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一种口服灭活产肠毒素大肠杆菌加霍乱毒素B亚单位疫苗在18至36月龄孟加拉国儿童中的安全性和免疫原性。

Safety and immunogenicity of an oral, inactivated enterotoxigenic Escherichia coli plus cholera toxin B subunit vaccine in Bangladeshi children 18-36 months of age.

作者信息

Qadri Firdausi, Ahmed Tanvir, Ahmed Firoz, Bradley Sack R, Sack David A, Svennerholm Ann Mari

机构信息

Laboratory Sciences Division, International Centre for Diarrhoeal Disease Research, GPO Box 128, Dhaka 1000, Bangladesh.

出版信息

Vaccine. 2003 Jun 2;21(19-20):2394-403. doi: 10.1016/s0264-410x(03)00077-x.

Abstract

A phase II safety and immunogenicity study of an oral-formalin inactivated enterotoxigenic Escherichia coli (ETEC) vaccine containing six colonization factors (CFA/I, CS1, CS2, CS3, CS4, CS5) and 1mg of recombinant cholera toxin B subunit (the CF-BS-ETEC vaccine) was carried out in an urban slum of Dhaka city in Bangladesh. The study was carried out in a double blinded, placebo controlled design in 158 children, 18-36 months of age. Children were given two doses of the CF-BS-ETEC vaccine or the placebo which consisted of E. coli K12. The vaccine was well tolerated. The immune response was studied in 60 children (30 each in the placebo and vaccine group). Significant vaccine specific IgA antibody-secreting cell (ASC) responses were seen 7 days after ingestion of the first and second dose of the vaccine. The responses to CFA/I (P<or=0.001), CS2 (P=0.021), CS4 (P=0.009) and rCTB (P<or=0.001) were elevated in the vaccines in comparison to the pre-immune values and in comparison to those seen in the placebo recipients (P=0.018 to <0.001). Vaccines but not placebo recipients also showed significantly increased IgM ASC responses to all three CF antigens that were tested (P=0.012 to <0.001) and IgG-ASCs to rCTB (P<0.001). Peak ASC levels were reached after one dose of the vaccine with no further increase or decrease after the second dose. The vaccine recipients also responded with IgA plasma antibodies to CFA/I, CS1, CS2, CS4 and rCTB after one or two doses of the vaccine (P=0.01 to <0.001). Subjects in the placebo group failed to mount responses to any of the antigens. The vaccine also induced responses in mucosal IgA antibodies in feces to CFA/I, CS2 and rCTB (61, 88 and 69% responder frequency, respectively) and the magnitude of the response was elevated in comparison to the pre-immune levels (P=0.031 to <0.001) and to the levels of the control group (P=0.003 to <0.001). This study thus shows that the CF-BS-ETEC vaccine is well tolerated in children, 18-36 months of age and gives rise to significant systemic and mucosal IgA antibody responses.

摘要

在孟加拉国达卡市的一个城市贫民窟开展了一项II期安全性和免疫原性研究,该研究针对一种口服福尔马林灭活的产肠毒素大肠杆菌(ETEC)疫苗,其包含六种定植因子(CFA/I、CS1、CS2、CS3、CS4、CS5)和1毫克重组霍乱毒素B亚单位(CF-BS-ETEC疫苗)。该研究采用双盲、安慰剂对照设计,针对158名年龄在18至36个月的儿童。给予儿童两剂CF-BS-ETEC疫苗或由大肠杆菌K12组成的安慰剂。疫苗耐受性良好。在60名儿童(安慰剂组和疫苗组各30名)中研究了免疫反应。在摄入第一剂和第二剂疫苗后7天,观察到显著的疫苗特异性IgA抗体分泌细胞(ASC)反应。与免疫前值相比以及与安慰剂接受者相比,疫苗中对CFA/I(P≤0.001)、CS2(P = 0.021)、CS4(P = 0.009)和rCTB(P≤0.001)的反应升高(P = 0.018至<0.001)。疫苗接受者而非安慰剂接受者还显示出对所有三种测试的CF抗原的IgM ASC反应显著增加(P = 0.012至<0.001)以及对rCTB的IgG-ASC反应显著增加(P<0.001)。一剂疫苗后达到ASC峰值水平,第二剂后无进一步升高或降低。疫苗接受者在接种一剂或两剂疫苗后也产生了针对CFA/I、CS1、CS2、CS4和rCTB的IgA血浆抗体(P = 0.01至<0.001)。安慰剂组的受试者对任何抗原均未产生反应。该疫苗还诱导了粪便中针对CFA/I、CS2和rCTB的黏膜IgA抗体反应(应答频率分别为61%、88%和69%),与免疫前水平相比以及与对照组水平相比,反应强度升高(P = 0.031至<0.001)。因此,这项研究表明CF-BS-ETEC疫苗在18至36个月的儿童中耐受性良好,并产生显著的全身和黏膜IgA抗体反应。

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