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  1. Article ; Online: Pathology of T-cell-mediated drug hypersensitivity reactions and impact of tolerance mechanisms on patient susceptibility.

    Line, James / Thomson, Paul / Naisbitt, Dean J

    Current opinion in allergy and clinical immunology

    2022  Volume 22, Issue 4, Page(s) 226–233

    Abstract: Purpose of review: T-cell-mediated drug hypersensitivity is responsible for significant morbidity and mortality, and represents a substantial clinical concern. The purpose of this article is to focus on T-cell reactions and discuss recent advances in ... ...

    Abstract Purpose of review: T-cell-mediated drug hypersensitivity is responsible for significant morbidity and mortality, and represents a substantial clinical concern. The purpose of this article is to focus on T-cell reactions and discuss recent advances in disease pathogenesis by exploring the impact of tolerance mechanisms in determining susceptibility in genetically predisposed patients.
    Recent findings: Certain drugs preferentially activate pathogenic T cells that have defined pathways of effector function. Thus, a critical question is what extenuating factors influence the direction of immune activation. A large effort has been given towards identifying phenotypic (e.g., infection) or genotypic (e.g., human leukocyte antigen) associations which predispose individuals to drug hypersensitivity. However, many individuals expressing known risk factors safely tolerate drug administration. Thus, mechanistic insight is needed to determine what confers this tolerance. Herein, we discuss recent clinical/mechanistic findings which indicate that the direction in which the immune system is driven relies upon a complex interplay between co-stimulatory/co-regulatory pathways which themselves depend upon environmental inputs from the innate immune system.
    Summary: It is becoming increasingly apparent that tolerance mechanisms impact on susceptibility to drug hypersensitivity. As the field moves forward it will be interesting to discover whether active tolerance is the primary response to drug exposure, with genetic factors such as HLA acting as a sliding scale, influencing the degree of regulation required to prevent clinical reactions in patients.
    MeSH term(s) Drug Hypersensitivity ; HLA Antigens/genetics ; Humans ; Hypersensitivity, Delayed ; Pharmaceutical Preparations ; T-Lymphocytes
    Chemical Substances HLA Antigens ; Pharmaceutical Preparations
    Language English
    Publishing date 2022-07-02
    Publishing country United States
    Document type Journal Article ; Review
    ZDB-ID 2088710-3
    ISSN 1473-6322 ; 1528-4050
    ISSN (online) 1473-6322
    ISSN 1528-4050
    DOI 10.1097/ACI.0000000000000834
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article ; Online: Pathology of drug hypersensitivity reactions and mechanisms of immune tolerance.

    Thomson, Paul / Hammond, Sean / Naisbitt, Dean J

    Clinical and experimental allergy : journal of the British Society for Allergy and Clinical Immunology

    2022  Volume 52, Issue 12, Page(s) 1379–1390

    Abstract: Immune-mediated type IV adverse drug reactions are idiosyncratic in nature, generally not related to the primary or secondary pharmacology of the drug. Due to their complex nature and rarity, these iatrogenic reactions are seldom predicted or encountered ...

    Abstract Immune-mediated type IV adverse drug reactions are idiosyncratic in nature, generally not related to the primary or secondary pharmacology of the drug. Due to their complex nature and rarity, these iatrogenic reactions are seldom predicted or encountered during preclinical/early clinical development stages, and often precipitate upon exposure to wider populations (i.e. phase III onwards). They confer a burden on the healthcare sector in both a clinical and financial sense presenting a severe impediment to the drug discovery and development process. Research over the past 50 years has improved our understanding of these reactions markedly as both in vitro and in vivo studies have placed the role of the immune system, in particular; drug-responsive T cells, firmly in the spotlight as the mediators of these reactions. Indeed, the role of different populations of T cells in adverse events and the interaction of drug molecules with HLA proteins expressed on the surface of antigen-presenting cells is of considerable interest. Herein, this review examines the pathways of immune-mediated adverse events including the various T cell subtypes implicated and the mechanisms of T cell activation. Additionally, we address the enigma of immunological tolerance and explore the role tolerance plays in determination of susceptibility to such adverse events even in individuals carrying immunogenic liabilities.
    MeSH term(s) Humans ; Drug Hypersensitivity/diagnosis ; Immune Tolerance ; T-Lymphocytes ; Lymphocyte Activation ; Drug-Related Side Effects and Adverse Reactions
    Language English
    Publishing date 2022-10-20
    Publishing country England
    Document type Journal Article ; Review
    ZDB-ID 645204-8
    ISSN 1365-2222 ; 0954-7894 ; 0960-2178
    ISSN (online) 1365-2222
    ISSN 0954-7894 ; 0960-2178
    DOI 10.1111/cea.14235
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  3. Article ; Online: Investigating the Immune Basis of Green Tea Extract Induced Liver Injury in Healthy Donors Expressing HLA-B*35:01.

    Line, James / Ali, Serat-E / Grice, Sophie / Rao, Tai / Naisbitt, Dean J

    Chemical research in toxicology

    2023  Volume 36, Issue 12, Page(s) 1872–1875

    Abstract: Epigallocatechin-3- ...

    Abstract Epigallocatechin-3-
    MeSH term(s) Humans ; Chemical and Drug Induced Liver Injury, Chronic ; Leukocytes, Mononuclear ; Antioxidants ; Tea ; HLA-B Antigens/genetics ; Plant Extracts/pharmacology ; Catechin/pharmacology
    Chemical Substances Antioxidants ; Tea ; HLA-B Antigens ; Plant Extracts ; Catechin (8R1V1STN48)
    Language English
    Publishing date 2023-12-06
    Publishing country United States
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 639353-6
    ISSN 1520-5010 ; 0893-228X
    ISSN (online) 1520-5010
    ISSN 0893-228X
    DOI 10.1021/acs.chemrestox.3c00253
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  4. Article ; Online: Does immune checkpoint inhibitor therapy increase the frequency of adverse reactions to concomitant medications?

    Hammond, Sean / Olsson-Brown, Anna / Grice, Sophie / Naisbitt, Dean J

    Clinical and experimental allergy : journal of the British Society for Allergy and Clinical Immunology

    2022  Volume 52, Issue 5, Page(s) 600–603

    MeSH term(s) Drug-Related Side Effects and Adverse Reactions/diagnosis ; Drug-Related Side Effects and Adverse Reactions/drug therapy ; Drug-Related Side Effects and Adverse Reactions/epidemiology ; Humans ; Immune Checkpoint Inhibitors/adverse effects ; Immunotherapy/adverse effects ; Neoplasms/etiology
    Chemical Substances Immune Checkpoint Inhibitors
    Language English
    Publishing date 2022-03-25
    Publishing country England
    Document type Editorial
    ZDB-ID 645204-8
    ISSN 1365-2222 ; 0954-7894 ; 0960-2178
    ISSN (online) 1365-2222
    ISSN 0954-7894 ; 0960-2178
    DOI 10.1111/cea.14134
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  5. Article ; Online: Activation of tolvaptan-responsive T-cell clones with the structurally-related mozavaptan.

    Hammond, Sean / Meng, Xiaoli / Mosedale, Merrie / Naisbitt, Dean J

    Toxicology letters

    2022  Volume 373, Page(s) 148–151

    Abstract: Tolvaptan is an effective drug for the treatment of autosomal dominant polycystic kidney disease, but its use is associated with a significant risk of T-cell-mediated liver injury in a small number of patients. An important clinical conundrum following ... ...

    Abstract Tolvaptan is an effective drug for the treatment of autosomal dominant polycystic kidney disease, but its use is associated with a significant risk of T-cell-mediated liver injury in a small number of patients. An important clinical conundrum following the contraindication of tolvaptan is whether administration of agents of similar pharmacological action and structure will be tolerated. Herein, we addressed this question through the exposure of tolvaptan-responsive T-cell clones to similar pharmaceutical agents. Whilst lixivaptan and conivaptan did not activate tolvaptan-responsive T-cells, mozavaptan evoked proliferative responses comparable with tolvaptan itself, indicating that there may be collateral immunological intolerance to this compound as a product of sensitization to tolvaptan.
    MeSH term(s) Humans ; Tolvaptan/toxicity ; Tolvaptan/therapeutic use ; Antidiuretic Hormone Receptor Antagonists/toxicity ; Antidiuretic Hormone Receptor Antagonists/therapeutic use ; T-Lymphocytes ; Polycystic Kidney, Autosomal Dominant/chemically induced ; Polycystic Kidney, Autosomal Dominant/complications ; Polycystic Kidney, Autosomal Dominant/drug therapy ; Clone Cells
    Chemical Substances Tolvaptan (21G72T1950) ; mozavaptan (17OJ42922Y) ; Antidiuretic Hormone Receptor Antagonists
    Language English
    Publishing date 2022-11-26
    Publishing country Netherlands
    Document type Journal Article
    ZDB-ID 433788-8
    ISSN 1879-3169 ; 0378-4274
    ISSN (online) 1879-3169
    ISSN 0378-4274
    DOI 10.1016/j.toxlet.2022.11.017
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  6. Article ; Online: Drug hapten-specific T-cell activation: Current status and unanswered questions.

    Adair, Kareena / Meng, Xiaoli / Naisbitt, Dean J

    Proteomics

    2021  Volume 21, Issue 17-18, Page(s) e2000267

    Abstract: Drug haptens are formed from the irreversible, covalent binding of drugs to nucleophilic moieties on proteins, which can warrant adverse reactions in the body including severe delayed-type, T-cell mediated, drug hypersensitivity reactions (DHRs). While ... ...

    Abstract Drug haptens are formed from the irreversible, covalent binding of drugs to nucleophilic moieties on proteins, which can warrant adverse reactions in the body including severe delayed-type, T-cell mediated, drug hypersensitivity reactions (DHRs). While three main pathways exist for the activation of T-cells in DHRs, namely the hapten model, the pharmacological interaction model and the altered peptide repertoire model, the exact antigenic determinants responsible have not yet been defined. In recent years, progress has been made using advanced mass spectrometry-based proteomic methods to identify protein carriers and characterise the structure of drug-haptenated proteins. Since genome-wide association studies discovered a link between human leukocyte antigens (HLA) and an individual's susceptibility to DHRs, much effort has been made to define the drug-associated HLA ligands driving T-cell activation, including the elution of natural HLA peptides from HLA molecules and the generation of HLA-binding peptides. In this review, we discuss our current methodology used to design and synthesise drug-modified HLA ligands to investigate their immunogenicity using T-cell models, and thus their implication in drug hypersensitivity.
    MeSH term(s) Genome-Wide Association Study ; Haptens ; Humans ; Pharmaceutical Preparations ; Proteomics ; T-Lymphocytes
    Chemical Substances Haptens ; Pharmaceutical Preparations
    Language English
    Publishing date 2021-07-05
    Publishing country Germany
    Document type Journal Article ; Review
    ZDB-ID 2032093-0
    ISSN 1615-9861 ; 1615-9853
    ISSN (online) 1615-9861
    ISSN 1615-9853
    DOI 10.1002/pmic.202000267
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  7. Article ; Online: Current perspective of the etiopathogenesis of delayed-type, and T-cell-mediated drug-related skin diseases.

    Vocanson, Marc / Naisbitt, Dean J / Nicolas, Jean-François

    The Journal of allergy and clinical immunology

    2020  Volume 145, Issue 4, Page(s) 1142–1144

    MeSH term(s) Animals ; Cell Degranulation ; Drug Hypersensitivity/immunology ; Humans ; Hypersensitivity, Delayed/immunology ; Mast Cells/immunology ; Nerve Tissue Proteins/metabolism ; Receptors, G-Protein-Coupled/metabolism ; Receptors, Neuropeptide/metabolism ; T-Lymphocytes, Cytotoxic/immunology ; Urticaria/immunology ; Xenobiotics/adverse effects
    Chemical Substances MRGPRX2 protein, human ; Nerve Tissue Proteins ; Receptors, G-Protein-Coupled ; Receptors, Neuropeptide ; Xenobiotics
    Language English
    Publishing date 2020-02-01
    Publishing country United States
    Document type Journal Article ; Review
    ZDB-ID 121011-7
    ISSN 1097-6825 ; 1085-8725 ; 0091-6749
    ISSN (online) 1097-6825 ; 1085-8725
    ISSN 0091-6749
    DOI 10.1016/j.jaci.2020.01.030
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  8. Article ; Online: Characterization of Teicoplanin-Specific T-Cells from Drug Naïve Donors Expressing HLA-A*32:01.

    Gardner, Joshua / Ogese, Monday / Betts, Catherine J / Pirmohamed, Munir / Naisbitt, Dean J

    Chemical research in toxicology

    2022  Volume 35, Issue 2, Page(s) 199–202

    Abstract: Teicoplanin is a glycopeptide antibiotic deployed to combat Gram-positive bacterial infection and has recently been associated with development of adverse drug reactions, particularly following previous exposure to vancomycin. In this study, we generated ...

    Abstract Teicoplanin is a glycopeptide antibiotic deployed to combat Gram-positive bacterial infection and has recently been associated with development of adverse drug reactions, particularly following previous exposure to vancomycin. In this study, we generated teicoplanin-specific monoclonal T-cell populations from healthy volunteers expressing HLA-A*32:01 and defined pathways of T-cell activation and HLA allele restriction. Teicoplanin-responsive T-cells were CD8+, HLA class I-restricted, and cross-reacted with the lipoglycopeptide daptomycin in proliferation and cytokine/cytolytic molecule (granzyme B, Perforin, and FasL) release assays. These data show that teicoplanin activates T-cells, which may play a role in the pathogenesis of teicoplanin-induced adverse events, in HLA-A*32:01 positive donors.
    MeSH term(s) Anti-Bacterial Agents/chemistry ; Anti-Bacterial Agents/pharmacology ; HLA-A Antigens/biosynthesis ; Healthy Volunteers ; Humans ; T-Lymphocytes/drug effects ; T-Lymphocytes/metabolism ; Teicoplanin/chemistry ; Teicoplanin/pharmacology
    Chemical Substances Anti-Bacterial Agents ; HLA-A Antigens ; Teicoplanin (61036-62-2)
    Language English
    Publishing date 2022-02-02
    Publishing country United States
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 639353-6
    ISSN 1520-5010 ; 0893-228X
    ISSN (online) 1520-5010
    ISSN 0893-228X
    DOI 10.1021/acs.chemrestox.1c00425
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  9. Article ; Online: Characterization of Drug-Specific CD4

    Jaruthamsophon, Kanoot / Thomson, Paul J / Hammond, Sean / Zhang, Eunice / Alfirevic, Ana / Sukasem, Chonlaphat / Naisbitt, Dean J / Pirmohamed, Munir

    Chemical research in toxicology

    2023  Volume 36, Issue 5, Page(s) 757–768

    Abstract: Carbamazepine (CBZ) is an aromatic anticonvulsant known to cause drug hypersensitivity reactions, which range in severity from relatively mild maculopapular exanthema to potentially fatal Stevens-Johnson syndrome and toxic epidermal necrolysis (SJS-TEN). ...

    Abstract Carbamazepine (CBZ) is an aromatic anticonvulsant known to cause drug hypersensitivity reactions, which range in severity from relatively mild maculopapular exanthema to potentially fatal Stevens-Johnson syndrome and toxic epidermal necrolysis (SJS-TEN). These reactions are known to be associated with human leukocyte antigen (HLA) class I alleles, and CBZ interacts preferentially with the related HLA proteins to activate CD8
    MeSH term(s) Humans ; CD8-Positive T-Lymphocytes ; HLA-DRB1 Chains/genetics ; Carbamazepine/adverse effects ; Anticonvulsants/adverse effects ; Drug Hypersensitivity/genetics ; HLA Antigens ; Stevens-Johnson Syndrome/genetics ; CD4-Positive T-Lymphocytes ; HLA-B Antigens
    Chemical Substances HLA-DRB1 Chains ; Carbamazepine (33CM23913M) ; Anticonvulsants ; HLA Antigens ; HLA-B Antigens
    Language English
    Publishing date 2023-04-19
    Publishing country United States
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 639353-6
    ISSN 1520-5010 ; 0893-228X
    ISSN (online) 1520-5010
    ISSN 0893-228X
    DOI 10.1021/acs.chemrestox.2c00414
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  10. Article ; Online: Patients with naproxen‐induced liver injury display T‐cell memory responses toward an oxidative (S)‐O‐desmethyl naproxen metabolite but not the acyl glucuronide

    Thomson, Paul / Fragkas, Nik / Kafu, Laila M. / Aithal, Guruprasad P. / Lucena, M. Isabel / Terracciano, Luigi / Meng, Xiaoli / Pirmohamed, Munir / Brees, Dominique / Kullak‐Ublick, Gerd A. / Odermatt, Alex / Hammond, Thomas / Kammüller, M. E. / Naisbitt, Dean J.

    Allergy. 2024 Jan., v. 79, no. 1, p. 200-214

    2024  , Page(s) 200–214

    Abstract: BACKGROUND: Exposure to nonsteroidal anti‐inflammatory drugs (NSAIDs) such as ibuprofen (IBU) and naproxen (NAP) is associated with idiosyncratic drug‐induced liver injury (DILI). Carboxylate bioactivation into reactive metabolites (e.g., acyl ... ...

    Abstract BACKGROUND: Exposure to nonsteroidal anti‐inflammatory drugs (NSAIDs) such as ibuprofen (IBU) and naproxen (NAP) is associated with idiosyncratic drug‐induced liver injury (DILI). Carboxylate bioactivation into reactive metabolites (e.g., acyl glucuronides, AG) and resulting T‐cell activation is hypothesized as causal for this adverse event. However, conclusive evidence supporting this is lacking. METHODS: In this work, we identify CD4⁺ and CD8⁺ T‐cell hepatic infiltration in a biopsy from an IBU DILI patient. Lymphocyte transformation test and IFN‐γ ELIspot, conducted on peripheral blood mononuclear cells (PBMCs) of patients with NAP‐DILI, were used to explore drug‐specific T‐cell activation. T‐cell clones (TCC) were generated and tested for drug specificity, phenotype/function, and pathways of T‐cell activation. Cells were exposed to NAP, its oxidative metabolite 6‐O‐desmethyl NAP (DM‐NAP), its AG or synthesized NAP‐AG human‐serum albumin adducts (NAP‐AG adduct). RESULTS: CD4⁺ and CD8⁺ T‐cells from patients expressing a range of different Vβ receptors were stimulated to proliferate and secrete IFN‐γ and IL‐22 when exposed to DM‐NAP, but not NAP, NAP‐AG or the NAP‐AG adduct. Activation of the CD4⁺ TCC was HLA‐DQ‐restricted and dependent on antigen presenting cells (APC); most TCC were activated with DM‐NAP‐pulsed APC, while fixation of APC blocked the T‐cell response. Cross‐reactivity was not observed with structurally‐related drugs. CONCLUSION: Our results confirm hepatic T‐cell infiltrations in NSAID‐induced DILI, and show a T‐cell memory response toward DM‐NAP indicating an immune‐mediated basis for the adverse event. Whilst bioactivation at the carboxylate group is widely hypothesized to be pathogenic for NSAID associated DILI, we found no evidence of this with NAP.
    Keywords T-lymphocytes ; albumins ; antigens ; biopsy ; cross reaction ; hypersensitivity ; ibuprofen ; liver ; lymphocyte proliferation ; memory ; metabolites ; patients ; phenotype
    Language English
    Dates of publication 2024-01
    Size p. 200-214
    Publishing place John Wiley & Sons, Ltd
    Document type Article ; Online
    Note JOURNAL ARTICLE
    ZDB-ID 391933-x
    ISSN 1398-9995 ; 0105-4538
    ISSN (online) 1398-9995
    ISSN 0105-4538
    DOI 10.1111/all.15830
    Database NAL-Catalogue (AGRICOLA)

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