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重度婴幼儿龋与单纯龋中淋巴细胞T(CD4)细胞表达的分析。

Analysis of lymphocyte T(CD4) cells expression on severe early childhood caries and free caries.

作者信息

Luthfi Muhammad, Rachmadi Priyawan, Oki Aqsa Sjuhada, Indrawati Retno, Sosiawan Agung, Rifa'i Muhaimin

机构信息

Department of Oral Biology.

Department of Dental Material.

出版信息

Infect Dis Rep. 2020 Jul 6;12(Suppl 1):8760. doi: 10.4081/idr.2020.8760. eCollection 2020 Jul 7.

Abstract

Early childhood caries (ECC) is still one of the many diseases found in children throughout the world. Cariogenic bacteria are a significant risk factor for ECC associated with early colonization and high levels of cariogenic microbes (, ). Lymphocyte T (CD4) cells known as helper T cells, are effector cells for mediated host immunity. Naive T cells (CD4) must be activated to initiate effector function. This activation occurs through interaction with professional antigen- presenting cells (pro-APC), especially dendritic cells that lead to intracellular pathways that regulate T cell receptor (TCR) more specifically against antigen in T cells. Lymphocyte cells from samples were collected from severe early childhood caries (S-ECC) and Free caries aged 5 to 6 years. The subjects were instructed to gargle 10 mL of sterile NaCl 1.5% solution for 30 seconds, and expectorate it into a sterile glass then analyzing T lymphocyte cell (CD4) expression using flow cytometry. Lymphocyte T (CD4) cell expression at SECC (6.2525±64482) while in free caries (8.4138±1.10397) with P-value (P=0. 000). Conclusion of lymphocyte T (CD4) cells expression at S-ECC is lower than that occurring in free caries.

摘要

幼儿龋齿(ECC)仍是全球儿童中常见的多种疾病之一。致龋菌是与早期定植和高水平致龋微生物相关的ECC的重要危险因素(,)。称为辅助性T细胞的淋巴细胞T(CD4)细胞是介导宿主免疫的效应细胞。幼稚T细胞(CD4)必须被激活才能启动效应功能。这种激活通过与专业抗原呈递细胞(pro-APC)相互作用发生,尤其是树突状细胞,其导致细胞内途径更特异性地调节T细胞受体(TCR)以对抗T细胞中的抗原。从5至6岁患有严重幼儿龋齿(S-ECC)和无龋齿的儿童中采集样本的淋巴细胞。受试者被指示用10 mL 1.5%无菌氯化钠溶液漱口30秒,然后将其吐入无菌玻璃杯中,接着使用流式细胞术分析T淋巴细胞(CD4)的表达。S-ECC组淋巴细胞T(CD4)细胞表达为(6.2525±6.4482),而无龋齿组为(8.4138±1.10397),P值(P = 0.000)。结论是S-ECC组淋巴细胞T(CD4)细胞表达低于无龋齿组。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/38a9/7447946/ae16d7c7becd/idr-12-s1-8760-g001.jpg

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