Microparticles as a source of extracellular DNA
Open accessAbstract
Microparticles are small membrane-bound vesicles that display pro-inflammatory and pro-thrombotic activities important in the pathogenesis of a wide variety of diseases. These particles are released from activated and dying cells and incorporate nuclear and cytoplasmic molecules for extracellular export. Of these molecules, DNA is a central autoantigen in systemic lupus erythematosus (SLE). As studies in our laboratory show, DNA occurs prominently in microparticles, translocating into these structures during apoptotic cell death. This DNA is antigenically active and can bind to lupus anti-DNA autoantibodies. These findings suggest that microparticles are an important source of extracellular DNA to serve as an autoantigen and autoadjuvant in SLE.
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
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?
Detection of mitochondrial motives by innate and adaptive immunity might elicit potent pro-inflammatory responses.
“Given the bacterial features of mitochondria, the detection of mitochondrial motives by cells of the innate and adaptive immunity might elicit potent pro-inflammatory responses147,276,277.”
From The role of mitochondria in rheumatic diseases (2022) · cites this paper as [276]
The Introduction discusses immune responses to bacterial CpG motifs and to DNA-containing immune complexes, but it does not address mitochondrial motifs or their detection by innate and adaptive immune cells. Searches for mitochondrial DNA, mitochondria, and mitochondrial motifs found no passage supporting the attributed claim. The available passages have no page numbers. (LLM, conf=0.75)
Experimental — accuracy not yet measured
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Cites
Shedding microvesicles: artefacts no more
Cocucci, E., Racchetti, G., & Meldolesi, J. (2009) · Trends in Cell Biology · doi:10.1016/j.tcb.2008.11.003 · Cited by 1,742 · see citing works
Casciola-Rosen, L. A., Anhalt, G. J., & Rosen, A. (1994) · The Journal of Experimental Medicine · doi:10.1084/jem.179.4.1317 · Cited by 1,723 · see citing works
Tian, J., Avalos, A. M., Mao, S.-Y., Chen, B., Senthil, K., Wu, H., Parroche, P., Drabic, S., Golenbock, D., Sirois, C., et al. (2007) · Nature Immunology · doi:10.1038/ni1457 · Cited by 1,372 · see citing works
Monocytic cells hyperacetylate chromatin protein HMGB1 to redirect it towards secretion
Bonaldi, T., Talamo, F., Scaffidi, P., Ferrera, D., Porto, A., Bachi, A., Rubartelli, A., Agresti, A., & Bianchi, M. E. (2003) · The EMBO Journal · doi:10.1093/emboj/cdg516 · Cited by 1,252 · see citing works
Gardella, S., Andrei, C., Ferrera, D., Lotti, L. V., Torrisi, M. R., Bianchi, M. E., & Rubartelli, A. (2002) · EMBO Reports · doi:10.1093/embo-reports/kvf198 · Cited by 926 · see citing works
Human lupus autoantibody–DNA complexes activate DCs through cooperation of CD32 and TLR9
Means, T. K., Latz, E., Hayashi, F., Murali, M. R., Golenbock, D. T., & Luster, A. D. (2005) · Journal of Clinical Investigation · doi:10.1172/jci23025 · Cited by 849 · see citing works
Hahn, B. H. (1998) · New England Journal of Medicine · doi:10.1056/nejm199805073381906 · Cited by 677 · see citing works
Microparticles in cardiovascular diseases
VANWIJK, M., VanBavel, E., Sturk, A., & Nieuwland, R. (2003) · Cardiovascular Research · doi:10.1016/s0008-6363(03)00367-5 · Cited by 610 · see citing works
The type I interferon system in systemic lupus erythematosus
Rönnblom, L., Eloranta, M., & Alm, G. V. (2006) · Arthritis & Rheumatism · doi:10.1002/art.21571 · Cited by 340 · see citing works
Flow cytometric analysis of circulating microparticles in plasma
Orozco, A. F., & Lewis, D. E. (2010) · Cytometry Part A · doi:10.1002/cyto.a.20886 · Cited by 333 · see citing works
The role of microparticles in the pathogenesis of rheumatic diseases
Beyer, C., & Pisetsky, D. S. (2009) · Nature Reviews Rheumatology · doi:10.1038/nrrheum.2009.229 · Cited by 324 · see citing works
Self-citationHarris, H. E., & Raucci, A. (2006) · EMBO Reports · doi:10.1038/sj.embor.7400759 · Cited by 278 · see citing works
Autoantigens are translocated into small apoptotic bodies during early stages of apoptosis
Schiller, M. R., Bekeredjian‐Ding, I., Heyder, P., Blank, N., Ho, A. D., & Lorenz, H.-M. (2007) · Cell Death and Differentiation · doi:10.1038/sj.cdd.4402239 · Cited by 210 · see citing works
Pisetsky, D. S., Erlandsson-Harris, H., & Andersson, U. (2008) · Arthritis Research & Therapy · doi:10.1186/ar2440 · Cited by 188 · see citing works
Self-citationJiang, W., Bell, C. W., & Pisetsky, D. S. (2007) · The Journal of Immunology · doi:10.4049/jimmunol.178.10.6495 · Cited by 134 · see citing works
Self-citationThe role of HMGB1 in the pathogenesis of rheumatic disease
Andersson, U., & Harris, H. E. (2010) · Biochimica et Biophysica Acta (BBA) - Gene Regulatory Mechanisms · doi:10.1016/j.bbagrm.2009.11.003 · Cited by 126 · see citing works
Reich, C. F., & Pisetsky, D. S. (2008) · Experimental Cell Research · doi:10.1016/j.yexcr.2008.12.014 · Cited by 121 · see citing works
Self-citationJiang, W., & Pisetsky, D. S. (2006) · The Journal of Immunology · doi:10.4049/jimmunol.177.5.3337 · Cited by 99 · see citing works
Self-citationClearance deficiency—A potential link between infections and autoimmunity
Schulze, C., Munoz, L. E., Franz, S., Sarter, K., Chaurio, R. A., Gaipl, U. S., & i, M. H. (2008) · Autoimmunity Reviews · doi:10.1016/j.autrev.2008.07.049 · Cited by 89 · see citing works
Ullal, A. J., Pisetsky, D. S., & Reich, C. F. (2010) · Cytometry Part A · doi:10.1002/cyto.a.20833 · Cited by 67 · see citing works
Self-citationToll-like receptors and innate immune responses in systemic lupus erythematosus
Lafyatis, R., & Marshak‐Rothstein, A. (2007) · Arthritis Research & Therapy · doi:10.1186/ar2321 · Cited by 59 · see citing works
The release of microparticles by RAW 264.7 macrophage cells stimulated with TLR ligands
Gauley, J., & Pisetsky, D. S. (2010) · Journal of Leukocyte Biology · doi:10.1189/jlb.0709465 · Cited by 54 · see citing works
Self-citationEffect of cytofectins on the immune response of murine macrophages to mammalian DNA
Zhu, F., Reich, C. F., & Pisetsky, D. S. (2003) · Immunology · doi:10.1046/j.1365-2567.2003.01653.x · Cited by 31 · see citing works
Self-citationUllal, A. J., & Pisetsky, D. S. (2010) · APOPTOSIS · doi:10.1007/s10495-010-0470-3 · Cited by 27 · see citing works
Self-citationPisetsky, D. S., & Reich, C. F. (1999) · Journal of Interferon & Cytokine Research · doi:10.1089/107999099313163 · Cited by 14 · see citing works
Self-citation
Flagged first, then by citations
Cited by
Sorted by citations
Emerging role of extracellular vesicles in inflammatory diseases
Buzás, E. I., György, B., Nagy, G., Falus, A., & Gay, S. (2014) · Nature Reviews Rheumatology · doi:10.1038/nrrheum.2014.19 · Cited by 673 · see citing works
Lee, T. H., D’Asti, E., Magnus, N., Al-Nedawi, K. N. I., Meehan, B., & Rak, J. W. (2011) · Seminars in Immunopathology · doi:10.1007/s00281-011-0250-3 · Cited by 496 · see citing works
Digestion of Chromatin in Apoptotic Cell Microparticles Prevents Autoimmunity
Sisirak, V., Sally, B., D’Agati, V. D., Martinez‐Ortiz, W., Özçakar, Z. B., David, J., Rashidfarrokhi, A., Yeste, A., Panea, C., Chida, A. S., et al. (2016) · Cell · doi:10.1016/j.cell.2016.05.034 · Cited by 450 · see citing works
Salivary biomarkers in cancer detection
Wang, X., Kaczor‐Urbanowicz, K. E., & Wong, D. T. (2016) · Medical Oncology · doi:10.1007/s12032-016-0863-4 · Cited by 231 · see citing works
Bioactive DNA from extracellular vesicles and particles
Malkin, E. Z., & Bratman, S. V. (2020) · Cell Death and Disease · doi:10.1038/s41419-020-02803-4 · Cited by 214 · see citing works
Soni, 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 205 · see citing works
Nielsen, C. T., Østergaard, O., Stener, L., Iversen, L. V., Truedsson, L., Gullstrand, B., Jacobsen, S., & Heegaard, N. H. H. (2012) · Arthritis & Rheumatism · doi:10.1002/art.34381 · Cited by 167 · see citing works
Extracellular vesicles: potential applications in cancer diagnosis, prognosis, and epidemiology
Verma, M., Lam, T. K., Hebert, E. F., & Divi, R. L. (2015) · BMC Clinical Pathology · doi:10.1186/s12907-015-0005-5 · Cited by 150 · see citing works
Extracellular vesicles arising from apoptosis: forms, functions, and applications
Gregory, C. D., & Rimmer, M. P. (2023) · The Journal of Pathology · doi:10.1002/path.6138 · Cited by 140 · see citing works
Emerging and critical issues in the pathogenesis of lupus
Gatto, M., Zen, M., Ghirardello, A., Bettio, S., Bassi, N., Iaccarino, L., Punzi, L., & Doria, A. (2012) · Autoimmunity Reviews · doi:10.1016/j.autrev.2012.09.003 · Cited by 127 · see citing works
Principe, S., Hui, A., Bruce, J., Sinha, A., Liu, F.-F., & Kislinger, T. (2013) · Proteomics · doi:10.1002/pmic.201200533 · Cited by 121 · see citing works
Microvesicles and intercellular communication in the context of parasitism
Barteneva, N. S., Maltsev, N., & Vorobjev, I. A. (2013) · Frontiers in Cellular and Infection Microbiology · doi:10.3389/fcimb.2013.00049 · Cited by 120 · see citing works
Extracellular vesicles: communication, coercion, and conditioning
Shifrin, D., Beckler, M. D., Coffey, R., & Tyska, M. (2013) · Molecular Biology of the Cell · doi:10.1091/mbc.e12-08-0572 · Cited by 105 · see citing works
Review: Cell Death, Nucleic Acids, and Immunity
Elkon, K. B. (2018) · Arthritis & Rheumatology · doi:10.1002/art.40452 · Cited by 99 · see citing works
Extracellular vesicle-associated DNA: ten years since its discovery in human blood
Tsering, T., Nadeau, A., Wu, T.-C., Dickinson, K., & Burnier, J. V. (2024) · Cell Death and Disease · doi:10.1038/s41419-024-07003-y · Cited by 97 · see citing works
Functional transferred DNA within extracellular vesicles
Cai, J., Wu, G., José, P. A., & Zeng, C. (2016) · Experimental Cell Research · doi:10.1016/j.yexcr.2016.10.012 · Cited by 93 · see citing works
Extracellular DNA in Pancreatic Cancer Promotes Cell Invasion and Metastasis
Wen, F., Shen, A., Choi, A., Gerner, E. W., & Shi, J. (2013) · Cancer Research · doi:10.1158/0008-5472.can-12-3287 · Cited by 90 · see citing works
The Alarmin Properties of DNA and DNA-associated Nuclear Proteins
Magna, M., & Pisetsky, D. S. (2016) · Clinical Therapeutics · doi:10.1016/j.clinthera.2016.02.029 · Cited by 89 · see citing works
Self-citationThe 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 · see citing works
Escamilla-Tilch, M., Filio‐Rodríguez, G., García‐Rocha, R., Mancilla‐Herrera, I., Mitchison, N. A., Ruiz‐Pacheco, J. A., Sánchez‐García, F. J., Sandoval‐Borrego, D., & Vázquez-Sánchez, E. A. (2013) · Immunology and Cell Biology · doi:10.1038/icb.2013.58 · Cited by 86 · see citing works
Cai, J., Wu, G., Tan, X., Han, Y., Chen, C., Li, C., Wang, N., Zou, X., Chen, X., Zhou, F., et al. (2014) · PLoS ONE · doi:10.1371/journal.pone.0105200 · Cited by 79 · see citing works
Schiller, M. R., Parčina, M., Heyder, P., Foermer, S., Ostrop, J., Leo, A., Heeg, K. M., i, M. H., Lorenz, H., & Bekeredjian‐Ding, I. (2012) · The Journal of Immunology · doi:10.4049/jimmunol.1100631 · Cited by 74 · see citing works
Mobarrez, F., Fuzzi, E., Gunnarsson, I., Larsson, A., Eketjäll, S., Pisetsky, D. S., & Svenungsson, E. (2019) · Journal of Autoimmunity · doi:10.1016/j.jaut.2019.05.003 · Cited by 68 · see citing works
Self-citationMicrovesicles in Autoimmune Diseases
Liu, M., Williams, K. J., & Werth, V. P. (2016) · Advances in clinical chemistry · doi:10.1016/bs.acc.2016.06.005 · Cited by 65 · see citing works
Mongini, P. K. A., Gupta, R., Boyle, E., Nieto, J., Lee, H., Stein, J., Bandovic, J., Stanković, T., Barrientos, J. C., Kolitz, J. E., et al. (2015) · The Journal of Immunology · doi:10.4049/jimmunol.1403189 · Cited by 63 · see citing works
LAMP3 induces apoptosis and autoantigen release in Sjögren’s syndrome patients
Tanaka, T., Warner, B. M., Odani, T., Ji, Y., Mo, Y., Nakamura, H., Jang, S.-I., Yin, H., Michael, D. G., Hirata, N., et al. (2020) · Scientific Reports · doi:10.1038/s41598-020-71669-5 · Cited by 60 · see citing works
Abdouh, M., Hamam, D., Gao, Z., Arena, V., Arena, M., & Arena, G. O. (2017) · Journal of Experimental & Clinical Cancer Research · doi:10.1186/s13046-017-0587-0 · Cited by 58 · see citing works
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 51 · see citing works
The effect of cell death in the initiation of lupus nephritis
Fenton, K. A. (2014) · Clinical & Experimental Immunology · doi:10.1111/cei.12417 · Cited by 51 · see citing works
Dye, J. R., Ullal, A. J., & Pisetsky, D. S. (2013) · Scandinavian Journal of Immunology · doi:10.1111/sji.12068 · Cited by 50 · see citing works
Self-citationNeutrophil Extracellular Traps: A Walk on the Wild Side of Exercise Immunology
Beiter, T., Fragasso, A., Hartl, D., & Niess, A. M. (2014) · Sports Medicine · doi:10.1007/s40279-014-0296-1 · Cited by 49 · see citing works
Hamam, D., Abdouh, M., Gao, Z., Arena, V., Arena, M., & Arena, G. O. (2016) · Journal of Experimental & Clinical Cancer Research · doi:10.1186/s13046-016-0360-9 · Cited by 40 · see citing works
A novel role for synaptic acetylcholinesterase as an apoptotic deoxyribonuclease
Du, A., Xie, J., Guo, K., Yang, L., Wan, Y., Ouyang, Q., Zhang, X., Niu, X., Lu, L., Wu, J., et al. (2015) · Cell Discovery · doi:10.1038/celldisc.2015.2 · Cited by 39 · see citing works
Microparticles That Form Immune Complexes as Modulatory Structures in Autoimmune Responses
Burbano, C., Rojas, M., Vásquez, G. M., & Castaño, D. (2015) · Mediators of Inflammation · doi:10.1155/2015/267590 · Cited by 38 · see citing works
Pfister, H. (2022) · Diagnostics · doi:10.3390/diagnostics12071715 · Cited by 36 · see citing works
Transfer of malignant trait to immortalized human cells following exposure to human cancer serum
Abdouh, M., Zhou, S., Arena, V., Arena, M., Lazaris, A., Onerheim, R. M., Metrakos, P. P., & Arena, G. O. (2014) · Journal of Experimental & Clinical Cancer Research · doi:10.1186/s13046-014-0086-5 · Cited by 34 · see citing works
Defining the molecular mechanisms of HIV‐1 Tat secretion: PtdIns(4,5)P2 at the epicenter
Mele, A. R., Marino, J., Chen, K., Pirrone, V., Janetopoulos, C., Wigdahl, B. L., Klase, Z. A., & Nonnemacher, M. R. (2018) · Traffic · doi:10.1111/tra.12578 · Cited by 35 · see citing works
Liu, X., Liang, H., Yan, Y., Wu, J., Bottini, M., Liu, L., & Chen, Y. (2021) · Bioactive Materials · doi:10.1016/j.bioactmat.2021.10.044 · Cited by 33 · see citing works
Hijacking homeostasis: Regulation of the tumor microenvironment by apoptosis
Gregory, C. D. (2023) · Immunological Reviews · doi:10.1111/imr.13259 · Cited by 28 · see citing works
Frank‐Bertoncelj, M., Pisetsky, D. S., Kolling, C., Michel, B. A., Gay, R. E., Jüngel, A., & Gay, S. (2018) · Frontiers in Immunology · doi:10.3389/fimmu.2018.00028 · Cited by 25 · see citing works
Self-citationLeleu, D., Levionnois, É., Laurent, P., Lazaro, E., Richez, C., Duffau, P., Blanco, P., Sisirak, V., Contin‐Bordes, C., & Truchetet, M. (2020) · Frontiers in Immunology · doi:10.3389/fimmu.2020.532177 · Cited by 24 · see citing works
Crompot, E., Damme, M. V., Duvillier, H., Pieters, K., Vermeesch, M., Pérez-Morga, D. L., Meuleman, N., Mineur, P., Bron, D., Lagneaux, L., et al. (2015) · PLoS ONE · doi:10.1371/journal.pone.0127209 · Cited by 22 · see citing works
Cellular and Molecular Mechanisms of Autoimmunity and Lupus Nephritis
Devarapu, S. K., Lorenz, G., Kulkarni, O. P., Anders, H., & Mulay, S. R. (2017) · International review of cytology · doi:10.1016/bs.ircmb.2016.12.001 · Cited by 21 · see citing works
Chen, X., Xiong, W., & Li, H. (2016) · Oncology Letters · doi:10.3892/ol.2016.5308 · Cited by 20 · see citing works
Extracellular DNA in blood products and its potential effects on transfusion
Li, Y., Yang, D., Yang, Q., Fu, C., & Huang, Y. (2020) · Bioscience Reports · doi:10.1042/bsr20192770 · Cited by 20 · see citing works
González‐Quintial, R., Nguyen, A., Kono, D. H., Oldstone, M. B. A., Theofilopoulos, A. N., & Baccalà, R. (2018) · PLoS ONE · doi:10.1371/journal.pone.0203118 · Cited by 19 · see citing works
Turbica, I., Gallais, Y., Guéguen, C., Tharinger, H., Sabbagh, C. A., Gorges, R., Gary‐Gouy, H., Kerdine‐Römer, S., Pallardy, M. J., Mascarell, L., et al. (2015) · Journal of Leukocyte Biology · doi:10.1189/jlb.3a0314-132rr · Cited by 19 · see citing works
Lü, L., Chen, X. M., Tao, H. M., Xiong, W., Jie, S. H., & LI, H. Y. (2015) · Genetics and Molecular Research · doi:10.4238/2015.october.5.2 · Cited by 19 · see citing works
Re-Examining Neutrophil Participation in GN
Caster, D. J., Powell, D. W., Miralda, I., Ward, R. A., & McLeish, K. R. (2017) · Journal of the American Society of Nephrology · doi:10.1681/asn.2016121271 · Cited by 18 · see citing works
Extracellular Vesicles: Evolving Contributors in Autoimmunity
Katsiougiannis, S. (2015) · Forum on Immunopathological Diseases and Therapeutics · doi:10.1615/forumimmundisther.2016016491 · Cited by 17 · see citing works
Microparticles in Autoimmunity: Cause or Consequence of Disease?
Rother, N., Yanginlar, C., Pieterse, E., Hilbrands, L. B., & van der Vlag, J. (2022) · Frontiers in Immunology · doi:10.3389/fimmu.2022.822995 · Cited by 17 · see citing works
Park, S., Baek, S., Shin, H.-J., Kim, J.-S., Gwon, H.-I., 배승희, & An, S. (2025) · Applied Sciences · doi:10.3390/app151910437 · Cited by 12 · see citing works
Yamaguchi, R., Yamamoto, T., Sakamoto, A., Ishimaru, Y., 楢原, 真., Sugiuchi, H., & Yamaguchi, Y. (2016) · Blood Cells Molecules and Diseases · doi:10.1016/j.bcmd.2016.01.006 · Cited by 11 · see citing works
Pathogenetic Mechanisms in Lupus Nephritis
Davidson, A., Berthier, C. C., & Kretzler, M. (2012) · Elsevier eBooks · doi:10.1016/b978-1-4377-1893-5.00018-2 · Cited by 10 · see citing works
Microvesicles released from ectopic endometrial foci as a potential biomarker of endometriosis
Kajdos, M., Szymański, J., Jerczyńska, H., Stetkiewicz, T., & Wilczyński, J. R. (2022) · Ginekologia Polska · doi:10.5603/gp.a2022.0096 · Cited by 9 · see citing works
Therapeutic and diagnostic potential of extracellular vesicles in amyotrophic lateral sclerosis
Ellison, T. J., Stice, S. L., & Yao, Y. (2022) · Extracellular Vesicle · doi:10.1016/j.vesic.2022.100019 · Cited by 8 · see citing works
Abuaf, N., Desgruelles, C., Moumaris, M., Boussa-Khettab, F., Rostane, H., Bellec, E., & Francès, C. (2019) · Journal of Immunology Research · doi:10.1155/2019/6047085 · Cited by 8 · see citing works
Extracellular vesicles: Regenerative medicine prospect in hematological malignancies
Masoumipour, M., Abbaspanah, B., & Mousavi, S. H. (2021) · Cell Biology International · doi:10.1002/cbin.11660 · Cited by 8 · see citing works
Kovalčíková, A. G., Novák, B., Roshko, O., Kovaľová, E., Pastorek, M., Vlková, B., & Celec, P. (2024) · Journal of Clinical Medicine · doi:10.3390/jcm13020468 · Cited by 7 · see citing works
Kajdos, M., Janas, Ł., Kolasa-Zwierzchowska, D., Wilczyński, J. R., & Stetkiewicz, T. (2015) · Menopause Review/Przegląd Menopauzalny · doi:10.5114/pm.2015.56540 · Cited by 7 · see citing works
The role of DNASE1L3 in systemic lupus erythematosus: from pathogenesis to clinical implications
Liu, X., Yu, Y., Cai, S., & Lingli, D. (2025) · Clinical and Experimental Medicine · doi:10.1007/s10238-025-02008-z · Cited by 6 · see citing works
Pre-Analytical Factors Affecting Extracellular DNA in Saliva
Janovičová, Ľ., Holániová, D., Vlková, B., & Celec, P. (2024) · Diagnostics · doi:10.3390/diagnostics14030249 · Cited by 6 · see citing works
CHRONIC MYELOGENOUS LEUKEMIA: A REVIEW AND UPDATE OF CURRENT AND FUTURE THERAPY
Darji, A., & Bharadia, P. D. (2016) · International Journal of Pharmacy and Pharmaceutical Sciences · Cited by 6 · see citing works
Circulating cell-free DNA and its clinical utility in cancer
Salviano‐Silva, A., Maire, C. L., Lamszus, K., & Ricklefs, F. L. (2022) · Journal of Laboratory Medicine · doi:10.1515/labmed-2022-0047 · Cited by 6 · see citing works
The Future of Kawasaki Disease Diagnosis: Liquid Biopsy May Hold the Key
Markandran, K., Clemente, K. N. M., Tan, E., Attal, K., Chee, Q. Z., Cheung, C., & Chen, C. K. (2024) · International Journal of Molecular Sciences · doi:10.3390/ijms25158062 · Cited by 5 · see citing works
Losada, P. X., Serrato, L. M., Zapata, A. M. D., Vanegas-García, A. L., Muñoz, C. H., Rodríguez, D., Diaz, J. C., Pineda, R., Lopez, M. R., & Vásquez, G. M. (2024) · Lupus Science & Medicine · doi:10.1136/lupus-2024-001243 · Cited by 5 · see citing works
Tumours and tissues: similar homeostatic systems?
Demicheli, R. (2013) · Targeted Oncology · doi:10.1007/s11523-013-0277-6 · Cited by 5 · see citing works
Extracellular DNA and Deoxyribonuclease Activity as Prognostic Markers in Sepsis
Janíková, M., Pribulová, N., Kmeťová, K., Macáková, K., Dobišová, A., Kopcova, M., Bucová, M., Vlková, B., & Celec, P. (2024) · Biomedicines · doi:10.3390/biomedicines12112565 · Cited by 4 · see citing works
B cell encounters with apoptotic cells
Bekeredjian‐Ding, I. (2012) · Autoimmunity · doi:10.3109/08916934.2012.750298 · Cited by 3 · see citing works
Janovičová, Ľ., Kmeťová, K., Tóthová, Ľ., Vlková, B., & Celec, P. (2023) · Molecular and Cellular Probes · doi:10.1016/j.mcp.2023.101900 · Cited by 3 · see citing works
Cell Death and Anti-DNA Antibodies
Hirabayashi, Y. (2012) · InTech eBooks · doi:10.5772/48343
Micropartículas como sustrato antigénico en lupus eritematoso sistémico
Muñoz‐Grajales, C., & Duque, G. M. V. (2012) · Inmunología · doi:10.1016/j.inmuno.2012.04.001
Mauricio Restrepo, E., Carolina Muñoz, G., Vanegas-García, A. L., González, L. A., & Gloria María Vásquez, D. (2012) · Revista Colombiana de Reumatología · doi:10.1016/s0121-8123(12)70039-7
Ultrastructure of Endothelium and Microparticles
Gönül, İ. I. (2013) · CRC Press eBooks · doi:10.1201/b14907-4
The Role of Microparticles as Biomarkers in the Development of Therapy for Autoimmune Disease
Pisetsky, D. S. (2017) · Springer eBooks · doi:10.1007/978-3-319-42252-7_3
Self-citationDemicheli, R. (2017) · Springer eBooks · doi:10.1007/978-3-319-57943-6_10
Yasasever, C. T., Duranyıldız, D., Bademler, S., & Oğuz, H. (2024) · Current Issues in Molecular Biology · doi:10.3390/cimb47010019
Lupus nephritis : the role of renal DNase I in the progression of the disease
Seredkina, N. (2011)
Lei, Z. (2026) · Cytometry Part B Clinical Cytometry · doi:10.1002/cytob.70011
DNASE1L3 maintains homeostatic levels of mitochondrial DNA on the mammalian cell surface
Porat, J., Sun, Y., Poli, V., Petkov, S., Almahayni, K., Crompton, A., George, B. M., Vitorino, F. N. D. L., Yi, L., Costa, C. B., et al. (2026) · Molecular Cell · doi:10.1016/j.molcel.2026.09.012 · Cited by 1 · see citing works
- Authors
- Pisetsky, D. S., Gauley, J., & Ullal, A. J.
- Affiliations
- Durham VA Medical Center (US)
- Duke Medical Center (US)
- Corresponding author
- Pisetsky, David S.
- Venue
- Immunologic Research
- Published
- 2010-12-04
- Volume
- 49
- Issue
- 1-3
- Pages
- 227-234
- ISSN
- 0257-277X (ISSN-L)
- 1559-0755
- PMC
- PMC3724471
- OpenAlex
- W2037870966
- Cited by
- 80
- References
- 25
- Citations by year
- 2026: 2 · 2025: 2 · 2024: 7 · 2023: 3 · 2022: 6 · 2021: 2 · 2020: 5 · 2019: 3 · 2018: 4 · 2017: 5 · 2016: 9 · 2015: 9 · 2014: 5 · 2013: 8 · 2012: 8
- FWCI
- 4.02
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Licence
- www.springer.com/tdm (tdm)
- Locations
- Immunologic Research (publishedVersion)
- PubMed (publishedVersion)
- Europe PMC (PubMed Central) (acceptedVersion)
- PubMed Central (acceptedVersion)
- Funders
- National Institutes of Health
- National Institute of Allergy and Infectious Diseases (AI083923, R21AI082402, R21AI083923, AI082402)
- Topics
- Health Sciences › Medicine › Rheumatology › Systemic Lupus Erythematosus Research
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Extracellular vesicles in disease
- Life Sciences › Immunology and Microbiology › Immunology › Immune Response and Inflammation
- Keywords
- microparticles, extracellular DNA, systemic lupus erythematosus, autoantigens, apoptosis, membrane vesicles, autoimmunity
- MeSH terms
- Antibodies, Antinuclear, Autoantibodies, Autoantigens, Cell Line, DNA, Extracellular Space, Humans, Lupus Erythematosus, Systemic, Cytokines, Apoptosis, Toll-Like Receptors, Cell-Derived Microparticles
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