Esposito Susanna, Garziano Micaela, Rainone Veronica, Trabattoni Daria, Biasin Mara, Senatore Laura, Marchisio Paola, Rossi Marta, Principi Nicola, Clerici Mario
Pediatric Highly Intensive Care Unit, Department of Pathophysiology and Transplantation, Università degli Studi di Milano, Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico, Via Commenda 9, 20122, Milan, Italy.
Immunology Unit, Department of Biomedical and Clinical Sciences, Luigi Sacco Hospital, Università degli Studi di Milano, Milan, Italy.
J Transl Med. 2015 Sep 3;13:288. doi: 10.1186/s12967-015-0649-z.
Several attempts to improve immune function in young children have been made and encouraging results have been collected with pidotimod (PDT), a synthetic dipeptide molecule that seems to have immunomodulatory activity on both innate and adaptive responses. Until now, the effects of PDT on the immune system have only been studied in vivo after long-term administration to evaluate whether its immunomodulatory activity might prevent the development of infections. This study was planned to evaluate the immunomodulatory activity of PDT administered together with standard antibiotic therapy in children hospitalized for community-acquired pneumonia (CAP).
A total of 20 children hospitalized for community-acquired pneumonia (CAP) were randomized at a 1:1 ratio to receive either standard antibiotics plus pidotimod (PDT) or standard antibiotics alone to evaluate the immunomodulatory activity of PDT. Blood samples for the evaluation of immunological parameters were drawn at the time of recruitment (T0) (i.e., before therapy administration), at T3 and T5 (i.e., 3 and 5 days after the initiation of therapy) as well as at T21 (i.e., 7 days after the therapy ended).
Following pneumococcal polysaccharide stimulation, the percentage of dendritic cells (DCs) expressing activation and costimulatory molecules was significantly higher in children receiving PDT plus antibiotics than in the controls. A significant increase in tumor necrosis factor-α and/or interleukin-12 secretion and expression of toll like receptor 2 was observed in PDT-treated children compared with controls; this was followed by an increased release of proinflammatory cytokines by monocytes. In the PDT-treated group, mRNA expression of antimicrobial peptides and genes involved in the inflammatory response were also augmented in comparison with the controls.
These results demonstrate, for the first time, that PDT administered together with standard antibiotics is associated with a favorable persistent immunomodulatory effect in children with CAP.
人们已多次尝试改善幼儿的免疫功能,并使用匹多莫德(PDT)取得了令人鼓舞的结果。匹多莫德是一种合成二肽分子,似乎对先天性和适应性免疫反应均具有免疫调节活性。到目前为止,仅在长期给药后对PDT在体内的免疫系统作用进行了研究,以评估其免疫调节活性是否可以预防感染的发生。本研究旨在评估在因社区获得性肺炎(CAP)住院的儿童中,将PDT与标准抗生素疗法联合使用时的免疫调节活性。
总共20名因社区获得性肺炎(CAP)住院的儿童按1:1比例随机分组,分别接受标准抗生素加匹多莫德(PDT)或仅接受标准抗生素治疗,以评估PDT的免疫调节活性。在入组时(T0)(即治疗给药前)、T3和T5(即治疗开始后3天和5天)以及T21(即治疗结束后7天)采集血样,用于评估免疫参数。
在接受肺炎球菌多糖刺激后,接受PDT加抗生素治疗的儿童中,表达激活分子和共刺激分子的树突状细胞(DC)百分比显著高于对照组。与对照组相比,接受PDT治疗的儿童中肿瘤坏死因子-α和/或白细胞介素-12的分泌以及Toll样受体2的表达显著增加;随后单核细胞释放的促炎细胞因子增加。在PDT治疗组中,与对照组相比,抗菌肽和参与炎症反应的基因的mRNA表达也有所增加。
这些结果首次证明,在患有CAP的儿童中,将PDT与标准抗生素联合使用可产生持续良好的免疫调节作用。