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Memory-Like Antigen-Specific Human NK Cells from TB Pleural Fluids Produced IL-22 in Response to IL-15 or Mycobacterium tuberculosis Antigens

Our previous result indicated that memory-like human natural killer (NK) cells from TB pleural fluid cells (PFCs) produced large amounts of IFN-γ in response to Bacille Calmette Guerin (BCG). Furthermore, recent studies have shown that human lymphoid tissues harbored a unique NK cell subset that spe...

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Autores principales: Fu, Xiaoying, Yu, Sifei, Yang, Binyan, Lao, Suihua, Li, Baiqing, Wu, Changyou
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4816314/
https://www.ncbi.nlm.nih.gov/pubmed/27031950
http://dx.doi.org/10.1371/journal.pone.0151721
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author Fu, Xiaoying
Yu, Sifei
Yang, Binyan
Lao, Suihua
Li, Baiqing
Wu, Changyou
author_facet Fu, Xiaoying
Yu, Sifei
Yang, Binyan
Lao, Suihua
Li, Baiqing
Wu, Changyou
author_sort Fu, Xiaoying
collection PubMed
description Our previous result indicated that memory-like human natural killer (NK) cells from TB pleural fluid cells (PFCs) produced large amounts of IFN-γ in response to Bacille Calmette Guerin (BCG). Furthermore, recent studies have shown that human lymphoid tissues harbored a unique NK cell subset that specialized in production of interleukin (IL)-22, a proinflammatory cytokine that mediates host defense against pathogens. Yet little information was available with regard to the properties of IL-22 production by memory-like human NK cells. In the present study, we found that cytokines IL-15 induced and IL-12 enhanced the levels of IL-22 by NK cells from TB PFCs. In addition, IL-22 but not IL-17 was produced by NK cells from PFCs in response to BCG and M.tb-related Ags. More importantly, the subset of specific IL-22-producing NK cells were distinct from IFN-γ-producing NK cells in PFCs. CD45RO(+) or CD45RO(-) NK cells were sorted, co-cultured with autologous monocytes and stimulated with BCG for the production of IL-22. The result demonstrated that CD45RO(+) but not CD45RO(-) NK cells produced significantly higher level of IL-22. Anti-IL-12Rβ1 mAbs (2B10) partially inhibit the expression of IL-22 by NK cells under the culture with BCG. Consistently, BCG specific IL-22-producing NK cells from PFCs expressed CD45RO(high)NKG2D(high)granzyme B(high). In conclusion, our data demonstrated that memory-like antigen-specific CD45RO(+) NK cells might participate in the recall immune response for M. tb infection via producing IL-22, which display a critical role to fight against M. tb.
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spelling pubmed-48163142016-04-14 Memory-Like Antigen-Specific Human NK Cells from TB Pleural Fluids Produced IL-22 in Response to IL-15 or Mycobacterium tuberculosis Antigens Fu, Xiaoying Yu, Sifei Yang, Binyan Lao, Suihua Li, Baiqing Wu, Changyou PLoS One Research Article Our previous result indicated that memory-like human natural killer (NK) cells from TB pleural fluid cells (PFCs) produced large amounts of IFN-γ in response to Bacille Calmette Guerin (BCG). Furthermore, recent studies have shown that human lymphoid tissues harbored a unique NK cell subset that specialized in production of interleukin (IL)-22, a proinflammatory cytokine that mediates host defense against pathogens. Yet little information was available with regard to the properties of IL-22 production by memory-like human NK cells. In the present study, we found that cytokines IL-15 induced and IL-12 enhanced the levels of IL-22 by NK cells from TB PFCs. In addition, IL-22 but not IL-17 was produced by NK cells from PFCs in response to BCG and M.tb-related Ags. More importantly, the subset of specific IL-22-producing NK cells were distinct from IFN-γ-producing NK cells in PFCs. CD45RO(+) or CD45RO(-) NK cells were sorted, co-cultured with autologous monocytes and stimulated with BCG for the production of IL-22. The result demonstrated that CD45RO(+) but not CD45RO(-) NK cells produced significantly higher level of IL-22. Anti-IL-12Rβ1 mAbs (2B10) partially inhibit the expression of IL-22 by NK cells under the culture with BCG. Consistently, BCG specific IL-22-producing NK cells from PFCs expressed CD45RO(high)NKG2D(high)granzyme B(high). In conclusion, our data demonstrated that memory-like antigen-specific CD45RO(+) NK cells might participate in the recall immune response for M. tb infection via producing IL-22, which display a critical role to fight against M. tb. Public Library of Science 2016-03-31 /pmc/articles/PMC4816314/ /pubmed/27031950 http://dx.doi.org/10.1371/journal.pone.0151721 Text en © 2016 Fu et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Fu, Xiaoying
Yu, Sifei
Yang, Binyan
Lao, Suihua
Li, Baiqing
Wu, Changyou
Memory-Like Antigen-Specific Human NK Cells from TB Pleural Fluids Produced IL-22 in Response to IL-15 or Mycobacterium tuberculosis Antigens
title Memory-Like Antigen-Specific Human NK Cells from TB Pleural Fluids Produced IL-22 in Response to IL-15 or Mycobacterium tuberculosis Antigens
title_full Memory-Like Antigen-Specific Human NK Cells from TB Pleural Fluids Produced IL-22 in Response to IL-15 or Mycobacterium tuberculosis Antigens
title_fullStr Memory-Like Antigen-Specific Human NK Cells from TB Pleural Fluids Produced IL-22 in Response to IL-15 or Mycobacterium tuberculosis Antigens
title_full_unstemmed Memory-Like Antigen-Specific Human NK Cells from TB Pleural Fluids Produced IL-22 in Response to IL-15 or Mycobacterium tuberculosis Antigens
title_short Memory-Like Antigen-Specific Human NK Cells from TB Pleural Fluids Produced IL-22 in Response to IL-15 or Mycobacterium tuberculosis Antigens
title_sort memory-like antigen-specific human nk cells from tb pleural fluids produced il-22 in response to il-15 or mycobacterium tuberculosis antigens
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4816314/
https://www.ncbi.nlm.nih.gov/pubmed/27031950
http://dx.doi.org/10.1371/journal.pone.0151721
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