Brenner M K, Reittie J G, Chadda H R, Pollock A, Asherson G L
Clin Exp Immunol. 1984 Dec;58(3):619-24.
Patients with acquired hypogammaglobulinaemia usually have near normal numbers of B cells and normal T cell function. When hypogammaglobulinaemia occurs in association with thymoma, then B cell numbers have been reported as low, and distinctive T cells are present which inhibit immunoglobulin production by normal cells. It has been suggested that these T cells are responsible for the observed hypogammaglobulinaemia. We report a patient with thymoma and hypogammaglobulinaemia who lacks these distinctive suppressor cells and has normal B cell numbers. It is therefore incorrect to propose a single pathogenic mechanism for hypogammaglobulinaemia in association with thymoma.
获得性低丙种球蛋白血症患者的B细胞数量通常接近正常,T细胞功能也正常。当低丙种球蛋白血症与胸腺瘤相关联时,有报道称B细胞数量减少,且存在独特的T细胞,这些T细胞会抑制正常细胞产生免疫球蛋白。有人认为这些T细胞是导致观察到的低丙种球蛋白血症的原因。我们报告了一名患有胸腺瘤和低丙种球蛋白血症的患者,该患者缺乏这些独特的抑制性细胞,且B细胞数量正常。因此,认为与胸腺瘤相关的低丙种球蛋白血症存在单一致病机制是不正确的。