Sulman Sadaf, Savidge Benjamin O, Alqaseer Kawther, Das Mrinal K, Nezam Abadi Neda, Pearl John E, Turapov Obolbek, Mukamolova Galina V, Akhtar M Waheed, Cooper Andrea May
Department Respiratory Sciences, University of Leicester, Leicester LE1 7RH, UK.
School of Biological Sciences, University of the Punjab, Lahore 54590, Pakistan.
Vaccines (Basel). 2021 May 18;9(5):519. doi: 10.3390/vaccines9050519.
Tuberculosis vaccines capable of reducing disease worldwide have proven difficult to develop. BCG is effective in limiting childhood disease, but adult TB is still a major public health issue. Development of new vaccines requires identification of antigens that are both spatially and temporally available throughout infection, and immune responses to which reduce bacterial burden without increasing pathologic outcomes. Subunit vaccines containing antigen require adjuvants to drive appropriate long-lived responses. We generated a triple-antigen fusion containing the virulence-associated EsxN (Rv1793), the PPE42 (Rv2608), and the latency associated Rv2628 to investigate the balance between bacterial reduction and weight loss in an animal model of aerosol infection. We found that in both a low pattern recognition receptor (PRR) engaging adjuvant and a high PRR-engaging adjuvant (MPL/TDM/DDA) the triple-antigen fusion could reduce the bacterial burden, but also induced weight loss in the mice upon aerosol infection. The weight loss was associated with an imbalance between TNFα and IL-17 transcription in the lung upon challenge. These data indicate the need to assess both protective and pathogenic responses when investigating subunit vaccine activity.
事实证明,开发能够在全球范围内减少结核病发病的疫苗颇具难度。卡介苗(BCG)在限制儿童结核病方面有效,但成人结核病仍是一个重大的公共卫生问题。开发新疫苗需要确定在整个感染过程中在空间和时间上均存在的抗原,并且针对这些抗原的免疫反应能够降低细菌载量而不增加病理结果。含有抗原的亚单位疫苗需要佐剂来驱动适当的长期免疫反应。我们构建了一种包含与毒力相关的EsxN(Rv1793)、PPE42(Rv2608)和与潜伏相关的Rv2628的三抗原融合体,以研究在气溶胶感染动物模型中细菌减少与体重减轻之间的平衡。我们发现,在低模式识别受体(PRR)结合佐剂和高PRR结合佐剂(MPL/TDM/DDA)中,三抗原融合体均可降低细菌载量,但在气溶胶感染后也会导致小鼠体重减轻。体重减轻与攻击后肺中TNFα和IL-17转录失衡有关。这些数据表明,在研究亚单位疫苗活性时需要同时评估保护性和致病性反应。