血友病
医学
血友病A
抗体
免疫系统
免疫学
临床意义
内科学
胃肠病学
外科
作者
Jenny Klintman,Andreas Hillarp,Erik Berntorp,Jan Astermark
摘要
Summary It has previously been shown that patients with haemophilia A may develop non‐neutralizing anti‐factor VIII ( FVIII ) antibodies ( NNA ) that escape detection by the Bethesda assay, but are detected using immune‐based assays. We and others found NNA s to be directed not only towards non‐functional parts of the protein, but towards all regions of the FVIII protein. We also showed a heterogeneous antibody response towards different FVIII products. However, the clinical relevance and the natural history of NNA remain unclear. Therefore, we followed a cohort of unrelated subjects with haemophilia A for 4 years with the goal of exploring the long‐term development of NNA using an enzyme‐linked immunosorbent assay ( ELISA ). Ten of 78 subjects (12·8%) exhibited an immune response that was transient and heterogeneous, and none of the subjects developed an FVIII inhibitor. The result of the ELISA was examined in relation to clinical variables and no significant associations between a positive ELISA and age, F 8 mutation, port‐à‐cath implantation and HCV infection were shown. Interestingly, patients with NNA had significantly fewer bleeding episodes ( P = 0·048) compared with NNA ‐negative subjects. The results indicate that the immune response to FVIII products within an individual may vary over time. However, the clinical impact of NNA remains unclear.
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