Barouch Dan H, Pau Maria G, Custers Jerome H H V, Koudstaal Wouter, Kostense Stefan, Havenga Menzo J E, Truitt Diana M, Sumida Shawn M, Kishko Michael G, Arthur Janelle C, Korioth-Schmitz Birgit, Newberg Michael H, Gorgone Darci A, Lifton Michelle A, Panicali Dennis L, Nabel Gary J, Letvin Norman L, Goudsmit Jaap
Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, MA 02215, USA.
J Immunol. 2004 May 15;172(10):6290-7. doi: 10.4049/jimmunol.172.10.6290.
The high prevalence of pre-existing immunity to adenovirus serotype 5 (Ad5) in human populations may substantially limit the immunogenicity and clinical utility of recombinant Ad5 vector-based vaccines for HIV-1 and other pathogens. A potential solution to this problem is to use vaccine vectors derived from adenovirus (Ad) serotypes that are rare in humans, such as Ad35. However, cross-reactive immune responses between heterologous Ad serotypes have been described and could prove a major limitation of this strategy. In particular, the extent of immunologic cross-reactivity between Ad5 and Ad35 has not previously been determined. In this study we investigate the impact of pre-existing anti-Ad5 immunity on the immunogenicity of candidate rAd5 and rAd35 vaccines expressing SIV Gag in mice. Anti-Ad5 immunity at levels typically found in humans dramatically blunted the immunogenicity of rAd5-Gag. In contrast, even high levels of anti-Ad5 immunity did not substantially suppress Gag-specific cellular immune responses elicited by rAd35-Gag. Low levels of cross-reactive Ad5/Ad35-specific CD4(+) T lymphocyte responses were observed, but were insufficient to suppress vaccine immunogenicity. These data demonstrate the potential utility of Ad35 as a candidate vaccine vector that is minimally suppressed by anti-Ad5 immunity. Moreover, these studies suggest that using Ad vectors derived from immunologically distinct serotypes may be an effective and general strategy to overcome the suppressive effects of pre-existing anti-Ad immunity.
人群中对5型腺病毒(Ad5)预先存在的免疫力的高流行率可能会极大地限制基于重组Ad5载体的HIV-1和其他病原体疫苗的免疫原性和临床效用。解决这一问题的一个潜在办法是使用源自人类中罕见的腺病毒(Ad)血清型的疫苗载体,如Ad35。然而,已有文献报道了不同Ad血清型之间的交叉反应性免疫应答,这可能是该策略的一个主要限制。特别是,此前尚未确定Ad5和Ad35之间免疫交叉反应的程度。在本研究中,我们调查了预先存在的抗Ad5免疫力对在小鼠中表达SIV Gag的候选rAd5和rAd35疫苗免疫原性的影响。人类中常见水平的抗Ad5免疫力显著削弱了rAd5-Gag的免疫原性。相比之下,即使是高水平的抗Ad5免疫力也没有实质性地抑制rAd35-Gag引发的Gag特异性细胞免疫应答。观察到低水平的Ad5/Ad35特异性CD4(+) T淋巴细胞交叉反应性应答,但不足以抑制疫苗的免疫原性。这些数据证明了Ad35作为候选疫苗载体的潜在效用,其受抗Ad5免疫力的抑制最小。此外,这些研究表明,使用源自免疫上不同血清型的Ad载体可能是克服预先存在的抗Ad免疫力抑制作用的一种有效且通用的策略。