A 16-year review of seroprevalence studies on measles and rubella

The determination of the seroprevalence of vaccine-preventable diseases is critical in monitoring the efficacy of vaccination programmes and to assess the gaps in population immunity but requires extensive organisation and is time and resource intensive. The results of the studies are frequently reported in peer-reviewed scientific, government and non-government publications. A review of scientific literature was undertaken to advise the development of WHO guidelines for the assessment of measles and rubella seroprevalence. A search of the National Library of Medicine’s PubMed online publications using key words of ‘measles’, ‘rubella’, combined with ‘serosurvey’, ‘seroprevalence’, ‘immunity’ and ‘population immunity’ was conducted. A total of 97 articles published between January 1998 and June 2014 were retrieved, 68 describing serosurveys for measles and 58 serosurveys for rubella, conducted in 37 and 36 different countries respectively. Only 13 (19%) and 8 (14%) respectively were UN classified “least developed countries”. The study sample varied markedly and included combinations of male and female infants, children, adolescents and adults. The study sizes also varied with 28% and 33% of measles and rubella studies respectively, having greater than 2000 participants. Microtitre plate enzyme immunoassays were used in 52 (76%) measles studies and 40 (69%) rubella studies. A total of 39 (57%) measles and 44 (76%) rubella studies reported quantitative test results. Seroprevalence ranged from 60.8% to 95.9% for measles and 53.0% to 99.3% for rubella studies. The review highlighted that infants lost maternally-acquired immunity within 9 months of birth and were unprotected until vaccination. Two groups at higher risk of infection were identified: young adults between the ages of 15 and 30 years and immigrants.     

Multiple sclerosis patients have reduced HLA class II-restricted cytotoxic responses specific for both measles and herpes virus

It has been previously demonstrated that the generation of measles virus (MV)-specific cytotoxicity (CTL) is reduced in patients with multiple sclerosis (MS). By contrast, CTL specific for influenza virus (FLU) and mumps virus is normal. It is uncertain if reduced CTL is limited to MV in MS patients, or if reduced CTL may be found to other viruses as well. Since MV-specific CTL is predominantly restricted by HLA class II molecules, while FLU-specific and mumps-specific CTL have large HLA class I-restricted components, reduced MV-specific CTL may reflect a broader reduction in HLA class II-restricted CTL in patients with MS. To examine this question we studied the generation of CTL specific for herpes simplex virus type I (HSV). HSV-specific CTL, like MV-specific CTL is predominantly restricted by HLA class II molecules. We found that patients with MS had reduced generation of CTL to both MV and HSV. Most, but not all patients who had reduced generation of CTL to one virus also had a similar impairment with respect to the second virus. Some patients, however, had a reduction in the generation of CTL only to MV or to HSV. These findings extend our earlier observations regarding reduced MV-specific CTL in patients with MS to a second HLA class II-restricted virus, HSV. Such a reduction may reflect discrete impairments in immune function to separate viruses, possibly those that are associated with viral persistence, or may reflect a more generalized defect in HLA class II-restricted CTL.     

2000年广西麻疹疑似病例血清学监测分析

目的了解麻疹的血清流行病学特征 ,探讨麻疹与风疹之间的血清学鉴别诊断。方法采用酶联免疫吸附法对714例RFIs的血清标本进行麻疹IgM和风疹IgM抗体检测 ,对204例麻疹IgM抗体阳性的血清标本进行麻疹IgG抗体检测。结果麻疹IgM阳性率为45.7 % ,风疹IgM抗体阳性率为27.5%。在出疹后4～14天采集的血清标本其麻疹IgM和风疹IgM抗体阳性检出率最高。麻疹IgM阳性数以1～14岁为主 ,1～6岁最高 (44.5% ) ,风疹IgM阳性数是7～14岁为最高 (73.5% ) ;麻疹IgG检出<1:200为76例 (27.7 % ) ,1:200为59例 (21.5% ) ,1:800为17例(6.2 %) ,1:3200为25例(9.1 %) ,≥1:12800为27例(9.8 %)。结论采血时间与检出率密切相关 ;采集血清标本要注意质量和采集时间 ;麻疹患者与风疹患者有一定的年龄差距 ,风疹是最主要的需要与麻疹相鉴别的RFIs,未经实验室诊断极易发生误诊 ;应提高麻疹实验室诊断的及时性、准确性和敏感性 ,建议有条件的地区开展麻疹抗体血清学检测     

山东省中小学生麻疹爆发原因的病例对照研究

为探讨山东省中小学生麻疹爆发的原因 ,采用 1∶2配比的病例对照方法对中小学生麻疹疫苗 (MV)效力进行了研究 ,同时对近年来中小学生MV接种率进行了估算。结果显示 :中小学生MV效力为 74 % ,95 %可信区间为4 7%～ 88% ;小学生MV效力明显高于中学生 ,分别为 82 %和 6 8% ;1999～ 2 0 0 1年学龄儿童的估算接种率分别为75 4 %、75 6 %和 5 5 7%。较低的MV效力和接种率是计划免疫工作薄弱地区中小学生麻疹爆发的主要原因。     

陕西省2000～2002年麻疹流行病学分析及控制策略探讨

为了解陕西省麻疹流行状况 ,以加速控制麻疹 ,对陕西省 2 0 0 0～ 2 0 0 2年麻疹发病资料进行流行病学分析。结果显示 :陕西省 2 0 0 0～ 2 0 0 2年麻疹年平均发病率比 1997～ 1999年上升了 6 5 7%。病例分布广泛 ,流行模式为爆发和散发并存 ,局部麻疹爆发影响着全省的麻疹发病水平。 3～ 6月为麻疹高发季节 ,0～ 2岁和 6～ 8岁为麻疹高发年龄组。对麻疹病例的免疫史分析表明 ,2 5 %的麻疹病例未接种麻疹疫苗 (MV) ,2 4 %的病例免疫史不详。报告病例的年龄和免疫史状况说明 ,MV的初种和复种需加强 ,同时要在全省范围开展一定年龄组儿童的MV强化免疫 ,调整现行MV的免疫程序 ,健全麻疹监测系统。     

河北省2001年麻疹流行病学分析与监测系统运转状况评价

为了掌握河北省麻疹的流行病学特点 ,对 2 0 0 1年麻疹监测系统运转情况进行了分析。全年共报告麻疹疑似病例 6 95例 ,临床诊断 73例 ,实验室确诊 2 76例 ,实验室排除 346例。根据分析结果 ,2 0 0 1年河北省麻疹的流行病学特征是 :春季高发 ;学龄前儿童和小学生为重点发病对象 ;18 6 %的报告病例无免疫史 ,4 7 9%免疫史不详。针对病例的地域和年龄分布 ,提出在 2 0 0 2年对重点地区和人群开展麻疹疫苗的后续强化免疫。分析相关年龄麻疹病例的免疫史 ,说明常规免疫工作存在一些问题 ,要着重提高麻疹疫苗接种的及时性和接种质量。一些监测指标 ,如报告及时率、病例调查率、标本采集率等有待提高。     

广东省2005-2007年麻疹病原学监测

目的 开展有效的麻疹病原学监测,分离麻疹病毒,了解广东省2005-2007年流行的麻疹野病毒分离株基因特征,为控制、消除麻疹提供科学依据.方法 用Veto/Slam细胞从暴发和散发麻疹疑似病例的咽拭子和尿液标本中分离麻疹病毒,并对所有分离到的麻疹病毒通过逆转录-聚合酶链反应(RT-PCR)方法,扩增出核蛋白(N)基因碳末端450个核苷酸片段,对其产物测定基因序列以定型.结果 2005-2007年共收到380份标本,包括咽拭子或尿液标本.共分离到82株麻疹野病毒.2005年病毒分离率为23.58%,2006年病毒分离率为17.11%,2007年病毒分离率为39.13%.病毒分离成功率与病例出疹天数和标本的采集质量有密切关系.结论 我省已经掌握了麻疹病毒的分离和分子生物学鉴定技术,分离率较高;我省多年来流行的麻疹毒株均为H1基因型,与国内流行的优势基因型一致.     

Transgenic expression of a CD46 (membrane cofactor protein) minigene: Studies of xenotransplantation and measles virus infection

CD46 (membrane cofactor protein) is a human cell-surface regulator of activated complement and a receptor for the measles virus. A CD46 transgenic mouse line with an expression pattern similar to that of human tissues has been produced, to develop an animal model of (i) the control of complement activation by complement regulators in hyperacute rejection of xenografts, and (ii) measles virus infection. The mouse line was made using a CD46 minigene that includes promoter sequence and the first two introns of genomic CD46, which was coinjected into mouse ova with chicken lysozyme matrix attachment region DNA. A high level of CD46 expression in homozygotic transgenic mice was obtained with spleen cells having approximately 75% of the level found on human peripheral blood mononuclear cells. CD46 was detected in all tissues examined by immunohistochemistry, radioimmunoassay and Western blotting, showing that these mice were suitable for transplantation and measles virus infection studies. It also indicated that the transgene included the important regulatory elements of the CD46 promoter. Transgenic spleen cells were significantly protected in vitro from human complement activated by either the classical or alternative pathways and from alternative pathway rat complement. Furthermore, transgenic mouse hearts transplanted to rats regulated complement deposition in an in vivo model of antibody-dependent hyperacute xenograft rejection. Similar to human lymphocytes, transgenic lymphoblasts could be infected in vitro with measles virus; infected cells expressed viral proteins and produced infectious viral particles. The data demonstrate the suitability of this minigene for obtaining high-level CD46 expression sufficient for enhanced resistance of transgenic cells to complement attack and for obtaining wide tissue distribution of CD46, analogous to human tissues and, therefore, useful for comparative studies.     

Measles virus-induced down-regulation of CD46 is associated with enhanced sensitivity to complement-mediated lysis of infected cells

CD46, the major component of the measles virus (MV) receptor complex and a member of the regulators of complement activity (RCA) gene cluster, is down-regulated in MV-infected cells. We investigated whether the reduction of surface CD46 correlates with enhanced sensitivity of lymphoid and monocytic cells to lysis by activated complement. On human U937 cells, acutely or persistently infected with MV-Edmonston (ED) vaccine strain, infection-dependent down-regulation of CD46 confers sensitivity to activated complement, regardless of the pathway of activation and the specificity of the activating antibodies. Interestingly, down-regulation of CD46 alone is sufficient to confer susceptibility of cells to complement lysis despite the continued surface expression of other RCA proteins such as CD35 and CD55. In primary cultures, both peripheral blood lymphocytes and macrophages are efficiently lysed in the presence of complement activated via the alternative pathway after MV infection. In contrast to the MV-ED infection, infection of cells with the lymphotropic MV wild-type strain WTF does not down-regulate CD46. Cells infected with MV-WTF do not exhibit enhanced susceptibility to complement lysis. These data suggest that MV strains similar to WTF that do not down-regulate CD46 may have an enhanced potential for replication and dissemination within the human host, whereas complement-mediated elimination of cells infected with CD46-down-regulating strains of MV, such as ED, may limit the spread of MV infection, and could thus represent an attenuating factor for MV.