Lipsit Sean, Facciuolo Antonio, Scruten Erin, Griebel Philip, Napper Scott
Vaccine and Infectious Disease Organization (VIDO), University of Saskatchewan, Saskatoon, SK, Canada.
Department of Biochemistry, Microbiology and Immunology, University of Saskatchewan, Saskatoon, SK, Canada.
Front Vet Sci. 2022 Jul 13;9:922992. doi: 10.3389/fvets.2022.922992. eCollection 2022.
Failure to mount an effective immune response to vaccination leaves individuals at risk for infection and can compromise herd immunity. Vaccine unresponsiveness can range from poor responses "low responders" to a failure to seroconvert "non-responders." Biomarkers of vaccine unresponsiveness, particularly those measured at the time of vaccination, could facilitate more strategic vaccination programs. We previously reported that pro-inflammatory cytokine signaling within peripheral blood mononuclear cells, elevated plasma interferon-gamma (IFNγ), and low birth weight correlated with vaccine-induced serum IgG titers in piglets that were below the threshold of detectable seroconversion (vaccine non-responders). These observations suggested that plasma IFNγ concentration and birth weight might serve as pre-vaccination biomarkers of vaccine unresponsiveness. To test this hypothesis, piglets ( = 67) from a different production facility were vaccinated with the same commercial bacterin (RespiSure-One) to determine if there was a consistent and significant association between vaccine-induced serum IgG titers and either plasma cytokine concentrations or birth weight. All piglets seroconverted following vaccination with significantly less variability in vaccine-induced serum IgG titers than observed in the previous vaccine trial. Piglets exhibited highly variable birth weights and plasma cytokine concentrations prior to vaccination, but there were no significant associations ( > 0.05) between these variables and vaccine-induced serum IgG titers. There were significant ( < 0.001) differences in plasma IFNγ concentrations among individual litters ( = 6), and plasma IFNγ concentrations decreased in all pigs from birth to 63-days of age. One of the six litters ( = 11 piglets) exhibited significantly elevated plasma IFNγ concentrations during the first 3 weeks of life ( < 0.001) and at the time of vaccination ( < 0.01). This litter, however, had similar vaccine-induced serum IgG titers when compared to the other piglets in this study. Collectively the two studies indicate that while plasma cytokines and birth weight can be associated with vaccine non-responsiveness, their temporal and individual variation, as well as the complexity of the vaccine responsiveness phenotype, make them inconsistent biomarkers for predicting the less extreme phenotype of vaccine low responders.
无法对疫苗接种产生有效的免疫反应会使个体面临感染风险,并可能损害群体免疫力。疫苗无反应性的范围可以从反应不佳的“低反应者”到未能血清转化的“无反应者”。疫苗无反应性的生物标志物,尤其是在接种疫苗时测量的那些标志物,可能有助于制定更具战略性的疫苗接种计划。我们之前报道过,外周血单核细胞内的促炎细胞因子信号传导、血浆干扰素-γ(IFNγ)升高以及低出生体重与血清转化检测阈值以下的仔猪(疫苗无反应者)中疫苗诱导的血清IgG滴度相关。这些观察结果表明,血浆IFNγ浓度和出生体重可能作为疫苗无反应性的接种前生物标志物。为了验证这一假设,来自不同生产设施的仔猪(n = 67)接种了相同的商业菌苗(RespiSure-One),以确定疫苗诱导的血清IgG滴度与血浆细胞因子浓度或出生体重之间是否存在一致且显著的关联。所有仔猪在接种疫苗后均发生血清转化,疫苗诱导的血清IgG滴度的变异性明显小于之前的疫苗试验。仔猪在接种疫苗前出生体重和血浆细胞因子浓度变化很大,但这些变量与疫苗诱导的血清IgG滴度之间没有显著关联(P > 0.05)。各窝仔猪(n = 6)之间的血浆IFNγ浓度存在显著差异(P < 0.001),并且所有仔猪从出生到63日龄血浆IFNγ浓度均下降。六窝仔猪中的一窝(n = 11头仔猪)在出生后的前3周(P < 0.001)和接种疫苗时(P < 0.01)血浆IFNγ浓度显著升高。然而,与本研究中的其他仔猪相比,这窝仔猪的疫苗诱导血清IgG滴度相似。总体而言,这两项研究表明,虽然血浆细胞因子和出生体重可能与疫苗无反应性相关,但它们的时间和个体变化以及疫苗反应性表型的复杂性,使其成为预测疫苗低反应者这种不太极端表型的不一致生物标志物。