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  1. Article ; Online: Sensitive detection of integrated and free transcripts in chimeric antigen receptor T-cell manufactured cell products using droplet digital polymerase chain reaction.

    Wiltshire, Timothy D / Milosevic, Dragana / Jacob, Eapen K / Grebe, Stefan K / Dietz, Allan B

    Cytotherapy

    2021  Volume 23, Issue 5, Page(s) 452–458

    Abstract: ... competent lentivirus (RCL) remains in the final product. An optimal CAR T-cell product should contain ...

    Abstract Background aims: Viral vectors are commonly used to introduce chimeric antigen receptor (CAR) constructs into cell therapy products for the treatment of human disease. They are efficient at gene delivery and integrate into the host genome for subsequent replication but also carry risks if replication-competent lentivirus (RCL) remains in the final product. An optimal CAR T-cell product should contain sufficient integrated viral material and no RCL. Current product testing methods include cell-based assays with slow turnaround times and rapid quantitative polymerase chain reaction (PCR)-based assays that suffer from high result variability. The authors describe the development of a droplet digital PCR (ddPCR) method for detection of the vesicular stomatitis virus G glycoprotein envelope sequence, required for viral assembly, and the replication response element to measure integration of the CAR construct.
    Methods: Assay validation included precision, linearity, sensitivity, specificity and reproducibility over a range of low to high concentrations.
    Results: The limit of detection was 10 copies/μL, whereas negative samples showed <1.3 copies/μL. Within and between assay imprecision coefficients of variation across the reportable range (10-10 000 copies/μL) were <25%. Accuracy and linearity were verified by comparing known copy numbers with measured copy numbers (R
    Conclusions: DDPCR has excellent reproducibility, linearity, specificity and sensitivity for detecting RCL and assuring the safety of patient products in a rapid manner. The technique can also likely be adapted for the rapid detection of other targets during cell product manufacturing, including purity, potency and sterility assays.
    MeSH term(s) Humans ; Lentivirus/genetics ; Polymerase Chain Reaction ; Real-Time Polymerase Chain Reaction ; Receptors, Chimeric Antigen/genetics ; Reproducibility of Results ; T-Lymphocytes
    Chemical Substances Receptors, Chimeric Antigen
    Language English
    Publishing date 2021-03-11
    Publishing country England
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 2039821-9
    ISSN 1477-2566 ; 1465-3249
    ISSN (online) 1477-2566
    ISSN 1465-3249
    DOI 10.1016/j.jcyt.2020.12.012
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article ; Online: Protein kinase CK2 enables regulatory T cells to suppress excessive TH2 responses in vivo.

    Ulges, Alexander / Klein, Matthias / Reuter, Sebastian / Gerlitzki, Bastian / Hoffmann, Markus / Grebe, Nadine / Staudt, Valérie / Stergiou, Natascha / Bohn, Toszka / Brühl, Till-Julius / Muth, Sabine / Yurugi, Hajime / Rajalingam, Krishnaraj / Bellinghausen, Iris / Tuettenberg, Andrea / Hahn, Susanne / Reißig, Sonja / Haben, Irma / Zipp, Frauke /
    Waisman, Ari / Probst, Hans-Christian / Beilhack, Andreas / Buchou, Thierry / Filhol-Cochet, Odile / Boldyreff, Brigitte / Breloer, Minka / Jonuleit, Helmut / Schild, Hansjörg / Schmitt, Edgar / Bopp, Tobias

    Nature immunology

    2015  Volume 16, Issue 3, Page(s) 267–275

    Abstract: ... helper T cell subsets, and the magnitude of an immune response is controlled by CD4(+)Foxp3(+) regulatory ... T cells (Treg cells). However, how a tissue- and cell type-specific suppressor program of Treg cells is ... we found that the suppression of allergic immune responses in the lungs mediated by T helper type 2 (TH2 ...

    Abstract The quality of the adaptive immune response depends on the differentiation of distinct CD4(+) helper T cell subsets, and the magnitude of an immune response is controlled by CD4(+)Foxp3(+) regulatory T cells (Treg cells). However, how a tissue- and cell type-specific suppressor program of Treg cells is mechanistically orchestrated has remained largely unexplored. Through the use of Treg cell-specific gene targeting, we found that the suppression of allergic immune responses in the lungs mediated by T helper type 2 (TH2) cells was dependent on the activity of the protein kinase CK2. Genetic ablation of the β-subunit of CK2 specifically in Treg cells resulted in the proliferation of a hitherto-unexplored ILT3(+) Treg cell subpopulation that was unable to control the maturation of IRF4(+)PD-L2(+) dendritic cells required for the development of TH2 responses in vivo.
    MeSH term(s) Animals ; CD4-Positive T-Lymphocytes/enzymology ; CD4-Positive T-Lymphocytes/immunology ; Casein Kinase II/immunology ; Cell Differentiation/immunology ; Cell Growth Processes/immunology ; Cell Line ; Dendritic Cells/enzymology ; Dendritic Cells/immunology ; Forkhead Transcription Factors/immunology ; Humans ; Hypersensitivity/blood ; Hypersensitivity/immunology ; Interferon Regulatory Factors/immunology ; Leukocytes, Mononuclear/immunology ; Male ; Mice ; Mice, Inbred BALB C ; Mice, Inbred C57BL ; Mice, Transgenic ; Receptors, Cell Surface/immunology ; T-Lymphocytes, Regulatory/enzymology ; T-Lymphocytes, Regulatory/immunology ; Th2 Cells/enzymology ; Th2 Cells/immunology
    Chemical Substances Forkhead Transcription Factors ; Interferon Regulatory Factors ; Receptors, Cell Surface ; interferon regulatory factor-4 ; Casein Kinase II (EC 2.7.11.1)
    Language English
    Publishing date 2015-03
    Publishing country United States
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 2016987-5
    ISSN 1529-2916 ; 1529-2908
    ISSN (online) 1529-2916
    ISSN 1529-2908
    DOI 10.1038/ni.3083
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  3. Article ; Online: Regulatory T cells facilitate the nuclear accumulation of inducible cAMP early repressor (ICER) and suppress nuclear factor of activated T cell c1 (NFATc1).

    Vaeth, Martin / Gogishvili, Tea / Bopp, Tobias / Klein, Matthias / Berberich-Siebelt, Friederike / Gattenloehner, Stefan / Avots, Andris / Sparwasser, Tim / Grebe, Nadine / Schmitt, Edgar / Hünig, Thomas / Serfling, Edgar / Bodor, Josef

    Proceedings of the National Academy of Sciences of the United States of America

    2011  Volume 108, Issue 6, Page(s) 2480–2485

    Abstract: ... and nuclear occurrence are elevated by high cAMP levels in naturally occurring regulatory T ... CREM, and thereby inhibit IL-2 synthesis in conventional CD4(+) T cells. Ablation of nTregs ... in depletion of regulatory T-cell (DEREG) mice resulted in cytosolic localization of ICER/CREM and increased IL ...

    Abstract Inducible cAMP early repressor (ICER) is a transcriptional repressor, which, because of alternate promoter use, is generated from the 3' region of the cAMP response modulator (Crem) gene. Its expression and nuclear occurrence are elevated by high cAMP levels in naturally occurring regulatory T cells (nTregs). Using two mouse models, we demonstrate that nTregs control the cellular localization of ICER/CREM, and thereby inhibit IL-2 synthesis in conventional CD4(+) T cells. Ablation of nTregs in depletion of regulatory T-cell (DEREG) mice resulted in cytosolic localization of ICER/CREM and increased IL-2 synthesis upon stimulation. Direct contacts between nTregs and conventional CD4(+) T cells led to nuclear accumulation of ICER/CREM and suppression of IL-2 synthesis on administration of CD28 superagonistic (CD28SA) Ab. In a similar way, nTregs communicated with B cells and induced the cAMP-driven nuclear localization of ICER/CREM. High levels of ICER suppressed the induction of nuclear factor of activated T cell c1 (Nfatc1) gene in T cells whose inducible Nfatc1 P1 promoter bears two highly conserved cAMP-responsive elements to which ICER/CREM can bind. These findings suggest that nTregs suppress T-cell responses by the cAMP-dependent nuclear accumulation of ICER/CREM and inhibition of NFATc1 and IL-2 induction.
    MeSH term(s) Active Transport, Cell Nucleus/drug effects ; Active Transport, Cell Nucleus/genetics ; Active Transport, Cell Nucleus/immunology ; Animals ; Antibodies/immunology ; Antibodies/pharmacology ; CD28 Antigens/genetics ; CD28 Antigens/immunology ; CD28 Antigens/metabolism ; Cell Nucleus/genetics ; Cell Nucleus/immunology ; Cell Nucleus/metabolism ; Cyclic AMP/genetics ; Cyclic AMP/immunology ; Cyclic AMP/metabolism ; Cyclic AMP Response Element Modulator/genetics ; Cyclic AMP Response Element Modulator/immunology ; Cyclic AMP Response Element Modulator/metabolism ; Interleukin-2/biosynthesis ; Interleukin-2/genetics ; Interleukin-2/immunology ; Lymphocyte Activation/drug effects ; Lymphocyte Activation/immunology ; Mice ; Mice, Inbred BALB C ; Mice, Knockout ; NFATC Transcription Factors/genetics ; NFATC Transcription Factors/immunology ; NFATC Transcription Factors/metabolism ; Response Elements/genetics ; Response Elements/immunology ; T-Lymphocytes, Regulatory/immunology ; T-Lymphocytes, Regulatory/metabolism
    Chemical Substances Antibodies ; CD28 Antigens ; Crem protein, mouse ; Interleukin-2 ; NFATC Transcription Factors ; Nfatc1 protein, mouse ; Cyclic AMP Response Element Modulator (135844-64-3) ; Cyclic AMP (E0399OZS9N)
    Language English
    Publishing date 2011-01-24
    Publishing country United States
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 209104-5
    ISSN 1091-6490 ; 0027-8424
    ISSN (online) 1091-6490
    ISSN 0027-8424
    DOI 10.1073/pnas.1009463108
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  4. Book ; Thesis: Untersuchung der Cytokinexpression beim peripheren T-Zell-Lymphom vom angioimmunoblastischen Typ und beim Lennert's Lymphom

    Hoffmann, Maren

    1999  

    Author's details vorgelegt von Maren Hoffmann, geb. Grebe
    Language German
    Size 55 Bl., Ill.
    Edition [Mikrofiche-Ausg.]
    Publishing country Germany
    Document type Book ; Thesis
    Thesis / German Habilitation thesis Berlin, Freie Univ., Diss., 1999
    HBZ-ID HT013116182
    Database Catalogue ZB MED Medicine, Health

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  5. Article ; Online: Selective inhibitors of bacterial t-RNA-(N(1)G37) methyltransferase (TrmD) that demonstrate novel ordering of the lid domain.

    Hill, Pamela J / Abibi, Ayome / Albert, Robert / Andrews, Beth / Gagnon, Moriah M / Gao, Ning / Grebe, Tyler / Hajec, Laurel I / Huang, Jian / Livchak, Stephania / Lahiri, Sushmita D / McKinney, David C / Thresher, Jason / Wang, Hongming / Olivier, Nelson / Buurman, Ed T

    Journal of medicinal chemistry

    2013  Volume 56, Issue 18, Page(s) 7278–7288

    Abstract: The tRNA-(N(1)G37) methyltransferase (TrmD) is essential for growth and highly conserved in both Gram-positive and Gram-negative bacterial pathogens. Additionally, TrmD is very distinct from its human orthologue TRM5 and thus is a suitable target for the ...

    Abstract The tRNA-(N(1)G37) methyltransferase (TrmD) is essential for growth and highly conserved in both Gram-positive and Gram-negative bacterial pathogens. Additionally, TrmD is very distinct from its human orthologue TRM5 and thus is a suitable target for the design of novel antibacterials. Screening of a collection of compound fragments using Haemophilus influenzae TrmD identified inhibitory, fused thieno-pyrimidones that were competitive with S-adenosylmethionine (SAM), the physiological methyl donor substrate. Guided by X-ray cocrystal structures, fragment 1 was elaborated into a nanomolar inhibitor of a broad range of Gram-negative TrmD isozymes. These compounds demonstrated no activity against representative human SAM utilizing enzymes, PRMT1 and SET7/9. This is the first report of selective, nanomolar inhibitors of TrmD with demonstrated ability to order the TrmD lid in the absence of tRNA.
    MeSH term(s) Adenosine/metabolism ; Amines/chemical synthesis ; Amines/chemistry ; Amines/metabolism ; Amines/pharmacology ; Anti-Bacterial Agents/chemical synthesis ; Anti-Bacterial Agents/chemistry ; Anti-Bacterial Agents/metabolism ; Anti-Bacterial Agents/pharmacology ; Drug Evaluation, Preclinical ; Enzyme Inhibitors/chemical synthesis ; Enzyme Inhibitors/chemistry ; Enzyme Inhibitors/metabolism ; Enzyme Inhibitors/pharmacology ; Haemophilus influenzae/drug effects ; Haemophilus influenzae/enzymology ; Humans ; Methionine/metabolism ; Microbial Sensitivity Tests ; Models, Molecular ; Protein Structure, Tertiary ; RNA, Transfer/chemistry ; RNA, Transfer/metabolism ; Structure-Activity Relationship ; Substrate Specificity ; tRNA Methyltransferases/antagonists & inhibitors ; tRNA Methyltransferases/chemistry ; tRNA Methyltransferases/metabolism
    Chemical Substances Amines ; Anti-Bacterial Agents ; Enzyme Inhibitors ; RNA, Transfer (9014-25-9) ; Methionine (AE28F7PNPL) ; tRNA Methyltransferases (EC 2.1.1.-) ; Adenosine (K72T3FS567)
    Language English
    Publishing date 2013-09-26
    Publishing country United States
    Document type Journal Article
    ZDB-ID 218133-2
    ISSN 1520-4804 ; 0022-2623
    ISSN (online) 1520-4804
    ISSN 0022-2623
    DOI 10.1021/jm400718n
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  6. Book ; Online ; Thesis: Analyse humaner regulatorischer T-Zellen im humanisierten Mausmodell

    Grebe, Nadine [Verfasser]

    2013  

    Author's details Nadine Grebe
    Keywords Biowissenschaften, Biologie ; Life Science, Biology
    Subject code sg570
    Language German
    Publisher Universitätsbibliothek Mainz
    Publishing place Mainz
    Document type Book ; Online ; Thesis
    Database Digital theses on the web

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  7. Article ; Online: Quantitating T cell cross-reactivity for unrelated peptide antigens.

    Ishizuka, Jeffrey / Grebe, Kristie / Shenderov, Eugene / Peters, Bjoern / Chen, Qiongyu / Peng, Yanchun / Wang, Lili / Dong, Tao / Pasquetto, Valerie / Oseroff, Carla / Sidney, John / Hickman, Heather / Cerundolo, Vincenzo / Sette, Alessandro / Bennink, Jack R / McMichael, Andrew / Yewdell, Jonathan W

    Journal of immunology (Baltimore, Md. : 1950)

    2009  Volume 183, Issue 7, Page(s) 4337–4345

    Abstract: Quantitating the frequency of T cell cross-reactivity to unrelated peptides is essential ... to understanding T cell responses in infectious and autoimmune diseases. Here we used 15 mouse or human CD8+ T ... T cells raised to viral or alloantigens. These findings provide the best estimate to date of the frequency ...

    Abstract Quantitating the frequency of T cell cross-reactivity to unrelated peptides is essential to understanding T cell responses in infectious and autoimmune diseases. Here we used 15 mouse or human CD8+ T cell clones (11 antiviral, 4 anti-self) in conjunction with a large library of defined synthetic peptides to examine nearly 30,000 TCR-peptide MHC class I interactions for cross-reactions. We identified a single cross-reaction consisting of an anti-self TCR recognizing a poxvirus peptide at relatively low sensitivity. We failed to identify any cross-reactions between the synthetic peptides in the panel and polyclonal CD8+ T cells raised to viral or alloantigens. These findings provide the best estimate to date of the frequency of T cell cross-reactivity to unrelated peptides ( approximately 1/30,000), explaining why cross-reactions between unrelated pathogens are infrequently encountered and providing a critical parameter for understanding the scope of self-tolerance.
    MeSH term(s) Animals ; CD8-Positive T-Lymphocytes/immunology ; CD8-Positive T-Lymphocytes/metabolism ; CD8-Positive T-Lymphocytes/microbiology ; CD8-Positive T-Lymphocytes/virology ; Cell Line, Tumor ; Clone Cells ; Cross Reactions ; Cross-Priming/immunology ; Epitopes, T-Lymphocyte/immunology ; Epitopes, T-Lymphocyte/metabolism ; Humans ; Male ; Mice ; Mice, Inbred BALB C ; Mice, Inbred C57BL ; Mice, Knockout ; Mice, Transgenic ; Peptide Fragments/agonists ; Peptide Fragments/immunology ; Peptide Fragments/metabolism ; Peptide Library ; Predictive Value of Tests ; Protein Binding/immunology
    Chemical Substances Epitopes, T-Lymphocyte ; Peptide Fragments ; Peptide Library
    Keywords covid19
    Language English
    Publishing date 2009-09-04
    Publishing country United States
    Document type Journal Article ; Research Support, N.I.H., Intramural ; Research Support, Non-U.S. Gov't
    ZDB-ID 3056-9
    ISSN 1550-6606 ; 0022-1767 ; 1048-3233 ; 1047-7381
    ISSN (online) 1550-6606
    ISSN 0022-1767 ; 1048-3233 ; 1047-7381
    DOI 10.4049/jimmunol.0901607
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  8. Article ; Online: Editorial: regulation of the regulator: sympathetic nervous system control of regulatory T cells.

    Grebe, Kristie M

    Journal of leukocyte biology

    2009  Volume 86, Issue 6, Page(s) 1269–1270

    MeSH term(s) Animals ; Antigen-Presenting Cells/immunology ; Encephalomyelitis, Autoimmune, Experimental/immunology ; Lymph Nodes/immunology ; Lymph Nodes/innervation ; Mice ; Mice, Knockout ; Oxidopamine/adverse effects ; Oxidopamine/pharmacology ; Spleen/immunology ; Spleen/innervation ; Stress, Physiological/immunology ; Sympathetic Nervous System/immunology ; Sympatholytics/adverse effects ; Sympatholytics/pharmacology ; T-Lymphocytes, Regulatory/immunology ; Transforming Growth Factor beta/immunology
    Chemical Substances Sympatholytics ; Transforming Growth Factor beta ; Oxidopamine (8HW4YBZ748)
    Language English
    Publishing date 2009-12
    Publishing country United States
    Document type Comment ; Editorial
    ZDB-ID 605722-6
    ISSN 1938-3673 ; 0741-5400
    ISSN (online) 1938-3673
    ISSN 0741-5400
    DOI 10.1189/jlb.0409249
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  9. Article ; Online: Regulatory T cells facilitate the nuclear accumulation of inducible cAMP early repressor (ICER) and suppress nuclear factor of activated T cell c1 (NFATc1).

    Vaeth, Martin / Gogishvili, Tea / Bopp, Tobias / Klein, Matthias / Berberich-Siebelt, Friederike / Gattenloehner, Stefan / Avots, Andris / Sparwasser, Tim / Grebe, Nadine / Schmitt, Edgar / Hünig, Thomas / Serfling, Edgar / Bodor, Josef

    2011  

    Abstract: ... and nuclear occurrence are elevated by high cAMP levels in naturally occurring regulatory T ... CREM, and thereby inhibit IL-2 synthesis in conventional CD4(+) T cells. Ablation of nTregs ... in depletion of regulatory T-cell (DEREG) mice resulted in cytosolic localization of ICER/CREM and increased IL ...

    Abstract Inducible cAMP early repressor (ICER) is a transcriptional repressor, which, because of alternate promoter use, is generated from the 3' region of the cAMP response modulator (Crem) gene. Its expression and nuclear occurrence are elevated by high cAMP levels in naturally occurring regulatory T cells (nTregs). Using two mouse models, we demonstrate that nTregs control the cellular localization of ICER/CREM, and thereby inhibit IL-2 synthesis in conventional CD4(+) T cells. Ablation of nTregs in depletion of regulatory T-cell (DEREG) mice resulted in cytosolic localization of ICER/CREM and increased IL-2 synthesis upon stimulation. Direct contacts between nTregs and conventional CD4(+) T cells led to nuclear accumulation of ICER/CREM and suppression of IL-2 synthesis on administration of CD28 superagonistic (CD28SA) Ab. In a similar way, nTregs communicated with B cells and induced the cAMP-driven nuclear localization of ICER/CREM. High levels of ICER suppressed the induction of nuclear factor of activated T cell c1 (Nfatc1) gene in T cells whose inducible Nfatc1 P1 promoter bears two highly conserved cAMP-responsive elements to which ICER/CREM can bind. These findings suggest that nTregs suppress T-cell responses by the cAMP-dependent nuclear accumulation of ICER/CREM and inhibition of NFATc1 and IL-2 induction.
    Keywords Active Transport ; Cell Nucleus ; Animals ; Antibodies ; Antigens ; CD28 ; Cyclic AMP ; Cyclic AMP Response Element Modulator ; Interleukin-2 ; Lymphocyte Activation ; Mice ; Inbred BALB C ; Knockout ; NFATC Transcription Factors ; Response Elements ; T-Lymphocytes ; Regulatory
    Subject code 570
    Language English
    Publishing date 2011-02-08
    Publishing country de
    Document type Article ; Online
    Database BASE - Bielefeld Academic Search Engine (life sciences selection)

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  10. Article ; Online: Regulatory T cells facilitate the nuclear accumulation of inducible cAMP early repressor (ICER) and suppress nuclear factor of activated T cell c1 (NFATc1).

    Vaeth, Martin / Gogishvili, Tea / Bopp, Tobias / Klein, Matthias / Berberich-Siebelt, Friederike / Gattenloehner, Stefan / Avots, Andris / Sparwasser, Tim / Grebe, Nadine / Schmitt, Edgar / Hünig, Thomas / Serfling, Edgar / Bodor, Josef

    2011  

    Abstract: ... and nuclear occurrence are elevated by high cAMP levels in naturally occurring regulatory T ... CREM, and thereby inhibit IL-2 synthesis in conventional CD4(+) T cells. Ablation of nTregs ... in depletion of regulatory T-cell (DEREG) mice resulted in cytosolic localization of ICER/CREM and increased IL ...

    Abstract Inducible cAMP early repressor (ICER) is a transcriptional repressor, which, because of alternate promoter use, is generated from the 3' region of the cAMP response modulator (Crem) gene. Its expression and nuclear occurrence are elevated by high cAMP levels in naturally occurring regulatory T cells (nTregs). Using two mouse models, we demonstrate that nTregs control the cellular localization of ICER/CREM, and thereby inhibit IL-2 synthesis in conventional CD4(+) T cells. Ablation of nTregs in depletion of regulatory T-cell (DEREG) mice resulted in cytosolic localization of ICER/CREM and increased IL-2 synthesis upon stimulation. Direct contacts between nTregs and conventional CD4(+) T cells led to nuclear accumulation of ICER/CREM and suppression of IL-2 synthesis on administration of CD28 superagonistic (CD28SA) Ab. In a similar way, nTregs communicated with B cells and induced the cAMP-driven nuclear localization of ICER/CREM. High levels of ICER suppressed the induction of nuclear factor of activated T cell c1 (Nfatc1) gene in T cells whose inducible Nfatc1 P1 promoter bears two highly conserved cAMP-responsive elements to which ICER/CREM can bind. These findings suggest that nTregs suppress T-cell responses by the cAMP-dependent nuclear accumulation of ICER/CREM and inhibition of NFATc1 and IL-2 induction.
    Keywords Active Transport ; Cell Nucleus ; Animals ; Antibodies ; Antigens ; CD28 ; Cyclic AMP ; Cyclic AMP Response Element Modulator ; Interleukin-2 ; Lymphocyte Activation ; Mice ; Inbred BALB C ; Knockout ; NFATC Transcription Factors ; Response Elements ; T-Lymphocytes ; Regulatory
    Subject code 570
    Language English
    Publishing date 2011-02-08
    Publishing country de
    Document type Article ; Online
    Database BASE - Bielefeld Academic Search Engine (life sciences selection)

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