Dalakas M C, Cupler E J
National Institute of Neurological Disorders and Stroke, National Institute of Health, Bethesda, MD 20892, USA.
Baillieres Clin Neurol. 1996 Mar;5(1):199-218.
Peripheral neuropathies represent the most common neurological manifestation in patients infected with HIV infection occurring either early in the infection or during the course of the illness. They present as acute or chronic demyelinating neuropathies (Guillain-Barré syndrome or chronic inflammatory demyelinating polyneuropathy), mononeuritis multiplex, ganglioneuronitis, cytomegalovirus-related polyradiculoneuropathy, autonomic neuropathy or distal painful sensory neuropathy. They are multifactorial in aetiology. Their putative cause (viral, autoimmune, toxic, nutritional, co-infections) are often dictated by the stage of the underlying HIV disease. The virus, which is not found within ganglionic neurones or Schwann cells but only within the endoneurial macrophages, may generate a tissue-specific autoimmune attack by secretion of cytokines that promote trafficking of activated T cells and macrophages within the endoneurial parenchyma. The wide use of the neurotoxic antiretroviral nucleoside analogues ddC, ddI, d4T and 3TC, exacerbate or trigger subclinical neuropathy in many of these patients.
周围神经病变是感染人类免疫缺陷病毒(HIV)患者最常见的神经表现,可发生于感染早期或病程中。它们表现为急性或慢性脱髓鞘性神经病变(格林-巴利综合征或慢性炎症性脱髓鞘性多发性神经病变)、多发性单神经炎、神经节神经元炎、巨细胞病毒相关性多发性神经根神经病、自主神经病变或远端疼痛性感觉神经病变。其病因是多因素的。其假定病因(病毒、自身免疫、毒性、营养、合并感染)通常取决于潜在HIV疾病的阶段。病毒不在神经节神经元或施万细胞内,而仅在内神经巨噬细胞内,可通过分泌促进活化T细胞和巨噬细胞在内神经实质内游走的细胞因子,引发组织特异性自身免疫攻击。神经毒性抗逆转录病毒核苷类似物ddC、ddI、d4T和3TC的广泛使用,使许多此类患者的亚临床神经病变加重或引发。