A brief review of recent data on some cytokine expressions at the materno-foetal interface which might challenge the classical Th1/Th2 dichotomy

Focussing attention on cytokines at the materno-foetal interface represents one of the major advances made in the field. This owes much to the visionary views of Tom Wegmann, and to the changes brought about in the field by immunotrophism and Th1/Th2 paradigms. We review these briefly and also point...

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Veröffentlicht in:Journal of reproductive immunology 2002, Vol.53 (1), p.241-256
Hauptverfasser: Chaouat, Gérard, Zourbas, Sandrine, Ostojic, Sasa, Lappree-Delage, Geneviève, Dubanchet, Sylvie, Ledee, Natalie, Martal, Jacques
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container_issue 1
container_start_page 241
container_title Journal of reproductive immunology
container_volume 53
creator Chaouat, Gérard
Zourbas, Sandrine
Ostojic, Sasa
Lappree-Delage, Geneviève
Dubanchet, Sylvie
Ledee, Natalie
Martal, Jacques
description Focussing attention on cytokines at the materno-foetal interface represents one of the major advances made in the field. This owes much to the visionary views of Tom Wegmann, and to the changes brought about in the field by immunotrophism and Th1/Th2 paradigms. We review these briefly and also point out some emerging problems. However, a certain number of newly discovered cytokines do not fit into the classical Th1/Th2 dichotomy. Yet, by their capacity to activate or downregulate NK cells, by their action on adhesion molecules, and by their regulatory effects on the vascularisation process, they are of possible interest within the materno-foetal relationship. Therefore, as a first step, we have undertaken a systematic study of the expression of IL-11, IL-12, IL-13, IL-15, IL-16, IL-17 and IL-18 in the uterus, the peri-implantation embryo, and later on decidual and placental tissues throughout pregnancy. These cytokines were detected in every case, with, in each case, a precise localisation, which will be detailed, and which indeed suggests important regulatory functions, especially during implantation. In some cases, as will be shown in the peri-implantation uterus, those cells are perfectly expressed by uterine GMG-NK-like cells. Comparative ELISAs and quantitative RT–PCR have been or are being conducted, but already the expression patterns that are observed, and the very precise window of appearance that is observed for some of the GMG NK-like cells, either around or in the implanting embryo, as well as the complexity of the respective distributions, strongly suggest that, as useful as it certainly was for a while, the Th1/Th2 paradigm must now be considered as an over-simplification. Rather, the existing data point to sequential windows and are suggestive of a system where an extreme complexity is allied to very precise timing and tuning. They also suggest that the materno-foetal relationship is not simply maternal tolerance of a foreign tissue, but a series of intricate mutual cytokine interactions governing selective immune regulation and also control of the adhesion and vascularisation processes during this dialogue.
doi_str_mv 10.1016/S0165-0378(01)00119-X
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This owes much to the visionary views of Tom Wegmann, and to the changes brought about in the field by immunotrophism and Th1/Th2 paradigms. We review these briefly and also point out some emerging problems. However, a certain number of newly discovered cytokines do not fit into the classical Th1/Th2 dichotomy. Yet, by their capacity to activate or downregulate NK cells, by their action on adhesion molecules, and by their regulatory effects on the vascularisation process, they are of possible interest within the materno-foetal relationship. Therefore, as a first step, we have undertaken a systematic study of the expression of IL-11, IL-12, IL-13, IL-15, IL-16, IL-17 and IL-18 in the uterus, the peri-implantation embryo, and later on decidual and placental tissues throughout pregnancy. These cytokines were detected in every case, with, in each case, a precise localisation, which will be detailed, and which indeed suggests important regulatory functions, especially during implantation. In some cases, as will be shown in the peri-implantation uterus, those cells are perfectly expressed by uterine GMG-NK-like cells. Comparative ELISAs and quantitative RT–PCR have been or are being conducted, but already the expression patterns that are observed, and the very precise window of appearance that is observed for some of the GMG NK-like cells, either around or in the implanting embryo, as well as the complexity of the respective distributions, strongly suggest that, as useful as it certainly was for a while, the Th1/Th2 paradigm must now be considered as an over-simplification. Rather, the existing data point to sequential windows and are suggestive of a system where an extreme complexity is allied to very precise timing and tuning. 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This owes much to the visionary views of Tom Wegmann, and to the changes brought about in the field by immunotrophism and Th1/Th2 paradigms. We review these briefly and also point out some emerging problems. However, a certain number of newly discovered cytokines do not fit into the classical Th1/Th2 dichotomy. Yet, by their capacity to activate or downregulate NK cells, by their action on adhesion molecules, and by their regulatory effects on the vascularisation process, they are of possible interest within the materno-foetal relationship. Therefore, as a first step, we have undertaken a systematic study of the expression of IL-11, IL-12, IL-13, IL-15, IL-16, IL-17 and IL-18 in the uterus, the peri-implantation embryo, and later on decidual and placental tissues throughout pregnancy. These cytokines were detected in every case, with, in each case, a precise localisation, which will be detailed, and which indeed suggests important regulatory functions, especially during implantation. 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Psychology</subject><subject>Gene Expression</subject><subject>Histocompatibility Antigens Class I</subject><subject>Humans</subject><subject>Inflammation - genetics</subject><subject>Inflammation - immunology</subject><subject>Killer Cells, Natural - immunology</subject><subject>Life Sciences</subject><subject>Maternal-Fetal Exchange - genetics</subject><subject>Maternal-Fetal Exchange - immunology</subject><subject>Materno-foetal interface</subject><subject>Mice</subject><subject>Mother. Fetoplacental unit. Mammary gland. Milk</subject><subject>Placenta - immunology</subject><subject>Pregnancy</subject><subject>Pregnancy. Parturition. Lactation</subject><subject>Th1 Cells - immunology</subject><subject>Th1/Th2 dichotomy</subject><subject>Th2 Cells - immunology</subject><subject>Uterus - immunology</subject><subject>Vertebrates: reproduction</subject><issn>0165-0378</issn><issn>1872-7603</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2002</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkc1u1DAQgC0EotvCI4B8AdFD2nGcxMmpWlXQVlqJQxepN8txJo0hsRfb27Jv0UfG-6P22IP_Rt-MR_MR8onBGQNWnd-mrcyAi_obsFMAxprs7g2ZsVrkmaiAvyWzZ-SIHIfwO0ECGvaeHDEmODQ5zMjTnLbeYE89Phh8pG5702gj7VRU1Fka3IRUb6L7YyxS_LfyGIJxNlAVaRyQTiqity7rHUY1UmPTs1ca6eNg9EAncz9Eqgc1jmjvcZeiR5Vq6EQvB3a-HHLaJdRFN20-kHe9GgN-PJwn5NeP78vL62zx8-rmcr7IdFFWMROizqHseCt4jqxqeaE0qKYUjW416E5g3vdthSIFIcFFr0tULeq2aIqmVfyEnO7rpsbkyptJ-Y10ysjr-UJuY5BXogQGDyyxX_fsyru_awxRTiZoHEdl0a2DFIxzLtJ6DWQ1a5paFAks96D2LgSP_XMLDOTWr9z5lVt5Epjc-ZV3Ke_z4YN1O2H3knUQmoAvB0CFNN_eK6tNeOF4kYOoy8Rd7DlMM07mvQzaoNXYmeQ_ys6ZV1r5Dz1-w0E</recordid><startdate>2002</startdate><enddate>2002</enddate><creator>Chaouat, Gérard</creator><creator>Zourbas, Sandrine</creator><creator>Ostojic, Sasa</creator><creator>Lappree-Delage, Geneviève</creator><creator>Dubanchet, Sylvie</creator><creator>Ledee, Natalie</creator><creator>Martal, Jacques</creator><general>Elsevier Ireland Ltd</general><general>Elsevier Science</general><general>Elsevier</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7T5</scope><scope>H94</scope><scope>7X8</scope><scope>1XC</scope></search><sort><creationdate>2002</creationdate><title>A brief review of recent data on some cytokine expressions at the materno-foetal interface which might challenge the classical Th1/Th2 dichotomy</title><author>Chaouat, Gérard ; Zourbas, Sandrine ; Ostojic, Sasa ; Lappree-Delage, Geneviève ; Dubanchet, Sylvie ; Ledee, Natalie ; Martal, Jacques</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c456t-778205d3b732e16b34ac0a9579cbc0cd7e2ffb6e70a907784fc5eabecb4949ba3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2002</creationdate><topic>Animals</topic><topic>Biological and medical sciences</topic><topic>Blastocyst - immunology</topic><topic>Cytokine expressions</topic><topic>Cytokines - genetics</topic><topic>Decidua - immunology</topic><topic>Female</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Gene Expression</topic><topic>Histocompatibility Antigens Class I</topic><topic>Humans</topic><topic>Inflammation - genetics</topic><topic>Inflammation - immunology</topic><topic>Killer Cells, Natural - immunology</topic><topic>Life Sciences</topic><topic>Maternal-Fetal Exchange - genetics</topic><topic>Maternal-Fetal Exchange - immunology</topic><topic>Materno-foetal interface</topic><topic>Mice</topic><topic>Mother. Fetoplacental unit. Mammary gland. Milk</topic><topic>Placenta - immunology</topic><topic>Pregnancy</topic><topic>Pregnancy. Parturition. 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In some cases, as will be shown in the peri-implantation uterus, those cells are perfectly expressed by uterine GMG-NK-like cells. Comparative ELISAs and quantitative RT–PCR have been or are being conducted, but already the expression patterns that are observed, and the very precise window of appearance that is observed for some of the GMG NK-like cells, either around or in the implanting embryo, as well as the complexity of the respective distributions, strongly suggest that, as useful as it certainly was for a while, the Th1/Th2 paradigm must now be considered as an over-simplification. Rather, the existing data point to sequential windows and are suggestive of a system where an extreme complexity is allied to very precise timing and tuning. They also suggest that the materno-foetal relationship is not simply maternal tolerance of a foreign tissue, but a series of intricate mutual cytokine interactions governing selective immune regulation and also control of the adhesion and vascularisation processes during this dialogue.</abstract><cop>Shannon</cop><pub>Elsevier Ireland Ltd</pub><pmid>11730920</pmid><doi>10.1016/S0165-0378(01)00119-X</doi><tpages>16</tpages></addata></record>
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subjects Animals
Biological and medical sciences
Blastocyst - immunology
Cytokine expressions
Cytokines - genetics
Decidua - immunology
Female
Fundamental and applied biological sciences. Psychology
Gene Expression
Histocompatibility Antigens Class I
Humans
Inflammation - genetics
Inflammation - immunology
Killer Cells, Natural - immunology
Life Sciences
Maternal-Fetal Exchange - genetics
Maternal-Fetal Exchange - immunology
Materno-foetal interface
Mice
Mother. Fetoplacental unit. Mammary gland. Milk
Placenta - immunology
Pregnancy
Pregnancy. Parturition. Lactation
Th1 Cells - immunology
Th1/Th2 dichotomy
Th2 Cells - immunology
Uterus - immunology
Vertebrates: reproduction
title A brief review of recent data on some cytokine expressions at the materno-foetal interface which might challenge the classical Th1/Th2 dichotomy
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