Raqib Rubhana, Ahmed Sultan, Ahsan Khalid Bin, Kippler Maria, Akhtar Evana, Roy Anjan Kumar, Lu Ying, Arifeen Shams El, Wagatsuma Yukiko, Vahter Marie
Infectious Diseases Division, icddr,b (International Centre for Diarrhoeal Disease Research, Bangladesh), Dhaka, Bangladesh
Institute of Environmental Medicine, Karolinska Institutet, Stockholm, Sweden
Environ Health Perspect. 2017 Jun 14;125(6):067006. doi: 10.1289/EHP318.
Early-life arsenic exposure has been associated with reduced cell-mediated immunity, but little is known about its effects on humoral immunity.
We evaluated whether prenatal and childhood arsenic exposure was associated with humoral immune function in school-aged children.
Children born in a prospective mother–child cohort in rural Bangladesh were immunized with measles, mumps, and rubella (MMR) vaccines at 9 years of age (n=525). Arsenic exposure was assessed in urine (U-As), from mothers during pregnancy and their children at 4.5 and 9 years of age. Total IgG (tIgG), tIgE, tIgA, and MMR-specific IgG concentrations were measured in plasma using immunoassays.
Arsenic exposure was positively associated with child tIgG and tIgE, but not tIgA. The association with tIgG was mainly apparent in boys ( for interaction=0.055), in whom each doubling of maternal U-As was related to an increase in tIgG by 28 mg/dL. The associations of U-As at 9 years with tIgG and tIgE were evident in underweight children ( for interaction <0.032). Childhood arsenic exposure tended to impair mumps-specific vaccine response, although the evaluation was complicated by high preimmunization titers. Postimmunization mumps–specific IgG titers tended to decrease with increasing U-As at 4.5 and 9 years of age [regression coefficient (β)=−0.16; 95% confidence interval (CI): −0.33, 0.01; p=0.064 and β=−0.12; 95% CI: −0.27, −0.029; p=0.113, respectively) in 25% children with the lowest preexisting mumps-specific IgG titers.
Arsenic exposure increased tIgG and tIgE in plasma, and tended to decrease mumps-specific IgG in children at 9 years of age. https://doi.org/10.1289/EHP318.
生命早期接触砷与细胞介导免疫功能降低有关,但对其对体液免疫的影响知之甚少。
我们评估了产前和儿童期接触砷是否与学龄儿童的体液免疫功能有关。
在孟加拉国农村的一个前瞻性母婴队列中出生的儿童在9岁时接种了麻疹、腮腺炎和风疹(MMR)疫苗(n = 525)。在母亲孕期以及孩子4.5岁和9岁时评估尿砷(U-As)水平来衡量砷暴露情况。使用免疫分析法测量血浆中的总IgG(tIgG)、总IgE(tIgE)、总IgA(tIgA)和MMR特异性IgG浓度。
砷暴露与儿童tIgG和tIgE呈正相关,但与tIgA无关。与tIgG的关联主要在男孩中明显(交互作用P = 0.055),母亲U-As每增加一倍,男孩的tIgG增加28 mg/dL。9岁时U-As与tIgG和tIgE的关联在体重不足的儿童中明显(交互作用P < 0.032)。儿童期砷暴露往往会损害腮腺炎特异性疫苗反应,尽管由于免疫前滴度高,评估较为复杂。在25%的腮腺炎特异性IgG滴度最低的儿童中,4.5岁和9岁时,接种疫苗后腮腺炎特异性IgG滴度往往随着U-As增加而降低[回归系数(β)= -0.16;95%置信区间(CI):-0.33,0.01;P = 0.064和β = -0.12;95% CI:-0.27,-0.029;P = 0.113]。
砷暴露增加了血浆中的tIgG和tIgE,并在9岁儿童中往往降低腮腺炎特异性IgG。https://doi.org/10.1289/EHP318