Monos D S, Papaioakim M, Ho T W, Li C Y, McKhann G M
Department of Pediatrics, University of Pennsylvania, Children's Hospital of Philadelphia, 19104, USA.
J Infect Dis. 1997 Dec;176 Suppl 2:S180-2. doi: 10.1086/513786.
Guillain-Barré syndrome in northern China occurs in two forms: acute inflammatory demyelinating polyneuropathy (AIDP) and acute motor axonal neuropathy (AMAN). AMAN and AIDP have an immunologic basis, and some cases are associated with preceding Campylobacter jejuni infection. The distribution of allelic forms of the histocompatibility genes HLA-DPB1, DQB1, DRB1, DRB3, DRB4, and DRB5 was examined by DNA-based technology in 34 control, 12 AIDP, and 31 AMAN cases. In AIDP patients, the DRB11301 allele showed a significant increase (18% vs. 0%, P = .055). In AMAN patients, alleles DRB11301-03 and DRB11312, taken collectively, were increased (19% vs. 0%, P = .009), but by itself, the DRB11301 allele was not increased, as in AIDP patients. With a larger number of persons, more definitive statements will be possible; however, the differential distribution of DR13 allelic forms between AIDP and AMAN cases may suggest that there are different immunologic mechanisms operating at the molecular level of these diseases.
中国北方的吉兰-巴雷综合征有两种形式:急性炎症性脱髓鞘性多发性神经病(AIDP)和急性运动轴索性神经病(AMAN)。AMAN和AIDP具有免疫基础,一些病例与先前的空肠弯曲菌感染有关。通过基于DNA的技术检测了34名对照者、12名AIDP患者和31名AMAN患者的组织相容性基因HLA-DPB1、DQB1、DRB1、DRB3、DRB4和DRB5等位基因形式的分布。在AIDP患者中,DRB11301等位基因显著增加(18%对0%,P = 0.055)。在AMAN患者中,DRB11301-03和DRB11312等位基因合计增加(19%对0%,P = 0.009),但与AIDP患者不同,DRB11301等位基因本身并未增加。如果有更多的人参与研究,就可能得出更明确的结论;然而,AIDP和AMAN病例之间DR13等位基因形式的差异分布可能表明,在这些疾病的分子水平上存在不同的免疫机制。