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  1. Article ; Online: Disease flares with baricitinib dose reductions and development of flare criteria in patients with CANDLE/PRAAS.

    Cetin Gedik, Kader / Ortega-Villa, Ana M / Materne, Grace / Rastegar, Andre / Montealegre Sanchez, Gina A / Reinhardt, Adam / Brogan, Paul A / Berkun, Yackov / Murias, Sara / Robles, Maria / Schalm, Susanne / de Jesus, Adriana A / Goldbach-Mansky, Raphaela

    Annals of the rheumatic diseases

    2024  

    Abstract: Objectives: Patients with chronic atypical neutrophilic dermatosis with lipodystrophy and elevated temperature/proteasome-associated autoinflammatory syndrome (CANDLE/PRAAS) respond to the janus kinase inhibitor 1/2 inhibition with baricitinib at ... ...

    Abstract Objectives: Patients with chronic atypical neutrophilic dermatosis with lipodystrophy and elevated temperature/proteasome-associated autoinflammatory syndrome (CANDLE/PRAAS) respond to the janus kinase inhibitor 1/2 inhibition with baricitinib at exposures higher than in rheumatoid arthritis. Baricitinib dose reductions to minimise exposure triggered disease flares which we used to develop 'flare criteria'.
    Methods: Of 10 patients with CANDLE/PRAAS treated with baricitinib in an open-label expanded-access programme, baricitinib doses were reduced 14 times in 9 patients between April 2014 and December 2019. Retrospective data analysis of daily diary scores and laboratory markers collected before and after the dose reductions were used to develop 'clinical' and 'subclinical' flare criteria. Disease flare rates were compared among patients with <25% and >25% dose reductions and during study visits when patients received recommended 'optimized' baricitinib doses (high-dose visits) versus lower than recommended baricitinib doses (low-dose visits) using two-sided χ
    Results: In the 9/10 patients with CANDLE with dose reduction, 7/14 (50%) times the dose was reduced resulted in a disease flare. All four dose reductions of >25% triggered a disease flare (p <0.05). Assessment of clinical and laboratory changes during disease flares allowed the development of disease flare criteria that were assessed during visits when patients received high or low doses of baricitinib. Disease flare criteria were reached during 43.14% of low-dose visits compared with 12.75% of high-dose visits (p <0.0001). Addition of an interferon score as an additional flare criterion increased the sensitivity to detect disease flares.
    Conclusion: We observed disease flares and rebound inflammation with baricitinib dose reductions and proposed flare criteria that can assist in monitoring disease activity and in designing clinical studies in CANDLE/PRAAS.
    Language English
    Publishing date 2024-04-23
    Publishing country England
    Document type Journal Article
    ZDB-ID 7090-7
    ISSN 1468-2060 ; 0003-4967
    ISSN (online) 1468-2060
    ISSN 0003-4967
    DOI 10.1136/ard-2023-225463
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article ; Online: Rash, Fever, and Pulmonary Hypertension in a 6-Year-Old Female.

    Buchbinder, David / Montealegre Sanchez, Gina A / Goldbach-Mansky, Raphaela / Brunner, Hermine / Shulman, Andrew I

    Arthritis care & research

    2018  Volume 70, Issue 5, Page(s) 785–790

    MeSH term(s) Child ; Child, Preschool ; Diagnosis, Differential ; Fatal Outcome ; Female ; Hereditary Autoinflammatory Diseases/complications ; Hereditary Autoinflammatory Diseases/diagnosis ; Hereditary Autoinflammatory Diseases/genetics ; Humans ; Hypertension, Pulmonary/etiology ; Proteasome Endopeptidase Complex/genetics ; Syndrome
    Chemical Substances LMP7 protein (EC 3.4.25.1) ; Proteasome Endopeptidase Complex (EC 3.4.25.1)
    Language English
    Publishing date 2018-04-02
    Publishing country United States
    Document type Case Reports ; Clinical Conference ; Journal Article ; Research Support, N.I.H., Intramural
    ZDB-ID 645059-3
    ISSN 2151-4658 ; 0893-7524 ; 2151-464X
    ISSN (online) 2151-4658
    ISSN 0893-7524 ; 2151-464X
    DOI 10.1002/acr.23506
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  3. Article ; Online: Deep immune profiling uncovers novel associations with clinical phenotypes of multisystem inflammatory syndrome in children (MIS-C).

    Redmond, Christopher John / Kitakule, Moses M / Son, Aran / Sylvester, McKella / Sacco, Keith / Delmonte, Ottavia / Licciardi, Francesco / Castagnoli, Riccardo / Poli, M Cecilia / Espinoza, Yasmin / Astudillo, Camila / Weber, Sarah E / Montealegre Sanchez, Gina A / Barron, Karyl S / Magliocco, Mary / Dobbs, Kerry / Zhang, Yu / Matthews, Helen / Oguz, Cihan /
    Su, Helen C / Notarangelo, Luigi D / Frischmeyer-Guerrerio, Pamela / Schwartz, Daniella M

    Annals of the rheumatic diseases

    2022  Volume 82, Issue 3, Page(s) 442–445

    MeSH term(s) Humans ; Systemic Inflammatory Response Syndrome ; COVID-19
    Language English
    Publishing date 2022-11-24
    Publishing country England
    Document type Journal Article ; Research Support, N.I.H., Intramural
    ZDB-ID 7090-7
    ISSN 1468-2060 ; 0003-4967
    ISSN (online) 1468-2060
    ISSN 0003-4967
    DOI 10.1136/ard-2022-223269
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  4. Article ; Online: Recurrent fevers, progressive lipodystrophy, and annular plaques in a child.

    Cardis, Michael A / Montealegre Sanchez, Gina A / Goldbach-Mansky, Raphaela / Richard Lee, Chyi-Chia / Cowen, Edward W

    Journal of the American Academy of Dermatology

    2018  Volume 80, Issue 1, Page(s) 291–295

    Abstract: KEY TEACHING POINTS. ...

    Abstract KEY TEACHING POINTS.
    MeSH term(s) Child ; Chronic Disease ; Disease Progression ; Female ; Fever/etiology ; Humans ; Lipodystrophy/etiology ; Neutrophils ; Recurrence ; Skin Diseases/complications ; Skin Diseases/diagnosis
    Language English
    Publishing date 2018-09-08
    Publishing country United States
    Document type Case Reports ; Journal Article
    ZDB-ID 603641-7
    ISSN 1097-6787 ; 0190-9622
    ISSN (online) 1097-6787
    ISSN 0190-9622
    DOI 10.1016/j.jaad.2018.08.043
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  5. Article ; Online: Insights from Mendelian Interferonopathies: Comparison of CANDLE, SAVI with AGS, Monogenic Lupus.

    Kim, Hanna / Sanchez, Gina A Montealegre / Goldbach-Mansky, Raphaela

    Journal of molecular medicine (Berlin, Germany)

    2016  Volume 94, Issue 10, Page(s) 1111–1127

    Abstract: Autoinflammatory disorders are sterile inflammatory conditions characterized by episodes of early-onset fever and disease-specific patterns of organ inflammation. Recently, the discoveries of monogenic disorders with strong type I interferon (IFN) ... ...

    Abstract Autoinflammatory disorders are sterile inflammatory conditions characterized by episodes of early-onset fever and disease-specific patterns of organ inflammation. Recently, the discoveries of monogenic disorders with strong type I interferon (IFN) signatures caused by mutations in proteasome degradation and cytoplasmic RNA and DNA sensing pathways suggest a pathogenic role of IFNs in causing autoinflammatory phenotypes. The IFN response gene signature (IGS) has been associated with systemic lupus erythematosus (SLE) and other autoimmune diseases. In this review, we compare the clinical presentations and pathogenesis of two IFN-mediated autoinflammatory diseases, CANDLE and SAVI, with Aicardi Goutières syndrome (AGS) and monogenic forms of SLE (monoSLE) caused by loss-of-function mutations in complement 1 (C1q) or the DNA nucleases, DNASE1 and DNASE1L3. We outline differences in intracellular signaling pathways that fuel a pathologic type I IFN amplification cycle. While IFN amplification is caused by predominantly innate immune cell dysfunction in SAVI, CANDLE, and AGS, autoantibodies to modified RNA and DNA antigens interact with tissues and immune cells including neutrophils and contribute to IFN upregulation in some SLE patients including monoSLE, thus justifying a grouping of "autoinflammatory" and "autoimmune" interferonopathies. Understanding of the differences in the cellular sources and signaling pathways will guide new drug development and the use of emerging targeted therapies.
    MeSH term(s) Animals ; Autoimmune Diseases/immunology ; Humans ; Inflammation/immunology ; Interferon Type I/immunology ; Interleukin-1/immunology
    Chemical Substances Interferon Type I ; Interleukin-1
    Language English
    Publishing date 2016-09-27
    Publishing country Germany
    Document type Journal Article ; Review ; Research Support, N.I.H., Intramural
    ZDB-ID 1223802-8
    ISSN 1432-1440 ; 0946-2716
    ISSN (online) 1432-1440
    ISSN 0946-2716
    DOI 10.1007/s00109-016-1465-5
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  6. Article: Deep immune profiling uncovers novel associations with clinical phenotypes of Multisystem Inflammatory Syndrome in Children (MIS-C).

    Redmond, Christopher / Kitakule, Moses M / Son, Aran / Sylvester, McKella / Sacco, Keith / Delmonte, Ottavia / Licciardi, Francesco / Castagnoli, Riccardo / Poli, Cecilia / Espinoza, Yasmin / Astudillo, Camila / Weber, Sarah E / Sanchez, Gina A Montealegre / Barron, Karyl / Magliocco, Mary / Dobbs, Kerry / Zhang, Yu / Matthews, Helen / Oguz, Cihan /
    Su, Helen C / Notarangelo, Luigi D / Frischmeyer-Guerrerio, Pamela A / Schwartz, Daniella M

    medRxiv : the preprint server for health sciences

    2022  

    Abstract: Multisystem Inflammatory Syndrome in Children (MIS-C) is a systemic inflammatory condition that follows SARS-CoV2 infection or exposure in children. Clinical presentations are highly variable and include fever, gastrointestinal (GI) disease, shock, and ... ...

    Abstract Multisystem Inflammatory Syndrome in Children (MIS-C) is a systemic inflammatory condition that follows SARS-CoV2 infection or exposure in children. Clinical presentations are highly variable and include fever, gastrointestinal (GI) disease, shock, and Kawasaki Disease-like illness (MIS-C/KD). Compared to patients with acute COVID, patients with MIS-C have a distinct immune signature and expansion of
    Language English
    Publishing date 2022-09-02
    Publishing country United States
    Document type Preprint
    DOI 10.1101/2022.08.31.22279265
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  7. Article ; Online: Novel proteasome assembly chaperone mutations in PSMG2/PAC2 cause the autoinflammatory interferonopathy CANDLE/PRAAS4.

    de Jesus, Adriana A / Brehm, Anja / VanTries, Rachel / Pillet, Pascal / Parentelli, Anne-Sophie / Montealegre Sanchez, Gina A / Deng, Zuoming / Paut, Isabelle Koné / Goldbach-Mansky, Raphaela / Krüger, Elke

    The Journal of allergy and clinical immunology

    2019  Volume 143, Issue 5, Page(s) 1939–1943.e8

    MeSH term(s) Chaperonins/genetics ; Child ; Female ; Humans ; Immunologic Deficiency Syndromes/genetics ; Interferons ; Molecular Chaperones/genetics ; Mutation ; Proteasome Endopeptidase Complex/genetics
    Chemical Substances Molecular Chaperones ; PSMG2 protein, human ; Interferons (9008-11-1) ; Proteasome Endopeptidase Complex (EC 3.4.25.1) ; Chaperonins (EC 3.6.1.-)
    Language English
    Publishing date 2019-01-18
    Publishing country United States
    Document type Case Reports ; Journal Article ; Research Support, N.I.H., Intramural ; Research Support, Non-U.S. Gov't
    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.2018.12.1012
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  8. Article ; Online: Autoantibodies Against Proteins Previously Associated With Autoimmunity in Adult and Pediatric Patients With COVID-19 and Children With MIS-C.

    Burbelo, Peter D / Castagnoli, Riccardo / Shimizu, Chisato / Delmonte, Ottavia M / Dobbs, Kerry / Discepolo, Valentina / Lo Vecchio, Andrea / Guarino, Alfredo / Licciardi, Francesco / Ramenghi, Ugo / Rey-Jurado, Emma / Vial, Cecilia / Marseglia, Gian Luigi / Licari, Amelia / Montagna, Daniela / Rossi, Camillo / Montealegre Sanchez, Gina A / Barron, Karyl / Warner, Blake M /
    Chiorini, John A / Espinosa, Yazmin / Noguera, Loreani / Dropulic, Lesia / Truong, Meng / Gerstbacher, Dana / Mató, Sayonara / Kanegaye, John / Tremoulet, Adriana H / Eisenstein, Eli M / Su, Helen C / Imberti, Luisa / Poli, Maria Cecilia / Burns, Jane C / Notarangelo, Luigi D / Cohen, Jeffrey I

    Frontiers in immunology

    2022  Volume 13, Page(s) 841126

    Abstract: The antibody profile against autoantigens previously associated with autoimmune diseases and other human proteins in patients with COVID-19 or multisystem inflammatory syndrome in children (MIS-C) remains poorly defined. Here we show that 30% of adults ... ...

    Abstract The antibody profile against autoantigens previously associated with autoimmune diseases and other human proteins in patients with COVID-19 or multisystem inflammatory syndrome in children (MIS-C) remains poorly defined. Here we show that 30% of adults with COVID-19 had autoantibodies against the lung antigen KCNRG, and 34% had antibodies to the SLE-associated Smith-D3 protein. Children with COVID-19 rarely had autoantibodies; one of 59 children had GAD65 autoantibodies associated with acute onset of insulin-dependent diabetes. While autoantibodies associated with SLE/Sjögren's syndrome (Ro52, Ro60, and La) and/or autoimmune gastritis (gastric ATPase) were detected in 74% (40/54) of MIS-C patients, further analysis of these patients and of children with Kawasaki disease (KD), showed that the administration of intravenous immunoglobulin (IVIG) was largely responsible for detection of these autoantibodies in both groups of patients. Monitoring
    MeSH term(s) Adaptor Proteins, Signal Transducing ; Adenosine Triphosphatases ; Adult ; Autoantibodies ; Autoantigens ; Autoimmune Diseases ; Autoimmunity ; COVID-19/complications ; Child ; Humans ; Immunoglobulins, Intravenous ; Lupus Erythematosus, Systemic ; Ribonucleoproteins ; Systemic Inflammatory Response Syndrome
    Chemical Substances Adaptor Proteins, Signal Transducing ; Autoantibodies ; Autoantigens ; Immunoglobulins, Intravenous ; KLHL12 protein, human ; Ribonucleoproteins ; Adenosine Triphosphatases (EC 3.6.1.-)
    Language English
    Publishing date 2022-03-11
    Publishing country Switzerland
    Document type Journal Article ; Research Support, N.I.H., Extramural ; Research Support, Non-U.S. Gov't
    ZDB-ID 2606827-8
    ISSN 1664-3224 ; 1664-3224
    ISSN (online) 1664-3224
    ISSN 1664-3224
    DOI 10.3389/fimmu.2022.841126
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  9. Article ; Online: The 2021 European Alliance of Associations for Rheumatology/American College of Rheumatology points to consider for diagnosis and management of autoinflammatory type I interferonopathies: CANDLE/PRAAS, SAVI and AGS.

    Cetin Gedik, Kader / Lamot, Lovro / Romano, Micol / Demirkaya, Erkan / Piskin, David / Torreggiani, Sofia / Adang, Laura A / Armangue, Thais / Barchus, Kathe / Cordova, Devon R / Crow, Yanick J / Dale, Russell C / Durrant, Karen L / Eleftheriou, Despina / Fazzi, Elisa M / Gattorno, Marco / Gavazzi, Francesco / Hanson, Eric P / Lee-Kirsch, Min Ae /
    Montealegre Sanchez, Gina A / Neven, Bénédicte / Orcesi, Simona / Ozen, Seza / Poli, M Cecilia / Schumacher, Elliot / Tonduti, Davide / Uss, Katsiaryna / Aletaha, Daniel / Feldman, Brian M / Vanderver, Adeline / Brogan, Paul A / Goldbach-Mansky, Raphaela

    Annals of the rheumatic diseases

    2022  Volume 81, Issue 5, Page(s) 601–613

    Abstract: Objective: Autoinflammatory type I interferonopathies, chronic atypical neutrophilic dermatosis with lipodystrophy and elevated temperature/proteasome-associated autoinflammatory syndrome (CANDLE/PRAAS), stimulator of interferon genes (STING)-associated ...

    Abstract Objective: Autoinflammatory type I interferonopathies, chronic atypical neutrophilic dermatosis with lipodystrophy and elevated temperature/proteasome-associated autoinflammatory syndrome (CANDLE/PRAAS), stimulator of interferon genes (STING)-associated vasculopathy with onset in infancy (SAVI) and Aicardi-Goutières syndrome (AGS) are rare and clinically complex immunodysregulatory diseases. With emerging knowledge of genetic causes and targeted treatments, a Task Force was charged with the development of 'points to consider' to improve diagnosis, treatment and long-term monitoring of patients with these rare diseases.
    Methods: Members of a Task Force consisting of rheumatologists, neurologists, an immunologist, geneticists, patient advocates and an allied healthcare professional formulated research questions for a systematic literature review. Then, based on literature, Delphi questionnaires and consensus methodology, 'points to consider' to guide patient management were developed.
    Results: The Task Force devised consensus and evidence-based guidance of 4 overarching principles and 17 points to consider regarding the diagnosis, treatment and long-term monitoring of patients with the autoinflammatory interferonopathies, CANDLE/PRAAS, SAVI and AGS.
    Conclusion: These points to consider represent state-of-the-art knowledge to guide diagnostic evaluation, treatment and management of patients with CANDLE/PRAAS, SAVI and AGS and aim to standardise and improve care, quality of life and disease outcomes.
    MeSH term(s) Autoimmune Diseases of the Nervous System ; Erythema Nodosum ; Fingers/abnormalities ; Humans ; Nervous System Malformations ; Quality of Life ; Rheumatology ; Skin Diseases
    Language English
    Publishing date 2022-01-27
    Publishing country England
    Document type Journal Article ; Systematic Review ; Research Support, N.I.H., Intramural ; Research Support, N.I.H., Extramural ; Research Support, Non-U.S. Gov't
    ZDB-ID 7090-7
    ISSN 1468-2060 ; 0003-4967
    ISSN (online) 1468-2060
    ISSN 0003-4967
    DOI 10.1136/annrheumdis-2021-221814
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  10. Article ; Online: The 2021 European Alliance of Associations for Rheumatology/American College of Rheumatology Points to Consider for Diagnosis and Management of Autoinflammatory Type I Interferonopathies: CANDLE/PRAAS, SAVI, and AGS.

    Cetin Gedik, Kader / Lamot, Lovro / Romano, Micol / Demirkaya, Erkan / Piskin, David / Torreggiani, Sofia / Adang, Laura A / Armangue, Thais / Barchus, Kathe / Cordova, Devon R / Crow, Yanick J / Dale, Russell C / Durrant, Karen L / Eleftheriou, Despina / Fazzi, Elisa M / Gattorno, Marco / Gavazzi, Francesco / Hanson, Eric P / Lee-Kirsch, Min Ae /
    Montealegre Sanchez, Gina A / Neven, Bénédicte / Orcesi, Simona / Ozen, Seza / Poli, M Cecilia / Schumacher, Elliot / Tonduti, Davide / Uss, Katsiaryna / Aletaha, Daniel / Feldman, Brian M / Vanderver, Adeline / Brogan, Paul A / Goldbach-Mansky, Raphaela

    Arthritis & rheumatology (Hoboken, N.J.)

    2022  Volume 74, Issue 5, Page(s) 735–751

    Abstract: Objective: Autoinflammatory type I interferonopathies, chronic atypical neutrophilic dermatosis with lipodystrophy and elevated temperature/proteasome-associated autoinflammatory syndrome (CANDLE/PRAAS), stimulator of interferon genes (STING)-associated ...

    Abstract Objective: Autoinflammatory type I interferonopathies, chronic atypical neutrophilic dermatosis with lipodystrophy and elevated temperature/proteasome-associated autoinflammatory syndrome (CANDLE/PRAAS), stimulator of interferon genes (STING)-associated vasculopathy with onset in infancy (SAVI), and Aicardi-Goutières syndrome (AGS) are rare and clinically complex immunodysregulatory diseases. With emerging knowledge of genetic causes and targeted treatments, a Task Force was charged with the development of "points to consider" to improve diagnosis, treatment, and long-term monitoring of patients with these rare diseases.
    Methods: Members of a Task Force consisting of rheumatologists, neurologists, an immunologist, geneticists, patient advocates, and an allied health care professional formulated research questions for a systematic literature review. Then, based on literature, Delphi questionnaires, and consensus methodology, "points to consider" to guide patient management were developed.
    Results: The Task Force devised consensus and evidence-based guidance of 4 overarching principles and 17 points to consider regarding the diagnosis, treatment, and long-term monitoring of patients with the autoinflammatory interferonopathies, CANDLE/PRAAS, SAVI, and AGS.
    Conclusion: These points to consider represent state-of-the-art knowledge to guide diagnostic evaluation, treatment, and management of patients with CANDLE/PRAAS, SAVI, and AGS and aim to standardize and improve care, quality of life, and disease outcomes.
    MeSH term(s) Autoimmune Diseases of the Nervous System/genetics ; Erythema Nodosum ; Fingers/abnormalities ; Humans ; Nervous System Malformations ; Quality of Life ; Rheumatology ; Skin Diseases
    Language English
    Publishing date 2022-03-21
    Publishing country United States
    Document type Journal Article ; Systematic Review ; Research Support, N.I.H., Intramural ; Research Support, Non-U.S. Gov't
    ZDB-ID 2756371-6
    ISSN 2326-5205 ; 2326-5191
    ISSN (online) 2326-5205
    ISSN 2326-5191
    DOI 10.1002/art.42087
    Database MEDical Literature Analysis and Retrieval System OnLINE

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