The DOI matches its Crossref record; 50 of the 51 references it cites were found in a registry or an index.
A CD4+ T cell population expanded in lupus blood provides B cell help through interleukin-10 and succinate
Open accessAbstract
Understanding the mechanisms underlying autoantibody development will accelerate therapeutic target identification in autoimmune diseases such as systemic lupus erythematosus (SLE)1. Follicular helper T cells (T FH cells) have long been implicated in SLE pathogenesis. Yet a fraction of autoantibodies in individuals with SLE are unmutated, supporting that autoreactive B cells also differentiate outside germinal centers 2. Here, we describe a CXCR5-CXCR3+ programmed death 1 (PD1)hi CD4+ helper T cell population distinct from T FH cells and expanded in both SLE blood and the tubulointerstitial areas of individuals with proliferative lupus nephritis. These cells produce interleukin-10 (IL-10) and accumulate mitochondrial reactive oxygen species as the result of reverse electron transport fueled by succinate. Furthermore, they provide B cell help, independently of IL-21, through IL-10 and succinate. Similar cells are generated in vitro upon priming naive CD4+ T cells with plasmacytoid dendritic cells activated with oxidized mitochondrial DNA, a distinct class of interferogenic toll-like receptor 9 ligand 3. Targeting this pathway might blunt the initiation and/or perpetuation of extrafollicular humoral responses in SLE.
Overview
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
The source backs part of the claim, not all of it — or backs it for a different population, condition or comparison.
In the citing paper
“In the blood of patients with SLE, concomitant oxidation of mtDNA and signalling through the Notch pathway induce the expansion of a unique population of CD4+ T cells (CXCR5−CXCR3+PD1hiCD4+ T cells, known as T helper 10 (TH10) cells)75,76”
From The role of mitochondria in rheumatic diseases (2022) · cites this paper as [75]
Experimental — accuracy not yet measuredThe source backs part of the claim, not all of it — or backs it for a different population, condition or comparison.
In the citing paper
“Accumulation of succinate in TH10 cells enables an altered type of electron transport chain activity, ultimately leading to the production of IL-10 and mtROS, and acquisition of B cell helper functions75”
From The role of mitochondria in rheumatic diseases (2022) · cites this paper as [75]
Experimental — accuracy not yet measuredThe cited source says what the claim attributes to it.
In the citing paper
“These cells might contribute to SLE pathogenesis and end organ damage via supporting extrafollicular humoral responses75”
From The role of mitochondria in rheumatic diseases (2022) · cites this paper as [75]
The cited source says what the claim attributes to it.
In the citing paper
“Moreover, pDCs activated by oxidized mtDNA induce a unique population of CD4+ T cells, TH10 (CXCR5−CXCR3+PD1hiCD4+ T cell), that have altered metabolic features; these cells have accumulated levels of mtROS and succinate and produce large amounts of IL-10 and IFNγ but not IL-21 (REF.75).”
From The role of mitochondria in rheumatic diseases (2022) · cites this paper as [75]
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Citations
Cites
Trimmomatic: a flexible trimmer for Illumina sequence data
Bolger, A. M., Lohse, M., & Usadel, B. (2014) · Bioinformatics · doi:10.1093/bioinformatics/btu170 · Cited by 65,548
Fast and accurate short read alignment with Burrows-Wheeler transform
Li, H., & Durbin, R. (2009) · Bioinformatics · doi:10.1093/bioinformatics/btp324 · Cited by 58,607
Heinz, S., Benner, C., Spann, N., Bertolino, E., Lin, Y. C., Laslo, P., Cheng, J. X., Murre, C., Singh, H., & Glass, C. K. (2010) · Molecular Cell · doi:10.1016/j.molcel.2010.05.004 · Cited by 13,382
Hochberg, M. C. (1997) · Arthritis & Rheumatism · doi:10.1002/art.1780400928 · Cited by 11,409
How mitochondria produce reactive oxygen species
Murphy, M. P. (2009) · Biochemical Journal · doi:10.1042/bj20081386 · Cited by 8,207
Interleukin-10 and the Interleukin-10 Receptor
Moore, K. W., de Waal Malefyt, R., Coffman, R. L., & O'Garra, A. (2001) · Annual Review of Immunology · doi:10.1146/annurev.immunol.19.1.683 · Cited by 6,737
Buenrostro, J. D., Giresi, P. G., Zaba, L. C., Chang, H. Y., & Greenleaf, W. J. (2013) · Nature Methods · doi:10.1038/nmeth.2688 · Cited by 6,422
PD-1 and Its Ligands in Tolerance and Immunity
Keir, M. E., Butte, M. J., Freeman, G. J., & Sharpe, A. H. (2008) · Annual Review of Immunology · doi:10.1146/annurev.immunol.26.021607.090331 · Cited by 5,378
ChIPseeker: an R/Bioconductor package for ChIP peak annotation, comparison and visualization
Yu, G., Wang, L.-G., & He, Q. (2015) · Bioinformatics · doi:10.1093/bioinformatics/btv145 · Cited by 4,399
Succinate is an inflammatory signal that induces IL-1β through HIF-1α
Tannahill, G. M., Curtis, A. M., Adamik, J., Palsson-McDermott, E. M., McGettrick, A. F., Goel, G., Frezza, C., Bernard, N. J., Kelly, B., Foley, N. H., et al. (2013) · Nature · doi:10.1038/nature11986 · Cited by 4,176
Cited by
Sorted by citations
IL-10 Family Cytokines IL-10 and IL-22: from Basic Science to Clinical Translation
Ouyang, W., & O’Garra, A. (2019) · Immunity · doi:10.1016/j.immuni.2019.03.020 · Cited by 1,141
ROS and diseases: role in metabolism and energy supply
Yang, S., & Lian, G. (2019) · Molecular and Cellular Biochemistry · doi:10.1007/s11010-019-03667-9 · Cited by 689
TLR7 gain-of-function genetic variation causes human lupus
Brown, G. J., Cañete, P. F., Wang, H., Medhavy, A., Bones, J., Roco, J. A., He, Y., Qin, Y., Cappello, J., Ellyard, J. I., et al. (2022) · Nature · doi:10.1038/s41586-022-04642-z · Cited by 596
Self-citationAutoimmunity and organ damage in systemic lupus erythematosus
Tsokos, G. C. (2020) · Nature Immunology · doi:10.1038/s41590-020-0677-6 · Cited by 589
IgG4-related disease: an update on pathophysiology and implications for clinical care
Perugino, C. A., & Stone, J. H. (2020) · Nature Reviews Rheumatology · doi:10.1038/s41584-020-0500-7 · Cited by 435
PD-1hiCXCR5– T peripheral helper cells promote B cell responses in lupus via MAF and IL-21
Bocharnikov, A. V., Keegan, J., Wacleche, V. S., Cao, Y., Fonseka, C. Y., Wang, G., Muise, E. S., Zhang, K. X., Arazi, A., Keras, G., et al. (2019) · JCI Insight · doi:10.1172/jci.insight.130062 · Cited by 320
Erythroid mitochondrial retention triggers myeloid-dependent type I interferon in human SLE
Caielli, S., Cardenas, J., de Jesus, A. A., Baisch, J., Walters, L., Blanck, J. P., Balasubramanian, P., Stagnar, C., Ohouo, M., Hong, S., et al. (2021) · Cell · doi:10.1016/j.cell.2021.07.021 · Cited by 228
Self-citationSystemic Lupus Erythematosus Pathogenesis: Interferon and Beyond
Caielli, S., Wan, Z., & Pascual, V. (2023) · Annual Review of Immunology · doi:10.1146/annurev-immunol-101921-042422 · Cited by 229
Self-citationSoni, C., Perez, O. A., Voss, W. N., Pucella, J. N., Serpas, L., Mehl, J., Ching, K. L., Goike, J., Georgiou, G., Ippolito, G. C., et al. (2020) · Immunity · doi:10.1016/j.immuni.2020.04.015 · Cited by 210
Shared and distinct roles of T peripheral helper and T follicular helper cells in human diseases
Yoshitomi, H., & Ueno, H. (2020) · Cellular and Molecular Immunology · doi:10.1038/s41423-020-00529-z · Cited by 206
Self-citationLi, H., Boulougoura, A., Endo, Y., & Tsokos, G. C. (2022) · Journal of Autoimmunity · doi:10.1016/j.jaut.2022.102870 · Cited by 211
Cytokine-like Roles for Metabolites in Immunity
Zasłona, Z., & O'Neill, L. A. J. (2020) · Molecular Cell · doi:10.1016/j.molcel.2020.04.002 · Cited by 202
T follicular helper cells and T follicular regulatory cells in rheumatic diseases
Deng, J., Wei, Y., Fonseca, V. R., Graça, L., & Yu, D. (2019) · Nature Reviews Rheumatology · doi:10.1038/s41584-019-0254-2 · Cited by 171
Cui, H., Chen, Y., Li, K., Zhan, R., Zhao, M., Xu, Y., Lin, Z., Fu, Y., He, Q., Tang, P. C. Y., et al. (2021) · European Heart Journal · doi:10.1093/eurheartj/ehab605 · Cited by 169
Peripheral CD4+ T cell subsets and antibody response in COVID-19 convalescent individuals
Gong, F., Dai, Y., Zheng, T., Cheng, L., Zhao, D., Wang, H., Liu, M., Pei, H., Jin, T., Yu, D., et al. (2020) · Journal of Clinical Investigation · doi:10.1172/jci141054 · Cited by 160
B cell targeted therapies in autoimmune disease
Barnas, J. L., Looney, R. J., & Anolik, J. H. (2019) · Current Opinion in Immunology · doi:10.1016/j.coi.2019.09.004 · Cited by 130
The immunology of systemic lupus erythematosus
Tsokos, G. C. (2024) · Nature Immunology · doi:10.1038/s41590-024-01898-7 · Cited by 142
CD4+ T cells that help B cells – a proposal for uniform nomenclature
Eisenbarth, S. C., Baumjohann, D., Craft, J. E., Fazilleau, N., Ma, C. S., Tangye, S. G., Vinuesa, C. G., & Linterman, M. A. (2021) · Trends in Immunology · doi:10.1016/j.it.2021.06.003 · Cited by 131
Physiology and pathology of T-cell aging
Minato, N., Hattori, M., & Hamazaki, Y. (2020) · International Immunology · doi:10.1093/intimm/dxaa006 · Cited by 124
Oxidized mitochondrial DNA induces gasdermin D oligomerization in systemic lupus erythematosus
Miao, N., Wang, Z., Wang, Q., Xie, H., Yang, N., Wang, Y., Wang, J., Kang, H., Bai, W., Wang, Y., et al. (2023) · Nature Communications · doi:10.1038/s41467-023-36522-z · Cited by 118
CD153/CD30 signaling promotes age-dependent tertiary lymphoid tissue expansion and kidney injury
Sato, Y., Oguchi, A., Fukushima, Y., Masuda, K., Toriu, N., Taniguchi, K., Yoshikawa, T., Cui, X., Kondo, M., Hosoi, T., et al. (2021) · Journal of Clinical Investigation · doi:10.1172/jci146071 · Cited by 115
Kidney tissue hypoxia dictates T cell–mediated injury in murine lupus nephritis
Chen, P.-M., Wilson, P. C., Shyer, J. A., Veselits, M., Steach, H. R., Cui, C., Moeckel, G. W., Clark, M. R., & Craft, J. E. (2020) · Science Translational Medicine · doi:10.1126/scitranslmed.aay1620 · Cited by 103
Trzupek, D., Dunstan, M., Cutler, A. J., Lee, M., Godfrey, L., Jarvis, L., Rainbow, D. B., Aschenbrenner, D., Jones, J. L., Uhlig, H. H., et al. (2020) · Genome Medicine · doi:10.1186/s13073-020-00756-z · Cited by 105
PD-1+CXCR5−CD4+T cells are correlated with the severity of systemic lupus erythematosus
Lin, J., Yu, Y., Ma, J., Ren, C., & Chen, W. (2019) · Rheumatology · doi:10.1093/rheumatology/kez228 · Cited by 103
CD4+ and CD8+ cytotoxic T lymphocytes may induce mesenchymal cell apoptosis in IgG4-related disease
Perugino, C. A., Kaneko, N., Maehara, T., Mattoo, H., Kers, J., Allard‐Chamard, H., Mahajan, V. S., Liu, H., Della‐Torre, E., Murphy, S. J. H., et al. (2020) · Journal of Allergy and Clinical Immunology · doi:10.1016/j.jaci.2020.05.022 · Cited by 104
B-cell depletion in autoimmune diseases
Schett, G. A., Nagy, G., Krönke, G., & Mielenz, D. (2024) · Annals of the Rheumatic Diseases · doi:10.1136/ard-2024-225727 · Cited by 113
T peripheral helper cells in autoimmune diseases*
Marks, K. E., & Rao, D. A. (2022) · Immunological Reviews · doi:10.1111/imr.13069 · Cited by 104
Makiyama, A., Chiba, A., Noto, D., Murayama, G., Yamaji, K., Tamura, N., & Miyake, S. (2019) · Rheumatology · doi:10.1093/rheumatology/kez077 · Cited by 102
Lessons learned: new insights on the role of cytokines in COVID-19
Buszko, M., Nita‐Lazar, A., Park, J., Schwartzberg, P. L., Verthelyi, D. I., Young, H. A., & Rosenberg, A. S. (2021) · Nature Immunology · doi:10.1038/s41590-021-00901-9 · Cited by 99
Splicing factor SRSF1 controls T cell hyperactivity and systemic autoimmunity
Katsuyama, T., Li, H., Comte, D., Tsokos, G. C., & Moulton, V. R. (2019) · Journal of Clinical Investigation · doi:10.1172/jci127949 · Cited by 96
T follicular regulatory cells and IL-10 promote food antigen–specific IgE
Xie, M. M., Chen, Q., Liu, H., Yang, K., Koh, B., Wu, H., Maleki, S. J., Hurlburt, B. K., Cook‐Mills, J. M., Kaplan, M. H., et al. (2020) · Journal of Clinical Investigation · doi:10.1172/jci132249 · Cited by 94
Succinate Receptor 1: An Emerging Regulator of Myeloid Cell Function in Inflammation
Krzak, G., Willis, C. M., Smith, J. A., Pluchino, S., & Peruzzotti‐Jametti, L. (2020) · Trends in Immunology · doi:10.1016/j.it.2020.11.004 · Cited by 91
The role of mitochondria in rheumatic diseases
Becker, Y. L. C., Duvvuri, B., Fortin, P. R., Lood, C., & Boilard, E. (2022) · Nature Reviews Rheumatology · doi:10.1038/s41584-022-00834-z · Cited by 81
Dendritic cells in systemic lupus erythematosus: From pathogenesis to therapeutic applications
Liu, J., Zhang, X., & Cao, X. (2022) · Journal of Autoimmunity · doi:10.1016/j.jaut.2022.102856 · Cited by 90
Guo, C., Liu, Q., Zong, D., Zhang, W., Zuo, Z.-Q., Yu, Q., Sha, Q., Zhu, L., Gao, X., Fang, J., et al. (2022) · Cell Reports · doi:10.1016/j.celrep.2022.111606 · Cited by 86
T follicular helper cells and T follicular regulatory cells in autoimmune diseases
Qi, J., Liu, C., Bai, Z., Li, X., & Yao, G. (2023) · Frontiers in Immunology · doi:10.3389/fimmu.2023.1178792 · Cited by 86
CD153/CD30 signaling promotes age-dependent tertiary lymphoid tissue expansion and kidney injury
Sato, Y., Oguchi, A., Fukushima, Y., Masuda, K., Toriu, N., Taniguchi, K., Yoshikawa, T., Cui, X., Kondo, M., Hosoi, T., et al. (2022) · Institutional Repositories DataBase (IRDB) · Cited by 82
IFN-I Mediates Lupus Nephritis From the Beginning to Renal Fibrosis
Ding, X., Ren, Y., & He, X. (2021) · Frontiers in Immunology · doi:10.3389/fimmu.2021.676082 · Cited by 80
IL-10 revisited in systemic lupus erythematosus
Biswas, S., Bieber, K., & Manz, R. A. (2022) · Frontiers in Immunology · doi:10.3389/fimmu.2022.970906 · Cited by 81
Koenig, A., & Buskiewicz, I. A. (2022) · Antioxidants and Redox Signaling · doi:10.1089/ars.2021.0073 · Cited by 78
Gudgeon, N. H., Munford, H., Bishop, E. L., Hill, J., Fulton-Ward, T., Bending, D., Roberts, J., Tennant, D. A., & Dimeloe, S. (2022) · Cell Reports · doi:10.1016/j.celrep.2022.111193 · Cited by 85
Integrative molecular profiling of autoreactive CD4 T cells in autoimmune hepatitis
Renand, A., Cervera-Marzal, I., Gil, L., Dong, C., Garcia, A., Kervagoret, E., Aublé, H., Habes, S., Chevalier, C., Vavasseur, F., et al. (2020) · Journal of Hepatology · doi:10.1016/j.jhep.2020.05.053 · Cited by 80
IL-10 producing regulatory and helper T-cells in systemic lupus erythematosus
Geginat, J., Vasco, M., Gerosa, M., Tas, S. W., Pagani, M., Grassi, F., Flavell, R. A., Meroni, P. L., & Abrignani, S. (2019) · Seminars in Immunology · doi:10.1016/j.smim.2019.101330 · Cited by 69
Cellular aspects of the pathogenesis of lupus nephritis
Chang, A., Clark, M. R., & Ko, K. (2020) · Current Opinion in Rheumatology · doi:10.1097/bor.0000000000000777 · Cited by 64
Type 1 regulatory T cell-mediated tolerance in health and disease
Freeborn, R. A., Strubbe, S., & Roncarolo, M. G. (2022) · Frontiers in Immunology · doi:10.3389/fimmu.2022.1032575 · Cited by 68
Facciotti, F., Larghi, P., Bosotti, R., Vasco, C., Gagliani, N., Cordiglieri, C., Mazzara, S., Ranzani, V., Rottoli, E., Curti, S., et al. (2020) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1917834117 · Cited by 63
Díaz-Gallo, L.-M., Oke, V., Lundström, E., Elvin, K., Wu, Y. L., Eketjäll, S., Zickert, A., Gustafsson, J. T., Jönsen, A., Leonard, D., et al. (2021) · ACR Open Rheumatology · doi:10.1002/acr2.11343 · Cited by 60
Gong, F., Zheng, T., & Zhou, P. (2019) · Frontiers in Immunology · doi:10.3389/fimmu.2019.02918 · Cited by 58
Age-associated CD4 + T cells with B cell–promoting functions are regulated by ZEB2 in autoimmunity
Goto, M., Takahashi, H., Yoshida, R., Itamiya, T., Nakano, M., Nagafuchi, Y., Harada, H., Shimizu, T., Maeda, M. H., Kubota, A., et al. (2024) · Science Immunology · doi:10.1126/sciimmunol.adk1643 · Cited by 59
Panwar, B., Schmiedel, B. J., Liang, S. Y., White, B. M., Rodriguez, E., KALUNIAN, K. C., McKnight, A. J., Soloff, R. S., Seumois, G., Vijayanand, P., et al. (2021) · Genome Research · doi:10.1101/gr.265249.120 · Cited by 53
Autoantibodies in Morphea: An Update
Khatri, S., Torok, K. S., Mirizio, E., Liu, C., & Astakhova, K. (2019) · Frontiers in Immunology · doi:10.3389/fimmu.2019.01487 · Cited by 54
Spatial and functional heterogeneity of follicular helper T cells in autoimmunity
Seth, A., & Craft, J. E. (2019) · Current Opinion in Immunology · doi:10.1016/j.coi.2019.06.005 · Cited by 49
Metabolic determinants of lupus pathogenesis
Teng, X., Brown, J., Choi, S., Li, W., & Morel, L. M. (2020) · Immunological Reviews · doi:10.1111/imr.12847 · Cited by 53
Self-DNA at the Epicenter of SLE: Immunogenic Forms, Regulation, and Effects
Soni, C., & Reizis, B. (2019) · Frontiers in Immunology · doi:10.3389/fimmu.2019.01601 · Cited by 54
Tsuji, N., & Agbor-Enoh, S. T. (2021) · The Journal of Heart and Lung Transplantation · doi:10.1016/j.healun.2021.03.007 · Cited by 50
Moleón, J., González‐Correa, C., Miñano, S., Robles‐Vera, I., de la Visitación, N., Barranco, A. M., Gómez‐Guzmán, M., Sánchez, M., Riesco, P., Guerra-Hernández, E. J., et al. (2023) · Pharmacological Research · doi:10.1016/j.phrs.2023.106997 · Cited by 53
Immune Profiling and Precision Medicine in Systemic Lupus Erythematosus
Nagafuchi, Y., Shoda, H., & Fujio, K. (2019) · Cells · doi:10.3390/cells8020140 · Cited by 49
IL‐10 induces MC3T3‐E1 cells differentiation towards osteoblastic fate in murine model
Xiong, Y., Yan, C., Chen, L., Endo, Y., Sun, Y. T., Zhou, W., Hu, Y., Hu, L., Chen, D., Xue, H., et al. (2019) · Journal of Cellular and Molecular Medicine · doi:10.1111/jcmm.14832 · Cited by 50
Update on the cellular and molecular aspects of lupus nephritis
Frangou, E. A., Georgakis, S., & Bertsias, G. K. (2020) · Clinical Immunology · doi:10.1016/j.clim.2020.108445 · Cited by 50
CD4+ T-cell-derived IL-10 promotes CNS inflammation in mice by sustaining effector T cell survival
Yogev, N., Bedke, T., Kobayashi, Y., Brockmann, L., Lukas, D., Regen, T., Croxford, A. L., Nikolaev, A., Hövelmeyer, N., von Stebut, E., et al. (2022) · Cell Reports · doi:10.1016/j.celrep.2022.110565 · Cited by 47
B cell activation via immunometabolism in systemic lupus erythematosus
Iwata, S., Hajime, M., & Tanaka, Y. (2023) · Frontiers in Immunology · doi:10.3389/fimmu.2023.1155421 · Cited by 44
Ding, X., Xiang, W., & He, X. (2020) · Frontiers in Immunology · doi:10.3389/fimmu.2020.581385 · Cited by 46
Chen, W., Hong, S., Jenks, S. A., Anam, F. A., Tipton, C. M., Woodruff, M. C., Hom, J., Cashman, K. S., Faliti, C. E., Wang, X., et al. (2024) · Nature Communications · doi:10.1038/s41467-024-46053-w · Cited by 40
T and B lymphocytes in fibrosis and systemic sclerosis
Pillai, S. S. (2019) · Current Opinion in Rheumatology · doi:10.1097/bor.0000000000000644 · Cited by 40
T follicular helper cells and T peripheral helper cells in rheumatic and musculoskeletal diseases
Akiyama, M., Alshehri, W., Yoshimoto, K., & Kaneko, Y. (2023) · Annals of the Rheumatic Diseases · doi:10.1136/ard-2023-224225 · Cited by 40
The role of hypoxic microenvironment in autoimmune diseases
Gong, X., Yang, S.-Y., Wang, Z.-Y., & Tang, M. (2024) · Frontiers in Immunology · doi:10.3389/fimmu.2024.1435306 · Cited by 44
Metabolic regulation of pathogenic autoimmunity: therapeutic targeting
Teng, X., Cornaby, C., Li, W., & Morel, L. M. (2019) · Current Opinion in Immunology · doi:10.1016/j.coi.2019.07.001 · Cited by 38
Wang, M., Guo, J., Zhao, Y., & Wang, J. (2020) · Aging · doi:10.18632/aging.103566 · Cited by 39
Mitochondrial DNA release and cGAS-STING activation: Emerging insights into anti-tumor immunity
Aloraini, G. S. (2025) · Pathology - Research and Practice · doi:10.1016/j.prp.2025.156158 · Cited by 41
Systemic lupus erythematosus: year in review 2019
Fan, Y., Hao, Y., & Zhang, Z. (2020) · Chinese Medical Journal · doi:10.1097/cm9.0000000000000983 · Cited by 36
Hoshino, Y., Noto, D., Sano, S., Tomizawa, Y., Yokoyama, K., Hattori, N., & Miyake, S. (2022) · Journal of Neuroinflammation · doi:10.1186/s12974-021-02375-w · Cited by 36
Association of Viral Infection With the Development and Pathogenesis of Systemic Lupus Erythematosus
Iwata, S., & Tanaka, Y. (2022) · Frontiers in Medicine · doi:10.3389/fmed.2022.849120 · Cited by 36
Senolytic treatment reverses obesity-mediated senescent cell accumulation in the ovary
Hense, J. D., Garcia, D. N., Isola, J. V. V., Rincón, J. A. A., Zanini, B. M., Prosczek, J. B., Stout, M. B., Mason, J. B., Walsh, P. T., Brieño‐Enríquez, M. A., et al. (2022) · GeroScience · doi:10.1007/s11357-022-00573-9 · Cited by 37
Wang, Z., Yao, Y., Chen, C., Guo, C., Ding, H.-X., Song, J., Wang, Z.-Z., Wang, N., Li, X., Liao, B., et al. (2021) · Journal of Allergy and Clinical Immunology · doi:10.1016/j.jaci.2021.06.023 · Cited by 35
Role of interferons (IFNs) in the differentiation of T peripheral helper (Tph) cells
Tanemura, S., Seki, N., Tsujimoto, H., Saito, S., Kikuchi, J., Sugahara, K., Yoshimoto, K., Suzuki, K., Kaneko, Y., Chiba, K., et al. (2022) · International Immunology · doi:10.1093/intimm/dxac032 · Cited by 32
Peripheral helper T cells, mavericks of peripheral immune responses
Yoshitomi, H. (2023) · International Immunology · doi:10.1093/intimm/dxad041 · Cited by 32
Immune cell metabolism in autoimmunity
Teng, X., Li, W., Cornaby, C., & Morel, L. M. (2019) · Clinical & Experimental Immunology · doi:10.1111/cei.13277 · Cited by 33
Oxidative Stress in SLE T Cells, Is NRF2 Really the Target to Treat?
Ohl, K., & Tenbrock, K. (2021) · Frontiers in Immunology · doi:10.3389/fimmu.2021.633845 · Cited by 31
Clinical relevance of T follicular helper cells in systemic lupus erythematosus
Nakayamada, S., & Tanaka, Y. (2021) · Expert Review of Clinical Immunology · doi:10.1080/1744666x.2021.1976146 · Cited by 31
T peripheral helper cells in autoimmune diseases: What do we know?
Huang, Y., Ba, X., Han, L., Wang, H., Lin, W., Chen, Z., & Tu, S. (2023) · Frontiers in Immunology · doi:10.3389/fimmu.2023.1145573 · Cited by 32
The IL‐12‐STAT4 axis in the pathogenesis of human systemic lupus erythematosus
Ueno, H. (2019) · European Journal of Immunology · doi:10.1002/eji.201948134 · Cited by 29
Self-citationZheng, M., Zhou, W., Huang, C., Hu, Z. Q., Zhang, B., Lu, Q., & Zhao, M. (2023) · Journal of Autoimmunity · doi:10.1016/j.jaut.2022.102989 · Cited by 29
Targeting plasma cells in systemic autoimmune rheumatic diseases – Promises and pitfalls
Steinmetz, T. D., Verstappen, G. M. P. J., Suurmond, J., & Kroese, F. G. M. (2023) · Immunology Letters · doi:10.1016/j.imlet.2023.06.005 · Cited by 31
Liu, Y., Chen, W., Ruan, R., Zhang, Z., Wang, Z., Guan, T., Lin, Q., Tang, W., Deng, J., Wang, Z., et al. (2024) · Journal of Translational Medicine · doi:10.1186/s12967-024-05262-z · Cited by 33
Opejin, A., Surnov, A., Misulovin, Z., Pherson, M., Gross, C. J., Iberg, C. A., Fallahee, I., Bourque, J., Dorsett, D., & Hawiger, D. (2020) · Cell Reports · doi:10.1016/j.celrep.2020.108424 · Cited by 29
Enhanced Fatty Acid Synthesis Leads to Subset Imbalance and IFN-γ Overproduction in T Helper 1 Cells
Iwata, S., Zhang, M., He, H., Trimova, G., Hajime, M., Miyazaki, Y., Ohkubo, N., Kanda, Y. S., Todoroki, Y., Miyata, H., et al. (2020) · Frontiers in Immunology · doi:10.3389/fimmu.2020.593103 · Cited by 29
Friedmann, D., Unger, S., Keller, B., Rakhmanov, M., Goldacker, S., Zissel, G., Frye, B. C., Schupp, J. C., Prasse, A., & Warnatz, K. (2021) · Frontiers in Immunology · doi:10.3389/fimmu.2020.616832 · Cited by 28
Emerging roles of circular RNAs in systemic lupus erythematosus
Wang, X., Ma, R., Shi, W., Wu, Z., & Shi, Y. (2021) · Molecular Therapy — Nucleic Acids · doi:10.1016/j.omtn.2021.02.028 · Cited by 28
A cellular overview of immunometabolism in systemic lupus erythematosus
Psarras, A., & Clarke, A. J. (2023) · Oxford Open Immunology · doi:10.1093/oxfimm/iqad005 · Cited by 29
Seki, N., Tsujimoto, H., Tanemura, S., Kojima, S., Miyoshi, F., Kikuchi, J., Saito, S., Akiyama, M., Sugahara, K., Yoshimoto, K., et al. (2024) · Communications Biology · doi:10.1038/s42003-024-05989-x · Cited by 29
Søndergaard, J. N., Tulyeu, J., Edahiro, R., Shirai, Y., Yamaguchi, Y., Murakami, T., Morita, T., Kato, Y., Hirata, H., Takeda, Y., et al. (2023) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2217902120 · Cited by 24
Christophersen, A. O., Zühlke, S., Lund, E. G., Snir, O., Dahal‐Koirala, S., Risnes, L. F., Jahnsen, J., Lundin, K. E. A., & Sollid, L. M. (2021) · Advanced Science · doi:10.1002/advs.202102778 · Cited by 26
Zhang, Y., Li, X., Gibson, A., Edberg, J. C., Kimberly, R. P., & Absher, D. (2020) · Human Molecular Genetics · doi:10.1093/hmg/ddaa131 · Cited by 25
Mitochondrial DNA on Tumor-Associated Macrophages Polarization and Immunity
Guo, Y., Tsai, H., Zhang, L., & Zhu, H. (2022) · Cancers · doi:10.3390/cancers14061452 · Cited by 26
Gong, M., Choi, S., Park, Y. P., Zou, X., Elshikha, A. S., Gerriets, V. A., Rathmell, J. C., Mohamazadeh, M., & Morel, L. M. (2023) · iScience · doi:10.1016/j.isci.2023.106774 · Cited by 24
PD ‐1/ PD‐L1 blockade: Prospectives for immunotherapy in cancer and autoimmunity
Hosseinzadeh, R., Feizisani, F., Shomali, N., Abdelbasset, W. K., Hemmatzadeh, M., Navashenaq, J. G., Jadidi‐Niaragh, F., Bokov, D. O., Janebifam, M., & Mohammadi, H. (2021) · IUBMB Life · doi:10.1002/iub.2558 · Cited by 25
Wen, Z., Xu, L., Xu, W., & Xiong, S. (2021) · Arthritis & Rheumatology · doi:10.1002/art.41687 · Cited by 24
Xu, L., Wang, L., Shi, Y., Deng, Y., Oates, J. C., Kamen, D. L., Gilkeson, G. S., Wang, F., Zhang, M., Tan, W., et al. (2021) · Arthritis & Rheumatology · doi:10.1002/art.41987 · Cited by 24
Dual Role of Interleukin-10 in Murine NZB/W F1 Lupus
Amend, A., Wickli, N., Schäfer, A.-L., Sprenger, D. T. L., Manz, R. A., Voll, R. E., & Chevalier, N. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22031347 · Cited by 24
Metabolic control of T cells in autoimmunity
Kono, M., Yoshida, N., & Tsokos, G. C. (2019) · Current Opinion in Rheumatology · doi:10.1097/bor.0000000000000685 · Cited by 23
Metadata
- Authors
- Caielli, S., Veiga, D. T., Balasubramanian, P., Athale, S., Domic, B., Murat, E., Banchereau, R., Xu, Z., Chandra, M., Chung, C.-H., Walters, L., Baisch, J., Wright, T., Punaro, M., Nassi, L., Stewart, K., Fuller, J., Ucar, D., Ueno, H., Zhou, J., Banchereau, J., & Pascual, V.
- Affiliations
- Weill Cornell Medicine (US)
- The Jackson Laboratory for Genomic Medicine (US)
- Texas Scottish Rite Hospital for Children (US)
- Icahn School of Medicine at Mount Sinai (US)
- Pathologist Bio-Medical Laboratories (US)
- Corresponding author
- Pascual, Virginia
- ORCID
- Venue
- Nature Medicine
- Published
- 2018-11-26
- Volume
- 25
- Issue
- 1
- Pages
- 75-81
- ISSN
- 1078-8956 (ISSN-L)
- 1546-170X
- PMC
- PMC6325012
- OpenAlex
- W2900950647
- Cited by
- 263
- References
- 51
- Citations by year
- 2026: 13 · 2025: 25 · 2024: 44 · 2023: 32 · 2022: 46 · 2021: 38 · 2020: 35 · 2019: 28 · 2018: 2
- FWCI
- 22.14
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Licence
- www.springer.com/tdm (tdm)
- Locations
- Nature Medicine (publishedVersion)
- PubMed (publishedVersion)
- Europe PMC (PubMed Central) (acceptedVersion)
- PubMed Central (acceptedVersion)
- The Mouseion at the JAXlibrary (Jackson Laboratory) (submittedVersion)
- Funders
- National Institute of Allergy and Infectious Diseases (U19AI082715)
- National Institute of Arthritis and Musculoskeletal and Skin Diseases (P50AR054083, P50AR070594)
- Topics
- Health Sciences › Medicine › Rheumatology › Systemic Lupus Erythematosus Research
- Life Sciences › Immunology and Microbiology › Immunology › T-cell and B-cell Immunology
- Life Sciences › Immunology and Microbiology › Immunology › Psoriasis: Treatment and Pathogenesis
- Keywords
- systemic lupus erythematosus, lupus nephritis, CD4+ T cells, B cell help, IL-10, succinic acid, reverse electron transfer, mitochondrial reactive oxygen species, PD-1, T follicular helper cells, plasmacytoid dendritic cells, oxidized mitochondrial DNA, TLR9, autoantibody production
- MeSH terms
- B-Lymphocytes, Dendritic Cells, DNA, Mitochondrial, Humans, Immunologic Memory, Lupus Erythematosus, Systemic, Lupus Nephritis, Oxidation-Reduction, CD4-Positive T-Lymphocytes, Interleukin-10, Succinic Acid, Cell Proliferation
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review