Joseph John
Center for Nanomedicine, Department of Anesthesiology, Perioperative and Pain Medicine, Brigham and Women's Hospital, Harvard Medical School, Boston, MA 02115, USA.
Vaccines (Basel). 2022 Nov 15;10(11):1932. doi: 10.3390/vaccines10111932.
Although parental vaccines offer long-term protection against homologous strains, they rely exclusively on adaptive immune memory to produce neutralizing antibodies that are ineffective against emerging viral variants. Growing evidence highlights the multifaceted functions of trained immunity to elicit a rapid and enhanced innate response against unrelated stimuli or pathogens to subsequent triggers. This review discusses the protective role of trained immunity against respiratory pathogens and the experimental models essential for evaluating novel inducers of trained immunity. The review further elaborates on the potential of trained immunity to leverage protection against pathogens via the molecular patterns of antigens by pathogen recognition receptors (PPRs) on innate immune cells. The review also focuses on integrating trained innate memory with adaptive memory to shape next-generation vaccines by coupling each one's unique characteristics.
尽管亲本疫苗能提供针对同源毒株的长期保护,但它们完全依赖适应性免疫记忆来产生中和抗体,而这些抗体对新出现的病毒变体无效。越来越多的证据凸显了训练有素的免疫的多方面功能,即引发针对后续触发因素的无关刺激或病原体的快速且增强的先天反应。本综述讨论了训练有素的免疫对呼吸道病原体的保护作用以及评估训练有素的免疫新诱导剂所必需的实验模型。该综述进一步阐述了训练有素的免疫通过先天免疫细胞上的病原体识别受体(PPR)利用抗原的分子模式来增强对病原体的保护的潜力。该综述还着重于通过结合各自独特的特征,将训练有素的先天记忆与适应性记忆整合起来,以塑造下一代疫苗。