Seman Brittany G, Robinson Cory M
Department of Microbiology, Immunology, and Cell Biology, West Virginia University School of Medicine, Morgantown, WV 26506, USA.
Vaccine Development Center, West Virginia University, Morgantown, WV 26506, USA.
Pathogens. 2021 Aug 27;10(9):1091. doi: 10.3390/pathogens10091091.
Low-density granulocytes (LDGs) have been characterized as important immune cells during healthy and disease states in humans, including microbial infections, cancer, and autoimmune dysfunction. However, the classification of this cell type is similar to other immune cells (e.g., neutrophils, myeloid-derived suppressor cells) and ambiguous functional standards have rendered LDG identification and isolation daunting. Furthermore, most research involving LDGs has mainly focused on adult cells and subjects, leaving increased uncertainty surrounding younger populations, especially in vulnerable neonatal groups where LDG numbers are elevated. This review aims to bring together the current research in the field of LDG biology in the context of immunity to disease, with a focus on infection. In addition, we propose to highlight the gaps in the field that, if filled, could improve upon isolation techniques and functional characterizations for LDGs separate from neutrophils and myeloid-derived suppressor cells (MDSCs). This will not only enhance understanding of LDGs during disease processes and how they differ from other cell types but will also aid in the interpretation of comparative studies and results with the potential to inform development of novel therapeutics to improve disease states in patients.
低密度粒细胞(LDGs)已被认定为人类健康和疾病状态下的重要免疫细胞,包括微生物感染、癌症和自身免疫功能障碍。然而,这种细胞类型的分类与其他免疫细胞(如中性粒细胞、髓源性抑制细胞)相似,模糊的功能标准使得LDG的识别和分离颇具挑战性。此外,大多数关于LDGs的研究主要集中在成年细胞和受试者身上,这使得围绕年轻人群体的不确定性增加,尤其是在LDG数量升高的脆弱新生儿群体中。本综述旨在将LDG生物学领域目前在疾病免疫背景下的研究汇集起来,重点关注感染。此外,我们建议突出该领域的空白,如果这些空白得以填补,可能会改进LDGs与中性粒细胞和髓源性抑制细胞(MDSCs)分离的分离技术和功能表征。这不仅将增进对疾病过程中LDGs的理解以及它们与其他细胞类型的差异,还将有助于解释比较研究和结果,有可能为开发改善患者疾病状态的新型疗法提供信息。