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Journal articles on the topic 'Immunity control'

Author: Grafiati

Published: 4 May 2024

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1

Bendelac, Albert, and Douglas T. Fearon. "Innate immunity Innate pathways that control acquired immunity." Current Opinion in Immunology 9, no. 1 (February 1997): 1–3. http://dx.doi.org/10.1016/s0952-7915(97)80151-3.

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2

Busslinger, M., and A. Tarakhovsky. "Epigenetic Control of Immunity." Cold Spring Harbor Perspectives in Biology 6, no. 6 (June 1, 2014): a019307. http://dx.doi.org/10.1101/cshperspect.a019307.

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3

Busslinger, M., and A. Tarakhovsky. "Epigenetic Control of Immunity." Cold Spring Harbor Perspectives in Biology 6, no. 7 (July 1, 2014): a024174. http://dx.doi.org/10.1101/cshperspect.a024174.

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4

Tracey, Kevin J. "Reflex control of immunity." Nature Reviews Immunology 9, no. 6 (June 2009): 418–28. http://dx.doi.org/10.1038/nri2566.

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5

Gamboa, Lena, Ali H. Zamat, and Gabriel A. Kwong. "Synthetic immunity by remote control." Theranostics 10, no. 8 (2020): 3652–67. http://dx.doi.org/10.7150/thno.41305.

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6

ALVAREZ, MARÍA E., FLORENCIA NOTA, and DAMIÁN A. CAMBIAGNO. "Epigenetic control of plant immunity." Molecular Plant Pathology 11, no. 4 (June 1, 2010): 563–76. http://dx.doi.org/10.1111/j.1364-3703.2010.00621.x.

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7

Chen, Huihui, Xiaohan Ning, and Zhengfan Jiang. "Caspases control antiviral innate immunity." Cellular & Molecular Immunology 14, no. 9 (July 10, 2017): 736–47. http://dx.doi.org/10.1038/cmi.2017.44.

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8

Bachère, Evelyne. "Shrimp immunity and disease control." Aquaculture 191, no. 1-3 (November 2000): 3–11. http://dx.doi.org/10.1016/s0044-8486(00)00413-0.

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9

Shanker, Anil. "Adaptive control of innate immunity." Immunology Letters 131, no. 2 (July 2010): 107–12. http://dx.doi.org/10.1016/j.imlet.2010.04.002.

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10

Kiberstis, P. A. "Oncogene control of antitumor immunity." Science 352, no. 6282 (April 7, 2016): 183. http://dx.doi.org/10.1126/science.352.6282.183-d.

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11

Fric, Jan, Teresa Zelante, Alicia Y. W. Wong, Alexandra Mertes, Hong-Bing Yu, and Paola Ricciardi-Castagnoli. "NFAT control of innate immunity." Blood 120, no. 7 (August 16, 2012): 1380–89. http://dx.doi.org/10.1182/blood-2012-02-404475.

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Abstract The calcineurin/nuclear factor of activated T cells (NFAT) signaling pathway mediates multiple adaptive T-cell functions, but recent studies have shown that calcineurin/NFAT signaling also contributes to innate immunity and regulates the homeostasis of innate cells. Myeloid cells, including granulocytes and dendritic cells, can promote inflammation, regulate adaptive immunity, and are essential mediators of early responses to pathogens. Microbial ligation of pattern-recognition receptors, such as TLR4, CD14, and dectin 1, is now known to induce the activation of calcineurin/NFAT signaling in myeloid cells, a finding that has provided new insights into the molecular pathways that regulate host protection. Inhibitors of calcineurin/NFAT binding, such as cyclosporine A and FK506, are broadly used in organ transplantation and can act as potent immunosuppressive drugs in a variety of different disorders. There is increasing evidence that these agents influence innate responses as well as inhibiting adaptive T-cell functions. This review focuses on the role of calcineurin/NFAT signaling in myeloid cells, which may contribute to the various unexplained effects of immunosuppressive drugs already being used in the clinic.

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12

Pouikli, Andromachi, and Christian Frezza. "Metabolic control of antitumor immunity." Science 381, no. 6664 (September 22, 2023): 1287–88. http://dx.doi.org/10.1126/science.adk1785.

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13

Akira, Shizuo, and Kazuhiko Maeda. "Control of RNA Stability in Immunity." Annual Review of Immunology 39, no. 1 (April 26, 2021): 481–509. http://dx.doi.org/10.1146/annurev-immunol-101819-075147.

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Posttranscriptional control of mRNA regulates various biological processes, including inflammatory and immune responses. RNA-binding proteins (RBPs) bind cis-regulatory elements in the 3′ untranslated regions (UTRs) of mRNA and regulate mRNA turnover and translation. In particular, eight RBPs (TTP, AUF1, KSRP, TIA-1/TIAR, Roquin, Regnase, HuR, and Arid5a) have been extensively studied and are key posttranscriptional regulators of inflammation and immune responses. These RBPs sometimes collaboratively or competitively bind the same target mRNA to enhance or dampen regulatory activities. These RBPs can also bind their own 3′ UTRs to negatively or positively regulate their expression. Both upstream signaling pathways and microRNA regulation shape the interactions between RBPs and target RNA. Dysregulation of RBPs results in chronic inflammation and autoimmunity. Here, we summarize the functional roles of these eight RBPs in immunity and their associated diseases.

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14

Ansaldo, Eduard, Taylor K. Farley, and Yasmine Belkaid. "Control of Immunity by the Microbiota." Annual Review of Immunology 39, no. 1 (April 26, 2021): 449–79. http://dx.doi.org/10.1146/annurev-immunol-093019-112348.

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The immune system has coevolved with extensive microbial communities living on barrier sites that are collectively known as the microbiota. It is increasingly clear that microbial antigens and metabolites engage in a constant dialogue with the immune system, leading to microbiota-specific immune responses that occur in the absence of inflammation. This form of homeostatic immunity encompasses many arms of immunity, including B cell responses, innate-like T cells, and conventional T helper and T regulatory responses. In this review we summarize known examples of innate-like T cell and adaptive immunity to the microbiota, focusing on fundamental aspects of commensal immune recognition across different barrier sites. Furthermore, we explore how this cross talk is established during development, emphasizing critical temporal windows that establish long-term immune function. Finally, we highlight how dysregulation of immunity to the microbiota can lead to inflammation and disease, and we pinpoint outstanding questions and controversies regarding immune system–microbiota interactions.

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15

Collins, Nicholas, and Yasmine Belkaid. "Control of immunity via nutritional interventions." Immunity 55, no. 2 (February 2022): 210–23. http://dx.doi.org/10.1016/j.immuni.2022.01.004.

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16

Machado, João Paulo B., Iara P. Calil, Anésia A. Santos, and Elizabeth P. B. Fontes. "Translational control in plant antiviral immunity." Genetics and Molecular Biology 40, no. 1 suppl 1 (February 13, 2017): 292–304. http://dx.doi.org/10.1590/1678-4685-gmb-2016-0092.

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17

Harjes, Ulrike. "Germline control of anti-tumour immunity." Nature Reviews Cancer 20, no. 8 (June 17, 2020): 414. http://dx.doi.org/10.1038/s41568-020-0282-x.

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18

Lau, Henry Y. K., Vicky W. K. Wong, and Ivan S. K. Lee. "Immunity-based autonomous guided vehicles control." Applied Soft Computing 7, no. 1 (January 2007): 41–57. http://dx.doi.org/10.1016/j.asoc.2005.02.003.

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19

Brave, Martina, Dana J. Lukin, and Sridhar Mani. "Microbial control of intestinal innate immunity." Oncotarget 6, no. 24 (July 3, 2015): 19962–63. http://dx.doi.org/10.18632/oncotarget.4780.

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20

Mehta, Manan M., Samuel E. Weinberg, and Navdeep S. Chandel. "Mitochondrial control of immunity: beyond ATP." Nature Reviews Immunology 17, no. 10 (July 3, 2017): 608–20. http://dx.doi.org/10.1038/nri.2017.66.

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21

Gray-Owen, Scott D., and Richard S. Blumberg. "CEACAM1: contact-dependent control of immunity." Nature Reviews Immunology 6, no. 6 (June 2006): 433–46. http://dx.doi.org/10.1038/nri1864.

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22

Pelgrom, Leonard R., and Bart Everts. "Metabolic control of type 2 immunity." European Journal of Immunology 47, no. 8 (July 14, 2017): 1266–75. http://dx.doi.org/10.1002/eji.201646728.

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23

Jerison, Elizabeth. "Dynamical control of immunity and inflammation." Biophysical Journal 123, no. 3 (February 2024): 309a. http://dx.doi.org/10.1016/j.bpj.2023.11.1908.

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24

Jin, Hyo Sun, Hyun-Woo Suh, Seong-Jun Kim, and Eun-Kyeong Jo. "Mitochondrial Control of Innate Immunity and Inflammation." Immune Network 17, no. 2 (2017): 77. http://dx.doi.org/10.4110/in.2017.17.2.77.

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25

Banchereau, Jacques, and Ralph M. Steinman. "Dendritic cells and the control of immunity." Nature 392, no. 6673 (March 1998): 245–52. http://dx.doi.org/10.1038/32588.

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26

Lau, H. Y. K., and V. W. K. Wong. "An immunity-based distributed multiagent-control framework." IEEE Transactions on Systems, Man, and Cybernetics - Part A: Systems and Humans 36, no. 1 (January 2006): 91–108. http://dx.doi.org/10.1109/tsmca.2005.859103.

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27

Moehlman, Andrew T., and Richard J. Youle. "Mitochondrial Quality Control and Restraining Innate Immunity." Annual Review of Cell and Developmental Biology 36, no. 1 (October 6, 2020): 265–89. http://dx.doi.org/10.1146/annurev-cellbio-021820-101354.

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Maintaining mitochondrial health is essential for the survival and function of eukaryotic organisms. Misfunctioning mitochondria activate stress-responsive pathways to restore mitochondrial network homeostasis, remove damaged or toxic proteins, and eliminate damaged organelles via selective autophagy of mitochondria, a process termed mitophagy. Failure of these quality control pathways is implicated in the pathogenesis of Parkinson's disease and other neurodegenerative diseases. Impairment of mitochondrial quality control has been demonstrated to activate innate immune pathways, including inflammasome-mediated signaling and the antiviral cyclic GMP-AMP synthase (cGAS)/stimulator of interferon genes (STING)–regulated interferon response. Immune system malfunction is a common hallmark in many neurodegenerative diseases; however, whether inflammation suppresses or exacerbates disease pathology is still unclear. The goal of this review is to provide a historical overview of the field, describe mechanisms of mitochondrial quality control, and highlight recent advances on the emerging role of mitochondria in innate immunity and inflammation.

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28

Park, Eun Jeong, Motomu Shimaoka, and Hiroshi Kiyono. "MicroRNA-mediated dynamic control of mucosal immunity." International Immunology 29, no. 4 (April 1, 2017): 157–63. http://dx.doi.org/10.1093/intimm/dxx019.

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29

Zhao, Ende, Huanbin Xu, Lin Wang, Ilona Kryczek, Ke Wu, Yu Hu, Guobin Wang, and Weiping Zou. "Bone marrow and the control of immunity." Cellular & Molecular Immunology 9, no. 1 (October 24, 2011): 11–19. http://dx.doi.org/10.1038/cmi.2011.47.

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30

Ottenhoff, Tom H. M., Frank A. W. Verreck, Marieke A. Hoeve, and Esther van de Vosse. "Control of human host immunity to mycobacteria." Tuberculosis 85, no. 1-2 (January 2005): 53–64. http://dx.doi.org/10.1016/j.tube.2004.09.011.

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31

Quintana, Francisco J., and David H. Sherr. "Aryl Hydrocarbon Receptor Control of Adaptive Immunity." Pharmacological Reviews 65, no. 4 (August 1, 2013): 1148–61. http://dx.doi.org/10.1124/pr.113.007823.

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32

Lau, Henry Y. K., and Vicky W. K. Wong. "An immunity approach to strategic behavioral control." Engineering Applications of Artificial Intelligence 20, no. 3 (April 2007): 289–306. http://dx.doi.org/10.1016/j.engappai.2006.06.002.

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33

Liu, Juan, Cheng Qian, and Xuetao Cao. "Post-Translational Modification Control of Innate Immunity." Immunity 45, no. 1 (July 2016): 15–30. http://dx.doi.org/10.1016/j.immuni.2016.06.020.

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34

Wakelin, D. "Genetic control of immunity to helminth infections." Parasitology Today 1, no. 1 (July 1985): 17–23. http://dx.doi.org/10.1016/0169-4758(85)90101-2.

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35

Potter, Tim, and Kat Baxter-Smith. "Modernising BRD control." Livestock 25, no. 6 (November 2, 2020): 292. http://dx.doi.org/10.12968/live.2020.25.6.292.

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36

Anandasabapathy, Niroshana, Rachel Feder, Shamim Mollah, Sze-Wah Tse, Maria Paula Longhi, Saurabh Mehandru, Ines Matos, et al. "Classical Flt3L-dependent dendritic cells control immunity to protein vaccine." Journal of Experimental Medicine 211, no. 9 (August 18, 2014): 1875–91. http://dx.doi.org/10.1084/jem.20131397.

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DCs are critical for initiating immunity. The current paradigm in vaccine biology is that DCs migrating from peripheral tissue and classical lymphoid-resident DCs (cDCs) cooperate in the draining LNs to initiate priming and proliferation of T cells. Here, we observe subcutaneous immunity is Fms-like tyrosine kinase 3 ligand (Flt3L) dependent. Flt3L is rapidly secreted after immunization; Flt3 deletion reduces T cell responses by 50%. Flt3L enhances global T cell and humoral immunity as well as both the numbers and antigen capture capacity of migratory DCs (migDCs) and LN-resident cDCs. Surprisingly, however, we find immunity is controlled by cDCs and actively tempered in vivo by migDCs. Deletion of Langerin+ DC or blockade of DC migration improves immunity. Consistent with an immune-regulatory role, transcriptomic analyses reveals different skin migDC subsets in both mouse and human cluster together, and share immune-suppressing gene expression and regulatory pathways. These data reveal that protective immunity to protein vaccines is controlled by Flt3L-dependent, LN-resident cDCs.

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37

Polushin, P. A., O. R. Nikitin, and I. R. Dubov. "Quasioptimal control in diversed signal transmission." IOP Conference Series: Materials Science and Engineering 1227, no. 1 (February 1, 2022): 012003. http://dx.doi.org/10.1088/1757-899x/1227/1/012003.

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Abstract To increase the noise immunity of signal transmission, diversity methods are now widely used, consisting in obtaining and combining several copies of the transmitted signal. In this case, it is possible to perform a combination either before the detection procedure or after it. If you do not take into account the possible use of non-linear types of modulation, then the pre-detector combination always has advantages over the post-detector combination. However, taking into account the nonlinear properties of the transmitted signals, new possibilities appear for increasing the noise immunity in combination and simplifying the processing. In the case of using analog signals, in particular frequency modulation, at certain points in time, the pre-detection combination can lose to the post-detection combination. At the same time, by combining pre-detector and post-detector combining circuits, it is possible to lower the threshold level during demodulation and increase noise immunity. In the case of using digital modes of modulation, it is possible to process only the signals after demodulation without reducing the noise immunity and to eliminate the need for preliminary phasing of the diversity signals before detection.

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38

Watts, Tania H. "Stepping up Th1 immunity to control phagosomal bacteria." Trends in Immunology 42, no. 6 (June 2021): 461–63. http://dx.doi.org/10.1016/j.it.2021.04.008.

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39

Schlosser, Thomas P. "Sovereign Immunity: Should the Sovereign Control the Purse?" American Indian Law Review 24, no. 2 (1999): 309. http://dx.doi.org/10.2307/20070637.

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40

Carter, Philip B. "Immunity to Parasites: How Animals Control Parasite Infections." American Journal of Tropical Medicine and Hygiene 34, no. 4 (July 1, 1985): 825. http://dx.doi.org/10.4269/ajtmh.1985.34.4.tm0340040825a.

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41

BACON, L. D., and R. R. DIETERT. "Genetic Control of Cell-Mediated Immunity in Chickens." Poultry Science 70, no. 5 (May 1991): 1187–99. http://dx.doi.org/10.3382/ps.0701187.

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42

Befus, A. Dean, Derek Wakelin, and Edward Arnold. "Immunity to Parasites: How Animals Control Parasite Infections." Journal of Parasitology 71, no. 3 (June 1985): 364. http://dx.doi.org/10.2307/3282019.

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43

Schiering, Chris, Emma Wincent, Amina Metidji, Andrea Iseppon, Ying Li, Alexandre J. Potocnik, Sara Omenetti, et al. "Feedback control of AHR signalling regulates intestinal immunity." Nature 542, no. 7640 (February 2017): 242–45. http://dx.doi.org/10.1038/nature21080.

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44

Asaturova, A. V., A. V. Tregubova, and D. V. Shushkanova. "Inhibition of immunity control points in ovarian cancer." CLINICAL AND EXPERIMENTAL MORPHOLOGY 9, no. 1 (2020): 11–19. http://dx.doi.org/10.31088/cem2020.9.1.11-19.

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45

Grant, Audrey V., Christian Roussilhon, Richard Paul, and Anavaj Sakuntabhai. "The genetic control of immunity to Plasmodium infection." BMC Immunology 16, no. 1 (2015): 14. http://dx.doi.org/10.1186/s12865-015-0078-z.

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46

Naik, S., N. Bouladoux, C. Wilhelm, M. J. Molloy, R. Salcedo, W. Kastenmuller, C. Deming, et al. "Compartmentalized Control of Skin Immunity by Resident Commensals." Science 337, no. 6098 (July 26, 2012): 1115–19. http://dx.doi.org/10.1126/science.1225152.

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47

Palm, Noah W., and Ruslan Medzhitov. "Pattern recognition receptors and control of adaptive immunity." Immunological Reviews 227, no. 1 (January 2009): 221–33. http://dx.doi.org/10.1111/j.1600-065x.2008.00731.x.

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48

Secher, Thomas, Olivier Gaillot, Bernhard Ryffel, and Mathias Chamaillard. "Remote Control of Intestinal Tumorigenesis by Innate Immunity." Cancer Research 70, no. 5 (February 28, 2010): 1749–52. http://dx.doi.org/10.1158/0008-5472.can-09-3401.

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49

Huang, Lei, and Andrew L. Mellor. "Metabolic control of tumour progression and antitumour immunity." Current Opinion in Oncology 26, no. 1 (January 2014): 92–99. http://dx.doi.org/10.1097/cco.0000000000000035.

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50

Wang, Tian. "Flavivirus Immunity in Disease Control and Viral Pathogenesis." Viral Immunology 33, no. 1 (February 1, 2020): 1–2. http://dx.doi.org/10.1089/vim.2019.29047.tjt.

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