Retinoic acid-adjuvanted vaccine induces antigen-specific secretory IgA in the gut of newborn piglets.

Vaccine Pub Date : 2025-02-06 Epub Date: 2024-12-28 DOI:10.1016/j.vaccine.2024.126672
Gitte Erbs, Jeanne Toft Jakobsen, Signe Tandrup Schmidt, Dennis Christensen, Mick Bailey, Gregers Jungersen
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Abstract

Mucosal secretory IgA (SIgA) produced by subepithelial plasma cells in the lamina propria is the major antigen-specific defense mechanism against mucosal infections. We investigated if a retinoic acid (RA)-containing adjuvant in parenteral immunization, can induce vaccine-specific SIgA in the jejunal lumen in a dose-dependent manner in neonatal pigs immunized with a Chlamydia hybrid antigen. To accurately quantify SIgA responses in mucosal secretions, an antigen-specific ELISA method with secondary detection of porcine secretory component rather than IgA was developed. RA facilitated a stronger (or faster) IgG, IgA, IgM and SIgA response in serum after primary immunization, and a more than 10-fold significantly increased level of vaccine-specific SIgA in jejunum at termination 2 weeks after the secondary boost, whereas IgA or SIgA responses in bronchoalveolar lavage (BAL) were not significantly increased after immunization with RA. Analyses of different isotype responses to vaccination and different sampling sites, revealed significant correlations between IgG and IgA responses in serum, and between IgG in serum and jejunum, while IgA in jejunum was neither correlated with IgA in serum nor with IgG in jejunum. This is indicative of IgG in jejunum being primarily a transudate from serum, while IgA is not. Jejunum SIgA correlated significantly with jejunum IgA and with both serum SIgA and IgA. Our results thus support the use of SC-specific reagents for mucosal SIgA responses, although IgA reagents to a lesser extent also reflects local antibodies. Although the IgA and SIgA levels in BAL were not significantly different with or without RA, we observed a significant correlation of vaccine-specific SIgA in jejunum and BAL, indicating a level of commonality in the regulation of mucosal antibodies in gut and respiratory system. In conclusion, an adjuvant with high concentration of RA was shown to increase the local intestinal mucosal antibody response after parenteral immunization in pigs.

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视黄酸佐剂疫苗诱导新生仔猪肠道抗原特异性分泌IgA。
粘膜分泌IgA (SIgA)是粘膜固有层上皮下浆细胞产生的主要抗原特异性防御机制。我们研究了肠外免疫中含有维甲酸(RA)的佐剂是否能在接种了衣原体杂交抗原的新生猪空肠腔中以剂量依赖的方式诱导疫苗特异性SIgA。为了准确定量猪粘膜分泌物中SIgA的反应,建立了一种抗原特异性ELISA方法,该方法对猪分泌物成分进行二次检测,而不是对IgA进行二次检测。初次免疫后,RA促进血清中IgG、IgA、IgM和SIgA反应更强(或更快),在二次增强后2周结束时,空肠中疫苗特异性SIgA水平显著增加10倍以上,而支气管肺泡灌洗(BAL)中IgA或SIgA反应在RA免疫后没有显著增加。对不同疫苗接种和不同采样点的同种型应答进行分析,发现血清中IgG和IgA应答、血清和空肠中IgG应答之间存在显著相关性,而空肠中IgA与血清中IgA和空肠中IgG均无相关性。这表明空肠中的IgG主要是从血清中漏出的,而IgA则不是。空肠SIgA与空肠IgA、血清SIgA和IgA均显著相关。因此,我们的结果支持sc特异性试剂用于粘膜SIgA反应,尽管IgA试剂在较小程度上也反映了局部抗体。虽然BAL中IgA和SIgA水平与RA无显著性差异,但我们观察到空肠中疫苗特异性SIgA与BAL存在显著相关性,表明肠道和呼吸系统粘膜抗体的调节水平具有共通性。综上所述,高浓度RA佐剂可提高猪肠外免疫后局部肠黏膜抗体应答。
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