Staats Richard, Rodrigues Raquel, Barros André, Bacelar-Nicolau Leonor, Aguiar Margarida, Fernandes Dina, Moreira Susana, Simões André, Silva-Santos Bruno, Rodrigues João Valença, Barbara Cristina, de Almeida António Bugalho, Moita Luis Ferreira
Departamento de Pneumologia, Hospital de Santa Maria, 1649-035, Lisbon, Portugal.
Instituto Gulbenkian de Ciência, Rua da Quinta Grande 6, 2780-156, Oeiras, Portugal.
Sleep Breath. 2018 Mar;22(1):211-221. doi: 10.1007/s11325-017-1602-6. Epub 2017 Dec 15.
Sleep related breathing disorders (SRBD) cause sleep fragmentation, intermittent hypoxia or a combination of both leading to homeostasis perturbations, including in the immune system. We investigated whether SRBD patients with or without intermittent hypoxia show substantial differences in perforin and granzyme-B positive peripheral blood lymphocytes.
A total of 87 subjects were included and distributed as follows: 24 controls (C), 19 patients with respiratory effort related arousals due to increased upper airway resistance (UAR) without hypoxic events, 24 obese patients with obstructive sleep apnea (OSA) (oOSA), and 20 without obesity (noOSA). After polysomnographic recording, we analyzed in fasting blood samples routine hematologic and biochemical parameters and the percentage of lymphocytes containing the proteins perforin and granzyme-B (GrB). Kruskal-Wallis tests and a posteriori multiple comparisons were applied for statistical analysis of results.
Perforin-positive γδ-cells revealed significant differences between groups (p = 0.017), especially between the Control group and the oOSA (p-value = 0.04); the remaining SRBD groups also showed differences from the control (C vs UAR: p = 0.08; C vs noOSA = 0.09), but they did not raise to statistical significance. There were no differences among the SRBD groups. Granzyme-B cells were decreased in SRBD patients, but the differences were not statistically significant. No additional statistical significant result was found in the other investigated lymphocyte subsets.
Obstructive sleep-disordered breathing is associated with a decrease in perforin-positive CD3γδ-T cells. Although this finding was detected in lean patients without intermittent hypoxia, the reduction was only statistically significant in obese patients with severe OSA. Because CD3γδ-T cells play an important role in the control of tumor cells, our findings are directly relevant for the study of the association of OSA and cancer.
睡眠相关呼吸障碍(SRBD)会导致睡眠片段化、间歇性缺氧或两者兼而有之,从而导致体内稳态紊乱,包括免疫系统的紊乱。我们研究了伴有或不伴有间歇性缺氧的SRBD患者在穿孔素和颗粒酶B阳性外周血淋巴细胞方面是否存在显著差异。
共纳入87名受试者,分布如下:24名对照组(C),19名因上气道阻力增加(UAR)导致呼吸努力相关觉醒且无缺氧事件的患者,24名肥胖阻塞性睡眠呼吸暂停(OSA)患者(oOSA),以及20名非肥胖患者(noOSA)。在进行多导睡眠图记录后,我们分析了空腹血样中的常规血液学和生化参数以及含有穿孔素和颗粒酶B(GrB)蛋白的淋巴细胞百分比。采用Kruskal-Wallis检验和事后多重比较对结果进行统计分析。
穿孔素阳性的γδ细胞在各组之间存在显著差异(p = 0.017),尤其是在对照组和oOSA组之间(p值 = 0.04);其余SRBD组与对照组也存在差异(C组与UAR组:p = 0.08;C组与noOSA组 = 0.09),但未达到统计学显著性。SRBD组之间没有差异。颗粒酶B细胞在SRBD患者中减少,但差异无统计学意义。在其他研究的淋巴细胞亚群中未发现其他统计学显著结果。
阻塞性睡眠呼吸障碍与穿孔素阳性CD3γδ-T细胞减少有关。尽管这一发现是在无间歇性缺氧的瘦患者中检测到的,但仅在重度OSA的肥胖患者中,这种减少具有统计学显著性。由于CD3γδ-T细胞在控制肿瘤细胞方面发挥重要作用,我们的发现与OSA和癌症关联的研究直接相关。