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231224s2015 xx |||||o 00| ||eng c |
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|a 10.1016/j.clim.2015.06.008
|2 doi
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|a pubmed24n0834.xml
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|a (DE-627)NLM250311461
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|a (PII)S1521-6616(15)00212-0
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|a DE-627
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|e rakwb
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|a eng
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|a Puff, R
|e verfasserin
|4 aut
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|a Compromised immune response in infants at risk for type 1 diabetes born by Caesarean Section
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|c 2015
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|a Text
|b txt
|2 rdacontent
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|a ƒaComputermedien
|b c
|2 rdamedia
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|a ƒa Online-Ressource
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|2 rdacarrier
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|a Date Completed 15.12.2015
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|a Date Revised 16.08.2019
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|a published: Print-Electronic
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|a Citation Status MEDLINE
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|a Copyright © 2015 Elsevier Inc. All rights reserved.
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|a Children born by Caesarean Section have a higher risk for type 1 diabetes. We aimed to investigate whether Caesarean Section leads to alterations of the immune response in children with familial risk for type 1 diabetes. We examined measures of innate and adaptive immune responses in 94 prospectively followed children, including 40 born by Caesarean Section. Proinflammatory serum cytokine concentrations were determined at age 6 months. As a measure of vaccine response, IgG1, IgG2, and IgG4 tetanus antibody titers and CD4(+) T cell proliferation against tetanus toxoid were quantified. Compared to infants born by vaginal delivery, infants born by Caesarean Section had lower concentrations of the cytokines IFN-ɣ (p=0.014) and IL-8 (p=0.005), and weaker CD4(+) T cell responses to tetanus measured in the first (p=0.007) and second year (p=0.047) of life. Overall, our findings provide evidence that the mode of delivery influences the immune status and responsiveness during childhood
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|a Journal Article
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|a Research Support, Non-U.S. Gov't
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|a Caesarean Section
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|a Cytokine
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|a Immune responsiveness
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|a Tetanus response
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|a Type 1 diabetes
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|a Antibodies, Bacterial
|2 NLM
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|a CXCL8 protein, human
|2 NLM
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|a IL10 protein, human
|2 NLM
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|a IL1B protein, human
|2 NLM
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|a IL2 protein, human
|2 NLM
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|a IL6 protein, human
|2 NLM
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|a Immunoglobulin G
|2 NLM
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|a Interleukin-1beta
|2 NLM
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|a Interleukin-2
|2 NLM
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|a Interleukin-6
|2 NLM
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|a Interleukin-8
|2 NLM
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|a Tetanus Toxin
|2 NLM
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|a Tetanus Toxoid
|2 NLM
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|a Tumor Necrosis Factor-alpha
|2 NLM
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|a Interleukin-10
|2 NLM
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|a 130068-27-8
|2 NLM
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|a Interleukin-12
|2 NLM
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|a 187348-17-0
|2 NLM
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|a Interferon-gamma
|2 NLM
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|a 82115-62-6
|2 NLM
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|a Granulocyte-Macrophage Colony-Stimulating Factor
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|a 83869-56-1
|2 NLM
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700 |
1 |
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|a D'Orlando, O
|e verfasserin
|4 aut
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|a Heninger, A-K
|e verfasserin
|4 aut
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|a Kühn, D
|e verfasserin
|4 aut
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|a Krause, S
|e verfasserin
|4 aut
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|a Winkler, C
|e verfasserin
|4 aut
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|a Beyerlein, A
|e verfasserin
|4 aut
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|a Bonifacio, E
|e verfasserin
|4 aut
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|a Ziegler, A-G
|e verfasserin
|4 aut
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773 |
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|i Enthalten in
|t Clinical immunology (Orlando, Fla.)
|d 1999
|g 160(2015), 2 vom: 26. Okt., Seite 282-5
|w (DE-627)NLM098196855
|x 1521-7035
|7 nnns
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|g volume:160
|g year:2015
|g number:2
|g day:26
|g month:10
|g pages:282-5
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|u http://dx.doi.org/10.1016/j.clim.2015.06.008
|3 Volltext
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|a AR
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|d 160
|j 2015
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|h 282-5
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