Center for Immunology and Inflammation, The Feinstein Institute for Medical Research, Manhasset, NY 11030, USA.
Center for Immunology and Inflammation, The Feinstein Institute for Medical Research, Manhasset, NY 11030, USA; Department of Surgery, Hofstra Northwell School of Medicine, Manhasset, NY 11030, USA.
Biochim Biophys Acta Mol Basis Dis. 2017 Oct;1863(10 Pt B):2584-2593. doi: 10.1016/j.bbadis.2017.01.014. Epub 2017 Jan 20.
Sepsis is a leading cause of mortality in intensive care units, and is more common in the geriatric population. The control of hyperinflammation has been suggested as a therapeutic approach in sepsis, but to date clinical trials utilizing this strategy have not lead to an effective treatment. In addition to hyperinflammation, patients with sepsis often experience a state of immunosuppression, which serves as an important determinant for increased morbidity and mortality. We previously used aged animals to demonstrate the effectiveness of combined treatment with human ghrelin (Ghr) and human growth hormone (GH) in improving organ injury and survival in septic animals. Here, we hypothesized that combined treatment with Ghr and GH could improve immune function in septic aged animals. Male 24-month-old rats were subjected to cecal ligation and puncture (CLP) for sepsis induction. Human Ghr (80nmol/kg BW) plus GH (50μg/kg BW) or vehicle (normal saline) was administrated subcutaneously at 5h after CLP. The ex vivo production of TNF-α, IL-6 and IL-10 to LPS-stimulation, as well as TNF-α, IL-6, IL-10 and IFN-γ production to anti-CD3/anti-CD28 antibody-stimulation, in splenocytes isolated 20h after CLP, was significantly decreased compared to production of these cytokines in splenocytes from sham animals. The production of cytokines from splenocytes isolated from septic animals that received the combined treatment, however, was significantly higher than from those isolated from vehicle-treated septic animals. Combined treatment prevented the loss of splenic CD4 and CD8 T cells in septic aged rats, and reduced lymphocyte apoptosis. Combined treatment also inhibited an increase in the regulatory T cell (T) population and expression of the immune co-inhibitory molecule PD-1 in the spleens of septic aged rats. In contrast, expression of HLA-DR was increased after combined treatment with Ghr and GH. Based on these findings, we conclude that co-administration of Ghr and GH is a promising therapeutic tool for reversing immunosuppression caused by sepsis in the geriatric population. This article is part of a Special Issue entitled: Immune and Metabolic Alterations in Trauma and Sepsis edited by Dr. Raghavan Raju.
脓毒症是重症监护病房死亡的主要原因,在老年人群中更为常见。过度炎症的控制已被认为是脓毒症的一种治疗方法,但迄今为止,利用这一策略的临床试验并未导致有效的治疗方法。除了过度炎症,脓毒症患者通常还会经历免疫抑制状态,这是增加发病率和死亡率的重要决定因素。我们之前使用老年动物证明了联合使用人 ghrelin (Ghr) 和人生长激素 (GH) 治疗可以改善脓毒症动物的器官损伤和存活率。在这里,我们假设联合使用 Ghr 和 GH 可以改善脓毒症老年动物的免疫功能。雄性 24 月龄大鼠接受盲肠结扎和穿刺 (CLP) 诱导脓毒症。CLP 后 5 小时,皮下给予人 Ghr(80nmol/kg BW)加 GH(50μg/kg BW)或载体 (生理盐水)。CLP 后 20 小时分离的脾细胞对 LPS 刺激的 TNF-α、IL-6 和 IL-10 的体外产生以及对抗 CD3/抗 CD28 抗体刺激的 TNF-α、IL-6、IL-10 和 IFN-γ的产生与假手术动物的脾细胞相比明显减少。然而,从接受联合治疗的脓毒症动物分离的脾细胞产生的细胞因子明显高于从载体处理的脓毒症动物分离的脾细胞。联合治疗防止了脓毒症老年大鼠脾脏 CD4 和 CD8 T 细胞的丢失,并减少了淋巴细胞凋亡。联合治疗还抑制了脓毒症老年大鼠脾脏调节性 T 细胞 (T) 群和免疫抑制分子 PD-1 表达的增加。相反,联合给予 Ghr 和 GH 后 HLA-DR 的表达增加。基于这些发现,我们得出结论,联合给予 Ghr 和 GH 是逆转老年人群脓毒症引起的免疫抑制的一种很有前途的治疗工具。本文是由 Raghavan Raju 博士编辑的特刊“创伤和脓毒症中的免疫和代谢改变”的一部分。