Is it possible to use the Toll-like receptors as biomarkers for neonatal sepsis? Review of the recent literature

Q4 Medicine Revista Romana de Pediatrie Pub Date : 2022-09-30 DOI:10.37897/rjp.2022.3.1
Irina Melinda Baizat, Corina Gabriela Zaharie, M. Hăşmăşanu, M. Matyas, L. Procopciuc
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Abstract

Background. Sepsis continues to be one of the main death causes in the neonate population. The toll-like receptors are molecules that express in the plasma or endosomal membrane and recognize endosomal or microorganism components. While aiming at the identification of new neonatal sepsis biomarkers, the toll-like receptors (TLR) have been considered that some of them overexpress in contact with the bacterial components. Methods. Research in the PubMed database has been made by the following criteria: Inclusion criteria (PubMed database, Period 2005-2022, English & Humans, generated 29, Meta-Analysis - 0, Review - 6, Systematic Review - 0), Exclusion criteria (Studies on animal models, Articles with merely didactical content, Articles regarding only one of the words researched either only neonatal sepsis or TLR in another context than together, Articles that are not directly connected with the topic). Based on the above-mentioned criteria 13 articles were consulted, of which 7 articles included in vivo studies, 6 with in vitro studies. Conclusions. The data of the present review and the current diagnostic method point at the fact that TLRs increase in the conditions of the presence of the inflammatory syndrome. Their dosing during in the neonatal sepsis is possible, but the non-specific overexpression is not a diagnostic.
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有可能使用Toll样受体作为新生儿败血症的生物标志物吗?近期文献综述
背景败血症仍然是新生儿死亡的主要原因之一。toll样受体是在血浆或内体膜中表达并识别内体或微生物成分的分子。在旨在鉴定新的新生儿败血症生物标志物的同时,toll样受体(TLR)被认为其中一些在与细菌成分接触时过度表达。方法。PubMed数据库中的研究是根据以下标准进行的:纳入标准(PubMed数据库,2005-2022年,英语与人类,生成29,荟萃分析-0,综述-6,系统综述-0),排除标准(关于动物模型的研究,仅具有教学内容的文章,仅关于其中一个词的文章,或者仅研究新生儿败血症或TLR,而不是在另一个上下文中一起研究,与主题没有直接联系的文章)。根据上述标准,查阅了13篇文章,其中7篇包含体内研究,6篇包含体外研究。结论。本综述的数据和当前的诊断方法指出,TLRs在炎症综合征存在的条件下增加。在新生儿败血症期间给药是可能的,但非特异性过表达不能诊断。
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0.10
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0.00%
发文量
15
审稿时长
4 weeks
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