Tostes Rafaella O, Rodrigues Tasson C, da Silva Josefa B, Schanoski Alessandra S, Oliveira Maria Leonor S, Miyaji Eliane N
Laboratório de Bacteriologia, Instituto Butantan, São Paulo, SP, Brazil.
PLoS One. 2017 Jan 19;12(1):e0170157. doi: 10.1371/journal.pone.0170157. eCollection 2017.
A promising alternative vaccine candidate to reduce the burden of pneumococcal diseases is the protein antigen PspA (Pneumococcal surface protein A). Since concomitant colonization with two or more pneumococcal strains is very common in children, we aimed to determine if immunization with PspA would be able to control co-colonization. We evaluated nasal immunization with recombinant PspA (rPspA) in a model of co-colonization with two strains expressing different PspAs. Mice were immunized intranasally with rPspAs from clades 1 to 4 (rPspA1, rPspA2, rPspA3 or rPspA4) using whole-cell pertussis vaccine (wP) as adjuvant. Mice were then challenged with a mixture of two serotype 6B isolates St491/00 (PspA1) and St472/96 (PspA4). Immunization with rPspA1+wP and rPspA4+wP reduced colonization with both strains and the mixture of rPspA1+rPspA4+wP induced greater reduction than a single antigen. Immunization rPspA1+rPspA4+wP also reduced colonization when challenge experiments were performed with a mixture of isolates of serotypes 6B (PspA3) and 23F (PspA2). Furthermore, none of the tested formulations led to a pronounced increase in colonization of one isolate over the other, showing that the vaccine strategy would not favor replacement. Interestingly, the adjuvant wP by itself already led to some reduction in pneumococcal colonization, indicating the induction of non-specific immune responses. Anti-rPspA IgG was observed in serum, nasal wash (NW) and bronchoalveolar lavage fluid (BALF) samples, whereas animals inoculated with formulations containing the adjuvant wP (with or without rPspA) showed higher levels of IL-6 and KC in NW and increase in tissue macrophages, B cells and CD4+T cells in BALF.
一种有望减轻肺炎球菌疾病负担的替代疫苗候选物是蛋白质抗原PspA(肺炎球菌表面蛋白A)。由于儿童中同时感染两种或更多种肺炎球菌菌株的情况非常普遍,我们旨在确定用PspA免疫是否能够控制共同感染。我们在与两种表达不同PspA的菌株共同感染的模型中评估了用重组PspA(rPspA)进行鼻腔免疫。使用全细胞百日咳疫苗(wP)作为佐剂,对小鼠进行鼻内免疫,免疫原分别为1至4分支的rPspA(rPspA1、rPspA2、rPspA3或rPspA4)。然后用两种6B血清型分离株St491/00(PspA1)和St472/96(PspA4)的混合物对小鼠进行攻击。用rPspA1+wP和rPspA4+wP免疫可减少两种菌株的定植,并且rPspA1+rPspA4+wP混合物诱导的减少幅度大于单一抗原。当用6B血清型(PspA3)和23F血清型(PspA2)的分离株混合物进行攻击实验时,rPspA1+rPspA4+wP免疫也减少了定植。此外,没有一种测试制剂导致一种分离株的定植相对于另一种分离株出现明显增加,这表明该疫苗策略不会促进替代。有趣的是,佐剂wP本身已经导致肺炎球菌定植有所减少,这表明诱导了非特异性免疫反应。在血清、鼻腔冲洗液(NW)和支气管肺泡灌洗液(BALF)样本中观察到了抗rPspA IgG,而接种含有佐剂wP(有或没有rPspA)制剂的动物在NW中显示出更高水平的IL-6和KC,并且BALF中的组织巨噬细胞、B细胞和CD4+T细胞增加。