Murdoch Children's Research Institute, Royal Children's Hospital, Parkville, Australia.
The University of Melbourne, Parkville, Australia.
BMC Immunol. 2024 Apr 30;25(1):24. doi: 10.1186/s12865-024-00611-5.
Bacillus Calmette-Guérin (BCG) vaccination has off-target protective effects against infections unrelated to tuberculosis. Among these, murine and human studies suggest that BCG vaccination may protect against malaria. We investigated whether BCG vaccination influences neonatal in vitro cytokine responses to Plasmodium falciparum. Blood samples were collected from 108 participants in the Melbourne Infant Study BCG for Allergy and Infection Reduction (MIS BAIR) randomised controlled trial (Clinical trials registration NCT01906853, registered July 2013), seven days after randomisation to neonatal BCG (n = 66) or no BCG vaccination (BCG-naïve, n = 42). In vitro cytokine responses were measured following stimulation with P. falciparum-infected erythrocytes (PfIE) or E. coli.
No difference in the measured cytokines were observed between BCG-vaccinated and BCG-naïve neonates following stimulation with PfIE or E. coli. However, age at which blood was sampled was independently associated with altered cytokine responses to PfIE. Being male was also independently associated with increased TNF-a responses to both PfIE and E. coli.
These findings do not support a role for BCG vaccination in influencing in vitro neonatal cytokine responses to P. falciparum. Older neonates are more likely to develop P. falciparum-induced IFN-γ and IFN-γ-inducible chemokine responses implicated in early protection against malaria and malaria pathogenesis.
卡介苗(BCG)接种具有针对与结核病无关的感染的靶向保护作用。在这些作用中,鼠类和人类研究表明,BCG 接种可能对疟疾有保护作用。我们研究了 BCG 接种是否会影响新生儿对恶性疟原虫的体外细胞因子反应。从墨尔本婴儿研究卡介苗用于过敏和感染减少(MIS BAIR)随机对照试验(临床试验注册 NCT01906853,2013 年 7 月注册)的 108 名参与者中采集血液样本,这些参与者在随机分配后 7 天内接受了新生儿 BCG(n=66)或无 BCG 接种(BCG-未接种,n=42)。在体外用恶性疟原虫感染的红细胞(PfIE)或大肠杆菌刺激后测量细胞因子反应。
BCG 接种和 BCG-未接种新生儿在 PfIE 或大肠杆菌刺激后,所测量的细胞因子没有差异。然而,采血时的年龄与 PfIE 细胞因子反应的改变独立相关。男性也是与 PfIE 和大肠杆菌的 TNF-α反应增加独立相关。
这些发现不支持 BCG 接种在影响新生儿对恶性疟原虫体外细胞因子反应中的作用。年龄较大的新生儿更有可能发展出 IFN-γ和 IFN-γ诱导的趋化因子反应,这些反应与早期对疟疾和疟疾发病机制的保护有关。