Langenberg A G, Burke R L, Adair S F, Sekulovich R, Tigges M, Dekker C L, Corey L
Chiron Biocine, Emeryville, California, USA.
Ann Intern Med. 1995 Jun 15;122(12):889-98. doi: 10.7326/0003-4819-122-12-199506150-00001.
To evaluate the safety and immunogenicity of a recombinant glycoprotein vaccine for herpes simplex virus type 2 (HSV-2), which contains glycoproteins gD2 and gB2 combined with the novel MF59 adjuvant emulsion, in HSV-2-seronegative persons.
Integrated summary of two phase I and two phase II studies.
University and private outpatient clinics.
137 persons seronegative for HSV-2 antibodies as determined by HSV Western blot assay.
Open-label vaccine administration with a dose-escalating design (phase I) was followed by randomized vaccine administration (phase II). Vaccine was administered intramuscularly into the deltoid at 0, 1, and 6 months.
Neutralizing, HSV-2-binding antibodies and HSV-2-stimulated proliferative responses were measured before and after immunization.
Among HSV-seronegative patients, the gD2 and gB2 enzyme-linked immunosorbent assay (ELISA) and HSV-2-neutralizing antibody titers increased to levels equal to or higher than those seen in naturally acquired HSV-2 infection after the full three-dose immunization schedule. Among HSV-1-seropositive patients, one immunization produced increases in gD2 and gB2 ELISA antibody titers and HSV-2-neutralizing antibody titers that were 3 to 5 times greater than those in persons with naturally acquired HSV-2 infection. Among HSV-seronegative patients, frequency analysis assays showed a marked increase in the precursor frequency of gD2- and gB2-specific T cells after vaccination: T-cell responses after two immunizations were equal to the responses of HSV-2-seropositive patients and were sustained at day 180. The vaccine was well tolerated.
This subunit vaccine induces both humoral and cellular responses to HSV-2 that are equal to or greater than those of persons with naturally acquired HSV-2 infection. Studies to evaluate this vaccine for the prevention of genital herpes appear warranted.
评估一种重组2型单纯疱疹病毒(HSV-2)糖蛋白疫苗的安全性和免疫原性,该疫苗包含糖蛋白gD2和gB2,并与新型MF59佐剂乳剂联合使用,用于HSV-2血清阴性者。
两项I期和两项II期研究的综合总结。
大学和私立门诊诊所。
137名经HSV免疫印迹法检测为HSV-2抗体血清阴性的人。
采用剂量递增设计的开放标签疫苗接种(I期),随后是随机疫苗接种(II期)。疫苗于0、1和6个月时通过肌肉注射至三角肌。
在免疫前后测量中和性、HSV-2结合抗体以及HSV-2刺激的增殖反应。
在HSV血清阴性患者中,经过完整的三剂免疫程序后,gD2和gB2酶联免疫吸附测定(ELISA)以及HSV-2中和抗体滴度升高至等于或高于自然获得HSV-2感染患者的水平。在HSV-1血清阳性患者中,一次免疫使gD2和gB2 ELISA抗体滴度以及HSV-2中和抗体滴度的升高幅度比自然获得HSV-2感染的人高3至5倍。在HSV血清阴性患者中,频率分析检测显示接种疫苗后gD2和gB2特异性T细胞的前体频率显著增加:两次免疫后的T细胞反应等同于HSV-2血清阳性患者的反应,并在第180天持续存在。该疫苗耐受性良好。
这种亚单位疫苗诱导的针对HSV-2的体液和细胞反应等于或大于自然获得HSV-2感染的人。评估该疫苗预防生殖器疱疹的研究似乎是必要的。