Singer Julian, Tunbridge Matthew J, Shi Bree, Perkins Griffith B, Chai Cheng Sheng, Salehi Tania, Sim Beatrice Z, Kireta Svjetlana, Johnston Julie K, Akerman Anouschka, Milogiannakis Vanessa, Aggarwal Anupriya, Turville Stuart, Hissaria Pravin, Ying Tracey, Wu Huiling, Grubor-Bauk Branka, Coates P Toby, Chadban Steven J
Department of Renal Medicine, Royal Prince Alfred Hospital, Sydney, NSW 2050, Australia.
Central Clinical School, Faculty of Medicine and Health, University of Sydney, Camperdown, NSW 2006, Australia.
Vaccines (Basel). 2024 Jun 3;12(6):608. doi: 10.3390/vaccines12060608.
Kidney transplant recipients are at an increased risk of hospitalisation and death from SARS-CoV-2 infection, and standard two-dose vaccination schedules are typically inadequate to generate protective immunity. Gut dysbiosis, which is common among kidney transplant recipients and known to effect systemic immunity, may be a contributing factor to a lack of vaccine immunogenicity in this at-risk cohort. The gut microbiota modulates vaccine responses, with the production of immunomodulatory short-chain fatty acids by bacteria such as associated with heightened vaccine responses in both observational and experimental studies. As SCFA-producing populations in the gut microbiota are enhanced by diets rich in non-digestible fibre, dietary supplementation with prebiotic fibre emerges as a potential adjuvant strategy to correct dysbiosis and improve vaccine-induced immunity. In a randomised, double-bind, placebo-controlled trial of 72 kidney transplant recipients, we found dietary supplementation with prebiotic inulin for 4 weeks before and after a third SARS-CoV2 mRNA vaccine to be feasible, tolerable, and safe. Inulin supplementation resulted in an increase in gut , as determined by 16S RNA sequencing, but did not increase in vitro neutralisation of live SARS-CoV-2 virus at 4 weeks following a third vaccination. Dietary fibre supplementation is a feasible strategy with the potential to enhance vaccine-induced immunity and warrants further investigation.
肾移植受者因感染严重急性呼吸综合征冠状病毒2(SARS-CoV-2)而住院和死亡的风险增加,标准的两剂疫苗接种方案通常不足以产生保护性免疫。肠道菌群失调在肾移植受者中很常见,并且已知会影响全身免疫,这可能是导致这一高危人群疫苗免疫原性缺乏的一个因素。肠道微生物群调节疫苗反应,在观察性和实验性研究中,诸如等细菌产生的免疫调节性短链脂肪酸与增强疫苗反应有关。由于富含不可消化纤维的饮食会增加肠道微生物群中产生短链脂肪酸的菌群数量,补充益生元纤维的饮食成为纠正菌群失调和改善疫苗诱导免疫的一种潜在辅助策略。在一项针对72名肾移植受者的随机、双盲、安慰剂对照试验中,我们发现在第三次接种严重急性呼吸综合征冠状病毒2(SARS-CoV-2)信使核糖核酸(mRNA)疫苗前后4周补充益生元菊粉的饮食是可行、可耐受且安全的。通过16S核糖体核糖核酸(RNA)测序确定,补充菊粉可使肠道增加,但在第三次接种疫苗后4周,并未增加对活的严重急性呼吸综合征冠状病毒2(SARS-CoV-2)病毒的体外中和作用。补充膳食纤维是一种可行的策略,有可能增强疫苗诱导的免疫,值得进一步研究。