Messina Nicole L, Germano Susie, Chung Amy W, van de Sandt Carolien E, Stevens Natalie E, Allen Lilith F, Bonnici Rhian, Croda Julio, Counoupas Claudio, Grubor-Bauk Branka, Haycroft Ebene R, Kedzierska Katherine, McDonald Ellie, McElroy Rebecca, Netea Mihai G, Novakovic Boris, Perrett Kirsten P, Pittet Laure F, Purcell Ruth A, Subbarao Kanta, Triccas James A, Lynn David J, Curtis Nigel
Infectious Diseases Group, Infection, Immunity and Global Health Theme Murdoch Children's Research Institute Parkville VIC Australia.
Department of Paediatrics The University of Melbourne Parkville VIC Australia.
Clin Transl Immunology. 2025 Jan 25;14(1):e70023. doi: 10.1002/cti2.70023. eCollection 2025.
Bacille Calmette-Guérin (BCG) vaccination has off-target effects on disease risk for unrelated infections and immune responses to vaccines. This study aimed to determine the immunomodulatory effects of BCG vaccination on immune responses to vaccines against SARS-CoV-2.
Blood samples, from a subset of 275 SARS-CoV-2-naïve healthcare workers randomised to BCG vaccination (BCG group) or no BCG vaccination (Control group) in the BRACE trial, were collected before and 28 days after the primary course (two doses) of ChAdOx1-S (Oxford-AstraZeneca) or BNT162b2 (Pfizer-BioNTech) vaccination. SARS-CoV-2-specific antibodies were measured using ELISA and multiplex bead array, whole blood cytokine responses to γ-irradiated SARS-CoV-2 (iSARS) stimulation were measured by multiplex bead array, and SARS-CoV-2-specific T-cell responses were measured by activation-induced marker and intracellular cytokine staining assays.
After randomisation (mean 11 months) but prior to COVID-19 vaccination, the BCG group had lower cytokine responses to iSARS stimulation than the Control group. After two doses of ChAdOx1-S, differences in iSARS-induced cytokine responses between the BCG group and Control group were found for three cytokines (CTACK, TRAIL and VEGF). No differences were found between the groups after BNT162b2 vaccination. There were also no differences between the BCG and Control groups in COVID-19 vaccine-induced antigen-specific antibody responses, T-cell activation or T-cell cytokine production.
BCG vaccination induced a broad and persistent reduction in cytokine responses to SARS-CoV-2. Following COVID-19 vaccination, this effect was abrogated, and BCG vaccination did not influence adaptive immune responses to COVID-19 vaccine antigens.
卡介苗(BCG)接种对无关感染的疾病风险和疫苗免疫反应具有非靶向效应。本研究旨在确定BCG接种对针对严重急性呼吸综合征冠状病毒2(SARS-CoV-2)疫苗的免疫反应的免疫调节作用。
在BRACE试验中,从275名未感染SARS-CoV-2的医护人员中随机抽取一部分,分为BCG接种组(BCG组)或未接种BCG组(对照组)。在接种ChAdOx1-S(牛津-阿斯利康)或BNT162b2(辉瑞-生物科技)疫苗的主要疗程(两剂)之前和之后28天采集血样。使用酶联免疫吸附测定(ELISA)和多重微珠阵列测量SARS-CoV-2特异性抗体,通过多重微珠阵列测量全血对γ射线照射的SARS-CoV-2(iSARS)刺激的细胞因子反应,并通过激活诱导标志物和细胞内细胞因子染色测定测量SARS-CoV-2特异性T细胞反应。
随机分组后(平均11个月)但在接种新冠疫苗之前,BCG组对iSARS刺激的细胞因子反应低于对照组。接种两剂ChAdOx1-S后,BCG组和对照组之间在三种细胞因子(皮肤T细胞趋化因子、肿瘤坏死因子相关凋亡诱导配体和血管内皮生长因子)的iSARS诱导细胞因子反应上存在差异。接种BNT162b2疫苗后,两组之间未发现差异。在新冠疫苗诱导的抗原特异性抗体反应、T细胞活化或T细胞细胞因子产生方面,BCG组和对照组之间也没有差异。
BCG接种导致对SARS-CoV-2的细胞因子反应广泛且持续降低。接种新冠疫苗后,这种效应被消除,且BCG接种不影响对新冠疫苗抗原的适应性免疫反应。