Spiking neural P systems are a class of distributed and parallel computing models inspired by the neurophysiological behavior of neurons sending electrical impulses (spikes) along axons to other... Show moreSpiking neural P systems are a class of distributed and parallel computing models inspired by the neurophysiological behavior of neurons sending electrical impulses (spikes) along axons to other neurons. In this thesis, we consider that the spiking neural P systems are universal even if the systems work in limited asynchronous mode. And we also investigated different variants of spiking neural P systems with other additional features, such as the axon functioning, the growth of dendritic trees in neurons, the positive or negative weights on synapses, and the astrocytes having excitatory and inhibitory influence on synapses. Show less
This thesis consists of two parts, focusing on CD4+CD25+ regulatory T cells (Tregs) (Part I) and IgG glycosylations (Part II), respectively. Part I (Chapter 2-5) is mainly dedicated to a better... Show moreThis thesis consists of two parts, focusing on CD4+CD25+ regulatory T cells (Tregs) (Part I) and IgG glycosylations (Part II), respectively. Part I (Chapter 2-5) is mainly dedicated to a better identification/characterization and generation of functional human Tregs in vitro. In Chapter 2, we investigated the dynamics of endogenous FOXP3 expression and its relation to the suppressive function in activated human CD4+ T cells. In Chapter 3, we discovered an inverse correlation between membrane-bound TNF-alpha expression and cell suppressive abilities within human CD4+CD25++ T-cell compartment. In Chapter 4 & 5, we developed efficient approaches to consistently convert effector T cells into Tregs both in mice and humans. The underlying mechanisms responsible for the inconsistency in Treg conversion were unraveled as well. Part II (Chapter 6-7) aims to analyze the glycosylation pattern of antigen-specific antibodies and to obtain more insights on how glycosylation is regulated during an active immune response. Chapter 6 describes a method for the microscale purification and Fc-glycosylation analysis of auto-antibodies in patients with rheumatoid arthritis. In Chapter 7, we identified, by using an in vitro culture system, some factors that can influence the gylcan pattern of secreted IgG1 during the activation and differentiation of B cells. Show less
