Kekow J, Plendl H, Gross W L
Clin Exp Immunol. 1986 May;64(2):376-81.
In addition to T cell abnormalities, patients with haemophilia A show a separate B cell dysfunction. Characteristic are elevated spontaneous IgG (not IgM) levels in the patient's sera and in the culture supernatants of peripheral blood mononuclear cells. It is also observed that these cells fail to show a differentiation response to T cell-independent B cell activators. The B cell dysfunction correlates with the amount of factor VIII concentrates given prophylactically to patients with severe haemophilia. In contrast to the acquired immune deficiency syndrome (AIDS), the proliferation response to B cell mitogens is not affected.
除了T细胞异常外,甲型血友病患者还表现出独立的B细胞功能障碍。患者血清和外周血单个核细胞培养上清液中自发IgG(而非IgM)水平升高是其特征。还观察到这些细胞对非T细胞依赖性B细胞激活剂未表现出分化反应。B细胞功能障碍与预防性给予重度血友病患者的凝血因子VIII浓缩物的量相关。与获得性免疫缺陷综合征(AIDS)不同,对B细胞有丝分裂原的增殖反应不受影响。