Immunomodulatory roles of red blood cells

被引:16
作者
Dobkin, Jane [1 ]
Mangalmurti, Nilam S. [2 ]
机构
[1] Univ Penn, Perelman Sch Med, 3450 Hamilton Walk, Philadelphia, PA 19104 USA
[2] Univ Penn, Div Pulm Allergy & Crit Care, Perelman Sch Med, Philadelphia, PA 19104 USA
关键词
coronavirus disease 2019; erythrocyte; immunity; toll-like receptors; vasculature; ACTIVATION; MORTALITY; FLUID; LUNG;
D O I
10.1097/MOH.0000000000000734
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Purpose of the Review To discuss recent advances supporting the role of red blood cells (RBCs) in the host immune response Recent Findings Over the last century, research has demonstrated that red blood cells exhibit functions beyond oxygen transport, including immune function. Recent work indicates that the nucleic acid sensing receptor, toll-like receptor 9 (TLR9), is expressed on the RBC surface and implicated in innate immune activation and red cell clearance during inflammatory states. In addition to this DNA-sensing role of RBCs, there is growing evidence that RBCs may influence immune function by inducing vascular dysfunction. RBC proteomics and metabolomics have provided additional insight into RBC immune function, with several studies indicating changes to RBC membrane structure and metabolism in response to severe acute respiratory syndrome coronavirus 2 infection. These structural RBC changes may even provide insight into the pathophysiology of the 'long-coronavirus disease 2019' phenomenon. Finally, evidence suggests that RBCs may influence host immune responses via complement regulation. Taken together, these recent findings indicate RBCs possess immune function. Further studies will be required to elucidate better how RBC immune function contributes to the heterogeneous host response during inflammatory states. The appreciation for nongas exchanging, red blood cell immune functions is rapidly growing. A better understanding of these RBC functions may provide insight into the heterogeneity observed in the host immune response to infection and inflammation.
引用
收藏
页码:306 / 309
页数:4
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