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1.
J Immunol ; 211(3): 443-452, 2023 08 01.
Article in English | MEDLINE | ID: mdl-37314415

ABSTRACT

"Adaptive" NK cells, characterized by FcRγ deficiency and enhanced responsiveness to Ab-bound, virus-infected cells, have been found in certain hCMV-seropositive individuals. Because humans are exposed to numerous microbes and environmental agents, specific relationships between hCMV and FcRγ-deficient NK cells (also known as g-NK cells) have been challenging to define. Here, we show that a subgroup of rhesus CMV (RhCMV)-seropositive macaques possesses FcRγ-deficient NK cells that stably persist and display a phenotype resembling human FcRγ-deficient NK cells. Moreover, these macaque NK cells resembled human FcRγ-deficient NK cells with respect to functional characteristics, including enhanced responsiveness to RhCMV-infected target in an Ab-dependent manner and hyporesponsiveness to tumor and cytokine stimulation. These cells were not detected in specific pathogen-free (SPF) macaques free of RhCMV and six other viruses; however, experimental infection of SPF animals with RhCMV strain UCD59, but not RhCMV strain 68-1 or SIV, led to induction of FcRγ-deficient NK cells. In non-SPF macaques, coinfection by RhCMV with other common viruses was associated with higher frequencies of FcRγ-deficient NK cells. These results support a causal role for specific CMV strain(s) in the induction of FcRγ-deficient NK cells and suggest that coinfection by other viruses further expands this memory-like NK cell pool.


Subject(s)
Coinfection , Cytomegalovirus Infections , Virus Diseases , Animals , Humans , Cytomegalovirus/genetics , Macaca mulatta , Killer Cells, Natural
2.
iScience ; 23(11): 101709, 2020 Nov 20.
Article in English | MEDLINE | ID: mdl-33205022

ABSTRACT

Adaptive human natural killer (NK) cells display significantly enhanced responsiveness to a broad-range of antibody-bound targets through the engagement of CD16 compared to conventional NK cells, yet direct reactivity against tumor targets is generally reduced. Adaptive NK cells also display a distinct phenotype and differential expression of numerous genes, including reduced expression of signaling adapter FcRγ and transcription factor PLZF. However, it is unclear whether differential expression of specific genes is responsible for the characteristics of adaptive NK cells. Using CRISPR-Cas9, we show deletion of FcRγ in conventional NK cells led to enhanced CD16 responsiveness, abolished cell surface expression of natural cytotoxicity receptors, NKp46 and NKp30, and dramatically reduced responsiveness to K562 and Raji tumor cells. However, deletion of PLZF had no notable effects. These results suggest multiple roles for FcRγ and identify its deficiency as an important factor responsible for the functional and phenotypic characteristics exhibited by adaptive NK cells.

3.
Immunity ; 42(3): 431-42, 2015 Mar 17.
Article in English | MEDLINE | ID: mdl-25786175

ABSTRACT

Long-lived "memory-like" NK cells have been identified in individuals infected by human cytomegalovirus (HCMV), but little is known about how the memory-like NK cell pool is formed. Here, we have shown that HCMV-infected individuals have several distinct subsets of memory-like NK cells that are often deficient for multiple transcription factors and signaling proteins, including tyrosine kinase SYK, for which the reduced expression was stable over time and correlated with epigenetic modification of the gene promoter. Deficient expression of these proteins was largely confined to the recently discovered FcRγ-deficient NK cells that display enhanced antibody-dependent functional activity. Importantly, FcRγ-deficient NK cells exhibited robust preferential expansion in response to virus-infected cells (both HCMV and influenza) in an antibody-dependent manner. These findings suggest that the memory-like NK cell pool is shaped and maintained by a mechanism that involves both epigenetic modification of gene expression and antibody-dependent expansion.


Subject(s)
Antibodies/immunology , Cytomegalovirus Infections/genetics , Epigenesis, Genetic/immunology , Immunologic Memory , Killer Cells, Natural/immunology , Cell Proliferation , Cytomegalovirus/immunology , Cytomegalovirus Infections/immunology , Cytomegalovirus Infections/pathology , Cytomegalovirus Infections/virology , DNA Methylation , GPI-Linked Proteins/genetics , GPI-Linked Proteins/immunology , Gene Expression Profiling , Humans , Immunophenotyping , Intracellular Signaling Peptides and Proteins/deficiency , Intracellular Signaling Peptides and Proteins/genetics , Intracellular Signaling Peptides and Proteins/immunology , Killer Cells, Natural/classification , Killer Cells, Natural/pathology , Killer Cells, Natural/virology , Microarray Analysis , NK Cell Lectin-Like Receptor Subfamily C/deficiency , NK Cell Lectin-Like Receptor Subfamily C/genetics , NK Cell Lectin-Like Receptor Subfamily C/immunology , Promoter Regions, Genetic , Protein-Tyrosine Kinases/deficiency , Protein-Tyrosine Kinases/genetics , Protein-Tyrosine Kinases/immunology , Receptors, IgG/deficiency , Receptors, IgG/genetics , Receptors, IgG/immunology , Signal Transduction , Syk Kinase
4.
J Immunol ; 190(4): 1402-6, 2013 Feb 15.
Article in English | MEDLINE | ID: mdl-23345329

ABSTRACT

Because NK cells lack gene-recombination machinery and are thought to be relatively short-lived, it is unclear whether NK cells can mount long-term effective recall responses to reinfections by diverse pathogens. In this article, we report that FcRγ-deficient NK cells, which we recently identified and termed g(-)NK cells, possess distinct memory features directed by FcR-mediated Ab-dependent target recognition. The presence of g(-)NK cells was associated with prior human CMV (HMCV) infection, yet g(-)NK cell responses were not restricted to HCMV-infected target cells. In the presence of virus-specific Abs, g(-)NK cells had greatly enhanced functional capabilities, superior to conventional NK cells, and were highly responsive to cells infected with either HCMV or HSV-1. Remarkably, the g(-)NK cell subset persisted long-term at nearly constant levels in healthy individuals. Therefore, FcRγ deficiency distinguishes an Ab-dependent memory-like NK cell subset with enhanced potential for broad antiviral responses.


Subject(s)
Antibody-Dependent Cell Cytotoxicity/immunology , Immunologic Memory , Killer Cells, Natural/immunology , Killer Cells, Natural/metabolism , Receptors, IgG/deficiency , Receptors, IgG/genetics , Cell Line , Cells, Cultured , Cytomegalovirus/immunology , Gene Targeting , Humans , Immunologic Memory/genetics , Immunophenotyping , Killer Cells, Natural/virology , Receptors, IgG/metabolism
5.
Int Immunol ; 24(12): 793-802, 2012 Dec.
Article in English | MEDLINE | ID: mdl-22962434

ABSTRACT

NK cells respond to tumor and virus-infected cells directly through several activation receptors, including natural cytotoxicity receptors, or indirectly through the activating Fc receptor CD16 for antibody-coated cells. Triggering of NK-cell effector functions through these receptors depends on physically associated transmembrane signaling adaptors, such as FcRγ (also known as FcεRIγ) and CD3ζ, both of which have been traditionally believed to be expressed by all mature NK cells. However, we have identified a distinct subset of human NK cells that are deficient for FcRγ expression but express normal levels of CD3ζ. FcRγ-deficient NK cells were readily detectable in about one-third of the healthy individuals examined. The deficiency was confined to the CD56(dim) population and was due to low FcRγ mRNA. FcRγ-deficient NK cells displayed dramatically reduced expression of the natural cytotoxicity receptors NKp46 and NKp30 but still expressed substantial levels of CD16. Compared to FcRγ-expressing NK cells, FcRγ-deficient NK cells showed poor direct reactivity toward tumor targets as measured by cytokine production and degranulation. Unexpectedly, however, FcRγ-deficient NK cells exhibited significantly more robust responsiveness upon stimulation through CD16, particularly for cytokine production, compared to FcRγ-expressing NK cells. Thus, our study reveals FcRγ-deficient NK cells as a novel subset of human NK cells that have remarkably potent responses toward antibody-coated targets. These findings also illustrate a differential contribution of FcRγ and CD3ζ for the expression and functional activity of their associated receptors.


Subject(s)
Antibodies/immunology , Killer Cells, Natural/immunology , Lymphocyte Subsets/immunology , Neoplasms/immunology , Receptors, IgG/metabolism , Antigens, Neoplasm/immunology , CD3 Complex/metabolism , Cells, Cultured , Cytokines/metabolism , Humans , Immunophenotyping , Natural Cytotoxicity Triggering Receptor 1/genetics , Natural Cytotoxicity Triggering Receptor 1/metabolism , Natural Cytotoxicity Triggering Receptor 3/genetics , Natural Cytotoxicity Triggering Receptor 3/metabolism , Receptor Cross-Talk , Receptors, IgG/deficiency , Receptors, IgG/immunology , Signal Transduction
6.
PLoS One ; 7(12): e51858, 2012.
Article in English | MEDLINE | ID: mdl-23300570

ABSTRACT

During early viral infection, activation of natural killer (NK) cells elicits the effector functions of target cell lysis and cytokine production. However, the cellular and molecular mechanisms leading to NK cell activation during viral infections are incompletely understood. In this study, using a model of acute viral infection, we investigated the mechanisms controlling cytotoxic activity and cytokine production in response to influenza (flu) virus. Analysis of cytokine receptor deficient mice demonstrated that type I interferons (IFNs), but not IL-12 or IL-18, were critical for the NK cell expression of both IFN-γ and granzyme B in response to flu infection. Further, adoptive transfer experiments revealed that NK cell activation was mediated by type I IFNs acting directly on NK cells. Analysis of signal transduction molecules showed that during flu infection, STAT1 activation in NK cells was completely dependent on direct type I IFN signaling, whereas STAT4 activation was only partially dependent. In addition, granzyme B induction in NK cells was mediated by signaling primarily through STAT1, but not STAT4, while IFN-γ production was mediated by signaling through STAT4, but not STAT1. Therefore, our findings demonstrate the importance of direct action of type I IFNs on NK cells to mount effective NK cell responses in the context of flu infection and delineate NK cell signaling pathways responsible for controlling cytotoxic activity and cytokine production.


Subject(s)
Influenza, Human/immunology , Killer Cells, Natural/immunology , Orthomyxoviridae/immunology , Receptors, Interleukin-12/physiology , Receptors, Interleukin-18/physiology , STAT1 Transcription Factor/physiology , STAT4 Transcription Factor/physiology , Adoptive Transfer , Animals , Cytokines/metabolism , Female , Flow Cytometry , Humans , Influenza, Human/metabolism , Influenza, Human/virology , Interferon-gamma/metabolism , Interleukin-12/metabolism , Interleukin-18/metabolism , Killer Cells, Natural/metabolism , Killer Cells, Natural/pathology , Lymphocyte Activation , Male , Mice , Mice, Inbred BALB C , Mice, Inbred C57BL , Signal Transduction
8.
J Gene Med ; 4(5): 480-9, 2002.
Article in English | MEDLINE | ID: mdl-12221641

ABSTRACT

BACKGROUND: Helper-dependent, or gutted, adenoviruses (Ad) lack viral coding sequences, resulting in reduced immunotoxicity compared with conventional Ad vectors. Gutted Ad growth requires a conventional Ad to supply replication and packaging functions in trans. Methods that allow high-titer growth of gutted vectors while reducing helper contamination, and which use safer helper viruses, will facilitate the use of gutted Ad vectors in vivo. METHODS: Replication-defective helper viruses were generated that are deleted for Ad E1, E2b and E3 genes, but which contain loxP sites flanking the packaging signal. Complementing Ad packaging cell lines (C7-cre cells) were also generated by transfecting 293 cells with the Ad E2b genes encoding DNA polymerase and pre-terminal protein, and with a cre-recombinase plasmid. RESULTS: We show that C7-cre cells allow efficient production of gutted Ad using deltaE1 + deltaE2b + deltaE3 helper viruses whose growth can be limited by cre-loxP-mediated excision of the packaging signal. Gutted Ad vectors carrying approximately 28 kb cassettes expressing full-length dystrophin were prepared at high titers, similar to those obtained with E2b+ helpers, with a resulting helper contamination of <1%. CONCLUSIONS: These new packaging cell lines and helper viruses offer several significant advantages for gutted Ad vector production. They allow gutted virus amplification using a reduced number of passages, which should reduce the chances of selecting rearranged products. Furthermore, the residual helper contamination in gutted vector preparations should be less able to elicit immunological reactions upon delivery to tissues, since E2b-deleted vectors display a profound reduction in viral gene expression.


Subject(s)
Adenoviridae , Adenovirus Early Proteins/genetics , Genetic Vectors , Helper Viruses/genetics , Adenoviridae/genetics , Adenoviridae/isolation & purification , Genetic Vectors/genetics , Genetic Vectors/isolation & purification , Humans , Integrases/genetics , Viral Proteins/genetics
9.
Proc Natl Acad Sci U S A ; 99(20): 12979-84, 2002 Oct 01.
Article in English | MEDLINE | ID: mdl-12271128

ABSTRACT

Duchenne muscular dystrophy is a lethal X-linked recessive disorder caused by mutations in the dystrophin gene. Delivery of functionally effective levels of dystrophin to immunocompetent, adult mdx (dystrophin-deficient) mice has been challenging because of the size of the gene, immune responses against viral vectors, and inefficient infection of mature muscle. Here we show that high titer stocks of three different gutted adenoviral vectors carrying full-length, muscle-specific, dystrophin expression cassettes are able to efficiently transduce muscles of 1-yr-old mdx mice. Single i.m. injections of viral vector restored dystrophin production to 25-30% of mouse limb muscle 1 mo after injection. Furthermore, functional tests of virally transduced muscles revealed almost 40% correction of their high susceptibility to contraction-induced injury. Our results show that functional abnormalities of dystrophic muscle can be corrected by delivery of full-length dystrophin to adult, immunocompetent mdx mice, raising the prospects for gene therapy of muscular dystrophies.


Subject(s)
Dystrophin/biosynthesis , Mice, Inbred mdx/genetics , Muscles/metabolism , Adenoviridae/genetics , Animals , Electrophoresis, Polyacrylamide Gel , Gene Transfer Techniques , Humans , Mice , Mice, Inbred C57BL , Mice, Inbred mdx/metabolism , Mice, Transgenic , Microscopy, Fluorescence , Models, Genetic
10.
Neuromuscul Disord ; 12 Suppl 1: S23-9, 2002 Oct.
Article in English | MEDLINE | ID: mdl-12206791

ABSTRACT

Gene therapy for Duchenne muscular dystrophy will require methods to deliver gene constructs encoding functional versions of dystrophin to the vast majority of a patient's musculature. Obstacles to achieving these goals include identifying which forms of dystrophin would be effective in a clinical setting and developing gene delivery shuttles capable of carrying and expressing dystrophin cassettes without toxic or adverse immunologic consequences. We review here recent work from our laboratory to identify sequences within dystrophin that are required to prevent development of dystrophic changes in muscle or which might be able to correct pre-existing damage. We also describe work aimed at developing viral shuttle vectors able to carry and express these dystrophin cassettes at high levels and in a muscle-specific fashion. While great challenges remain in developing methods for systemic gene delivery, we show that a variety of viral vectors are able to carry and express therapeutic levels of dystrophin when delivered directly to mouse skeletal muscle.


Subject(s)
Dystrophin/genetics , Gene Transfer Techniques , Genetic Therapy/methods , Genetic Vectors , Muscular Dystrophy, Duchenne/therapy , Adenoviridae , Animals , Dependovirus , Gene Transfer Techniques/trends , Genetic Therapy/trends , Humans , Lentivirus , Mice , Mice, Inbred mdx , Muscle, Skeletal/pathology , Muscular Dystrophies/therapy , Muscular Dystrophy, Duchenne/genetics
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