Liu Peng, Sang Zunmeng, Liu Kangkang, Zhang Minghao, Niu Yuanjie
Medical College of Nankai University, Tianjin, China; The Second Hospital of Tianjin Medical University, Tianjin, China.
WeiFang People's Hospital, Shandong Second Medical University, China.
Vaccine. 2025 Jul 12;62:127493. doi: 10.1016/j.vaccine.2025.127493.
Heat shock proteins (HSPs), particularly the 70 kDa heat shock protein (Hsp70), are crucial for cellular functions such as protein folding, refolding, and regulation of protein activity. Mycobacterium tuberculosis Hsp70 (DnaK) has attracted attention for its potential as a vaccine adjuvant due to its immunostimulatory properties. This review covers the following topics: an overview of cancer vaccines, introduction to Hsp70, research on DnaK in dendritic cells (DCs), DnaK's role in the tumor immune microenvironment, its safety profile, and insights for vaccine design. DnaK consists of an N-terminal nucleotide-binding domain and a C-terminal peptide substrate-binding domain, connected by a flexible linker. It has been shown to enhance DC maturation, facilitate antigen presentation, and activate T cells. DnaK stimulates Toll-like receptor 4 (TLR4) and CD40 on antigen-presenting cells, promoting both maturation and the secretion of pro-inflammatory cytokines. Additionally, DnaK can enhance antigen presentation through CD91 and DC-SIGN receptors on DCs. However, the immunosuppressive environment within tumors poses challenges to DC activation. DnaK may influence this tumor microenvironment by interacting with macrophages, scavenger receptors, and natural killer (NK) cells, potentially overcoming some of these barriers. Compared to traditional adjuvants like lipopolysaccharide (LPS), DnaK has a favorable safety profile. Its conserved structure and low toxicity make it a promising candidate for vaccine development. Insights from studies on DnaK suggest strategies to improve vaccine efficacy, such as combining it with TLR agonists and leveraging its interaction with DC-SIGN to promote targeted activation of DCs. In conclusion, DnaK shows significant potential as an adjuvant in vaccine design. Understanding its structural and functional roles, as well as its effects on the immune microenvironment, provides valuable insights for the development of more effective and targeted vaccines against infectious diseases and cancer. Further research is needed to elucidate its specific mechanisms of action and optimize its use in vaccine formulations.
热休克蛋白(HSPs),尤其是70 kDa热休克蛋白(Hsp70),对于蛋白质折叠、重折叠以及蛋白质活性调节等细胞功能至关重要。结核分枝杆菌Hsp70(DnaK)因其免疫刺激特性作为疫苗佐剂的潜力而备受关注。本综述涵盖以下主题:癌症疫苗概述、Hsp70介绍、树突状细胞(DCs)中DnaK的研究、DnaK在肿瘤免疫微环境中的作用、其安全性概况以及疫苗设计见解。DnaK由一个N端核苷酸结合结构域和一个C端肽底物结合结构域组成,通过一个柔性接头相连。已证明它可增强DC成熟、促进抗原呈递并激活T细胞。DnaK刺激抗原呈递细胞上的Toll样受体4(TLR4)和CD40,促进成熟以及促炎细胞因子的分泌。此外,DnaK可通过DC上的CD91和DC-SIGN受体增强抗原呈递。然而,肿瘤内的免疫抑制环境对DC激活构成挑战。DnaK可能通过与巨噬细胞、清道夫受体和自然杀伤(NK)细胞相互作用来影响这种肿瘤微环境,有可能克服其中一些障碍。与脂多糖(LPS)等传统佐剂相比,DnaK具有良好的安全性。其保守结构和低毒性使其成为疫苗开发的有希望的候选者。对DnaK的研究见解提出了提高疫苗效力的策略,例如将其与TLR激动剂结合,并利用其与DC-SIGN的相互作用促进DC的靶向激活。总之,DnaK在疫苗设计中显示出作为佐剂的巨大潜力。了解其结构和功能作用以及对免疫微环境的影响,为开发针对传染病和癌症的更有效、更具针对性的疫苗提供了有价值的见解。需要进一步研究以阐明其具体作用机制并优化其在疫苗制剂中的应用。