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  1. Article ; Online: Transforming mutations in the development of pathogenic B cell clones and autoantibodies.

    Reed, Joanne H

    Immunological reviews

    2022  Volume 307, Issue 1, Page(s) 101–115

    Abstract: Autoimmune diseases are characterized by serum autoantibodies, some of which are pathogenic, causing severe manifestations and organ injury. However, autoantibodies of the same antigenic reactivity are also present in the serum of asymptomatic people ... ...

    Abstract Autoimmune diseases are characterized by serum autoantibodies, some of which are pathogenic, causing severe manifestations and organ injury. However, autoantibodies of the same antigenic reactivity are also present in the serum of asymptomatic people years before they develop any clinical signs of autoimmunity. Autoantibodies can arise during multiple stages of B cell development, and various genetic and environmental factors drive their production. However, what drives the development of pathogenic autoantibodies is poorly understood. Advances in single-cell technology have enabled the deep analysis of rare B cell clones producing pathogenic autoantibodies responsible for vasculitis in patients with primary Sjögren's syndrome complicated by mixed cryoglobulinaemia. These findings demonstrated a cascade of genetic events involving stereotypic immunoglobulin V(D)J recombination and transforming somatic mutations in lymphoma genes and V(D)J regions that disrupted antibody quality control mechanisms and decreased autoantibody solubility. Most studies consider V(D)J mutations that enhance autoantibody affinity to drive pathology; however, V(D)J mutations that increase autoantibody propensity to form insoluble complexes could be a major contributor to autoantibody pathogenicity. Defining the molecular characteristics of pathogenic autoantibodies and failed tolerance checkpoints driving their formation will improve prognostication, enabling early treatment to prevent escalating organ damage and B cell malignancy.
    MeSH term(s) Autoantibodies ; Autoimmunity/genetics ; B-Lymphocytes ; Clone Cells ; Humans ; Mutation/genetics
    Chemical Substances Autoantibodies
    Language English
    Publishing date 2022-01-09
    Publishing country England
    Document type Journal Article ; Review ; Research Support, Non-U.S. Gov't
    ZDB-ID 391796-4
    ISSN 1600-065X ; 0105-2896
    ISSN (online) 1600-065X
    ISSN 0105-2896
    DOI 10.1111/imr.13064
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article: Seronegative Sjögren Syndrome: A Forgotten Entity?

    Lee, Adrian Y S / Rischmueller, Maureen / Reed, Joanne H

    The Journal of rheumatology

    2023  

    Abstract: As a highly varied disease, Sjögren syndrome (SS; also ... ...

    Abstract As a highly varied disease, Sjögren syndrome (SS; also termed
    Language English
    Publishing date 2023-10-15
    Publishing country Canada
    Document type Editorial
    ZDB-ID 194928-7
    ISSN 1499-2752 ; 0315-162X
    ISSN (online) 1499-2752
    ISSN 0315-162X
    DOI 10.3899/jrheum.2023-0247
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  3. Article ; Online: Anti-Ro52/TRIM21 serological subsets identify differential clinical and laboratory parameters.

    Lee, Adrian Y S / Lin, Ming-Wei / Reed, Joanne H

    Clinical rheumatology

    2022  Volume 41, Issue 11, Page(s) 3495–3501

    Abstract: Introduction: Anti-Ro52/tripartite motif-containing protein 21 (TRIM21) IgG is one of the most common autoantibodies found in systemic autoimmune diseases and is typically found in conjunction with anti-Ro60 and/or anti-La. A retrospective, cross- ... ...

    Abstract Introduction: Anti-Ro52/tripartite motif-containing protein 21 (TRIM21) IgG is one of the most common autoantibodies found in systemic autoimmune diseases and is typically found in conjunction with anti-Ro60 and/or anti-La. A retrospective, cross-sectional study was undertaken to examine the clinical and laboratory features of two serological subsets: patients with anti-Ro52/TRIM21 autoantibodies in the absence of anti-Ro60 and anti-La (isolated anti-Ro52/TRIM21) and patients with anti-Ro52/TRIM21 in the presence of anti-Ro60 and/or anti-La.
    Methods: Over a 12-month period, patients tested positive for anti-Ro52/TRIM21 via line immunoassay (LIA) at the Westmead Hospital (Australia) immunopathology laboratory were included. The presence of anti-Ro60 and/or anti-La via same LIA was noted. Associated laboratory and medical records were perused to extract demographic, laboratory, and clinical information.
    Results: There were 346 patients within the study period, and 39.9% of the patients positive for anti-Ro52/TRIM21 lacked anti-Ro60/anti-La autoantibodies. Isolated anti-Ro52/TRIM21 patients tend to be older, have lower anti-Ro52/TRIM21 titres, have lower rheumatoid factors, and have lower proportions of neutropaenia compared to patients who were positive for anti-Ro52/TRIM21 and anti-Ro60/La. This occurred independent to diagnoses of Sjögren's syndrome or systemic lupus erythematosus. Coexisting neurological syndromes, pulmonary pathologies, and malignancies were more prevalent in the isolated anti-Ro52/TRIM21 subset.
    Conclusions: Patients with isolated anti-Ro52/TRIM21 tend to have distinct and important clinical and laboratory associations. It is unclear if these patients evolve or remain a stable subset and how they originate immunologically. Longitudinal and prospective studies are required to ascertain the overall predictive and prognostic value of this stratification. Key Points • Anti-Ro52/TRIM21 is an autoantibody found in autoimmunity and non-immunological conditions. • Sixty percent of anti-Ro52/TRIM21 patients are positive for anti-Ro60. • Isolated anti-Ro52/TRIM21 has reduced anti-Ro52/TRIM21 and rheumatoid factor titres. • Isolated anti-Ro52/TRIM21 is associated with anaemia and malignancies.
    MeSH term(s) Autoantibodies ; Cross-Sectional Studies ; Humans ; Immunoglobulin G ; Retrospective Studies ; Rheumatoid Factor ; Sjogren's Syndrome
    Chemical Substances Autoantibodies ; Immunoglobulin G ; Rheumatoid Factor (9009-79-4)
    Language English
    Publishing date 2022-07-23
    Publishing country Germany
    Document type Journal Article
    ZDB-ID 604755-5
    ISSN 1434-9949 ; 0770-3198
    ISSN (online) 1434-9949
    ISSN 0770-3198
    DOI 10.1007/s10067-022-06299-5
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  4. Article ; Online: Anti-Ro60 and anti-Ro52/TRIM21: Two distinct autoantibodies in systemic autoimmune diseases.

    Lee, Adrian Y S / Reed, Joanne H / Gordon, Tom P

    Journal of autoimmunity

    2021  Volume 124, Page(s) 102724

    Abstract: As iconic and important diagnostic autoantibodies, anti-Ro60 and anti-Ro52/tri-partite motif-containing 21 (TRIM21) make a common appearance in a number of systemic autoimmune disorders such as systemic lupus erythematosus (SLE). These autoantibodies ... ...

    Abstract As iconic and important diagnostic autoantibodies, anti-Ro60 and anti-Ro52/tri-partite motif-containing 21 (TRIM21) make a common appearance in a number of systemic autoimmune disorders such as systemic lupus erythematosus (SLE). These autoantibodies often co-exist together; yet despite their close relationship, there is no evidence that they are physically linked and probably reflect a convergence of separate processes of failed immunological tolerance. Confusingly, they are sometimes classed together as the "SSA" or "Ro" autoantibody system without clear distinction between the two. In this Short Communication, we discuss the diagnostic merits for separate detection and reporting of these two autoantibodies, and discuss avenues for future research. Indeed, further insight into their fascinating origins and pathogenic roles in autoimmunity will surely shed light on how we can prevent and treat devastating autoimmune disorders.
    MeSH term(s) Antibodies, Antinuclear/metabolism ; Autoimmunity ; Humans ; Immune Tolerance ; Lupus Erythematosus, Systemic/diagnosis ; Lupus Erythematosus, Systemic/immunology ; Ribonucleoproteins/immunology
    Chemical Substances Antibodies, Antinuclear ; Ribonucleoproteins ; SS-A antigen
    Language English
    Publishing date 2021-08-28
    Publishing country England
    Document type Journal Article
    ZDB-ID 639452-8
    ISSN 1095-9157 ; 0896-8411
    ISSN (online) 1095-9157
    ISSN 0896-8411
    DOI 10.1016/j.jaut.2021.102724
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  5. Article ; Online: Phases and Natural History of Sjögren's Disease: A New Model for an Old Disease?

    Lee, Adrian Y S / Wang, Jing Jing / Gordon, Tom P / Reed, Joanne H

    Arthritis care & research

    2023  Volume 75, Issue 7, Page(s) 1580–1587

    Abstract: Sjögren's disease (SjD) is an archetypal and heterogenous autoimmune disorder that is characterized by exocrine glandular dysfunction. A proportion of patients develop severe extraglandular manifestations, such as cryoglobulinemia, and have an increased ... ...

    Abstract Sjögren's disease (SjD) is an archetypal and heterogenous autoimmune disorder that is characterized by exocrine glandular dysfunction. A proportion of patients develop severe extraglandular manifestations, such as cryoglobulinemia, and have an increased risk of lymphoma, both of which can adversely affect quality of life and occasionally mortality. As with most autoimmune disorders, the pathogenesis is poorly understood and difficult to predict, and, frustratingly, there is a lack of targeted therapies to cure this disease. We review the disease manifestations of SjD and propose a staged model for understanding the evolution of pathology. In longitudinal studies, most patients remain relatively stable in terms of their laboratory and clinical parameters. However, in the setting of various risk factors, a proportion of patients develop severe symptoms and/or lymphoma. We discuss potential underlying mechanisms for disease progression and the strengths and limitations of using a staged model to correlate the pathogenesis and spectrum of manifestations in SjD. Ultimately, understanding how and why some patients remain relatively stable, whereas others progress and develop florid systemic disease and a fraction develop lymphoma, is key to developing preventative and therapeutic treatments.
    MeSH term(s) Humans ; Quality of Life ; Sjogren's Syndrome ; Autoimmune Diseases ; Risk Factors ; Lymphoma
    Language English
    Publishing date 2023-01-05
    Publishing country United States
    Document type Journal Article ; Review ; Research Support, Non-U.S. Gov't
    ZDB-ID 645059-3
    ISSN 2151-4658 ; 0893-7524 ; 2151-464X
    ISSN (online) 2151-4658
    ISSN 0893-7524 ; 2151-464X
    DOI 10.1002/acr.25011
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  6. Article ; Online: Anti-Ro52/TRIM21 serological subsets identify differential clinical and laboratory parameters

    Lee, Adrian Y. S. / Lin, Ming-Wei / Reed, Joanne H.

    Clin Rheumatol 2022 Nov., v. 41, no. 11, p. 3495-3501

    2022  , Page(s) 3495–3501

    Abstract: INTRODUCTION: Anti-Ro52/tripartite motif-containing protein 21 (TRIM21) IgG is one of the most common autoantibodies found in systemic autoimmune diseases and is typically found in conjunction with anti-Ro60 and/or anti-La. A retrospective, cross- ... ...

    Abstract INTRODUCTION: Anti-Ro52/tripartite motif-containing protein 21 (TRIM21) IgG is one of the most common autoantibodies found in systemic autoimmune diseases and is typically found in conjunction with anti-Ro60 and/or anti-La. A retrospective, cross-sectional study was undertaken to examine the clinical and laboratory features of two serological subsets: patients with anti-Ro52/TRIM21 autoantibodies in the absence of anti-Ro60 and anti-La (isolated anti-Ro52/TRIM21) and patients with anti-Ro52/TRIM21 in the presence of anti-Ro60 and/or anti-La. METHODS: Over a 12-month period, patients tested positive for anti-Ro52/TRIM21 via line immunoassay (LIA) at the Westmead Hospital (Australia) immunopathology laboratory were included. The presence of anti-Ro60 and/or anti-La via same LIA was noted. Associated laboratory and medical records were perused to extract demographic, laboratory, and clinical information. RESULTS: There were 346 patients within the study period, and 39.9% of the patients positive for anti-Ro52/TRIM21 lacked anti-Ro60/anti-La autoantibodies. Isolated anti-Ro52/TRIM21 patients tend to be older, have lower anti-Ro52/TRIM21 titres, have lower rheumatoid factors, and have lower proportions of neutropaenia compared to patients who were positive for anti-Ro52/TRIM21 and anti-Ro60/La. This occurred independent to diagnoses of Sjögren’s syndrome or systemic lupus erythematosus. Coexisting neurological syndromes, pulmonary pathologies, and malignancies were more prevalent in the isolated anti-Ro52/TRIM21 subset. CONCLUSIONS: Patients with isolated anti-Ro52/TRIM21 tend to have distinct and important clinical and laboratory associations. It is unclear if these patients evolve or remain a stable subset and how they originate immunologically. Longitudinal and prospective studies are required to ascertain the overall predictive and prognostic value of this stratification. Key Points • Anti-Ro52/TRIM21 is an autoantibody found in autoimmunity and non-immunological conditions. • Sixty percent of anti-Ro52/TRIM21 patients are positive for anti-Ro60. • Isolated anti-Ro52/TRIM21 has reduced anti-Ro52/TRIM21 and rheumatoid factor titres. • Isolated anti-Ro52/TRIM21 is associated with anaemia and malignancies.
    Keywords anemia ; autoantibodies ; autoimmunity ; cross-sectional studies ; hospitals ; immunoassays ; immunopathology ; lupus erythematosus ; neutropenia ; Australia
    Language English
    Dates of publication 2022-11
    Size p. 3495-3501
    Publishing place Springer International Publishing
    Document type Article ; Online
    Note Use and reproduction
    ZDB-ID 604755-5
    ISSN 0770-3198
    ISSN 0770-3198
    DOI 10.1007/s10067-022-06299-5
    Database NAL-Catalogue (AGRICOLA)

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  7. Article: When B cells break bad: development of pathogenic B cells in Sjögren's syndrome.

    Reed, Joanne H / Verstappen, Gwenny Matthea / Rischmueller, Maureen / Bryant, Vanessa L

    Clinical and experimental rheumatology

    2020  Volume 38 Suppl 126, Issue 4, Page(s) 271–282

    Abstract: Primary Sjögren's syndrome (pSS) is often considered a B cell-mediated disease, yet the precise role of B cells in the pathogenesis is not fully understood. This is exemplified by the failure of multiple clinical trials directed at B cell depletion or ... ...

    Abstract Primary Sjögren's syndrome (pSS) is often considered a B cell-mediated disease, yet the precise role of B cells in the pathogenesis is not fully understood. This is exemplified by the failure of multiple clinical trials directed at B cell depletion or inhibition. To date, most prognostic markers for severe disease outcomes are autoantibodies, but the underlying mechanisms by which B cells drive diverse disease presentations in pSS likely extend beyond autoantibody production. Here we outline an expanded role of B cells in disease pathogenesis drawing on examples from animal models of SS, and from other autoimmune diseases that share similar clinical or immunological abnormalities. We focus on recent findings from the detailed analysis of pathogenic B cells in patients with pSS to propose strategies for patient stratification to improve clinical trial outcomes. We conclude that an integrated cellular, molecular and genetic analysis of patients with pSS will reveal the underlying pathogenic mechanisms and guide precision medicine.
    MeSH term(s) Animals ; Autoantibodies ; Autoimmune Diseases ; B-Lymphocytes ; Humans ; Sjogren's Syndrome/diagnosis
    Chemical Substances Autoantibodies
    Language English
    Publishing date 2020-09-22
    Publishing country Italy
    Document type Journal Article ; Review
    ZDB-ID 605886-3
    ISSN 1593-098X ; 0392-856X
    ISSN (online) 1593-098X
    ISSN 0392-856X
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  8. Article ; Online: Autoimmunity: Ro60-associated RNA takes its toll on disease pathogenesis.

    Reed, Joanne H / Gordon, Tom P

    Nature reviews. Rheumatology

    2016  Volume 12, Issue 3, Page(s) 136–138

    MeSH term(s) Alu Elements ; Autoantigens/metabolism ; Gene Expression Regulation ; Humans ; Lupus Erythematosus, Systemic/genetics ; RNA, Small Cytoplasmic/metabolism ; Ribonucleoproteins/metabolism ; Sjogren's Syndrome/genetics
    Chemical Substances Autoantigens ; RNA, Small Cytoplasmic ; Ribonucleoproteins
    Language English
    Publishing date 2016-03
    Publishing country United States
    Document type Comment ; Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 2491532-4
    ISSN 1759-4804 ; 1759-4790
    ISSN (online) 1759-4804
    ISSN 1759-4790
    DOI 10.1038/nrrheum.2015.148
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  9. Article ; Online: Uncontrolled CD21

    Masle-Farquhar, Etienne / Peters, Timothy J / Miosge, Lisa A / Parish, Ian A / Weigel, Christoph / Oakes, Christopher C / Reed, Joanne H / Goodnow, Christopher C

    Cell reports

    2022  Volume 38, Issue 3, Page(s) 110259

    Abstract: ... ...

    Abstract CD21
    MeSH term(s) Animals ; Autoimmune Diseases/immunology ; Autoimmune Diseases/metabolism ; Autoimmunity/immunology ; B-Lymphocyte Subsets/immunology ; B-Lymphocyte Subsets/metabolism ; B-Lymphocytes/immunology ; B-Lymphocytes/metabolism ; Clonal Anergy/immunology ; Early Growth Response Protein 2/immunology ; Early Growth Response Protein 2/metabolism ; Early Growth Response Protein 3/immunology ; Early Growth Response Protein 3/metabolism ; Humans ; Leukemia, Lymphocytic, Chronic, B-Cell/immunology ; Leukemia, Lymphocytic, Chronic, B-Cell/metabolism ; Male ; Mice ; Receptors, Complement 3d/immunology
    Chemical Substances Early Growth Response Protein 2 ; Receptors, Complement 3d ; Early Growth Response Protein 3 (144516-98-3)
    Language English
    Publishing date 2022-01-19
    Publishing country United States
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 2649101-1
    ISSN 2211-1247 ; 2211-1247
    ISSN (online) 2211-1247
    ISSN 2211-1247
    DOI 10.1016/j.celrep.2021.110259
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  10. Article ; Online: Clonal redemption and clonal anergy as mechanisms to balance B cell tolerance and immunity.

    Burnett, Deborah L / Reed, Joanne H / Christ, Daniel / Goodnow, Christopher C

    Immunological reviews

    2019  Volume 292, Issue 1, Page(s) 61–75

    Abstract: The adaptive immune system is tasked with producing antibodies that recognize a wide scope of potential pathogens, including those never before encountered, and concurrently avoiding formation of antibodies binding host tissues. The diverse repertoire of ...

    Abstract The adaptive immune system is tasked with producing antibodies that recognize a wide scope of potential pathogens, including those never before encountered, and concurrently avoiding formation of antibodies binding host tissues. The diverse repertoire of antibodies produced by V(D)J recombination inevitably includes autoantibodies that bind to self-antigens, estimated to be as much as 70% of nascent antibodies on immature B cells. Early theoretical models of tolerance hypothesized that such self-reactive clones could not possibly be allowed to survive and mature. However from the first direct view of the fate of nascent B cells carrying a self-binding antibody it was clear that many "forbidden clones" circulate to secondary lymphoid tissues, where they adopt an IgM
    MeSH term(s) Animals ; Autoantibodies/immunology ; Autoantigens/immunology ; Autoantigens/metabolism ; B-Lymphocytes/immunology ; B-Lymphocytes/metabolism ; Clonal Anergy/immunology ; Germinal Center/immunology ; Germinal Center/metabolism ; Humans ; Immune Tolerance/immunology ; Immunity/immunology ; Receptors, Antigen, B-Cell/immunology ; Receptors, Antigen, B-Cell/metabolism
    Chemical Substances Autoantibodies ; Autoantigens ; Receptors, Antigen, B-Cell
    Language English
    Publishing date 2019-09-26
    Publishing country England
    Document type Journal Article ; Research Support, Non-U.S. Gov't ; Review
    ZDB-ID 391796-4
    ISSN 1600-065X ; 0105-2896
    ISSN (online) 1600-065X
    ISSN 0105-2896
    DOI 10.1111/imr.12808
    Database MEDical Literature Analysis and Retrieval System OnLINE

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