Yanai-Landau H, Amital H, Bar-Dayan Y, Levy Y, Gur H, Lin H C, Alosachie I J, Peter J B, Shoenfeld Y
Department of Medicine B, Sheba Medical Center, Tel Hashomer, Israel.
Pathobiology. 1995;63(2):71-5. doi: 10.1159/000163936.
Although primary pulmonary hypertension (PPH) is considered to be an idiopathic condition, it has been postulated that autoimmunity may play a role in the pathogenesis of the disease. This argument has been based on frequent coexisting clinical and serological rheumatic findings. Moreover, approximately in a third of the patients with PPH, and antinuclear factor can be detected. Pulmonary hypertension may appear as a secondary complication to various autoimmune conditions. In light of these findings we examined sera derived from 40 patients diagnosed as having PPH for the presence of 18 different autoantibodies by the ELISA and immunofluorescent techniques. Of the 40 patients, 62.4% had circulating autoantibodies and 47.5% presented with multiantibody responses. Autoantibodies most commonly observed were antinuclear (42.5%), anti-ssDNA (25%) and antithyroglobulin (30%) antibodies. These results may imply that in a subgroup of patients with PPH the disease may be ascribed to an immune dysregulation or alternatively that autoantibodies accompany the disease progression as an epiphenomenon.
虽然原发性肺动脉高压(PPH)被认为是一种特发性疾病,但据推测自身免疫可能在该疾病的发病机制中起作用。这一观点基于临床和血清学方面常见的风湿性表现共存。此外,大约三分之一的PPH患者可检测到抗核因子。肺动脉高压可能作为各种自身免疫性疾病的继发并发症出现。鉴于这些发现,我们通过酶联免疫吸附测定(ELISA)和免疫荧光技术检测了40例被诊断为PPH的患者血清中18种不同自身抗体的存在情况。在这40例患者中,62.4%有循环自身抗体,47.5%呈现多抗体反应。最常观察到的自身抗体是抗核抗体(42.5%)、抗单链DNA抗体(25%)和抗甲状腺球蛋白抗体(30%)。这些结果可能意味着在一部分PPH患者中,疾病可能归因于免疫失调,或者自身抗体作为一种附带现象伴随疾病进展。