Academic literature on the topic 'Immunocomputers'

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Journal articles on the topic "Immunocomputers"

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Mezentseva, A. V., L. V. Olkhova, E. B. Machneva, V. V. Konstantinova, A. E. Burya, Yu A. Nikolaeva, O. A. Filina, et al. "Successful use of hydroxymethylquinoxaline dioxide in complex antimicrobial therapy in patients with fulminant infectious complications in induced hematopoesis aplasia by gram-negative agents." Russian Journal of Pediatric Hematology and Oncology 8, no. 1 (April 7, 2021): 23–34. http://dx.doi.org/10.21682/2311-1267-2021-8-1-23-34.

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Relevance. Infectious septic complications caused by polyresistant gram-negative micro-organisms are a pressing issue in the treatment of patients after polychemotherapy (PCT) and hematopoietic stem cell transplantation at the high risk of the fulminant current and high lethality against the background of hematopoesis aplasia. One of the therapeutic strategies of antimicrobial treatment is the systematic use of 0.5 % hydroxymethylquinoxaline dioxide (dioxidine) solution in the complex antibacterial therapy of patients with severe infectious-septic complications. The preparation has a bactericidal type of action, a wide spectrum of antibacterial activity. Experience in adult clinical practice has demonstrated the effectiveness of dioxidine in the treatment of the most severe forms of aerobic and anaerobic infection. Strict dose enforcement and injection technique to avoid the appearance of side effects. Data on the intravenous use of dioxin in children are presented in a limited number of scientific literature.The aim of the study was to demonstrate the efficacy of systemic use of hydroxymethylquinoxaline dioxide (0.5 % dioxidine solution) in children with infectious complications progressing against the background of aplasia of hematopoiesis caused by multidrug-resistant pathogens Pseudomonas aeruginosa, Klebsiella pneumoniae, Enterobacter cloacae, Stenotrophomonas maltophilia.Materials and methods. 16 patients with a verified gram-negative infection were prescribed 0.5 % hydroxymethylquinoxaline dioxide solution as part of a combination antimicrobial therapy were included in the retrospective study. The median age of patients was 5 years (6 months – 16 years), 11 (69 %) were boys and 5 (31 %) girls.All children included in the study has infectious-septic complications at the PCT-induced hematopoietic aplasia, obtained according to the protocols of the main disease: severe combined immune deficiency (n = 2), idiopathic aplastic anaemia (n = 3), solid tumor (n = 2), acute myeloblastic leukemia (n = 7), acute lymphoblastic leukemia (n = 2). The main criterion for adding to the study was the existence at the least one site with a verified gram-negative infection (Pseudomonas aeruginosa, Klebsiella pneumoniae, Enterobacter cloacae, Stenotrophomonas maltophilia): bacteriemia (n = 11), oral mucosa (n = 6), ulcerative necrotic damage of perineum (n = 6), enterocolite (n = 6), infectionseptic compartments in the subcutaneous fat (n = 4), pleuropneumonia (n = 4), abscesses and inflammatory infiltration of the liver, spleen, pancreas, kidneys, lymph nodes (n = 1), infection of soft tissues in the area of the ventricular bypass with inflammatory changes of the brain membranes (n = 1).All patients received 0.5 % of the solution of dioxin by injection according of vital importance, as they had pathogens with confirmed laboratory resistance or clinical progression of the infectious process against the background of combined antibacterial therapy.Discussion. There is a complete control of fulminant developing infectious-septic processes caused by polyresistant micro-organisms against the background of hydroxymethylquinoxaline dioxide therapy in all 16 patients. The eradication of the pathogen, according to the microbiological study, has been confirmed in almost all observed patients, the efficacy of the drug has been preserved throughout the period of treatment, and the resistance of micro-organisms has not been observed. Strict adherence to the dosing and infusion technique of hydroxymethylquinoxaline dioxide has helped to achieve the full resolution of the infection process in all children without side-effects.Conclusion. On the basis of the experience presented, in immunocomputed patients of young age, 0.5 % dioxidine solution can be used as a necessary reserve preparation for the treatment of the most severe forms of infections of different localization, caused by polyresistant strains of gram-negative micro-organisms.
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Dissertations / Theses on the topic "Immunocomputers"

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Middlemiss, Melanie Jane, and n/a. "Aspects of a computational model inspired by immunological principles." University of Otago. Department of Information Science, 2007. http://adt.otago.ac.nz./public/adt-NZDU20071220.150157.

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Nature and biological systems have provided the basis for many computational models and systems, such as neural computing and evolutionary computation. This thesis examines the vertebrate immune system which formed the original basis for Artificial Immune Systems (AIS). The vertebrate immune system is highly complex and, for the most part, is successful at providing us with protection from harmful stimuli. Such a system is attractive as a model to inspire a computational system as it exhibits many desirable behaviours: adaptability, diversity, robustness, efficiency and multiple layers of detection. There has been an increasing volume of research in the field of artificial immune systems. However, as the field has expanded, immunological analogies have been reduced at the expense of problem specific optimisation. Hence, this thesis takes a different approach and returns to the immune system which initially inspired research in this field. In this thesis a set of key immunological properties based on immune system concepts and mechanisms are formalised in a model for an artificial immune system. This leads to an AIS framework that is more closely aligned with the immune system, and incorporates both innate and adaptive immune concepts. In particular, antigen presenting cells (APCs), major histocompatibility complex (MHC) molecules and T-cells are modelled within the framework. The differential signalling hypothesis is explored as a model for T-cell development, and provides a novel method for T-cell generation within an AIS. Extensive empirical analysis is performed at an individual level to examine the behaviour of the AIS framework components. These results show that the artificial immune system components exhibit similar properties to the real immune components that inspired them. However, the MHC component of the AIS is found to be of limited value within an individual AIS. The AIS framework is subsequently extended to model a population of artificial immune systems. Further empirical analysis is performed at a population level, and MHC is found to improve the adaptability of an evolving population of artificial immune systems within a dynamic environment. Such a model of immune system function is likely to be useful for immunologists, as it could provide a method of examining immune behaviour under various conditions in a cheaper and more rapid manner than in-vivo or in-vitro. Indeed, it may also provide a solution for examining properties that are unable to be tested using these traditional methods. Finally, the results of these empirical findings are discussed in terms of the relevance and applicability of immunological principles with regard to artificial immune systems for real world problems.
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Wong, Yin-cheung Eugene, and 黃彥璋. "A hybrid evolutionary algorithm for optimization of maritime logisticsoperations." Thesis, The University of Hong Kong (Pokfulam, Hong Kong), 2010. http://hub.hku.hk/bib/B44526763.

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Vasudevan, Swetha. "Immune Based Event-Incident Model for Intrusion Detection Systems: A Nature Inspired Approach to Secure Computing." [Kent, Ohio] : Kent State University, 2007. http://rave.ohiolink.edu/etdc/view?acc%5Fnum=kent1182821562.

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Thesis (M.S.)--Kent State University, 2007.
Title from PDF t.p. (viewed Mar. 19, 2009). Advisor: Michael Rothstein. Keywords: intrusion detection systems, immune system, immune detectors, intrusion detection squad, multi-agent system. Includes bibliographical references (p. 62-66).
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Hur, Jaeho 1965. "Multi-robot system control using artificial immune system." Thesis, 2007. http://hdl.handle.net/2152/3574.

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For the successful deployment of task-achieving multi-robot systems (MRS), the interactions must be coordinated among the robots within the MRS and between the robots and the task environment. There have been a number of impressive experimentally demonstrated coordinated MRS. However it is still of a premature stage for real world applications. This dissertation presents an MRS control scheme using Artificial Immune Systems (AIS). This methodology is firmly grounded in the biological sciences and provides robust performance for the intertwined entities involved in any task-achieving MRS. Based on its formal foundation, it provides a platform to characterize interesting relationships and dependencies among MRS task requirements, individual robot control, capabilities, and the resulting task performance. The work presented in this dissertation is a first of its kind wherein the principles of AIS have been used to model and organize the group behavior of the MRS. This has been presented in the form of a novel algorithm. In addition to the above, generic environments for computer simulation and real experiment have been realized to demonstrate the working of an MRS. These could potentially be used as a test bed to implement other algorithms onto the MRS. The experiment in this research is a bomb disposal task which involves a team of three heterogeneous robots with different sensors and actuators. And the algorithm has been tested practically through computer simulations.
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Books on the topic "Immunocomputers"

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ICARIS 2010 (2010 Edinburgh, Scotland). Artificial immune systems: 9th international conference, ICARIS 2010, Edinburgh, UK, July 26029, 2010 : proceedings. Berlin: Springer, 2010.

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Immunity-based systems: A design perspective. Berlin: Springer, 2004.

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ICARIS, 2010 (2010 Edinburgh Scotland). Artificial immune systems: 9th international conference, ICARIS 2010, Edinburgh, UK, July 26029, 2010 : proceedings. Berlin: Springer, 2010.

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Dasgupta, D. Immunological computation: Theory and applications. Boca Raton: Auerbach Publications, 2009.

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Dasgupta, D. Immunological computation: Theory and applications. Boca Raton: Auerbach Publications, 2009.

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De Castro, Leandro N., 1974-, Von Zuben Fernando J, and Knidel Helder, eds. Artificial immune systems: 6th international conference, ICARIS 2007, Santos, Brazil, August 26-29, 2007 ; proceedings. Berlin: Springer, 2007.

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M, Tyrrell Andy, Aickelin Uwe, Owens Nick D. L, Timmis Jonathan 1970-, Hart Emma, Hone Andrew, and SpringerLink (Online service), eds. Artificial Immune Systems: 8th International Conference, ICARIS 2009, York, UK, August 9-12, 2009. Proceedings. Berlin, Heidelberg: Springer Berlin Heidelberg, 2009.

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Julie, Greensmith, Krasnogor Natalio, Liò Pietro, Nicosia Giuseppe, Pavone Mario, and SpringerLink (Online service), eds. Artificial Immune Systems: 11th International Conference, ICARIS 2012, Taormina, Italy, August 28-31, 2012. Proceedings. Berlin, Heidelberg: Springer Berlin Heidelberg, 2012.

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In Silico Immunology. Springer, 2006.

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Tarakanov, Alexander O., Victor A. Skormin, and S. P. Sokolova. Immunocomputing: Principles and Applications. Springer New York, 2011.

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