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Characterization of Tissue Immunity Defense Factors of the Lip in Primary Dentition Children with Bilateral Cleft Lip Palate.

作者信息

Ozola Laura, Pilmane Mara

机构信息

Institute of Anatomy and Anthropology, Riga Stradins University, Kronvalda Boulevard 9, LV-1010 Riga, Latvia.

Children's Clinical University Hospital, Vienības Gatve 45, LV-1004 Riga, Latvia.

出版信息

J Pers Med. 2024 Sep 11;14(9):965. doi: 10.3390/jpm14090965.


DOI:10.3390/jpm14090965
PMID:39338219
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11433168/
Abstract

BACKGROUND: Bilateral cleft lip palate is a severe congenital birth defect of the mouth and face. Immunity factors modulate immune response, inflammation, and healing; therefore, they are vital in the assessment of the immunological status of the patient. The aim of this study is to assess the distribution of Gal-10, CD-163, IL-4, IL-6, IL-10, HBD-2, HBD-3, and HBD-4 in tissue of the bilateral cleft lip palate in primary dentition children. METHODS: Five patients underwent cheiloplasty surgery, where five tissue samples of lip were obtained. Immunohistochemical staining, semi-quantitative evaluation, and non-parametric statistical analysis were used. RESULTS: A statistically significant increase in HBD-2, HBD-3, and HBD-4 was found in skin and mucosal epithelium, hair follicles, and blood vessels. A notable increase was also noted in IL-4, IL-6, and IL-10 in the mucosal epithelium and CD163 in blood vessels. The connective tissue of patients presented with a statistically significant decrease in Gal-10, IL-10, and HBD-3. Spearman's rank correlation revealed multiple significant positive and negative correlations between the factors. CONCLUSIONS: Upregulation of CD163 points to increased angiogenesis but the increase in IL-4 and IL-10 as well as the decrease in Gal-10 points to suppression of excessive inflammatory damage. Decreased connective tissue healing and excessive scarring are suggested by the decrease in HBD-3 and IL-10 and the increase in IL-6.

摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6558/11433168/6f9811207de5/jpm-14-00965-g013.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6558/11433168/349d064e27d0/jpm-14-00965-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6558/11433168/1232ba7adf72/jpm-14-00965-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6558/11433168/1a83ec2a9588/jpm-14-00965-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6558/11433168/d51fab7b6bd6/jpm-14-00965-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6558/11433168/c188bb9549f1/jpm-14-00965-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6558/11433168/9e29bb0cc2ea/jpm-14-00965-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6558/11433168/e7653205e7c9/jpm-14-00965-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6558/11433168/824e42770460/jpm-14-00965-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6558/11433168/7669550f4803/jpm-14-00965-g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6558/11433168/a7ab4e5261b1/jpm-14-00965-g010.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6558/11433168/e11ea14dc08a/jpm-14-00965-g011.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6558/11433168/56540adc9166/jpm-14-00965-g012.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6558/11433168/6f9811207de5/jpm-14-00965-g013.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6558/11433168/349d064e27d0/jpm-14-00965-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6558/11433168/1232ba7adf72/jpm-14-00965-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6558/11433168/1a83ec2a9588/jpm-14-00965-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6558/11433168/d51fab7b6bd6/jpm-14-00965-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6558/11433168/c188bb9549f1/jpm-14-00965-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6558/11433168/9e29bb0cc2ea/jpm-14-00965-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6558/11433168/e7653205e7c9/jpm-14-00965-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6558/11433168/824e42770460/jpm-14-00965-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6558/11433168/7669550f4803/jpm-14-00965-g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6558/11433168/a7ab4e5261b1/jpm-14-00965-g010.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6558/11433168/e11ea14dc08a/jpm-14-00965-g011.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6558/11433168/56540adc9166/jpm-14-00965-g012.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6558/11433168/6f9811207de5/jpm-14-00965-g013.jpg

相似文献

[1]
Characterization of Tissue Immunity Defense Factors of the Lip in Primary Dentition Children with Bilateral Cleft Lip Palate.

J Pers Med. 2024-9-11

[2]
Local Defense Factors in Cleft-Affected Palate in Children before and during Milk Dentition Age: A Pilot Study.

J Pers Med. 2023-12-25

[3]
Antimicrobial Peptides and Interleukins in Cleft Soft Palate.

Children (Basel). 2023-7-2

[4]
Characterization of Cytokines and Proliferation Marker Ki67 in Cleft Affected Lip Tissue.

Medicina (Kaunas). 2019-8-22

[5]
Barx1, growth factors and apoptosis in facial tissue of children with clefts.

Stomatologija. 2008

[6]
Immunohistochemical analysis of nestin, CD34 and TGFβ3 in facial tissue of children with complete unilateral and bilateral cleft lip and palate.

Stomatologija. 2016

[7]
Gingivosupraperiosteoplasty following Presurgical Maxillary Orthopedics Is Associated with Normal Midface Growth in Complete Unilateral and Bilateral Cleft Patients at Mixed Dentition.

Plast Reconstr Surg. 2021-12-1

[8]
Condition of oral tissues in children with congenital cleft lip and palate.

Wiad Lek. 2024

[9]
, and Expression in Cleft Affected Tissue.

Medicina (Kaunas). 2021-10-8

[10]
A Longitudinal Study of the Presence of Dental Anomalies in the Primary and Permanent Dentitions of Cleft Lip and/or Palate Patients.

Cleft Palate Craniofac J. 2017-5

引用本文的文献

[1]
Characterization of Factors Associated with Tissue Immunity, Cellular Activity and Angiogenesis in Children with Unilateral Cleft Lip and Palate Before and During Primary Dentition: A Comparative Cross-Sectional Study.

J Clin Med. 2025-7-12

本文引用的文献

[1]
Local Defense Factors in Cleft-Affected Palate in Children before and during Milk Dentition Age: A Pilot Study.

J Pers Med. 2023-12-25

[2]
Investigating Inflammatory Markers in Wound Healing: Understanding Implications and Identifying Artifacts.

ACS Pharmacol Transl Sci. 2024-1-3

[3]
Mediators of Periodontitis complementing the development of Neural Disorders.

Pak J Med Sci. 2024

[4]
Ym1 protein crystals promote type 2 immunity.

Elife. 2024-1-9

[5]
Interleukin-4 during post-exercise recovery negatively correlates with the production of phagocyte-generated oxidants.

Front Physiol. 2023-12-12

[6]
Postmenopausal women with HIV have increased tooth loss.

BMC Oral Health. 2024-1-8

[7]
Natural Killer T Cell Diversity and Immunotherapy.

Cancers (Basel). 2023-12-7

[8]
Atopic Dermatitis in the Elderly Population.

Acta Derm Venereol. 2023-12-14

[9]
Galectin-10 Expression in Placentas of Women with Gestational Diabetes.

Curr Issues Mol Biol. 2023-11-2

[10]
Osteoprotective effect by interleukin-4 (IL-4) on lipoprotein-induced periodontitis.

Cytokine. 2023-12

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