Hoffmann Peter R, Kench Jennifer A, Vondracek Andrea, Kruk Ellen, Daleke David L, Jordan Michael, Marrack Philippa, Henson Peter M, Fadok Valerie A
Department of Pediatrics, Program in Cell Biology, National Jewish Medical and Research Center, Denver, CO 80206, USA.
J Immunol. 2005 Feb 1;174(3):1393-404. doi: 10.4049/jimmunol.174.3.1393.
Phosphatidylserine (PS) on apoptotic cells promotes their uptake and induces anti-inflammatory responses in phagocytes, including TGF-beta release. Little is known regarding the effects of PS on adaptive immune responses. We therefore investigated the effects of PS-containing liposomes on immune responses in mice in vivo. PS liposomes specifically inhibited responses to Ags as determined by decreased draining lymph node tissue mass, with reduced numbers of total leukocytes and Ag-specific CD4(+) T cells. There was also a decrease in formation and size of germinal centers in spleen and lymph nodes, accompanied by decreased levels of Ag-specific IgG in blood. Many of these effects were mimicked by an agonistic Ab-specific for the PS receptor. TGF-beta appears to play a critical role in this inhibition, as the inhibitory effects of PS were reversed by in vivo administration of anti-TGF-beta Ab. PS-containing liposomes did not appear to directly inhibit dendritic cell maturation in vitro in response to a variety of stimuli, nor did it prevent their migration to regional lymph nodes in vivo, suggesting that the inhibitory effects may have resulted from complicated interactions between tissue cells and dendritic cells, subsequently inhibiting their ability to productively activate T lymphocytes.
凋亡细胞上的磷脂酰丝氨酸(PS)可促进其被摄取,并在吞噬细胞中诱导抗炎反应,包括释放转化生长因子-β(TGF-β)。关于PS对适应性免疫反应的影响,人们了解甚少。因此,我们研究了含PS脂质体对小鼠体内免疫反应的影响。PS脂质体通过减少引流淋巴结组织质量、降低总白细胞和抗原特异性CD4(+) T细胞数量,特异性抑制对抗原的反应。脾脏和淋巴结中生发中心的形成和大小也有所减少,同时血液中抗原特异性IgG水平降低。许多这些效应可被PS受体特异性激动性抗体模拟。TGF-β似乎在这种抑制中起关键作用,因为体内给予抗TGF-β抗体可逆转PS的抑制作用。含PS脂质体在体外似乎不会直接抑制树突状细胞对多种刺激的成熟,也不会阻止其在体内迁移至局部淋巴结,这表明抑制作用可能是由于组织细胞与树突状细胞之间复杂的相互作用,随后抑制了它们有效激活T淋巴细胞的能力。
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