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What is Clonal Selection

Handbook of Research on Artificial Immune Systems and Natural Computing: Applying Complex Adaptive Technologies
Human immune response relies on the prior formation of an incredibly diverse population of B cells and T cells. The specificity of both the B-cell receptors and T-cell receptors, that is, the epitope to which a given receptor can bind, is created by a remarkable genetic mechanism. Each receptor is created even though the epitope it recognizes may never have been present in the body. If an antigen with that epitope should enter the body, those few lymphocytes able to bind to it will do so. If they also receive a second co-stimulatory signal, they may begin repeated rounds of mitosis. In this way, clones of antigen-specific lymphocytes (B and T) develop providing the basis of the immune response. This phenomenon is called clonal selection
Published in Chapter:
An Artificial Immune Dynamical System for Optimization
Licheng Jiao (Xidian University, China), Maoguo Gong (Xidian University, China), and Wenping Ma (Xidian University, China)
DOI: 10.4018/978-1-60566-310-4.ch003
Abstract
Many immue-inspired algorithms are based on the abstractions of one or several immunology theories, such as clonal selection, negative selection, positive selection, rather than the whole process of immune response to solve computational problems. In order to build a general computational framework by simulating immune response process, this chapter introduces a population-based artificial immune dynamical system, termed as PAIS, and applies it to numerical optimization problems. PAIS models the dynamic process of human immune response as a quaternion (G, I, R, Al), where G denotes exterior stimulus or antigen, I denotes the set of valid antibodies, R denotes the set of reaction rules describing the interactions between antibodies, and Al denotes the dynamic algorithm describing how the reaction rules are applied to antibody population. Some general descriptions of reaction rules, including the set of clonal selection rules and the set of immune memory rules are introduced in PAIS. Based on these reaction rules, a dynamic algorithm, termed as PAISA, is designed for numerical optimization. In order to validate the performance of PAISA, 9 benchmark functions with 20 to 10,000 dimensions and a practical optimization problem, optimal approximation of linear systems are solved by PAISA, successively. The experimental results indicate that PAISA has high performance in optimizing some benchmark functions and practical optimization problems.
Full Text Chapter Download: US $37.50 Add to Cart
More Results
Feature Selection Based on Clonal Selection Algorithm: Evaluation and Application
Human immune response relies on the prior formation of an incredibly diverse population of B cells and T cells. The specificity of both the B-cell receptors and T-cell receptors, that is, the epitope to which a given receptor can bind, is created by a remarkable genetic mechanism. Each receptor is created even though the epitope it recognizes may never have been present in the body. If an antigen with that epitope should enter the body, those few lymphocytes able to bind to it will do so. If they also receive a second co-stimulatory signal, they may begin repeated rounds of mitosis. In this way, clones of antigen-specific lymphocytes (B and T) develop providing the basis of the immune response. This phenomenon is called clonal selection
Full Text Chapter Download: US $37.50 Add to Cart
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