Onwubalili J K, Scott G M, Smith H
Q J Med. 1986 Jun;59(230):599-610.
Two patients with non-miliary pulmonary tuberculosis developed a syndrome resembling adult respiratory distress following initiation of drug treatment. They were studied clinically and with a representative range of in vitro and in vivo tests of immune function. Both were alcoholic, malnourished and presented with radiologically widespread, smear-positive disease and lymphocytopenia. One had cutaneous anergy in vivo and profound reduction on mononuclear cell proliferative and interferon responses to tuberculoprotein (PPD) in vitro; the other patient, who died two weeks after starting treatment, had relatively normal values for these measures of cell-mediated immunity. In both cases there was a progressive increase during treatment, in peripheral blood lymphocyte counts, skin reactions and in vitro cellular responses to PPD, and a sudden rise in ESR at the time of their deterioration. We propose that the reactions may represent local manifestations of heightened delayed hypersensitivity, mounted by increasing numbers of 'resuscitated' lymphocytes against immunogenic cell wall substances released from dying tubercle bacilli in patients whose level of cellular immunity is being enhanced as a result of chemotherapy. The likelihood of an acute respiratory reaction during treatment may therefore depend on the bacillary load, the extent of lung disease present, and its severity may be related to the pre-treatment immune status of the patient.
两名非粟粒性肺结核患者在开始药物治疗后出现了类似成人呼吸窘迫的综合征。对他们进行了临床研究,并进行了一系列具有代表性的体外和体内免疫功能测试。两人均为酗酒者,营养不良,影像学表现为广泛的涂片阳性疾病和淋巴细胞减少。其中一人在体内有皮肤无反应性,体外对结核菌素(PPD)的单核细胞增殖和干扰素反应显著降低;另一例患者在开始治疗两周后死亡,其细胞介导免疫的这些指标相对正常。在两例患者中,治疗期间外周血淋巴细胞计数、皮肤反应和体外对PPD的细胞反应均逐渐增加,病情恶化时血沉突然升高。我们认为,这些反应可能代表迟发型超敏反应增强的局部表现,是由于化疗使细胞免疫水平增强,越来越多“复苏”的淋巴细胞针对死亡结核杆菌释放的免疫原性细胞壁物质引发的。因此,治疗期间发生急性呼吸反应的可能性可能取决于细菌负荷、现存肺部疾病的程度,其严重程度可能与患者治疗前的免疫状态有关。