首页> 外文期刊>Drugs: International Journal of Current Therapeutics and Applied Pharmacology Reviews, Featuring Evaluations on New Drugs, Review Articles on Drugs and Drug Therapy, and Drug Literature Abstracts >AS04-adjuvanted human papillomavirus (HPV) types 16 and 18 vaccine (Cervarix(R)): a review of its use in the prevention of premalignant cervical lesions and cervical cancer causally related to certain oncogenic HPV types.
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AS04-adjuvanted human papillomavirus (HPV) types 16 and 18 vaccine (Cervarix(R)): a review of its use in the prevention of premalignant cervical lesions and cervical cancer causally related to certain oncogenic HPV types.

机译:AS04辅助的16型和18型人乳头瘤病毒(HPV)疫苗(Cervarix(R)):其在预防癌前宫颈病变和与某些致癌HPV类型因果相关的宫颈癌中的用途的综述。

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The AS04-adjuvanted human papillomavirus (HPV) 16/18 vaccine (Cervarix(R)) is a noninfectious recombinant vaccine produced using purified virus-like particles (VLPs) that induce a strong immunogenic response eliciting high levels of anti-L1 VLP antibodies that persist at levels markedly greater than those observed with natural infection. The vaccine adjuvant (AS04) is composed of monophosphoryl-lipid A, which enhances cellular and humoral immune response, adsorbed to aluminium hydroxide. The vaccine is indicated for the prevention of premalignant cervical lesions and cervical cancer causally related to certain oncogenic HPV types in females aged >/=10 years. The AS04-adjuvanted HPV 16/18 vaccine administered in a three-dose schedule over 6 months elicits a high immunogenic response and is highly protective against cervical intraepithelial neoplasia and infection causally related to high-risk oncogenic HPV types. In well designed clinical trials in young women aged 15-25 years who were HPV 16/18 seronegative and DNA negative to 14 HPV high-risk types, high levels of immunogenicity and protection were sustained for follow-up periods of up to 8.4 years. High and persistent immunogenicity against infection with HPV 16/18 has also been demonstrated in older and younger females (aged 10-55 years) who were seronegative for vaccine HPV types. The AS04-adjuvanted HPV 16/18 vaccine elicited a greater immunogenic response than the quadrivalent HPV vaccine in women aged 18-45 years who were seronegative and DNA negative for HPV 16/18. The AS04-adjuvanted HPV 16/18 vaccine confers cross protection against certain non-vaccine, high-risk HPV types. A rapid and strong anamnestic humoral immune response was elicited following a fourth dose of the vaccine. The AS04-adjuvanted HPV 16/18 vaccine is generally well tolerated, and pharmacoeconomic analyses have demonstrated the potential for public health benefits and cost effectiveness when vaccination programmes are run in conjunction with screening programmes. Thus, the AS04-adjuvanted HPV 16/18 vaccine prevents cervical disease associated with certain oncogenic HPV types, thereby reducing the burden of premalignant cervical lesions and, very likely, cervical cancer.
机译:AS04佐剂型人乳头瘤病毒(HPV)16/18疫苗(Cervarix®)是使用纯化的病毒样颗粒(VLP)生产的非感染性重组疫苗,该病毒样颗粒诱导强烈的免疫原性应答,引发高水平的抗L1 VLP抗体,持续存在的水平明显高于自然感染所观察到的水平。疫苗佐剂(AS04)由单磷酰脂质A组成,可增强细胞和体液免疫反应,并吸附到氢氧化铝上。该疫苗适用于预防年龄≥10岁女性与某些致癌HPV类型相关的癌前宫颈病变和子宫颈癌。在六个月内以三剂量方案给予AS04辅助的HPV 16/18疫苗,可引起高免疫原性应答,并对宫颈上皮内瘤变和与高危致癌HPV类型相关的感染具有高度保护作用。在针对15至25岁的HPV 16/18血清阴性且DNA对14种HPV高风险类型阴性的年轻女性中,精心设计的临床试验中,高水平的免疫原性和保护作用持续了8.4年。在对疫苗HPV类型呈血清反应阴性的年龄较大和较年轻的女性(年龄在10-55岁之间)中,也证明了针对HPV 16/18感染具有高度持久的免疫原性。与AS04佐剂的HPV 16/18疫苗相比,HPV 16/18血清阴性且DNA阴性的18-45岁女性比四价HPV疫苗产生更大的免疫原性应答。 AS04佐剂的HPV 16/18疫苗可针对某些非疫苗,高风险的HPV类型提供交叉保护。第四剂疫苗后引起快速而强烈的记忆消除体液免疫反应。通常,AS04佐剂的HPV 16/18疫苗耐受性良好,药物经济学分析表明,将疫苗接种计划与筛查计划一起运行时,具有潜在的公共卫生效益和成本效益。因此,AS04佐剂的HPV 16/18疫苗可预防与某些致癌HPV类型相关的宫颈疾病,从而减轻癌前病变和非常可能的宫颈癌的负担。

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