Vrethem M, Dahle C, Ekerfeldt C, Nilsson J, Ekstedt B, Ernerudh J
Department of Neurology, University Hospital, Linköping, Sweden.
J Neurol Sci. 1994 Apr;122(2):171-8. doi: 10.1016/0022-510x(94)90296-8.
Patients with monoclonal gammopathy secrete monoclonal antibodies (M-component), that in some patients are associated with polyneuropathy. The M-component has been shown to react with peripheral nerve myelin in some of these patients. However, it is not known whether the M-component secreting B-cells are autonomous or subject to regulation by T-cells or if other cellular abnormalities may occur. In order to define circulating lymphocyte subpopulations, flow cytometry was done on blood samples from patients with monoclonal gammopathy and demyelinating polyneuropathy (n = 13) and patients with monoclonal gammopathy without polyneuropathy (n = 11), and were compared to healthy controls. Significantly increased proportions of primed T-helper (CD4+) cells, i.e. those expressing helper/inducer function (CD29+ CD4+), providing help for antibody secretion, as well as decreased proportions of naive, unprimed suppressor/inducer (CD45RA+ CD4+) T-helper cells were found in patients with M-component associated polyneuropathy. Within the T-cytotoxic/suppressor population (CD8+) we found an increased proportion of killer/effector (S6F1+ CD8+) cells and a decreased proportion of suppressor/effector (S6F1- CD8+) cells in patients with monoclonal gammopathy and polyneuropathy. Similar findings were found in monoclonal gammopathy patients without polyneuropathy, although the deviations in general were less pronounced and did not reach statistical significance compared to the controls. The proportion of natural killer (NK) cells (CD56+) was markedly decreased in all patients with monoclonal gammopathy. In the whole group of patients with monoclonal gammopathy, we found clear proportions of interleukin-2 receptor (CD25+) expressing lymphocytes, indicating the presence of activated T-cells. No clear correlation between abberations in T-cell subtypes and clinical severity of the demyelinating polyneuropathy or titres of anti-PNM antibodies was found.(ABSTRACT TRUNCATED AT 250 WORDS)
单克隆丙种球蛋白病患者分泌单克隆抗体(M成分),在一些患者中,该成分与多发性神经病相关。在其中一些患者中,已证明M成分可与周围神经髓鞘发生反应。然而,尚不清楚分泌M成分的B细胞是自主的还是受T细胞调节,或者是否可能发生其他细胞异常。为了确定循环淋巴细胞亚群,对患有单克隆丙种球蛋白病和脱髓鞘性多发性神经病的患者(n = 13)以及无多发性神经病的单克隆丙种球蛋白病患者(n = 11)的血样进行了流式细胞术检测,并与健康对照进行比较。在与M成分相关的多发性神经病患者中,发现引发的辅助性T(CD4 +)细胞比例显著增加,即那些表达辅助/诱导功能(CD29 + CD4 +)、为抗体分泌提供帮助的细胞,同时幼稚的、未引发的抑制/诱导(CD45RA + CD4 +)辅助性T细胞比例降低。在细胞毒性/抑制性T细胞群体(CD8 +)中,我们发现患有单克隆丙种球蛋白病和多发性神经病的患者中杀伤/效应(S6F1 + CD8 +)细胞比例增加,而抑制/效应(S6F1 - CD8 +)细胞比例降低。在无多发性神经病的单克隆丙种球蛋白病患者中也发现了类似的结果,尽管总体偏差不太明显,与对照组相比未达到统计学显著性。所有单克隆丙种球蛋白病患者的自然杀伤(NK)细胞(CD56 +)比例均显著降低。在整个单克隆丙种球蛋白病患者组中,我们发现表达白细胞介素-2受体(CD25 +)的淋巴细胞比例明显,表明存在活化的T细胞。未发现T细胞亚型异常与脱髓鞘性多发性神经病的临床严重程度或抗PNM抗体滴度之间存在明显相关性。(摘要截选至250字)