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Immunity in the Cervix: Interphase between Immune and Cervical Epithelial Cells
The cervix is divided into two morphologically and immunologically distinct regions, namely, (1) the microbe-laden ectocervix, which is proximal to the vagina, and (2) the “sterile” endocervix, which is distal to the uterus. The two cervical regions are bordered by the cervical transformation zone (...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6501150/ https://www.ncbi.nlm.nih.gov/pubmed/31143785 http://dx.doi.org/10.1155/2019/7693183 |
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author | Barrios De Tomasi, Jorgelina Opata, Michael Makokha Mowa, Chishimba Nathan |
author_facet | Barrios De Tomasi, Jorgelina Opata, Michael Makokha Mowa, Chishimba Nathan |
author_sort | Barrios De Tomasi, Jorgelina |
collection | PubMed |
description | The cervix is divided into two morphologically and immunologically distinct regions, namely, (1) the microbe-laden ectocervix, which is proximal to the vagina, and (2) the “sterile” endocervix, which is distal to the uterus. The two cervical regions are bordered by the cervical transformation zone (CTZ), an area of changing cells, and are predominantly composed of cervical epithelial cells. Epithelial cells are known to play a crucial role in the initiation, maintenance, and regulation of innate and adaptive response in collaboration with immune cells in several tissue types, including the cervix, and their dysfunction can lead to a spectrum of clinical syndromes. For instance, epithelial cells block progression and neutralize or kill microorganisms through multiple ways. These (ways) include mounting physical (intercellular junctions, secretion of mucus) and immune barriers (pathogen-recognition receptor-mediated pathways), which collectively and ultimately lead to the release of specific chemokines and or cytokines. The cytokines subsequently recruit subsets of immune cells appropriate to a particular immune context and response, such as dendritic cells (DCs), T, B, and natural killer (NK) cells. The immune response, as most biological processes in the female reproductive tract (FRT), is mainly regulated by estrogen and progesterone and their (immune cells) responses vary during different physiological phases of reproduction, such as menstrual cycle, pregnancy, and post menopause. The purpose of the present review is to compare the immunological profile of the mucosae and immune cells in the ecto- and endocervix and their interphase during the different phases of female reproduction. |
format | Online Article Text |
id | pubmed-6501150 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Hindawi |
record_format | MEDLINE/PubMed |
spelling | pubmed-65011502019-05-29 Immunity in the Cervix: Interphase between Immune and Cervical Epithelial Cells Barrios De Tomasi, Jorgelina Opata, Michael Makokha Mowa, Chishimba Nathan J Immunol Res Review Article The cervix is divided into two morphologically and immunologically distinct regions, namely, (1) the microbe-laden ectocervix, which is proximal to the vagina, and (2) the “sterile” endocervix, which is distal to the uterus. The two cervical regions are bordered by the cervical transformation zone (CTZ), an area of changing cells, and are predominantly composed of cervical epithelial cells. Epithelial cells are known to play a crucial role in the initiation, maintenance, and regulation of innate and adaptive response in collaboration with immune cells in several tissue types, including the cervix, and their dysfunction can lead to a spectrum of clinical syndromes. For instance, epithelial cells block progression and neutralize or kill microorganisms through multiple ways. These (ways) include mounting physical (intercellular junctions, secretion of mucus) and immune barriers (pathogen-recognition receptor-mediated pathways), which collectively and ultimately lead to the release of specific chemokines and or cytokines. The cytokines subsequently recruit subsets of immune cells appropriate to a particular immune context and response, such as dendritic cells (DCs), T, B, and natural killer (NK) cells. The immune response, as most biological processes in the female reproductive tract (FRT), is mainly regulated by estrogen and progesterone and their (immune cells) responses vary during different physiological phases of reproduction, such as menstrual cycle, pregnancy, and post menopause. The purpose of the present review is to compare the immunological profile of the mucosae and immune cells in the ecto- and endocervix and their interphase during the different phases of female reproduction. Hindawi 2019-04-17 /pmc/articles/PMC6501150/ /pubmed/31143785 http://dx.doi.org/10.1155/2019/7693183 Text en Copyright © 2019 Jorgelina Barrios De Tomasi et al. https://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Review Article Barrios De Tomasi, Jorgelina Opata, Michael Makokha Mowa, Chishimba Nathan Immunity in the Cervix: Interphase between Immune and Cervical Epithelial Cells |
title | Immunity in the Cervix: Interphase between Immune and Cervical Epithelial Cells |
title_full | Immunity in the Cervix: Interphase between Immune and Cervical Epithelial Cells |
title_fullStr | Immunity in the Cervix: Interphase between Immune and Cervical Epithelial Cells |
title_full_unstemmed | Immunity in the Cervix: Interphase between Immune and Cervical Epithelial Cells |
title_short | Immunity in the Cervix: Interphase between Immune and Cervical Epithelial Cells |
title_sort | immunity in the cervix: interphase between immune and cervical epithelial cells |
topic | Review Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6501150/ https://www.ncbi.nlm.nih.gov/pubmed/31143785 http://dx.doi.org/10.1155/2019/7693183 |
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