Innate immune response in retinal homeostasis and inflammatory disorders

Personalized Proteomics in Proliferative Vitreoretinopathy Implicate Hematopoietic Cell Recruitment and mTOR as a Therapeutic Target

Roybal, C. N., Velez, G., Toral, M. A., Tsang, S. H., Bassuk, A. G., & Mahajan, V. B. (2017) · American Journal of Ophthalmology · doi:10.1016/j.ajo.2017.11.025 · Cited by 47

Myeloid Suppressor Cells Induced by Retinal Pigment Epithelial Cells Inhibit Autoreactive T-Cell Responses That Lead to Experimental Autoimmune Uveitis

Tu, Z., Li, Y., Smith, D. G., Doller, C. M., Sugita, S., Chan, C., Qian, S., Fung, J. J., Caspi, R. R., Lü, L., et al. (2012) · Investigative Ophthalmology & Visual Science · doi:10.1167/iovs.11-8377 · Cited by 46

A New Look at Immune Privilege of the Eye: Dual Role for the Vision-Related Molecule Retinoic Acid

Zhou, R., Horai, R., Mattapallil, M. J., & Caspi, R. R. (2011) · The Journal of Immunology · doi:10.4049/jimmunol.1101634 · Cited by 46

Optical Coherence Tomography Angiography Reveals Spatial Bias of Macular Capillary Dropout in Diabetic Retinopathy

Kaizu, Y., Nakao, S., Yoshida, S., Hayami, T., Arima, M., Yamaguchi, M., Wada, I., Hisatomi, T., Ikeda, Y., Ishibashi, T., et al. (2017) · Investigative Ophthalmology & Visual Science · doi:10.1167/iovs.17-22306 · Cited by 46

Leukotriene B4 promotes neovascularization and macrophage recruitment in murine wet-type AMD models

Sasaki, F., Koga, T., Ohba, M., Saeki, K., Okuno, T., Ishikawa, K., Nakama, T., Nakao, S., Yoshida, S., Ishibashi, T., et al. (2018) · JCI Insight · doi:10.1172/jci.insight.96902 · Cited by 45

APCs in the Anterior Uveal Tract Do Not Migrate to Draining Lymph Nodes

Dullforce, P. A., Garman, K. L., Seitz, G. W., Fleischmann, R. J., Crespo, S. M., Planck, S. R., Parker, D. C., & Rosenbaum, J. T. (2004) · The Journal of Immunology · doi:10.4049/jimmunol.172.11.6701 · Cited by 44

Inhibition of choroidal fibrovascular membrane formation by new class of RNA interference therapeutic agent targeting periostin

Nakama, T., Yoshida, S., Ishikawa, K., Kobayashi, Y., Zhou, Y., Nakao, S., Sassa, Y., Oshima, Y., Takao, K., Shimahara, A., et al. (2014) · Gene Therapy · doi:10.1038/gt.2014.112 · Cited by 44

Relationship Between Aqueous Flare and Visual Function in Retinitis Pigmentosa

Murakami, Y., Yoshida, N., Ikeda, Y., Nakatake, S., Fujiwara, K., Notomi, S., Nabeshima, T., Nakao, S., Hisatomi, T., Enaida, H., et al. (2015) · American Journal of Ophthalmology · doi:10.1016/j.ajo.2015.02.001 · Cited by 44

Cellular and Molecular Mechanisms of Anterior Chamber-Associated Immune Deviation (ACAID): What We Have Learned from Knockout Mice

Vendomèle, J., Khebizi, Q., & Fisson, S. (2017) · Frontiers in Immunology · doi:10.3389/fimmu.2017.01686 · Cited by 44

A Major Review: Current Aspects of Ocular Behçet's Disease in Japan

Namba, K., Gotô, H., Kaburaki, T., Kitaichi, N., Mizuki, N., Asukata, Y., Fujino, Y., Meguro, A., Sakamoto, S., Shibuya, E., et al. (2015) · Ocular Immunology and Inflammation · doi:10.3109/09273948.2014.981547 · Cited by 43

Bone marrow-derived monocyte lineage cells recruited by MIP-1β promote physiological revascularization in mouse model of oxygen-induced retinopathy

Ishikawa, K., Yoshida, S., Nakao, S., Sassa, Y., Asato, R., Kohno, R.-I., Arima, M., Kita, T., Yoshida, A., Ohuchida, K., et al. (2011) · Laboratory Investigation · doi:10.1038/labinvest.2011.141 · Cited by 43

Caspase-1 Ablation Protects Photoreceptors in a Model of Autosomal Dominant Retinitis Pigmentosa

Samardzija, M., Wenzel, A., Thiersch, M., Frigg, R., Remé, C., & Grimm, C. (2006) · Investigative Ophthalmology & Visual Science · doi:10.1167/iovs.06-0556 · Cited by 42

Prediction of Proliferative Vitreoretinopathy after Retinal Detachment Surgery: Potential of Biomarker Profiling

Ricker, L. J. A. G., Kessels, A. G. H., de Jager, W., Hendrikse, F., Kijlstra, A., & Heij, E. C. L. (2012) · American Journal of Ophthalmology · doi:10.1016/j.ajo.2012.02.004 · Cited by 42

Nutritional and Therapeutic Interventions for Diabetes and Metabolic Syndrome

Terán-Garcı́a, M. (2019) · Journal of Nutrition Education and Behavior · doi:10.1016/j.jneb.2019.03.018 · Cited by 42

Retinal Hemorheologic Characterization of Early-Stage Diabetic Retinopathy Using Adaptive Optics Scanning Laser Ophthalmoscopy

Arichika, S., Uji, A., Murakami, T., Unoki, N., Yoshitake, S., Dodo, Y., Ooto, S., Miyamoto, K., & Yoshimura, N. (2014) · Investigative Ophthalmology & Visual Science · doi:10.1167/iovs.14-15121 · Cited by 39

Superior sensitivity of novel molecular imaging probe: simultaneously targeting two types of endothelial injury markers

Sun, D., Nakao, S., Xie, F., Zandi, S., Schering, A., & Hafezi‐Moghadam, A. (2010) · The FASEB Journal · doi:10.1096/fj.09-148981 · Cited by 38

IL-10 Is Significantly Involved in HSP70-Regulation of Experimental Subretinal Fibrosis

Yang, Y., Takeda, A., Yoshimura, T., Oshima, Y., Sonoda, K.-H., & Ishibashi, T. (2013) · PLoS ONE · doi:10.1371/journal.pone.0080288 · Cited by 38

Histopathology of the Star-Figure of the Macular Area in Diabetic and Angiospastic Retinopathy

Wolter, J. R., GOLDSMITH, R. I., & Phillips, R. L. (1957) · Archives of Ophthalmology · doi:10.1001/archopht.1957.00930050388009 · Cited by 37

Involvement of Innate Immune System in Late Stages of Inherited Photoreceptor Degeneration

Sudharsan, R., Beiting, D. P., Aguirre, G. D., & Beltran, W. A. (2017) · Scientific Reports · doi:10.1038/s41598-017-18236-7 · Cited by 37

A review of the immunologic findings observed in retinitis pigmentosa

McMurtrey, J. J., & Tso, M. O. M. (2018) · Survey of Ophthalmology · doi:10.1016/j.survophthal.2018.03.002 · Cited by 36

Infliximab reduces Zaprinast-induced retinal degeneration in cultures of porcine retina

de la Cámara, C. M.-F., Olivares‐González, L., Hervás, D., Salom, D., Millán, J. M., & Rodrigo, R. (2014) · Journal of Neuroinflammation · doi:10.1186/s12974-014-0172-9 · Cited by 35

Association Between Aqueous Flare and Epiretinal Membrane in Retinitis Pigmentosa

Fujiwara, K., Ikeda, Y., Murakami, Y., Nakatake, S., Tachibana, T., Yoshida, N., Nakao, S., Hisatomi, T., Yoshida, S., Yoshitomi, T., et al. (2016) · Investigative Ophthalmology & Visual Science · doi:10.1167/iovs.16-19686 · Cited by 35

MUTYH promotes oxidative microglial activation and inherited retinal degeneration

Nakatake, S., Murakami, Y., Ikeda, Y., Morioka, N., Tachibana, T., Fujiwara, K., Yoshida, N., Notomi, S., Hisatomi, T., Yoshida, S., et al. (2016) · JCI Insight · doi:10.1172/jci.insight.87781 · Cited by 35

The HMGB1–CXCL12 Complex Promotes Inflammatory Cell Infiltration in Uveitogenic T Cell-Induced Chronic Experimental Autoimmune Uveitis

Yun, J., Jiang, G., Wang, Y., Xiao, T., Zhao, Y., Sun, D., Kaplan, H. J., & Shao, H. (2017) · Frontiers in Immunology · doi:10.3389/fimmu.2017.00142 · Cited by 35

Myeloid-Derived Suppressor Cells Mediate Inflammation Resolution in Humans and Mice with Autoimmune Uveoretinitis

Jeong, H. J., Lee, H. J., Ko, J. H., Cho, B., Park, S. Y., Park, J. W., Choi, S. R., Heo, J. W., Yoon, S.-O., & Oh, J. Y. (2018) · The Journal of Immunology · doi:10.4049/jimmunol.1700617 · Cited by 34

Cytokine Signaling Protein 3 Deficiency in Myeloid Cells Promotes Retinal Degeneration and Angiogenesis through Arginase-1 Up-Regulation in Experimental Autoimmune Uveoretinitis

Chen, M., Zhao, J., Ali, I. H. A., Marry, S., Augustine, J., Bhuckory, M. B., Lynch, A., Kissenpfennig, A., & Xu, H. (2018) · American Journal Of Pathology · doi:10.1016/j.ajpath.2017.12.021 · Cited by 34

High Mobility Group Box Protein-1 in Experimental Autoimmune Uveoretinitis

Watanabe, T., Keino, H., Sato, Y., Kudo, A., Kawakami, H., & Okada, A. A. (2009) · Investigative Ophthalmology & Visual Science · doi:10.1167/iovs.08-2709 · Cited by 31

The use of real-world evidence for evaluating anti–vascular endothelial growth factor treatment of neovascular age-related macular degeneration

Talks, J. S., Daïen, V., Finger, R. P., Eldem, B. M., Sakamoto, T., Cardillo, J. A., Mitchell, P., Wong, T. Y., & Korobelnik, J. (2019) · Survey of Ophthalmology · doi:10.1016/j.survophthal.2019.02.008 · Cited by 30

Differential association of elevated inflammatory cytokines with postoperative fibrous proliferation and neovascularization after unsuccessful vitrectomy in eyes with proliferative diabetic retinopathy

Yoshida, S., Kobayashi, Y., Nakao, S., Sassa, Y., Hisatomi, T., Ikeda, Y., Oshima, Y., Kono, T., Ishibashi, T., & Sonoda, K. (2017) · Clinical ophthalmology · doi:10.2147/opth.s141821 · Cited by 29

Dendritic Cells Augment Choroidal Neovascularization

Nakai, K., Fainaru, O., Bazinet, L. F., Pakneshan, P., Benny, O., Pravda, E. A., Folkman, J., & D’Amato, R. J. (2008) · Investigative Ophthalmology & Visual Science · doi:10.1167/iovs.07-1640 · Cited by 28

Necrotic enlargement of cone photoreceptor cells and the release of high-mobility group box-1 in retinitis pigmentosa

Murakami, Y., Ikeda, Y., Nakatake, S., Tachibana, T., Fujiwara, K., Yoshida, N., Notomi, S., Nakao, S., Hisatomi, T., Miller, J. W., et al. (2015) · Cell Death Discovery · doi:10.1038/cddiscovery.2015.58 · Cited by 28

NK cells are negatively regulated by sCD83 in experimental autoimmune uveitis

Lin, W., Man, X., Li, P., Song, N., Yue, Y., Li, B., Li, Y., Sun, Y., & Fu, Q. (2017) · Scientific Reports · doi:10.1038/s41598-017-13412-1 · Cited by 28

Cell Death Pathways in Mutant Rhodopsin Rat Models Identifies Genotype-Specific Targets Controlling Retinal Degeneration

viringipurampeer, I. A., Gregory, C. Y., Metcalfe, A. L., Bashar, E., Moritz, O. L., & Gregory-Evans, K. (2018) · Molecular Neurobiology · doi:10.1007/s12035-018-1192-8 · Cited by 27

Proliferative Vitreoretinopathy: Cytologic Findings in Vitreous Samples

Martín, F., Jimeno, J. C. P., Rodríguez-de-la-Rúa-Franch, E., Mayo-Íscar, A., García‐Arumí, J., Martínez-Castillo, V. J., Fernández, N., & Saornil, M. A. (2003) · Ophthalmic Research · doi:10.1159/000071175 · Cited by 26

Altered cellular immunity and suppressor cell activity in patients with primary retinitis pigmentosa.

Heredia, C. D., Vich, J. M., Huguet, J., GARCÍA‐CALDERÓN, J. V., & García-Calderón, P. A. (1981) · British Journal of Ophthalmology · doi:10.1136/bjo.65.12.850 · Cited by 26

ALTERED VASCULAR MICROENVIRONMENT BY BEVACIZUMAB IN DIABETIC FIBROVASCULAR MEMBRANE

Nakao, S., Ishikawa, K., Yoshida, S., Kohno, R.-I., Miyazaki, M., Enaida, H., Kono, T., & Ishibashi, T. (2013) · Retina · doi:10.1097/iae.0b013e3182753b41 · Cited by 25

Amelioration of endotoxin-induced uveitis treated with an IκB kinase β inhibitor in rats.

Lennikov, A., Kitaichi, N., Noda, K., Andõ, R., Dong, Z., Fukuhara, J., Kinoshita, S., Namba, K., Mizutani, M., Fujikawa, T., et al. (2012) · Europe PMC (PubMed Central) · Cited by 25

Correction: Toll-Like Receptor (TLR) 2 and TLR4 Differentially Regulate Doxorubicin Induced Cardiomyopathy in Mice

Ma, Y., Zhang, X., Bao, H., Mi, S., Cai, W., Yan, H., Wang, Q., Wang, Z., Yan, J., Fan, G., et al. (2012) · PLoS ONE · doi:10.1371/annotation/e82f77a8-3d29-44be-a9ef-7abc6c7e584a · Cited by 25

HMGB1 is an early and critical mediator in an animal model of uveitis induced by IRBP-specific T cells

Jiang, G., Sun, D., Yang, H., Lu, Q., Kaplan, H. J., & Shao, H. (2013) · Journal of Leukocyte Biology · doi:10.1189/jlb.0613337 · Cited by 24

Granulocytapheresis in patients with refractory ocular Behcet's disease

Namba, K., Sonoda, K., Kitamei, H., Shiratori, K., Ariyama, A., Iwabuchi, K., Onoé, K., Saniabadi, A. R., Inaba, S., Ishibashi, T., et al. (2006) · Journal of Clinical Apheresis · doi:10.1002/jca.20076 · Cited by 24

Local S100A8 Levels Correlate With Recurrence of Experimental Autoimmune Uveitis and Promote Pathogenic T Cell Activity

Yun, J., Xiao, T., Zhou, L., Beuerman, R. W., Li, J., Zhao, Y., Hadayer, A., Zhang, X., Sun, D., Kaplan, H. J., et al. (2018) · Investigative Ophthalmology & Visual Science · doi:10.1167/iovs.17-23127 · Cited by 24

Microaneurysm Detection in Diabetic Retinopathy Using OCT Angiography May Depend on Intramicroaneurysmal Turbulence

Nakao, S., Yoshida, S., Kaizu, Y., Yamaguchi, M., Wada, I., Ishibashi, T., & Sonoda, K. (2018) · Ophthalmology Retina · doi:10.1016/j.oret.2018.06.001 · Cited by 24

Increased aqueous flare is associated with thickening of inner retinal layers in eyes with retinitis pigmentosa

Nagasaka, Y., Ito, Y., Ueno, S., & Terasaki, H. (2016) · Scientific Reports · doi:10.1038/srep33921 · Cited by 23

Circulating S100A8/A9 Levels Reflect Intraocular Inflammation in Uveitis Patients

Wang, Y., Dai, X., Ran, Y., Cao, Y., Lan, C., Guan, J.-T., Liu, C., Yang, F., Gan, Y.-J., Liu, B.-J., et al. (2018) · Ocular Immunology and Inflammation · doi:10.1080/09273948.2018.1538461 · Cited by 23

Macrophages Acquire Fibroblast Characteristics in a Rat Model of Proliferative Vitreoretinopathy

Lin, M., Li, Y., Li, Z., Lin, J., Zhou, X., & Liang, D. (2010) · Ophthalmic Research · doi:10.1159/000320496 · Cited by 22

High-Resolution Imaging by Adaptive Optics Scanning Laser Ophthalmoscopy Reveals Two Morphologically Distinct Types of Retinal Hard Exudates

Yamaguchi, M., Nakao, S., Kaizu, Y., Kobayashi, Y., Nakama, T., Arima, M., Yoshida, S., Oshima, Y., Takeda, A., Ikeda, Y., et al. (2016) · Scientific Reports · doi:10.1038/srep33574 · Cited by 22

Capillary dropout is dominant in deep capillary plexus in early diabetic retinopathy in optical coherence tomography angiography

Kaizu, Y., Nakao, S., Arima, M., Wada, I., Yamaguchi, M., Sekiryu, H., Hayami, T., Ishikawa, K., Ikeda, Y., & Sonoda, K. (2019) · Acta Ophthalmologica · doi:10.1111/aos.14041 · Cited by 22

Classical complement activation and acquired immune response pathways are not essential for retinal degeneration in the rd1 mouse

Rohrer, B., Demos, C., Frigg, R., & Grimm, C. (2006) · Experimental Eye Research · doi:10.1016/j.exer.2006.08.017 · Cited by 21

Lack of Lymphatics and Lymph Node–Mediated Immunity in Choroidal Neovascularization

Nakao, S., Zandi, S., Kohno, R.-I., Sun, D., Nakama, T., Ishikawa, K., Yoshida, S., Enaida, H., Ishibashi, T., & Hafezi‐Moghadam, A. (2013) · Investigative Ophthalmology & Visual Science · doi:10.1167/iovs.12-10341 · Cited by 21

Association of High-Mobility Group Box-1 With Th Cell–Related Cytokines in the Vitreous of Ocular Sarcoidosis Patients

Takeuchi, M., Taguchi, M., Sato, T., Karasawa, K., Sakurai, Y., Harimoto, K., & Ito, M. (2017) · Investigative Ophthalmology & Visual Science · doi:10.1167/iovs.16-20324 · Cited by 21

Role of autoimmunity in retinitis pigmentosa.

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Retinal flow density by optical coherence tomography angiography is useful for detection of nonperfused areas in diabetic retinopathy

Kaizu, Y., Nakao, S., Sekiryu, H., Wada, I., Yamaguchi, M., Hisatomi, T., Ikeda, Y., Kishimoto, J., & Sonoda, K. (2018) · Graefe s Archive for Clinical and Experimental Ophthalmology · doi:10.1007/s00417-018-4122-6 · Cited by 18

CD83+CCR7+ NK cells induced by interleukin 18 by dendritic cells promote experimental autoimmune uveitis

Fu, Q., Man, X., Wang, X., Song, N., Li, Y., Xue, J., Sun, Y., & Lin, W. (2018) · Journal of Cellular and Molecular Medicine · doi:10.1111/jcmm.14081 · Cited by 18

Periostin in vitreoretinal diseases

Yoshida, S., Nakama, T., Ishikawa, K., Nakao, S., Sonoda, K., & Ishibashi, T. (2017) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-017-2651-5 · Cited by 17

Correlation between aqueous flare and residual visual field area in retinitis pigmentosa

Nishiguchi, K. M., Yokoyama, Y., Kunikata, H., Abe, T., & Nakazawa, T. (2018) · British Journal of Ophthalmology · doi:10.1136/bjophthalmol-2018-312225 · Cited by 16

Therapeutic Neutrophil Apheresis in Patients With Ocular Behçet Disease

Sonoda, K. (2005) · Archives of Ophthalmology · doi:10.1001/archopht.123.2.267 · Cited by 16

The Neuropeptides of Ocular Immune Privilege, α-MSH and NPY, Suppress Phagosome Maturation in Macrophages

Benque, I. J., Xia, P., Shannon, R., Ng, T. F., & Taylor, A. W. (2018) · ImmunoHorizons · doi:10.4049/immunohorizons.1800049 · Cited by 16

High-mobility group box 1 protein in endophthalmitis

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S100A12 and S100A8/9 proteins are biomarkers of articular disease activity in Blau syndrome

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CXCR2 Expression on Neutrophils is Upregulated During the Relapsing Phase of Ocular Behçet Disease

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Assessment of the innate and adaptive immune system in proliferative vitreoretinopathy

Zhang, W., Tan, J. Y., Liu, Y., Li, W., Gao, Q., & Lehmann, P. V. (2012) · Eye · doi:10.1038/eye.2012.52 · Cited by 14

Invariant natural killer T cells play dual roles in the development of experimental autoimmune uveoretinitis

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Clinicopathologic Correlation of Progressive Fibrovascular ProliferationAssociated With Occult Choroidal Neovascularization in Age-Related MacularDegeneration

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Novel immunodeficient Pde6b rd1 mouse model of retinitis pigmentosa to investigate potential therapeutics and pathogenesis of retinal degeneration

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Molecular Imaging of Retinal Endothelial Injury in Diabetic Animals

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DIABETIC RETINITIS

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EVOLUTION TIME AND LONGITUDINAL STUDIES OF THE ANTI-S-ANTIGEN ANTIBODY TITERS IN RETINITIS PIGMENTOSA

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An Overview of Diabetic Retinopathy

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Immune responses to injury and their links to eye disease

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Mechanisms of Photoreceptor Death in Retinitis Pigmentosa

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Retinitis Pigmentosa: Progress in Molecular Pathology and Biotherapeutical Strategies

Liu, W., Liu, S., Li, P., & Yao, K. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms23094883 · Cited by 192

Retinal Inflammation, Cell Death and Inherited Retinal Dystrophies

Olivares‐González, L., Velasco, S., Campillo, I., & Rodrigo, R. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22042096 · Cited by 135

The innate immune system in diabetic retinopathy

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Retinal innate immune activation in health and disease

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Ocular Vascular Diseases: From Retinal Immune Privilege to Inflammation

Wang, X., Wang, T., Lam, E., Álvarez, D., & Sun, Y. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms241512090 · Cited by 71

Immune regulation in the retina

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Road to fulfillment (not perdition): taming immune response to restore vision

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Innate immunity and retinal angiogenesis

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