The challenge of developing a herpes simplex virus 2 vaccine

被引:0
作者
Dropulic, Lesia K. [1 ]
Cohen, Jeffrey I. [1 ]
机构
[1] NIAID, Med Virol Sect, Infect Dis Lab, NIH, Bethesda, MD 20892 USA
关键词
animal models; genital herpes; herpes simplex virus; immune response; prophylactic vaccine; therapeutic vaccine; RECURRENT GENITAL HERPES; PLACEBO-CONTROLLED TRIAL; CD8(+) T-CELLS; GLYCOPROTEIN-D; GUINEA-PIGS; RECOMBINANT GLYCOPROTEIN; DOUBLE-BLIND; PAPILLOMAVIRUS INFECTION; AOTUS-TRIVIRGATUS; DELETION MUTANT;
D O I
10.1586/ERV.12.129
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Expert Rev. Vaccines 11(12), 1429-1440 (2012) HSV infections are prevalent worldwide. A vaccine to prevent genital herpes would have a significant impact on this disease. Several vaccines have shown promise in animal models; however, so far these have not been successful in human clinical studies. Prophylactic HSV vaccines to prevent HSV infection or disease have focused primarily on eliciting antibody responses. Potent antibody responses are needed to result in sufficiently high levels of virus-specific antibody in the genital tract. Therapeutic vaccines that reduce recurrences need to induce potent T-cell responses at the site of infection. With the increasing incidence of HSV-1 genital herpes, an effective herpes vaccine should protect against both HSV-1 and HSV-2. Novel HSV vaccines, such as replication-defective or attenuated viruses, have elicited humoral and cellular immune responses in preclinical studies. These vaccines and others hold promise in future clinical studies.
引用
收藏
页码:1429 / 1440
页数:12
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