与全长 FVIII 产物相比,BDD-FVIII 蛋白与血浆抗体的反应性明显更强。BDD-FVIII 的更强免疫反应性表明,B 结构域缺失可能会通过 FVIII 结构域的构象重排暴露新的 B 细胞表位。