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Regulation of immune responses by L-arginine metabolism
Abstract
L-Arginine is an essential amino acid for birds and young mammals, and it is a conditionally essential amino acid for adult mammals, as it is important in situations in which requirements exceed production, such as pregnancy. Recent findings indicate that increased metabolism of L-arginine by myeloid cells can result in the impairment of lymphocyte responses to antigen during immune responses and tumour growth. Two enzymes that compete for L-arginine as a substrate - arginase and nitric-oxide synthase - are crucial components of this lymphocyte-suppression pathway, and the metabolic products of these enzymes are important moderators of T-cell function. This Review article focuses on the relevance of L-arginine metabolism by myeloid cells for immunity under physiological and pathological conditions.
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“Along with activation of innate or adaptive immune cells, neutrophils, by releasing arginase or ROS, can inhibit NK-cell or T-cell activation by depriving extracellular levels of L-arginine, necessary for T-cell activation [225].”
From Superoxide Anion Chemistry—Its Role at the Core of the Innate Immunity (2023) · cites this paper as [225]
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Cites
Alternative activation of macrophages
Gordon, S. (2003) · Nature Reviews Immunology · doi:10.1038/nri978 · Cited by 6,189
Nitric oxide synthases: structure, function and inhibition
ALDERTON, W. K., COOPER, C. E., & KNOWLES, R. G. (2001) · Biochemical Journal · doi:10.1042/bj3570593 · Cited by 4,110
Blood Monocytes Consist of Two Principal Subsets with Distinct Migratory Properties
Geissmann, F., Jung, S., & Littman, D. R. (2003) · Immunity · doi:10.1016/s1074-7613(03)00174-2 · Cited by 3,504
Nitric oxide and the immune response
Bogdan, C. (2001) · Nature Immunology · doi:10.1038/ni1001-907 · Cited by 3,447
M-1/M-2 Macrophages and the Th1/Th2 Paradigm
Mills, C. D., Kincaid, K., Alt, J. M., Heilman, M. J., & Hill, A. M. (2000) · The Journal of Immunology · doi:10.4049/jimmunol.164.12.6166 · Cited by 3,287
Arginine metabolism: nitric oxide and beyond
WU, G., & MORRIS, S. M. (1998) · Biochemical Journal · doi:10.1042/bj3360001 · Cited by 2,811
Ido expression by dendritic cells: tolerance and tryptophan catabolism
Mellor, A. L., & Munn, D. H. (2004) · Nature Reviews Immunology · doi:10.1038/nri1457 · Cited by 2,341
Uyttenhove, C., Pilotte, L., Théate, I., Stroobant, V., Colau, D., Parmentier, N., Boon, T., & Van den Eynde, B. J. (2003) · Nature Medicine · doi:10.1038/nm934 · Cited by 2,305
Inhibition of T Cell Proliferation by Macrophage Tryptophan Catabolism
Munn, D. H., Shafizadeh, E., Attwood, J. T., Bondarev, I. E., Pashine, A., & Mellor, A. L. (1999) · The Journal of Experimental Medicine · doi:10.1084/jem.189.9.1363 · Cited by 1,640
Dendritic-cell control of pathogen-driven T-cell polarization
Kapsenberg, M. L. (2003) · Nature reviews. Immunology · doi:10.1038/nri1246 · Cited by 1,495
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Azeredo, R., Pérez‐Sánchez, J., Sitjà‐Bobadilla, A., Fouz, B., Tort, L., Aragão, C., Oliva‐Teles, A., & Costas, B. (2015) · PLoS ONE · doi:10.1371/journal.pone.0139967 · Cited by 69
Parasitic antigens alter macrophage polarization during Schistosoma japonicum infection in mice
Zhu, J., Xu, Z., Chen, X., Zhou, S., Zhang, W., Chi, Y., Li, W., Song, X., Liu, F., & Su, C. (2014) · Parasites & Vectors · doi:10.1186/1756-3305-7-122 · Cited by 69
Comprehensive metabolomic profiling of nutrients in fish and shrimp
Shao, C., Su, Y., Meng, D., Li, Y., Dong, Y., Hao, H., & Ye, H. (2022) · Food Chemistry · doi:10.1016/j.foodchem.2022.135037 · Cited by 68
Wang, J., Shirota, Y., Bayık, D., Shirota, H., Tross, D., Gulley, J. L., Wood, L. V., Berzofsky, J. A., & Klinman, D. M. (2015) · The Journal of Immunology · doi:10.4049/jimmunol.1402004 · Cited by 69
Immune Suppression: The Hallmark of Myeloid Derived Suppressor Cells
Haile, L. A., Greten, T. F., & Korangy, F. (2012) · Immunological Investigations · doi:10.3109/08820139.2012.680635 · Cited by 67
RETRACTED: Foxp3-positive macrophages display immunosuppressive properties and promote tumor growth
Manrique, S. Z., Correa, M. A. D., Hoelzinger, D. B., Dominguez, A. L., Mirza, N. N., Lin, H., Stein‐Streilein, J., Gordon, S., & Lustgarten, J. (2011) · The Journal of Experimental Medicine · doi:10.1084/jem.20100730 · Cited by 72
RetractedLee, W., Kang, J.-S., Choi, W. Y., Zhang, Q., Kim, C. H., Choi, U. Y., Kim‐Ha, J., & Kim, Y. (2016) · Nature Communications · doi:10.1038/ncomms11322 · Cited by 69
Tomé, D. (2021) · European Journal of Clinical Nutrition · doi:10.1038/s41430-021-00943-0 · Cited by 73
Local Increase of Arginase Activity in Lesions of Patients with Cutaneous Leishmaniasis in Ethiopia
Abebe, T., Hailu, A., Woldeyes, M., Mekonen, W., Bilcha, K. D., Cloke, T., Fry, L., al Basatena, N.-K. S., Corware, K., Modolell, M., et al. (2012) · PLoS neglected tropical diseases · doi:10.1371/journal.pntd.0001684 · Cited by 66
Overcoming immunosuppression in the melanoma microenvironment induced by chronic inflammation
Umansky, V., & Sevko, A. (2011) · Cancer Immunology Immunotherapy · doi:10.1007/s00262-011-1164-6 · Cited by 69
Reverting Immune Suppression to Enhance Cancer Immunotherapy
Guerrouahen, B. S., Maccalli, C., Cugno, C., Rutella, S., & Akporiaye, E. T. (2020) · Frontiers in Oncology · doi:10.3389/fonc.2019.01554 · Cited by 71
Tumor associated macrophages and ‘NO’
Nath, N., & Kashfi, K. (2020) · Biochemical Pharmacology · doi:10.1016/j.bcp.2020.113899 · Cited by 67
CD84 is a regulator of the immunosuppressive microenvironment in multiple myeloma
Lewinsky, H., Gunes, E. G., David, K., Radomir, L., Kramer, M. P., Pellegrino, B., Shahor, M. P., Chen, J., He, T.-F., Mansour, A. G., et al. (2021) · JCI Insight · doi:10.1172/jci.insight.141683 · Cited by 65
Immune-based therapies in penile cancer
Joshi, V. B., Spiess, P. E., Necchi, A., Pettaway, C. A., & Chahoud, J. (2022) · Nature Reviews Urology · doi:10.1038/s41585-022-00617-x · Cited by 66
Wang, L., Opland, D. M., Tsai, S. J., Luk, C. T., Schroer, S. A., Allison, M. B., Elia, A., Furlonger, C. L., Suzuki, A., Paige, C. J., et al. (2014) · Nature Medicine · doi:10.1038/nm.3527 · Cited by 67
LncRNA MALAT1 negatively regulates MDSCs in patients with lung cancer
Zhou, Q., Tang, X., Tian, X., Tian, J., Zhang, Y., Ma, J., Xu, H., & Wang, S. (2018) · Journal of Cancer · doi:10.7150/jca.24796 · Cited by 66
Mao, F.-Y., Zhao, Y., Lv, Y.-P., Teng, Y., Kong, H., Liu, Y., Wu, X., Hao, C.-J., Chen, W., Duan, M., et al. (2018) · Cell Death and Disease · doi:10.1038/s41419-018-0803-7 · Cited by 66
Hmgb1-IL-23-IL-17-IL-6-Stat3 Axis Promotes Tumor Growth in Murine Models of Melanoma
Tang, Q., Li, J., Zhu, H., Li, P., Zou, Z., & Xiao, Y. (2013) · Mediators of Inflammation · doi:10.1155/2013/713859 · Cited by 67
Overexpression of Arginase-1 is an indicator of poor prognosis in patients with colorectal cancer
Ma, Z., Lian, J., Yang, M., Wuyang, J., Zhao, C., Chen, W., Liu, C., Zhao, Q., Lou, C., Han, J., et al. (2019) · Pathology - Research and Practice · doi:10.1016/j.prp.2019.03.012 · Cited by 65
Morales, J. K., Kmieciak, M., Graham, L., Feldmesser, M., Bear, H. D., & Manjili, M. H. (2008) · Cancer Immunology Immunotherapy · doi:10.1007/s00262-008-0609-z · Cited by 64
Immunological Mechanisms in the Pathophysiology of Non-Alcoholic Steatohepatitis
Vonghia, L., Michielsen, P. P., & Francque, S. (2013) · International Journal of Molecular Sciences · doi:10.3390/ijms141019867 · Cited by 68
Proline Catabolism Modulates Innate Immunity in Caenorhabditis elegans
Tang, H., & Pang, S. (2016) · Cell Reports · doi:10.1016/j.celrep.2016.11.038 · Cited by 61
Gasotransmitters and the immune system: Mode of action and novel therapeutic targets
Fagone, P., Mazzon, E., Bramanti, P., Bendtzen, K., & Nicoletti, F. (2018) · European Journal of Pharmacology · doi:10.1016/j.ejphar.2018.07.026 · Cited by 62
Androgen-Regulated Expression of Arginase 1, Arginase 2 and Interleukin-8 in Human Prostate Cancer
Gannon, P. O., Godin-Ethier, J., Hassler, M. R., Delvoye, N., Aversa, M. M., Poisson, A. O., Péant, B., Fahmy, M. A., Fred Saad, C., Lapointe, R., et al. (2010) · PLoS ONE · doi:10.1371/journal.pone.0012107 · Cited by 63
MLean, N. A., & Verge, V. M. K. (2016) · Glia · doi:10.1002/glia.23021 · Cited by 62
Lee, H.-Y., Kim, H., Seo, J., Choi, K.-B., Lee, Y., Park, K., Kim, S., Mobasheri, A., & Choi, H. (2020) · Inflammopharmacology · doi:10.1007/s10787-020-00738-y · Cited by 62
Hofer, F., Sario, G. D., Musiu, C., Sartoris, S., Sanctis, F. D., & Ugel, S. (2021) · Cells · doi:10.3390/cells10102700 · Cited by 64
Role of inflammation and oxidative stress in chemotherapy-induced neurotoxicity
Gupta, P., Makkar, T. K., Goel, L., & Pahuja, M. (2022) · Immunologic Research · doi:10.1007/s12026-022-09307-7 · Cited by 71
Arginine depletion increases susceptibility to serious infections in preterm newborns
Badurdeen, S., Mulongo, M. M., & Berkley, J. A. (2014) · Pediatric Research · doi:10.1038/pr.2014.177 · Cited by 63
TGFβ in T cell biology and tumor immunity: Angel or devil?
Tu, E., Chia, P. Z. C., & Chen, W. (2014) · Cytokine & Growth Factor Reviews · doi:10.1016/j.cytogfr.2014.07.014 · Cited by 61
Banik, S., Viveros, P. R., Seeber, F., Klotz, C., Ignatius, R., & Aebischer, T. (2013) · Infection and Immunity · doi:10.1128/iai.00004-13 · Cited by 62
Won, H., Moreira, D., Gao, C., Duttagupta, P. A., Zhao, X., Manuel, E. R., Diamond, D. J., Yuan, Y., Liu, Z., Jones, J. O., et al. (2017) · Journal of Leukocyte Biology · doi:10.1189/jlb.3ma1016-451rr · Cited by 62
Kuś, K., Kij, A., Zakrzewska, A., Jasztal, A., Stojak, M., Walczak, M., & Chłopicki, S. (2018) · Breast Cancer Research · doi:10.1186/s13058-018-1075-y · Cited by 63
Ding, L., Li, Q., Chakrabarti, J. L., Munoz, A., Faure-Kumar, E., Ocádiz-Ruiz, R., Razumilava, N., Zhang, G., Hayes, M. H., Sontz, R. A., et al. (2020) · Gut · doi:10.1136/gutjnl-2019-318817 · Cited by 62
Li, D., Cao, D., Sun, Y., Cui, Y., Zhang, Y., Jiang, J., & Cao, X. (2024) · Frontiers in Immunology · doi:10.3389/fimmu.2024.1331641 · Cited by 67
Reenergizing T cell anti-tumor immunity by harnessing immunometabolic checkpoints and machineries
Ho, P., & Kaech, S. M. (2017) · Current Opinion in Immunology · doi:10.1016/j.coi.2017.04.003 · Cited by 62
Crump, N. T., Hadjinicolaou, A. V., Meng, X., Walsby-Tickle, J., Gileadi, U., Chen, J., Setshedi, M., Olsen, L. R., Lau, I., Godfrey, L., et al. (2021) · Cell Reports · doi:10.1016/j.celrep.2021.109101 · Cited by 61
Benoit, M. E., Ghigo, É., Capo, C., Raoult, D., & Mège, J. (2008) · PLoS Pathogens · doi:10.1371/journal.ppat.1000066 · Cited by 60
RetractedImmunopathogenesis of chronic hepatitis B
Балмасова, И. П. (2014) · World Journal of Gastroenterology · doi:10.3748/wjg.v20.i39.14156 · Cited by 62
Poggi, A. D., & Zocchi, M. R. (2006) · Archivum Immunologiae et Therapiae Experimentalis · doi:10.1007/s00005-006-0038-7 · Cited by 62
Transcription factors in myeloid-derived suppressor cell recruitment and function
Sonda, N., Chioda, M., Zilio, S., Simonato, F., & Bronte, V. (2011) · Current Opinion in Immunology · doi:10.1016/j.coi.2010.12.006 · Cited by 58
Self-citationWen, Z., Sun, H., Zhang, Z., Zheng, Y., Zheng, S., Bin, J., Liao, Y., Shi, M., Zhou, R., & Liao, W. (2023) · 癌症:英文版 · doi:10.1002/cac2.12420 · Cited by 58
Human Embryonic Stem Cells Suppress T Cell Responses via Arginase I-Dependent Mechanism
Yachimovich‐Cohen, N., Even‐Ram, S., Shufaro, Y., Rachmilewitz, J., & Reubinoff, B. E. (2009) · The Journal of Immunology · doi:10.4049/jimmunol.0804261 · Cited by 59
Vaccinology in the era of high-throughput biology
Nakaya, H. I., & Pulendran, B. (2015) · Philosophical Transactions of the Royal Society B Biological Sciences · doi:10.1098/rstb.2014.0146 · Cited by 65
Arginase Activity - A Marker of Disease Status in Patients with Visceral Leishmaniasis in Ethiopia
Abebe, T., Takele, Y., Weldegebreal, T., Cloke, T., Closs, E. I., Corset, C., Hailu, A., Hailu, W., Yifru, S., Corware, K., et al. (2013) · PLoS neglected tropical diseases · doi:10.1371/journal.pntd.0002134 · Cited by 59
Elahi, S. (2014) · Frontiers in Immunology · doi:10.3389/fimmu.2014.00376 · Cited by 59
Systems biological approaches to measure and understand vaccine immunity in humans
Li, S., Nakaya, H. I., Kazmin, D. A., Oh, J. Z., & Pulendran, B. (2013) · Seminars in Immunology · doi:10.1016/j.smim.2013.05.003 · Cited by 61
Macrophage heterogeneity and energy metabolism
Verdeguer, F., & Aouadi, M. (2017) · Experimental Cell Research · doi:10.1016/j.yexcr.2017.03.043 · Cited by 58
Disruption of Renal Arginine Metabolism Promotes Kidney Injury in Hepatorenal Syndrome in Mice
Varga, Z. V., Erdélyi, K., Pálóczi, J., Çınar, R., Zsengellér, Z. K., Jourdan, T., Mátyás, C., Németh, B. T., Guillot, A., Xiang, X., et al. (2018) · Hepatology · doi:10.1002/hep.29915 · Cited by 59
Lee, Y., Su, Y., Liu, T., Tsai, C., Chang, C., & Yu, H. (2018) · Frontiers in Immunology · doi:10.3389/fimmu.2018.02911 · Cited by 62
Myeloid-Derived Suppressor Cells in Prostate Cancer: Present Knowledge and Future Perspectives
Koinis, F., Xagara, A., Chantzara, E., Leontopoulou, V., Aidarinis, C., & Kotsakis, A. P. (2021) · Cells · doi:10.3390/cells11010020 · Cited by 62
Here, There, and Everywhere: Myeloid-Derived Suppressor Cells in Immunology
Ostrand‐Rosenberg, S., Lamb, T. J., & Pawelec, G. (2023) · The Journal of Immunology · doi:10.4049/jimmunol.2200914 · Cited by 63
Bacteria‐Based Backpacks to Enhance Adoptive Macrophage Transfer against Solid Tumors
An, J., Han, Z., Qin, Y., Li, C., He, J., & Zhang, X. (2023) · Advanced Materials · doi:10.1002/adma.202305384 · Cited by 58
Eastman, A. J., He, X., Qiu, Y., Davis, M. J., Vedula, P., Lyons, D. M., Park, Y., Hardison, S. E., Malachowski, A. N., Osterholzer, J. J., et al. (2015) · The Journal of Immunology · doi:10.4049/jimmunol.1402719 · Cited by 57
Bian, Z., Abdelaal, A. M., Shi, L., Liang, H., Xiong, L., Kidder, K., Venkataramani, M., Culpepper, C. D., Zen, K., & Liu, Y. (2018) · European Journal of Immunology · doi:10.1002/eji.201747355 · Cited by 59
Myeloid Cell Mediated Immune Suppression in Pancreatic Cancer
Kemp, S. B., di Magliano, M. P., & Crawford, H. C. (2021) · Cellular and Molecular Gastroenterology and Hepatology · doi:10.1016/j.jcmgh.2021.07.006 · Cited by 64
Inhibition of Tumor-Induced Myeloid-Derived Suppressor Cell Function by a Nanoparticulated Adjuvant
Fernández, A., Mesa, C., Marigo, I., Dolcetti, L., Clavell, M., Oliver, L., Fernandez, L. E., & Bronte, V. (2010) · The Journal of Immunology · doi:10.4049/jimmunol.1001465 · Cited by 58
Self-citationDressel, R. (2011) · Seminars in Immunopathology · doi:10.1007/s00281-011-0266-8 · Cited by 58
Bhatt, S., Qin, J., Bennett, C. D., Qian, S., Fung, J. J., Hamilton, T. A., & Lü, L. (2014) · The Journal of Immunology · doi:10.4049/jimmunol.1303073 · Cited by 61
Gai, Z., Wang, Q., Yang, C., Wang, L., Deng, W., & Wu, G. (2016) · Cell Discovery · doi:10.1038/celldisc.2016.51 · Cited by 58
Immunosuppressive Role of Myeloid-Derived Suppressor Cells and Therapeutic Targeting in Lung Cancer
Ma, J., Xu, H., & Wang, S. (2018) · Journal of Immunology Research · doi:10.1155/2018/6319649 · Cited by 57
Efficacy of arginine depletion by ADI-PEG20 in an intracranial model of GBM
Przystal, J. M., Hajji, N., Khozoie, C., Renziehausen, A., Zeng, Q., Abaitua, F., Hajitou, A., Suwan, K., Want, E. J., Bomalaski, J. S., et al. (2018) · Cell Death and Disease · doi:10.1038/s41419-018-1195-4 · Cited by 57
Strmiska, V., Michálek, P., Eckschlager, T., Stiborová, M., Adam, V., Křížková, S., & Heger, Z. (2019) · Biochimica et Biophysica Acta (BBA) - Reviews on Cancer · doi:10.1016/j.bbcan.2019.01.001 · Cited by 62
Amino Acid Metabolism in Rheumatoid Arthritis: Friend or Foe?
Panfili, E., Gerli, R., Grohmann, U., & Pallotta, M. T. (2020) · Biomolecules · doi:10.3390/biom10091280 · Cited by 58
Elahi, S., Vega‐López, M. A., Herman-Miguel, V., Ramírez-Estudillo, C., Mancilla-Ramı́rez, J., Motyka, B., West, L. J., & Oyegbami, O. (2020) · Frontiers in Immunology · doi:10.3389/fimmu.2020.597433 · Cited by 57
Immunotherapeutic modulation of the suppressive liver and tumor microenvironments
Chan, T., Wiltrout, R. H., & Weiss, J. M. (2011) · International Immunopharmacology · doi:10.1016/j.intimp.2010.12.024 · Cited by 56
Zhang, J., Chen, H.-M., Ma, G., Zhou, Z., Raulet, D. H., Rivera, A. L., Chen, S., & Pan, P. (2019) · Leukemia · doi:10.1038/s41375-019-0394-z · Cited by 56
Fleet, J. C., Burcham, G. N., Calvert, R. D., Elzey, B. D., & Ratliff, T. L. (2019) · The Journal of Steroid Biochemistry and Molecular Biology · doi:10.1016/j.jsbmb.2019.105557 · Cited by 58
Chimeric antigen receptor T cells in solid tumors: a war against the tumor microenvironment
Zhao, Z., Xiao, X., Saw, P. E., Wu, W., Huang, H., Chen, J., & Nie, Y. (2019) · Science China Life Sciences · doi:10.1007/s11427-019-9665-8 · Cited by 56
Less Yin, More Yang: Confronting the Barriers to Cancer Immunotherapy
Lizee, G. A., Cantu, M. A., & Hwu, P. (2007) · Clinical Cancer Research · doi:10.1158/1078-0432.ccr-07-1722 · Cited by 59
Immunometabolism: signaling pathways, homeostasis, and therapeutic targets
Xu, R., He, X., Xu, J., Yu, G., & Wu, Y. (2024) · MedComm · doi:10.1002/mco2.789 · Cited by 64
Aribi, M., Meziane, W., Habi, S., Boulatika, Y., Marchandin, H., & Aymeric, J. L. (2015) · PLoS ONE · doi:10.1371/journal.pone.0135515 · Cited by 55
The role of nitric oxide in the regulation of adaptive immune responses
Ibiza, S., & Serrador, J. M. (2008) · Inmunología · doi:10.1016/s0213-9626(08)70058-1 · Cited by 59
Egelston, C. A., Kurkó, J., Besenyei, T., Tryniszewska, B., Rauch, T. A., Glant, T. T., & Mikecz, K. (2012) · Arthritis & Rheumatism · doi:10.1002/art.34494 · Cited by 55
Luckett, J., Darch, O., Watters, C., AbuOun, M., Wright, V. J., Paredes-Osses, E., Ward, J., Goto, H., Heeb, S., Pommier, S., et al. (2012) · PLoS Pathogens · doi:10.1371/journal.ppat.1002854 · Cited by 55
Phenotypic Alteration of Neutrophils in the Blood of HIV Seropositive Patients
Cloke, T., Munder, M., Bergin, P. J., Herath, S., Modolell, M., Taylor, G. P., Müller, I., & Kropf, P. (2013) · PLoS ONE · doi:10.1371/journal.pone.0072034 · Cited by 55
Increased Level of Arginase Activity Correlates with Disease Severity in HIV‐Seropositive Patients
Cloke, T., Garvey, L. J., Choi, B., Abebe, T., Hailu, A., Hancock, M., Kadolsky, U. D., Bangham, C. R. M., Munder, M., Müller, I., et al. (2010) · The Journal of Infectious Diseases · doi:10.1086/653736 · Cited by 55
Tate, D. J., Vonderhaar, D. J., Caldas, Y. A., Metoyer, T., Patterson, J. R., Avilés, D., & Zea, A. H. (2008) · Journal of Hematology & Oncology · doi:10.1186/1756-8722-1-14 · Cited by 56
Su, L., Xu, Q., Zhang, P., Michalek, S. M., & Katz, J. (2017) · Infection and Immunity · doi:10.1128/iai.00213-17 · Cited by 55
Brin, E., Wu, K., Lu, H.-T., He, Y., Dai, Z., & He, W. (2017) · Oncotarget · doi:10.18632/oncotarget.19564 · Cited by 55
Trichomonas vaginalisandMycoplasma hominis: new tales of two old friends
Dessì, D., Margarita, V., Cocco, A. R., Marongiu, A., Fiori, P. L., & Rappelli, P. (2019) · Parasitology · doi:10.1017/s0031182018002135 · Cited by 55
Takeuchi, T., Iizumi, Y., Yudasaka, M., Kizaka‐Kondoh, S., & Okazaki, T. (2019) · Bioconjugate Chemistry · doi:10.1021/acs.bioconjchem.9b00088 · Cited by 59
Supplementation of l ‐arginine boosts the therapeutic efficacy of anticancer chemoimmunotherapy
Satoh, Y., Kotani, H., Iida, Y., Taniura, T., Notsu, Y., & Harada, M. (2020) · Cancer Science · doi:10.1111/cas.14490 · Cited by 55
Metabolic regulation in the immune response to cancer
Wu, Q., Yu, X., Li, J., Sun, S., & Tu, Y. (2021) · 癌症:英文版 · doi:10.1002/cac2.12182 · Cited by 57
Are oncoantigens suitable targets for anti-tumour therapy?
Cavallo, F., Calogero, R., & Forni, G. (2007) · Nature reviews. Cancer · doi:10.1038/nrc2208 · Cited by 55
Volpedo, G., Pacheco‐Fernández, T., Bhattacharya, P., Oljuskin, T., Dey, R., Gannavaram, S., Satoskar, A. R., & Nakhasi, H. L. (2021) · Frontiers in Immunology · doi:10.3389/fimmu.2021.748325 · Cited by 57
Chang, J., Thangamani, S., Kim, M. H., Ulrich, B. J., Morris, S. M., & Kim, C. H. (2013) · European Journal of Immunology · doi:10.1002/eji.201242772 · Cited by 54
Sunpaweravong, S., Puttawibul, P., Ruangsin, S., Laohawiriyakamol, S., Sunpaweravong, P., Sangthawan, D., Pradutkanchana, J., Raungkhajorn, P., & Geater, A. F. (2013) · Nutrition and Cancer · doi:10.1080/01635581.2014.847473 · Cited by 54
Zhang, H., Han, G., Liu, H., Ji, C. H. E. N., Ji, X., Zhou, F., Zhou, Y., & Xie, C. (2011) · Journal of Radiation Research · doi:10.1269/jrr.11054 · Cited by 58
Immune modulation by Lacto-N-fucopentaose III in experimental autoimmune encephalomyelitis
Zhu, B., Trikudanathan, S., Zozulya, A. L., Sandoval-Garcia, C., Kennedy, J. K., Atochina, O., Norberg, T., Castagner, B., Seeberger, P. H., Fábry, Z., et al. (2011) · Clinical Immunology · doi:10.1016/j.clim.2011.12.006 · Cited by 53
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Metadata
- Authors
- Bronte, V., & Zanovello, P.
- Affiliations
- University of Padua (IT)
- Corresponding author
- Bronte, Vincenzo
- Venue
- Nature Reviews Immunology
- Published
- 2005-08
- Volume
- 5
- Issue
- 8
- Pages
- 641-654
- ISSN
- 1474-1733 (ISSN-L)
- 1474-1741
- OpenAlex
- W1977179270
- Cited by
- 1,775
- References
- 146
- Citations by year
- 2026: 69 · 2025: 78 · 2024: 75 · 2023: 96 · 2022: 81 · 2021: 114 · 2020: 100 · 2019: 92 · 2018: 97 · 2017: 89 · 2016: 119 · 2015: 92 · 2014: 95 · 2013: 96 · 2012: 97
- FWCI
- 3.93
- Type
- journal article
- Language
- en
- Open access
- closed
- Licence
- www.springer.com/tdm (tdm)
- Locations
- Nature reviews. Immunology (publishedVersion)
- PubMed (publishedVersion)
- Padua Research Archive (University of Padova) (submittedVersion)
- Topics
- Life Sciences › Immunology and Microbiology › Immunology › Immune cells in cancer
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Biochemistry › Amino Acid Enzymes and Metabolism
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Biotechnology › Bacterial Cancer Therapy
- Keywords
- arginine metabolism, immune regulation, arginase, nitric oxide synthase, myeloid cells, T cell function, lymphocyte suppression, tumor growth, immunosuppression, essential amino acids
- MeSH terms
- Animals, Arginase, Arginine, Humans, Immunity, Cellular, Suppressor Factors, Immunologic, T-Lymphocytes, Reactive Oxygen Species, Nitric Oxide Synthase, Myeloid Cells, Reactive Nitrogen Species
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