Human memory-like NK cells migrating to tuberculous pleural fluid via IP-10/CXCR3 and SDF-1/CXCR4 axis produce IFN-γ in response to Bacille Calmette Guerin

Abstract We have previously shown that human memory-like NK cells were persistent in tuberculous pleurisy but it was unclear how NK cells migrated into the pleural fluids. At present, we found that NK cells from TB pleural fluid cells (PFCs) expressed significantly higher levels of CXCR3 and CXCR4 t...

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Published inClinical immunology (Orlando, Fla.) Vol. 148; no. 1; pp. 113 - 123
Main Authors Fu, Xiaoying, Yang, Binyan, Lao, Suihua, Fan, Yanying, Wu, Changyou
Format Journal Article
LanguageEnglish
Published United States Elsevier Inc 01.07.2013
Subjects
Adolescent
Adult
Aged
Allergy and Immunology
BCG
BCG Vaccine - administration & dosage
BCG Vaccine - immunology
Cell Movement - immunology
CXCR3/IP-10
CXCR4/SDF-1
Female
Flow Cytometry
Humans
IFN-γ
Immunologic Memory - immunology
Interferon-gamma - immunology
Killer Cells, Natural - immunology
Male
Memory
Middle Aged
Mycobacterium
Mycobacterium tuberculosis - immunology
NK Cells
Receptors, CXCR3 - biosynthesis
Receptors, CXCR3 - immunology
Receptors, CXCR4 - biosynthesis
Receptors, CXCR4 - immunology
Tuberculosis, Pleural - immunology
Young Adult
peripheral blood mononuclear cells
APCs
NK cells
PFCs
pleural fluid cells
Memory
BCG
tuberculosis
interferon
PBMCs
TB
IFN
natural killer cells
IFN-γ
Bacille Calmette Guerin
Mycobacterium tuberculosis
CXCR4/SDF-1
CXCR3/IP-10
TP
antigen presenting cells
tuberculous pleuritis
M. tb
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Abstract Abstract We have previously shown that human memory-like NK cells were persistent in tuberculous pleurisy but it was unclear how NK cells migrated into the pleural fluids. At present, we found that NK cells from TB pleural fluid cells (PFCs) expressed significantly higher levels of CXCR3 and CXCR4 than NK cells from PBMCs. Migration assay demonstrated that IP-10 and SDF-1 induced more migration of NK cells from PFCs than PBMCs. CD45RO+ or CD45RO− NK cells from PFCs were co-cultured with autologous monocytes and stimulated with BCG. The results showed CD45RO+ but not CD45RO− NK cells produced significantly higher levels of IFN-γ, which was IL-12-dependent since anti-IL-12Rβ1 mAbs could significantly inhibit the IFN-γ by NK cells. Collectively, our data demonstrated that human Mycobacterium tuberculosis -specific NK cells were migrated into the local site of TB infection mainly via IP-10/CXCR3 and SDF-1/CXCR4 axis, memory-like NK cells might display an important role against M. tuberculosis infection.
AbstractList Abstract We have previously shown that human memory-like NK cells were persistent in tuberculous pleurisy but it was unclear how NK cells migrated into the pleural fluids. At present, we found that NK cells from TB pleural fluid cells (PFCs) expressed significantly higher levels of CXCR3 and CXCR4 than NK cells from PBMCs. Migration assay demonstrated that IP-10 and SDF-1 induced more migration of NK cells from PFCs than PBMCs. CD45RO+ or CD45RO− NK cells from PFCs were co-cultured with autologous monocytes and stimulated with BCG. The results showed CD45RO+ but not CD45RO− NK cells produced significantly higher levels of IFN-γ, which was IL-12-dependent since anti-IL-12Rβ1 mAbs could significantly inhibit the IFN-γ by NK cells. Collectively, our data demonstrated that human Mycobacterium tuberculosis -specific NK cells were migrated into the local site of TB infection mainly via IP-10/CXCR3 and SDF-1/CXCR4 axis, memory-like NK cells might display an important role against M. tuberculosis infection.
We have previously shown that human memory-like NK cells were persistent in tuberculous pleurisy but it was unclear how NK cells migrated into the pleural fluids. At present, we found that NK cells from TB pleural fluid cells (PFCs) expressed significantly higher levels of CXCR3 and CXCR4 than NK cells from PBMCs. Migration assay demonstrated that IP-10 and SDF-1 induced more migration of NK cells from PFCs than PBMCs. CD45RO(+) or CD45RO(-) NK cells from PFCs were co-cultured with autologous monocytes and stimulated with BCG. The results showed CD45RO(+) but not CD45RO(-) NK cells produced significantly higher levels of IFN-γ, which was IL-12-dependent since anti-IL-12Rβ1 mAbs could significantly inhibit the IFN-γ by NK cells. Collectively, our data demonstrated that human Mycobacterium tuberculosis-specific NK cells were migrated into the local site of TB infection mainly via IP-10/CXCR3 and SDF-1/CXCR4 axis, memory-like NK cells might display an important role against M. tuberculosis infection.
We have previously shown that human memory-like NK cells were persistent in tuberculous pleurisy but it was unclear how NK cells migrated into the pleural fluids. At present, we found that NK cells from TB pleural fluid cells (PFCs) expressed significantly higher levels of CXCR3 and CXCR4 than NK cells from PBMCs. Migration assay demonstrated that IP-10 and SDF-1 induced more migration of NK cells from PFCs than PBMCs. CD45RO+ or CD45RO− NK cells from PFCs were co-cultured with autologous monocytes and stimulated with BCG. The results showed CD45RO+ but not CD45RO− NK cells produced significantly higher levels of IFN-γ, which was IL-12-dependent since anti-IL-12Rβ1 mAbs could significantly inhibit the IFN-γ by NK cells. Collectively, our data demonstrated that human Mycobacterium tuberculosis-specific NK cells were migrated into the local site of TB infection mainly via IP-10/CXCR3 and SDF-1/CXCR4 axis, memory-like NK cells might display an important role against M. tuberculosis infection. •NK cells from PFCs expressed significantly higher level of CXCR3 and CXCR4.•Memory NK cells increased CXCR3 but decreased CXCR4 than naïve NK cells form PFCs.•NK cells in PF were more migrated in response to IP-10 and SDF-1 than PBMCs.•CD45RO+ NK cells induced higher level of IFN-γ, which was IL-12-dependent.
We have previously shown that human memory-like NK cells were persistent in tuberculous pleurisy but it was unclear how NK cells migrated into the pleural fluids. At present, we found that NK cells from TB pleural fluid cells (PFCs) expressed significantly higher levels of CXCR3 and CXCR4 than NK cells from PBMCs. Migration assay demonstrated that IP-10 and SDF-1 induced more migration of NK cells from PFCs than PBMCs. CD45RO+ or CD45RO- NK cells from PFCs were co-cultured with autologous monocytes and stimulated with BCG. The results showed CD45RO+ but not CD45RO- NK cells produced significantly higher levels of IFN- gamma , which was IL-12-dependent since anti-IL-12R beta 1 mAbs could significantly inhibit the IFN- gamma by NK cells. Collectively, our data demonstrated that human Mycobacterium tuberculosis-specific NK cells were migrated into the local site of TB infection mainly via IP-10/CXCR3 and SDF-1/CXCR4 axis, memory-like NK cells might display an important role against M. tuberculosis infection.
Author Fan, Yanying
Wu, Changyou
Yang, Binyan
Fu, Xiaoying
Lao, Suihua
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Issue 1
Keywords peripheral blood mononuclear cells
APCs
NK cells
PFCs
pleural fluid cells
Memory
BCG
tuberculosis
interferon
PBMCs
TB
IFN
natural killer cells
IFN-γ
Bacille Calmette Guerin
Mycobacterium tuberculosis
CXCR4/SDF-1
CXCR3/IP-10
TP
antigen presenting cells
tuberculous pleuritis
M. tb
Language English
License Copyright © 2013 Elsevier Inc. All rights reserved.
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Snippet Abstract We have previously shown that human memory-like NK cells were persistent in tuberculous pleurisy but it was unclear how NK cells migrated into the...
We have previously shown that human memory-like NK cells were persistent in tuberculous pleurisy but it was unclear how NK cells migrated into the pleural...
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StartPage 113
SubjectTerms Adolescent
Adult
Aged
Allergy and Immunology
BCG
BCG Vaccine - administration & dosage
BCG Vaccine - immunology
Cell Movement - immunology
CXCR3/IP-10
CXCR4/SDF-1
Female
Flow Cytometry
Humans
IFN-γ
Immunologic Memory - immunology
Interferon-gamma - immunology
Killer Cells, Natural - immunology
Male
Memory
Middle Aged
Mycobacterium
Mycobacterium tuberculosis - immunology
NK Cells
Receptors, CXCR3 - biosynthesis
Receptors, CXCR3 - immunology
Receptors, CXCR4 - biosynthesis
Receptors, CXCR4 - immunology
Tuberculosis, Pleural - immunology
Young Adult
Title Human memory-like NK cells migrating to tuberculous pleural fluid via IP-10/CXCR3 and SDF-1/CXCR4 axis produce IFN-γ in response to Bacille Calmette Guerin
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https://dx.doi.org/10.1016/j.clim.2013.04.003
https://www.ncbi.nlm.nih.gov/pubmed/23685221
https://search.proquest.com/docview/1366578013
https://search.proquest.com/docview/1627970950
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