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231225s2021 xx |||||o 00| ||eng c |
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|a 10.1016/j.clim.2021.108859
|2 doi
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|a pubmed24n1103.xml
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|a (DE-627)NLM331053373
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|a (PII)S1521-6616(21)00196-0
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|a DE-627
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|e rakwb
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|a eng
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|a de Araújo, Thádia Evelyn
|e verfasserin
|4 aut
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|a Long-term impact of congenital toxoplasmosis on phenotypic and functional features of circulating leukocytes from infants one year after treatment onset
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|c 2021
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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
|b cr
|2 rdacarrier
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|a Date Completed 26.11.2021
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|a Date Revised 26.11.2021
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|a published: Print-Electronic
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|a Citation Status MEDLINE
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|a Copyright © 2021 Elsevier Inc. All rights reserved.
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|a Changes in immune response of children with congenital toxoplasmosis (CT) regarding infection evolution and therapeutic intervention was addressed. Infants with CT presented increased counts of monocytes, CD3-CD16-CD56High, CD3+CD56+ and CD4+ T-cells 1-year after treatment onset (TOXO1-yearAT). Smaller numbers of CD3-CD16-CD56+ and TCRγδ+ T-cells were specifically observed in infants with retinochoroidal lesions (L(+)). When infants were classified based on the baseline status, expansion of CD3-CD16-CD56High and CD4+ T-cells were observed in L(+) who had active, active/cicatricial or cicatricial lesions. Infants who had active or active/cicatricial lesions display augmented numbers of monocytes, CD3-CD16+CD56+, CD3+CD56+, CD8+DR+ and TCRγδ+ T-cells and those with active/cicatricial or cicatricial at baseline displayed increase in CD14+CD64+ monocytes. Moreover, all L(+) had increased IFN-γ+ and IL-10+ CD4+ T-cells, while L(-) had increased ratios of TNF+, IFN-γ+ and IL-4+ NK-cells upon antigen-specific stimulation. Persistent alterations in leukocytes in TOXO1-yearAT suggest long-term sequels in the immune system of infants with CT
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|a Journal Article
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|a Observational Study
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|a Research Support, Non-U.S. Gov't
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|a Congenital
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|a Immune response
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|a Infants
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|a Phenotypic and functional biomarkers
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|a Toxoplasmosis
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|a Antiprotozoal Agents
|2 NLM
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|a Sulfadiazine
|2 NLM
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|a 0N7609K889
|2 NLM
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|a Pyrimethamine
|2 NLM
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|a Z3614QOX8W
|2 NLM
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1 |
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|a Gomes, Angelica Oliveira
|e verfasserin
|4 aut
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|a Coelho-Dos-Reis, Jordana Grazziela
|e verfasserin
|4 aut
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|a Carneiro, Ana Carolina Aguiar Vasconcelos
|e verfasserin
|4 aut
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|a Machado, Anderson Silva
|e verfasserin
|4 aut
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1 |
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|a Andrade, Gláucia Manzan Queiroz
|e verfasserin
|4 aut
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1 |
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|a Vasconcelos-Santos, Daniel Vitor
|e verfasserin
|4 aut
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1 |
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|a Januário, José Nélio
|e verfasserin
|4 aut
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1 |
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|a Peruhype-Magalhães, Vanessa
|e verfasserin
|4 aut
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|a Teixeira-Carvalho, Andréa
|e verfasserin
|4 aut
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|a Vitor, Ricardo Wagner Almeida
|e verfasserin
|4 aut
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|a Antonelli, Lis Ribeiro do Valle
|e verfasserin
|4 aut
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|a Ferro, Eloisa Amalia Vieira
|e verfasserin
|4 aut
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|a Martins-Filho, Olindo Assis
|e verfasserin
|4 aut
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|a UFMG Congenital Toxoplasmosis Brazilian Group - UFMG-CTBG
|e verfasserin
|4 aut
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1 |
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|a Machado Azevedo, Danuza O
|e investigator
|4 oth
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|a Machado Carellos, Ericka V
|e investigator
|4 oth
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|a Resende, Luciana Macedo
|e investigator
|4 oth
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|a Castro Romanelli, Roberta M
|e investigator
|4 oth
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|i Enthalten in
|t Clinical immunology (Orlando, Fla.)
|d 1999
|g 232(2021) vom: 01. Nov., Seite 108859
|w (DE-627)NLM098196855
|x 1521-7035
|7 nnns
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|g volume:232
|g year:2021
|g day:01
|g month:11
|g pages:108859
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|u http://dx.doi.org/10.1016/j.clim.2021.108859
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