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231225s2019 xx |||||o 00| ||eng c |
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|a 10.1016/j.clim.2019.02.010
|2 doi
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|a pubmed24n0981.xml
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|a (DE-627)NLM294423834
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|a (NLM)30817998
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|a (PII)S1521-6616(19)30022-1
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|a DE-627
|b ger
|c DE-627
|e rakwb
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|a eng
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1 |
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|a Nabatanzi, Rose
|e verfasserin
|4 aut
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|a Aberrant natural killer (NK) cell activation and dysfunction among ART-treated HIV-infected adults in an African cohort
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|c 2019
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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 21.01.2020
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|a Date Revised 07.12.2022
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|a published: Print-Electronic
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|a Citation Status MEDLINE
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|a Copyright © 2019 The Authors. Published by Elsevier Inc. All rights reserved.
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|a BACKGROUND: We examined NK cell phenotypes and functions after seven years of ART and undetectable viral loads (<50 copies/ml) with restored CD4 T-cell counts (≥500 cells/μl) and age-matched healthy-HIV-uninfected individuals from the same community
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|a METHODS: Using flow-cytometry, NK cell phenotypes were described using lineage markers (CD56+/-CD16+/-). NK cell activation was determined by expression of activation receptors (NKG2D, NKp44 and NKp46) and activation marker CD69. NK cell function was determined by CD107a, granzyme-b, and IFN-gamma production
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|a RESULTS: CD56 dim and CD56 bright NK cells were lower among ART-treated-HIV-infected than among age-matched-HIV-negative individuals; p = 0.0016 and p = 0.05 respectively. Production of CD107a (P = 0.004) and Granzyme-B (P = 0.005) was lower among ART-treated-HIV-infected relative to the healthy-HIV-uninfected individuals. NKG2D and NKp46 were lower, while CD69 expression was higher among ART-treated-HIV-infected than healthy-HIV-uninfected individuals
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|a CONCLUSION: NK cell activation and dysfunction persisted despite seven years of suppressive ART with "normalization" of peripheral CD4 counts
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|a Journal Article
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|a Research Support, Non-U.S. Gov't
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|a 107a
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|a Antiretroviral therapy
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|a Granzyme-B
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|a Interferon gamma
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|a NK Cytolytic function
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|a NK cell activation
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|a NK cell dysfunction
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|a NK degranulation
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|a NKG2D
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|a NKp46
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|a Natural killer cells
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|a Sub-Saharan Africa
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|a Anti-Retroviral Agents
|2 NLM
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|a Antigens, CD
|2 NLM
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|a Antigens, Differentiation, T-Lymphocyte
|2 NLM
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|a CD69 antigen
|2 NLM
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|a KLRK1 protein, human
|2 NLM
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|a Lectins, C-Type
|2 NLM
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|a Lysosomal-Associated Membrane Protein 1
|2 NLM
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|a NCR1 protein, human
|2 NLM
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|a NK Cell Lectin-Like Receptor Subfamily K
|2 NLM
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|a Natural Cytotoxicity Triggering Receptor 1
|2 NLM
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|a Granzymes
|2 NLM
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|a EC 3.4.21.-
|2 NLM
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|a Bayigga, Lois
|e verfasserin
|4 aut
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|a Cose, Stephen
|e verfasserin
|4 aut
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|a Rowland-Jones, Sarah
|e verfasserin
|4 aut
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1 |
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|a Canderan, Glenda
|e verfasserin
|4 aut
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1 |
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|a Joloba, Moses
|e verfasserin
|4 aut
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|a Nakanjako, Damalie
|e verfasserin
|4 aut
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773 |
0 |
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|i Enthalten in
|t Clinical immunology (Orlando, Fla.)
|d 1999
|g 201(2019) vom: 20. Apr., Seite 55-60
|w (DE-627)NLM098196855
|x 1521-7035
|7 nnns
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|g volume:201
|g year:2019
|g day:20
|g month:04
|g pages:55-60
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|u http://dx.doi.org/10.1016/j.clim.2019.02.010
|3 Volltext
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|a GBV_USEFLAG_A
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|a SYSFLAG_A
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|a GBV_NLM
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|a GBV_ILN_11
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|a GBV_ILN_24
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|a GBV_ILN_350
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|a AR
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|d 201
|j 2019
|b 20
|c 04
|h 55-60
|