Ball L K, Ball R, Pratt R D
Division of Vaccines and Related Products Applications, Office of Vaccines Research and Review, Center for Biologics Evaluation and Research, Foodand Drug Administration, Rockville, Maryland 20852, USA.
Pediatrics. 2001 May;107(5):1147-54. doi: 10.1542/peds.107.5.1147.
On July 7, 1999, the American Academy of Pediatrics and the US Public Health Service issued a joint statement calling for removal of thimerosal, a mercury-containing preservative, from vaccines. This action was prompted in part by a risk assessment from the Food and Drug Administration that is presented here.
The risk assessment consisted of hazard identification, dose-response assessment, exposure assessment, and risk characterization. The literature was reviewed to identify known toxicity of thimerosal, ethylmercury (a metabolite of thimerosal) and methylmercury (a similar organic mercury compound) and to determine the doses at which toxicity occurs. Maximal potential exposure to mercury from vaccines was calculated for children at 6 months old and 2 years, under the US childhood immunization schedule, and compared with the limits for mercury exposure developed by the Environmental Protection Agency (EPA), the Agency for Toxic Substance and Disease Registry, the Food and Drug Administration, and the World Health Organization.
Delayed-type hypersensitivity reactions from thimerosal exposure are well-recognized. Identified acute toxicity from inadvertent high-dose exposure to thimerosal includes neurotoxicity and nephrotoxicity. Limited data on toxicity from low-dose exposures to ethylmercury are available, but toxicity may be similar to that of methylmercury. Chronic, low-dose methylmercury exposure may cause subtle neurologic abnormalities. Depending on the immunization schedule, vaccine formulation, and infant weight, cumulative exposure of infants to mercury from thimerosal during the first 6 months of life may exceed EPA guidelines.
Our review revealed no evidence of harm caused by doses of thimerosal in vaccines, except for local hypersensitivity reactions. However, some infants may be exposed to cumulative levels of mercury during the first 6 months of life that exceed EPA recommendations. Exposure of infants to mercury in vaccines can be reduced or eliminated by using products formulated without thimerosal as a preservative.
1999年7月7日,美国儿科学会和美国公共卫生服务部发表联合声明,呼吁从疫苗中去除硫柳汞(一种含汞防腐剂)。这一行动部分是由美国食品药品监督管理局的一项风险评估引发的,本文对此评估进行介绍。
风险评估包括危害识别、剂量反应评估、暴露评估和风险特征描述。查阅文献以确定硫柳汞、乙基汞(硫柳汞的一种代谢产物)和甲基汞(一种类似的有机汞化合物)已知的毒性,并确定出现毒性的剂量。根据美国儿童免疫接种计划,计算6个月大及2岁儿童从疫苗中最大可能接触汞的量,并与美国环境保护局(EPA)、有毒物质和疾病登记署、食品药品监督管理局及世界卫生组织制定的汞暴露限值进行比较。
硫柳汞暴露引起的迟发型超敏反应已得到充分认识。意外高剂量接触硫柳汞导致的急性毒性包括神经毒性和肾毒性。关于低剂量接触乙基汞毒性的资料有限,但毒性可能与甲基汞相似。长期低剂量接触甲基汞可能会导致细微的神经异常。根据免疫接种计划、疫苗配方和婴儿体重,婴儿在出生后头6个月内通过硫柳汞累积接触汞的量可能超过EPA指南。
我们的综述显示,除局部超敏反应外,没有证据表明疫苗中硫柳汞剂量会造成危害。然而,一些婴儿在出生后头6个月内接触的汞累积量可能超过EPA的建议值。使用不含硫柳汞作为防腐剂的产品可减少或消除婴儿接触疫苗中汞的情况。