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  1. Article: Activation of Autoreactive Lymphocytes in the Lung by STING Gain-of-function Mutation Radioresistant Cells.

    Gao, Kevin MingJie / Nündel, Kerstin / Chiang, Kristy / Yin, Xihui / Utz, Paul J / Fitzgerald, Kate / Marshak-Rothstein, Ann

    bioRxiv : the preprint server for biology

    2023  

    Abstract: Gain-of-function mutations in the dsDNA sensing adaptor STING lead to a severe autoinflammatory syndrome known as STING-associated vasculopathy with onset in Infancy (SAVI). SAVI patients develop interstitial lung disease (ILD) and commonly produce anti- ... ...

    Abstract Gain-of-function mutations in the dsDNA sensing adaptor STING lead to a severe autoinflammatory syndrome known as STING-associated vasculopathy with onset in Infancy (SAVI). SAVI patients develop interstitial lung disease (ILD) and commonly produce anti-nuclear antibodies (ANAs), indicative of concomitant autoimmunity. Mice heterozygous for the most common SAVI mutation, V154M (VM), also develop ILD, triggered by nonhematopoietic VM cells, but exhibit severe peripheral lymphopenia, low serum Ig titers and fail to produce autoantibodies. In contrast, we now show that lethally irradiated VM mice reconstituted with WT stem cells (WT→VM chimeras) develop ANAs and lung-reactive autoantibodies associated with accumulation of activated lymphocytes and formation of germinal centers in lung tissues. Moreover, when splenocytes from WT→VM chimeras were adoptively transferred into unmanipulated Rag1
    Summary: Chimeric mice expressing STING only in non-hematopoietic cells develop systemic and lung directed autoimmunity which recapitulates what is seen in pediatric patients with SAVI disease.
    Language English
    Publishing date 2023-07-28
    Publishing country United States
    Document type Preprint
    DOI 10.1101/2023.07.28.551002
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article ; Online: Endothelial cell expression of a STING gain-of-function mutation initiates pulmonary lymphocytic infiltration.

    Gao, Kevin MingJie / Chiang, Kristy / Jiang, Zhaozhao / Korkmaz, Filiz T / Janardhan, Harish P / Trivedi, Chinmay M / Quinton, Lee J / Gingras, Sebastien / Fitzgerald, Katherine A / Marshak-Rothstein, Ann

    Cell reports

    2024  Volume 43, Issue 4, Page(s) 114114

    Abstract: Patients afflicted with Stimulator of interferon gene (STING) gain-of-function mutations frequently present with debilitating interstitial lung disease (ILD) that is recapitulated in mice expressing the ... ...

    Abstract Patients afflicted with Stimulator of interferon gene (STING) gain-of-function mutations frequently present with debilitating interstitial lung disease (ILD) that is recapitulated in mice expressing the STING
    MeSH term(s) Animals ; Membrane Proteins/metabolism ; Membrane Proteins/genetics ; Endothelial Cells/metabolism ; Endothelial Cells/pathology ; Gain of Function Mutation ; Mice ; Lung/pathology ; Lung/metabolism ; Lymphocytes/metabolism ; Lung Diseases, Interstitial/pathology ; Lung Diseases, Interstitial/genetics ; Lung Diseases, Interstitial/metabolism ; Mice, Inbred C57BL ; Humans
    Chemical Substances Membrane Proteins ; Sting1 protein, mouse
    Language English
    Publishing date 2024-04-15
    Publishing country United States
    Document type Journal Article ; Research Support, N.I.H., Extramural ; 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.2024.114114
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  3. Article ; Online: Cutting Edge: Systemic Autoimmunity in Murine STAT3 Gain-of-Function Syndrome Is Characterized by Effector T Cell Expansion in the Absence of Overt Regulatory T Cell Dysfunction.

    Woods, Jonathan / Pemberton, Sarah E / Largent, Andrea D / Chiang, Kristy / Liggitt, Denny / Oukka, Mohamed / Rawlings, David J / Jackson, Shaun W

    Journal of immunology (Baltimore, Md. : 1950)

    2022  Volume 209, Issue 6, Page(s) 1033–1038

    Abstract: Germline gain-of-function mutations in the transcriptional ... ...

    Abstract Germline gain-of-function mutations in the transcriptional factor
    MeSH term(s) Animals ; Autoimmunity ; CD8-Positive T-Lymphocytes/metabolism ; Cell Differentiation ; Gain of Function Mutation ; Gene Knock-In Techniques ; Humans ; Inflammation/pathology ; Mice ; Mice, Transgenic ; STAT3 Transcription Factor/genetics ; T-Lymphocytes, Regulatory ; Th17 Cells
    Chemical Substances STAT3 Transcription Factor ; STAT3 protein, human ; Stat3 protein, mouse
    Language English
    Publishing date 2022-08-22
    Publishing country United States
    Document type Journal Article
    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.2100920
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  4. Article: Expression of a STING Gain-of-function Mutation in Endothelial Cells Initiates Lymphocytic Infiltration of the Lungs.

    Gao, Kevin MingJie / Chiang, Kristy / Korkmaz, Filiz T / Janardhan, Harish Palleti / Trivedi, Chinmay M / Quinton, Lee J / Gingras, Sebastien / Fitzgerald, Katherine A / Marshak-Rothstein, Ann

    bioRxiv : the preprint server for biology

    2023  

    Abstract: Patients afflicted with STING gain-of-function mutations frequently present with debilitating interstitial lung disease ( : Summary: Patients with STING gain-of-function (GOF) mutations develop life-threatening lung autoinflammation. In this study, ... ...

    Abstract Patients afflicted with STING gain-of-function mutations frequently present with debilitating interstitial lung disease (
    Summary: Patients with STING gain-of-function (GOF) mutations develop life-threatening lung autoinflammation. In this study, Gao et al. utilize a mouse model of conditional STING GOF to demonstrate a role for endothelial STING GOF in initiating immune cell recruitment into lung tissues of SAVI mice.
    Language English
    Publishing date 2023-07-27
    Publishing country United States
    Document type Preprint
    DOI 10.1101/2023.07.27.550897
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  5. Article ; Online: Dysregulated IFN-γ signals promote autoimmunity in STAT1 gain-of-function syndrome.

    Largent, Andrea D / Lambert, Katharina / Chiang, Kristy / Shumlak, Natali / Liggitt, Denny / Oukka, Mohammed / Torgerson, Troy R / Buckner, Jane H / Allenspach, Eric J / Rawlings, David J / Jackson, Shaun W

    Science translational medicine

    2023  Volume 15, Issue 703, Page(s) eade7028

    Abstract: Heterozygous signal transducer and activator of transcription 1 ( ...

    Abstract Heterozygous signal transducer and activator of transcription 1 (
    MeSH term(s) Humans ; Child ; Mice ; Animals ; Autoimmunity/genetics ; Gain of Function Mutation ; Interferon-gamma/metabolism ; Syndrome ; Inflammation ; STAT1 Transcription Factor/genetics ; STAT1 Transcription Factor/metabolism
    Chemical Substances Interferon-gamma (82115-62-6) ; STAT1 Transcription Factor ; STAT1 protein, human
    Language English
    Publishing date 2023-07-05
    Publishing country United States
    Document type Journal Article ; Research Support, N.I.H., Extramural ; Research Support, Non-U.S. Gov't
    ZDB-ID 2518854-9
    ISSN 1946-6242 ; 1946-6234
    ISSN (online) 1946-6242
    ISSN 1946-6234
    DOI 10.1126/scitranslmed.ade7028
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  6. Article ; Online: Cutting Edge: A Threshold of B Cell Costimulatory Signals Is Required for Spontaneous Germinal Center Formation in Autoimmunity.

    Chiang, Kristy / Largent, Andrea D / Arkatkar, Tanvi / Thouvenel, Christopher D / Du, Samuel W / Shumlak, Natali / Woods, Jonathan / Li, Quan-Zhen / Liu, Yifan / Hou, Baidong / Rawlings, David J / Jackson, Shaun W

    Journal of immunology (Baltimore, Md. : 1950)

    2021  Volume 207, Issue 9, Page(s) 2217–2222

    Abstract: Cognate interactions between autoreactive B and T cells promote systemic lupus erythematosus pathogenesis by inter alia facilitating spontaneous germinal center (GC) formation. Whereas both myeloid and B cell APCs express B7 ligands (CD80 and CD86), the ... ...

    Abstract Cognate interactions between autoreactive B and T cells promote systemic lupus erythematosus pathogenesis by inter alia facilitating spontaneous germinal center (GC) formation. Whereas both myeloid and B cell APCs express B7 ligands (CD80 and CD86), the prevailing model holds that dendritic cell costimulation is sufficient for CD28-dependent T cell activation. In this study, we report that B cell-intrinsic CD80/CD86 deletion unexpectedly abrogates GCs in murine lupus. Interestingly, absent GCs differentially impacted serum autoantibodies. In keeping with distinct extrafollicular and GC activation pathways driving lupus autoantibodies, lack of GCs correlated with loss of RNA-associated autoantibodies but preserved anti-dsDNA and connective tissue autoantibody titers. Strikingly, even heterozygous B cell CD80/CD86 deletion was sufficient to prevent autoimmune GCs and RNA-associated autoantibodies. Together, these findings identify a key mechanism whereby B cells promote lupus pathogenesis by providing a threshold of costimulatory signals required for autoreactive T cell activation.
    MeSH term(s) Animals ; Autoantibodies/metabolism ; Autoimmunity ; B-Lymphocytes/immunology ; B7-1 Antigen/genetics ; B7-1 Antigen/metabolism ; B7-2 Antigen/genetics ; B7-2 Antigen/metabolism ; Cells, Cultured ; Disease Models, Animal ; Germinal Center/immunology ; Humans ; Lupus Erythematosus, Systemic/immunology ; Lupus Nephritis/immunology ; Lymphocyte Activation ; Mice ; Mice, Knockout ; Receptor Cross-Talk ; T-Lymphocytes, Helper-Inducer/immunology
    Chemical Substances Autoantibodies ; B7-1 Antigen ; B7-2 Antigen
    Language English
    Publishing date 2021-09-29
    Publishing country United States
    Document type Journal Article ; Research Support, N.I.H., Extramural ; 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.2100548
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  7. Article ; Online: Intratumoral activation of the necroptotic pathway components RIPK1 and RIPK3 potentiates antitumor immunity.

    Snyder, Annelise G / Hubbard, Nicholas W / Messmer, Michelle N / Kofman, Sigal B / Hagan, Cassidy E / Orozco, Susana L / Chiang, Kristy / Daniels, Brian P / Baker, David / Oberst, Andrew

    Science immunology

    2019  Volume 4, Issue 36

    Abstract: Although the signaling events that induce different forms of programmed cell death are well defined, the subsequent immune responses to dying cells in the context of cancer remain relatively unexplored. Necroptosis occurs downstream of the receptor- ... ...

    Abstract Although the signaling events that induce different forms of programmed cell death are well defined, the subsequent immune responses to dying cells in the context of cancer remain relatively unexplored. Necroptosis occurs downstream of the receptor-interacting protein kinases RIPK1 and RIPK3, whose activation leads to lytic cell death accompanied by de novo production of proinflammatory mediators. Here, we show that ectopic introduction of necroptotic cells to the tumor microenvironment promotes BATF3
    MeSH term(s) Animals ; CD8-Positive T-Lymphocytes/immunology ; Dendritic Cells/immunology ; Dependovirus/genetics ; Female ; HEK293 Cells ; Humans ; Male ; Mice ; Mice, Inbred C57BL ; Mice, Transgenic ; NIH 3T3 Cells ; Necroptosis/immunology ; Neoplasms/immunology ; Programmed Cell Death 1 Receptor/immunology ; Receptor-Interacting Protein Serine-Threonine Kinases/genetics ; Receptor-Interacting Protein Serine-Threonine Kinases/immunology ; Signal Transduction ; Tumor Microenvironment/immunology
    Chemical Substances Pdcd1 protein, mouse ; Programmed Cell Death 1 Receptor ; Receptor-Interacting Protein Serine-Threonine Kinases (EC 2.7.11.1) ; Ripk1 protein, mouse (EC 2.7.11.1) ; Ripk3 protein, mouse (EC 2.7.11.1)
    Language English
    Publishing date 2019-06-21
    Publishing country United States
    Document type Journal Article ; Research Support, N.I.H., Extramural ; Research Support, Non-U.S. Gov't ; Research Support, U.S. Gov't, Non-P.H.S.
    ISSN 2470-9468
    ISSN (online) 2470-9468
    DOI 10.1126/sciimmunol.aaw2004
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  8. Article ; Online: Functional Characterization of CD11c

    Du, Samuel W / Arkatkar, Tanvi / Al Qureshah, Fahd / Jacobs, Holly M / Thouvenel, Christopher D / Chiang, Kristy / Largent, Andrea D / Li, Quan-Zhen / Hou, Baidong / Rawlings, David J / Jackson, Shaun W

    Journal of immunology (Baltimore, Md. : 1950)

    2019  Volume 203, Issue 11, Page(s) 2817–2826

    Abstract: Age-associated B cells (ABCs) are a unique subset of B cells defined by surface CD11b and CD11c expression. Although ABC expansion has been observed in both human and animal studies in the setting of advanced age, during humoral autoimmunity and ... ...

    Abstract Age-associated B cells (ABCs) are a unique subset of B cells defined by surface CD11b and CD11c expression. Although ABC expansion has been observed in both human and animal studies in the setting of advanced age, during humoral autoimmunity and following viral infection, the functional properties of this cellular subset remain incompletely defined. In the current study, we demonstrate that ABCs fulfill the criteria for memory B cells (MBCs), based on evidence of Ag-dependent expansion and persistence in a state poised for rapid differentiation into Ab-secreting plasma cells during secondary responses. First, we show that a majority of ABCs are not actively cycling but exhibit an extensive replication history consistent with prior Ag engagement. Second, despite unswitched surface IgM expression, ABCs show evidence of activation-induced cytidine deaminase (AID)-dependent somatic hypermutation. Third, BCRs cloned from sorted ABCs exhibit broad autoreactivity and polyreactivity. Although the overall level of ABC self-reactivity was not increased relative to naive B cells, ABCs lacked features of functional anergy characteristic of autoreactive B cells. Fourth, ABCs express MBC surface markers consistent with being poised for rapid plasma cell differentiation during recall responses. Finally, in a murine model of viral infection, adoptively transferred CD11c
    MeSH term(s) Aging/immunology ; Animals ; B-Lymphocytes/immunology ; CD11c Antigen/immunology ; Immunologic Memory/immunology ; Mice ; Mice, Inbred C57BL ; Mice, Knockout
    Chemical Substances CD11c Antigen
    Language English
    Publishing date 2019-10-21
    Publishing country United States
    Document type Journal Article ; Research Support, N.I.H., Extramural ; 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.1900404
    Database MEDical Literature Analysis and Retrieval System OnLINE

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