Division of Infectious Disease, Case Western Reserve University School of Medicine. 10900 Euclid Ave, BRB 1001, Cleveland, OH 44106-4984, USA.
Clin Immunol. 2012 Aug;144(2):172-7. doi: 10.1016/j.clim.2012.06.005. Epub 2012 Jun 24.
In this study we examine the effects of aging on antigen presentation of B cells and monocytes. We compared the antigen presentation function of peripheral blood B cells from young and old subjects using a system that specifically measures the B cell receptor (BCR)-mediated MHC-II antigen presentation. Monocytes were studied as well. Overall the mean magnitude of antigen presentation of soluble antigen and peptide was not different in older and younger subjects for both B cells and monocytes. Older subjects, however, showed increased heterogeneity of BCR-mediated antigen presentation by their B cells. The magnitude and variability of peptide presentation, which do not require uptake and processing, were the same between groups. Presentation by monocytes had similar variability between the older and younger subjects. These data suggest that poor B cell antigen processing, which results in diminished presentation in some older individuals may contribute to poor vaccine responses.
在这项研究中,我们研究了衰老对 B 细胞和单核细胞抗原呈递的影响。我们使用一种专门测量 B 细胞受体 (BCR) 介导的 MHC-II 抗原呈递的系统,比较了年轻和老年受试者外周血 B 细胞的抗原呈递功能。我们也研究了单核细胞。总的来说,对于 B 细胞和单核细胞,可溶性抗原和肽的抗原呈递的平均幅度在老年和年轻受试者之间没有差异。然而,老年受试者的 B 细胞 BCR 介导的抗原呈递异质性增加。不需要摄取和处理的肽呈递的幅度和可变性在两组之间相同。单核细胞的呈递在老年和年轻受试者之间具有相似的可变性。这些数据表明,导致某些老年人呈递减少的 B 细胞抗原加工不良可能导致疫苗反应不良。