Chakravarti Anita, Jain Manisha
Department of Microbiology, Maulana Azad Medical College, New Delhi.
Indian J Pathol Microbiol. 2006 Jan;49(1):54-6.
Rubella is a major cause of birth defects among the TORCH group of agents causing congenital anomalies. Almost all the symptomatic infected infants have long-term neurological sequelae & many asymptomatic infants also develop deafness or psychomotor retardation later in life. In India need for rubella prevention & control is being recognized. Before formulating any kind of rubella vaccination policies, data on the burden of disease is important. Hence the prevalence of rubella in children and their transmission was evaluated. Paired sera of 146 babies with suspected intra uterine infection and their mothers from lower socioeconomic strata was tested for IgM antibodies by commercially available Enzyme immunoassay (EIA) kits. Congenital Rubella Syndrome (CRS) was confirmed in babies presenting with rubella compatible defects with positive IgM antibodies against rubella. It was seen that out of 146-paired samples evaluated, 15-paired samples (10.27%) were positive for IgM antibodies. The transmission rate of rubella virus from mother to child when the mother was infected was around 55.55% according to this study. CRS prevalence of 10.27% among symptomatic infants is significant as a large majority of rubella infection remains undetected and hence the actual burden of the disease may be higher. Since the disease is preventable by an effective vaccination, strategies for rubella immunization should be developed and enhanced.
风疹是导致先天性异常的TORCH病原体组中出生缺陷的主要原因。几乎所有有症状的受感染婴儿都有长期的神经后遗症,许多无症状婴儿在以后的生活中也会出现耳聋或精神运动发育迟缓。在印度,风疹的预防和控制需求正在得到认可。在制定任何风疹疫苗接种政策之前,疾病负担数据很重要。因此,对儿童风疹的患病率及其传播情况进行了评估。使用市售酶免疫分析(EIA)试剂盒,对146名疑似宫内感染的婴儿及其来自社会经济地位较低阶层的母亲的配对血清进行IgM抗体检测。对出现与风疹相符的缺陷且风疹IgM抗体呈阳性的婴儿确诊为先天性风疹综合征(CRS)。结果发现,在评估的146对样本中,有15对样本(10.27%)的IgM抗体呈阳性。根据这项研究,母亲感染风疹病毒时,母婴传播率约为55.55%。有症状婴儿中CRS患病率为10.27%,这一数字很可观,因为大多数风疹感染仍未被发现,因此该疾病的实际负担可能更高。由于这种疾病可以通过有效的疫苗接种预防,因此应制定并加强风疹免疫策略。