VCL-CB01, an injectable bivalent plasmid DNA vaccine for potential protection against CMV disease and infection.

Mark R Schleiss
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Abstract

Vaccines for the prevention of human CMV (hCMV) infection and disease are a major public health priority. Immunization with DNA vaccines encoding key proteins involved in the immune response to hCMV has emerged as a major focus of hcmv vaccine research. Validation of the protective effect of DNA vaccination in animal models has provided support for clinical trials. VCL-CB01, under development by Vical Inc for the prevention of hCMV infection and disease, is a poloxamer-formulated, bivalent DNA vaccine that contains plasmids encoding hCMV tegument phosphoprotein 65 and the major hCMV surface glycoprotein B. In a phase I trial in healthy adults, VCL-CB01 was well tolerated. In interim results from a phase II trial in hCMV-seropositive hematopoietic cell transplant recipients, VCL-CB01 increased T-cell responses compared with placebo. The final results from the phase II trial will be of value for developing strategies to prevent hCMV disease in hCMV-seropositive transplant recipients, and may lead to other trials of VCL-CB01 or related vaccines for the prevention of congenital hCMV infection.

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VCL-CB01,一种可注射的二价质粒DNA疫苗,对巨细胞病毒疾病和感染具有潜在的保护作用。
预防人类巨细胞病毒(hCMV)感染和疾病的疫苗是一项主要的公共卫生重点。利用编码hCMV免疫应答关键蛋白的DNA疫苗进行免疫接种已成为hCMV疫苗研究的主要焦点。在动物模型上验证DNA疫苗的保护作用为临床试验提供了支持。VCL-CB01由Vical公司开发,用于预防hCMV感染和疾病,是一种由poloxmer配制的二价DNA疫苗,含有编码hCMV被膜磷酸化蛋白65和主要hCMV表面糖蛋白b的质粒。在健康成人的I期试验中,VCL-CB01耐受性良好。在一项针对hcmv血清阳性造血细胞移植受者的II期试验的中期结果中,与安慰剂相比,VCL-CB01增加了t细胞应答。II期试验的最终结果将对制定预防hCMV血清阳性移植受者hCMV疾病的策略具有价值,并可能导致VCL-CB01或相关疫苗预防先天性hCMV感染的其他试验。
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来源期刊
Current Opinion in Molecular Therapeutics
Current Opinion in Molecular Therapeutics 医学-生物工程与应用微生物
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