Kalimuddin Shirin, Tham Christine Y L, Chan Yvonne F Z, Hang Shou Kit, Kunasegaran Kamini, Chia Adeline, Chan Candice Y Y, Ng Dorothy H L, Sim Jean X Y, Tan Hwee-Cheng, Syenina Ayesa, Ngoh An Qi, Hamis Noor Zayanah, Chew Valerie, Leong Yan Shan, Yee Jia Xin, Low Jenny G, Chan Kuan Rong, Ong Eugenia Z, Bertoletti Antonio, Ooi Eng Eong
Department of Infectious Diseases, Singapore General Hospital, Singapore, Singapore.
Program in Emerging Infectious Diseases, Duke-NUS Medical School, Singapore, Singapore.
Nat Microbiol. 2025 Feb;10(2):374-387. doi: 10.1038/s41564-024-01903-7. Epub 2025 Jan 10.
T cells have been identified as correlates of protection in viral infections. However, the level of vaccine-induced T cells needed and the extent to which they alone can control acute viral infection in humans remain uncertain. Here we conducted a double-blind, randomized controlled trial involving vaccination and challenge in 33 adult human volunteers, using the live-attenuated yellow fever (YF17D) and chimeric Japanese encephalitis-YF17D (JE/YF17D) vaccines. Both Orthoflavivirus vaccines share T cell epitopes but have different neutralizing antibody epitopes. The primary objective was to assess the extent to which vaccine-induced T cell responses, independent of neutralizing antibodies, were able to reduce post-challenge viral RNAaemia levels. Secondary objectives included an assessment of surrogate measures of viral control, including post-challenge antibody titres and symptomatic outcomes. YF17D vaccinees had reduced levels of JE/YF17D challenge viraemia, compared with those without previous YF17D vaccination (mean log(area under the curve genome copies per ml): 2.23 versus 3.22; P = 0.039). Concomitantly, YF17D vaccinees had lower post-JE/YF17D challenge antibody titres that reduced JE virus plaque number by 50%, or PRNT (mean log(PRNT titre): 1.87 versus 2.5; P < 0.0001) and symptomatic rates (6% (n = 1/16) versus 53% (n = 9/17), P = 0.007). There were no unexpected safety events. Importantly, after challenge infection, several vaccinees had undetectable viraemia and no seroconversion, even in the absence of neutralizing antibodies. Indeed, high vaccine-induced T cell responses, specifically against the capsid protein, were associated with a level of viral control conventionally interpreted as sterilizing immunity. Our findings reveal the importance of T cells in controlling acute viral infection and suggests a potential correlate of protection against orthoflaviviral infections. ClinicalTrials.gov registration: NCT05568953 .
T细胞已被确定为病毒感染中保护作用的相关因素。然而,所需的疫苗诱导T细胞水平以及它们单独控制人类急性病毒感染的程度仍不确定。在此,我们对33名成年人类志愿者进行了一项双盲、随机对照试验,涉及使用减毒活黄热病疫苗(YF17D)和嵌合日本脑炎-YF17D疫苗(JE/YF17D)进行接种和攻毒。这两种黄病毒科疫苗都有共同的T细胞表位,但具有不同的中和抗体表位。主要目的是评估疫苗诱导的T细胞反应(独立于中和抗体)能够降低攻毒后病毒RNA血症水平的程度。次要目的包括评估病毒控制的替代指标,包括攻毒后抗体滴度和症状结果。与未接种过YF17D疫苗的人相比,YF17D疫苗接种者的JE/YF17D攻毒病毒血症水平降低(每毫升曲线下面积基因组拷贝数的对数平均值:2.23对3.22;P = 0.039)。同时,YF17D疫苗接种者攻毒后JE/YF17D的抗体滴度较低,使日本脑炎病毒蚀斑数量减少50%,或使血浆中和试验(PRNT)滴度降低(对数平均值:1.87对2.5;P < 0.0001),且症状发生率较低(6%(n = 1/16)对53%(n = 9/17),P = 0.007)。未发生意外安全事件。重要的是,在攻毒感染后,即使没有中和抗体,一些疫苗接种者的病毒血症也无法检测到且没有血清转化。实际上,疫苗诱导的针对衣壳蛋白的高T细胞反应与通常解释为无菌免疫的病毒控制水平相关。我们的研究结果揭示了T细胞在控制急性病毒感染中的重要性,并提示了针对黄病毒科感染的潜在保护相关因素。ClinicalTrials.gov注册号:NCT05568953 。