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免疫标志物和疫苗诱导免疫应答的保护相关性。

Immune markers and correlates of protection for vaccine induced immune responses.

机构信息

Adaptive Immunology and Parasitology, National Veterinary Institute, Technical University of Denmark, Bϋlowsvej 27, 1870 Frederiksberg C, Denmark.

出版信息

Vaccine. 2012 Jul 13;30(33):4907-20. doi: 10.1016/j.vaccine.2012.05.049. Epub 2012 May 30.

Abstract

Vaccines have been a major innovation in the history of mankind and still have the potential to address the challenges posed by chronic intracellular infections including tuberculosis, HIV and malaria which are leading causes of high morbidity and mortality across the world. Markers of an appropriate humoral response currently remain the best validated correlates of protective immunity after vaccination. Despite advancements in the field of immunology over the past few decades currently there are, however, no sufficiently validated immune correlates of vaccine induced protection against chronic infections in neither human nor veterinary medicine. Technological and conceptual advancements within cell-mediated immunology have led to a number of new immunological read-outs with the potential to emerge as correlates of vaccine induced protection. For T(H)1 type responses, antigen-specific production of interferon-gamma (IFN-γ) has been promoted as a quantitative marker of protective cell-mediated immune responses over the past couple of decades. More recently, however, evidence from several infections has pointed towards the quality of the immune response, measured through increased levels of antigen-specific polyfunctional T cells capable of producing a triad of relevant cytokines, as a better correlate of sustained protective immunity against this type of infections. Also the possibilities to measure antigen-specific cytotoxic T cells (CTL) during infection or in response to vaccination, through recombinant major histocompatibility complex (MHC) class I tetramers loaded with relevant peptides, has opened a new vista to include CTL responses in the evaluation of protective immune responses. Here, we review different immune markers and new candidates for correlates of a protective vaccine induced immune response against chronic infections and how successful they have been in defining the protective immunity in human and veterinary medicine.

摘要

疫苗是人类历史上的一项重大创新,仍然有潜力应对慢性细胞内感染带来的挑战,包括结核病、艾滋病病毒和疟疾,这些疾病是全世界高发病率和高死亡率的主要原因。体液免疫反应的标志物仍然是疫苗接种后保护性免疫的最佳验证相关性。尽管在过去几十年中免疫学领域取得了进展,但目前在人类和兽医医学中,针对慢性感染,既没有足够验证的免疫相关性,也没有疫苗诱导保护的免疫相关性。细胞介导免疫领域的技术和概念进步,已经产生了一些新的免疫检测方法,有可能成为疫苗诱导保护的相关性。对于 T(H)1 型反应,抗原特异性产生干扰素-γ(IFN-γ)在过去几十年中一直被作为保护性细胞介导免疫反应的定量标志物。然而,最近来自几种感染的证据表明,免疫反应的质量,通过增加能够产生三联相关细胞因子的抗原特异性多功能 T 细胞的水平来衡量,是针对这种类型感染的持续保护性免疫的更好相关性。此外,通过用相关肽装载重组主要组织相容性复合物(MHC)I 四聚体,在感染期间或接种疫苗后测量抗原特异性细胞毒性 T 细胞(CTL)的可能性,为包括 CTL 反应在内的保护性免疫反应的评估开辟了新的前景。在这里,我们回顾了不同的免疫标志物和新的候选物,以作为针对慢性感染的保护性疫苗诱导免疫反应的相关性,并评估它们在人类和兽医医学中定义保护性免疫的成功程度。

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