Department of Immunobiology, Yale University School of Medicine, New Haven, Connecticut 06520, USA.
Biol Psychiatry. 2010 Apr 1;67(7):679-83. doi: 10.1016/j.biopsych.2009.09.034. Epub 2009 Dec 14.
Postinfectious autoimmunity has been implicated in Tourette's syndrome and obsessive-compulsive disorder (TS/OCD), whereas increased frequency of upper respiratory tract infections (URTI) in TS/OCD patients suggests immune deficiency. We hypothesized that antineuronal antibodies may be elevated in patients (reflecting autoimmune processes), and levels of total immunoglobulins (Igs) may be decreased (reflecting immune deficiency).
We analyzed plasma of TS/OCD patients (n = 24) and healthy age- and sex-matched control subjects (n = 22) by enzyme-linked immunosorbent assay (ELISA) for the levels of total and specific IgG, IgM, and IgA against antigens previously identified in multiple sclerosis (myelin basic protein and myelin-associated glycoprotein) and Sydenham's chorea (ganglioside-GM1, lysoganglioside, and tubulin).
Total IgA was decreased in TS/OCD patients (median 115 mg/100 mL) compared with control subjects (141 mg/100 mL; p = .02). Specific IgA against all antigens, except tubulin were also decreased in the patients (MPB 0 vs. 13 [ELISA units [EU]; myelin-associated glycoprotein 29 vs. 44 EU, p = .04; ganglioside GM1 21 vs. 35 EU, p = .01; lysoganglioside 44 vs. 56 EU, p = .03; tubulin 44 vs. 44 EU, p = .8). The levels of total IgA and anti-myelin basic protein (MBP) IgA were significantly lower in the subgroup of pediatric autoimmune neuropsychiatric disorder associated with Streptococcus (PANDAS) cases (n = 10) than in non-PANDAS cases (n = 9; total IgA 98 mg/100 mL vs. 133 mg/mL, p = .03; anti-MBP IgA 1 vs. 6 EU, p = .03) or healthy control subjects (total IgA 141 mg/100 mL, p = .02; anti-MBP IgA 13 EU, p = .005).
At least some TS/OCD patients may suffer IgA dysgammaglobulinemia, possibly rendering the children more prone to URTI.
感染后自身免疫与妥瑞氏症候群和强迫症(TS/OCD)有关,而 TS/OCD 患者上呼吸道感染(URTI)的频率增加表明免疫缺陷。我们假设神经元抗体可能在患者中升高(反映自身免疫过程),而总免疫球蛋白(Ig)的水平可能降低(反映免疫缺陷)。
我们通过酶联免疫吸附试验(ELISA)分析了 24 名 TS/OCD 患者(n=24)和 22 名年龄和性别匹配的健康对照者(n=22)的血浆,以检测针对先前在多发性硬化症(髓鞘碱性蛋白和髓鞘相关糖蛋白)和 Sydenham's 舞蹈病(神经节苷脂-GM1、溶神经节苷脂和微管蛋白)中鉴定的抗原的总 IgG、IgM 和 IgA 的水平。
与对照组(141mg/100mL;p=0.02)相比,TS/OCD 患者的总 IgA 降低(中位数 115mg/100mL)。患者中针对所有抗原的特异性 IgA 也降低(除外微管蛋白)(髓鞘碱性蛋白 0 与 13[ELISA 单位(EU)];髓鞘相关糖蛋白 29 与 44EU,p=0.04;神经节苷脂 GM1 21 与 35EU,p=0.01;溶神经节苷脂 44 与 56EU,p=0.03;微管蛋白 44 与 44EU,p=0.8)。在与链球菌相关的自身免疫性神经精神障碍相关的儿科病例亚组(n=10)中,总 IgA 和抗髓鞘碱性蛋白(MBP)IgA 的水平明显低于非 PANDAS 病例(n=9;总 IgA 98mg/100mL 与 133mg/mL,p=0.03;抗-MBP IgA 1 与 6EU,p=0.03)或健康对照组(总 IgA 141mg/100mL,p=0.02;抗-MBP IgA 13EU,p=0.005)。
至少一些 TS/OCD 患者可能患有 IgA 免疫球蛋白血症,这可能使儿童更容易发生 URTI。