Oscherwitz Jon, Feldman Daniel, Yu Fen, Cease Kemp B
Division of Hematology-Oncology, Department of Internal Medicine, University of Michigan Medical School, Ann Arbor, MI 48105, USA; Veterans Administration Ann Arbor Healthcare System, 2215 Fuller Road, Ann Arbor, MI 48105, USA.
University of Michigan Medical School, Ann Arbor, MI 48105, USA.
Vaccine. 2015 Jan 9;33(3):430-6. doi: 10.1016/j.vaccine.2014.11.042. Epub 2014 Nov 30.
Anthrax represents a formidable bioterrorism threat for which new, optimized vaccines are required. We previously demonstrated that epitope-focused multiple antigenic peptides or a recombinant protein in Freund's adjuvant can elicit Ab against the loop neutralizing determinant (LND), a cryptic linear neutralizing epitope in the 2ß2-2ß3 loop of protective antigen from Bacillus anthracis, which mediated protection of rabbits from inhalation challenge with B. anthracis Ames strain. However, demonstration of efficacy using human-use adjuvants is required before proceeding with further development of an LND vaccine for testing in non-human primates and humans.
To optimize the LND immunogen, we first evaluated the protective efficacy and immune correlates associated with immunization of rabbits with mixtures containing two molecular variants of multiple antigenic peptides in Freunds adjuvant, termed BT-LND(2) and TB-LND(2). TB-LND(2) was then further evaluated for protective efficacy in rabbits employing human-use adjuvants.
Immunization of rabbits with TB-LND(2) in human-use adjuvants elicited protection from Ames strain spore challenge which was statistically indistinguishable from that elicited through immunization with protective antigen. All TB-LND(2) rabbits with any detectable serum neutralization prior to challenge were protected from aerosolized spore exposure. Remarkably, rabbits immunized with TB-LND(2) in Alhydrogel/CpG had significant anamnestic increases in post-challenge LND-specific Ab and neutralization titers despite little evidence of spore germination in these rabbits.
An LND-specific epitope-focused vaccine may complement PA-based vaccines and may represent a complementary stand-alone vaccine for anthrax.
炭疽构成了严重的生物恐怖主义威胁,因此需要新型优化疫苗。我们之前证明,表位聚焦的多抗原肽或弗氏佐剂中的重组蛋白可引发针对环中和决定簇(LND)的抗体,LND是炭疽杆菌保护性抗原2β2 - 2β3环中的一个隐蔽线性中和表位,介导了对兔免受炭疽杆菌Ames株吸入攻击的保护作用。然而,在继续开发用于非人类灵长类动物和人类测试的LND疫苗之前,需要证明其在人用佐剂中的有效性。
为了优化LND免疫原,我们首先评估了在弗氏佐剂中用含有两种多抗原肽分子变体(称为BT - LND(2)和TB - LND(2))的混合物免疫兔的保护效果和免疫相关性。然后进一步评估TB - LND(2)在人用佐剂中的兔保护效果。
用人用佐剂中的TB - LND(2)免疫兔可使其免受Ames株孢子攻击,其保护效果在统计学上与用保护性抗原免疫所引发的效果无差异。所有在攻击前有任何可检测到的血清中和作用的TB - LND(2)兔都免受雾化孢子暴露。值得注意的是,用Alhydrogel/CpG中的TB - LND(2)免疫的兔在攻击后LND特异性抗体和中和效价有显著的回忆性增加,尽管这些兔中几乎没有孢子萌发的证据。
一种LND特异性表位聚焦疫苗可能补充基于PA的疫苗,并且可能代表一种用于炭疽的补充性独立疫苗。