625 research outputs found
Randomly Evolving Idiotypic Networks: Structural Properties and Architecture
We consider a minimalistic dynamic model of the idiotypic network of
B-lymphocytes. A network node represents a population of B-lymphocytes of the
same specificity (idiotype), which is encoded by a bitstring. The links of the
network connect nodes with complementary and nearly complementary bitstrings,
allowing for a few mismatches. A node is occupied if a lymphocyte clone of the
corresponding idiotype exists, otherwise it is empty. There is a continuous
influx of new B-lymphocytes of random idiotype from the bone marrow.
B-lymphocytes are stimulated by cross-linking their receptors with
complementary structures. If there are too many complementary structures,
steric hindrance prevents cross-linking. Stimulated cells proliferate and
secrete antibodies of the same idiotype as their receptors, unstimulated
lymphocytes die.
Depending on few parameters, the autonomous system evolves randomly towards
patterns of highly organized architecture, where the nodes can be classified
into groups according to their statistical properties. We observe and describe
analytically the building principles of these patterns, which allow to
calculate number and size of the node groups and the number of links between
them. The architecture of all patterns observed so far in simulations can be
explained this way. A tool for real-time pattern identification is proposed.Comment: 19 pages, 15 figures, 4 table
Immunization and Aging: a Learning Process in the Immune Network
The immune system can be thought as a complex network of different
interacting elements. A cellular automaton, defined in shape-space, was
recently shown to exhibit self-regulation and complex behavior and is,
therefore, a good candidate to model the immune system. Using this model to
simulate a real immune system we find good agreement with recent experiments on
mice. The model exhibits the experimentally observed refractory behavior of the
immune system under multiple antigen presentations as well as loss of its
plasticity caused by aging.Comment: 4 latex pages, 3 postscript figures attached. To be published in
Physical Review Letters (Tentatively scheduled for 5th Oct. issue
A Hebbian approach to complex network generation
Through a redefinition of patterns in an Hopfield-like model, we introduce
and develop an approach to model discrete systems made up of many, interacting
components with inner degrees of freedom. Our approach clarifies the intrinsic
connection between the kind of interactions among components and the emergent
topology describing the system itself; also, it allows to effectively address
the statistical mechanics on the resulting networks. Indeed, a wide class of
analytically treatable, weighted random graphs with a tunable level of
correlation can be recovered and controlled. We especially focus on the case of
imitative couplings among components endowed with similar patterns (i.e.
attributes), which, as we show, naturally and without any a-priori assumption,
gives rise to small-world effects. We also solve the thermodynamics (at a
replica symmetric level) by extending the double stochastic stability
technique: free energy, self consistency relations and fluctuation analysis for
a picture of criticality are obtained
A statistical mechanics approach to autopoietic immune networks
The aim of this work is to try to bridge over theoretical immunology and
disordered statistical mechanics. Our long term hope is to contribute to the
development of a quantitative theoretical immunology from which practical
applications may stem. In order to make theoretical immunology appealing to the
statistical physicist audience we are going to work out a research article
which, from one side, may hopefully act as a benchmark for future improvements
and developments, from the other side, it is written in a very pedagogical way
both from a theoretical physics viewpoint as well as from the theoretical
immunology one.
Furthermore, we have chosen to test our model describing a wide range of
features of the adaptive immune response in only a paper: this has been
necessary in order to emphasize the benefit available when using disordered
statistical mechanics as a tool for the investigation. However, as a
consequence, each section is not at all exhaustive and would deserve deep
investigation: for the sake of completeness, we restricted details in the
analysis of each feature with the aim of introducing a self-consistent model.Comment: 22 pages, 14 figur
Equilibrium statistical mechanics on correlated random graphs
Biological and social networks have recently attracted enormous attention
between physicists. Among several, two main aspects may be stressed: A non
trivial topology of the graph describing the mutual interactions between agents
exists and/or, typically, such interactions are essentially (weighted)
imitative. Despite such aspects are widely accepted and empirically confirmed,
the schemes currently exploited in order to generate the expected topology are
based on a-priori assumptions and in most cases still implement constant
intensities for links. Here we propose a simple shift in the definition of
patterns in an Hopfield model to convert frustration into dilution: By varying
the bias of the pattern distribution, the network topology -which is generated
by the reciprocal affinities among agents - crosses various well known regimes
(fully connected, linearly diverging connectivity, extreme dilution scenario,
no network), coupled with small world properties, which, in this context, are
emergent and no longer imposed a-priori. The model is investigated at first
focusing on these topological properties of the emergent network, then its
thermodynamics is analytically solved (at a replica symmetric level) by
extending the double stochastic stability technique, and presented together
with its fluctuation theory for a picture of criticality. At least at
equilibrium, dilution simply decreases the strength of the coupling felt by the
spins, but leaves the paramagnetic/ferromagnetic flavors unchanged. The main
difference with respect to previous investigations and a naive picture is that
within our approach replicas do not appear: instead of (multi)-overlaps as
order parameters, we introduce a class of magnetizations on all the possible
sub-graphs belonging to the main one investigated: As a consequence, for these
objects a closure for a self-consistent relation is achieved.Comment: 30 pages, 4 figure
The Role of I Region Gene Products in Macrophage - T Lymphocyte Interaction
Peer Reviewedhttp://deepblue.lib.umich.edu/bitstream/2027.42/73965/1/j.1600-065X.1978.tb00400.x.pd
A new alloantigen, Ly-8, recognized by C3H anti-AKR serum
A new membrane alloantigen, designated Ly-8.2, is defined by a C3H anti-AKR serum. The locus, Ly-8 , which controls this determinant is not linked to Thy-1, Ly-4, Ly-6, H-2 , albino (c), or brown ( b ). Ly-8.2 has a unique strain distribution, and appears to be present on both T and B lymphocytes.Peer Reviewedhttp://deepblue.lib.umich.edu/bitstream/2027.42/46747/1/251_2005_Article_BF01576977.pd
Dendritic Cells Transfected with scFv from Mab 7.B12 Mimicking Original Antigen gp43 Induces Protection against Experimental Paracoccidioidomycosis
Paracoccidioidomycosis (PCM), endemic in Latin America, is a progressive systemic mycosis caused by Paracoccidioides brasiliensis (P. brasiliensis), which primarily attacks lung tissue. Dendritic cells (DCs) are able to initiate a response in naïve T cells, and they also participate in Th-cell education. Furthermore, these cells have been used for therapy in several disease models. Here we transfected DCs with a plasmid (pMAC/PS-scFv) encoding a single chain variable fragment (scFv) of an anti-Id antibody that is capable of mimicking gp43, the main antigenic component of P. brasiliensis. First, Balb/c mice were immunized subcutaneously with pMAC/PS-scFv and, after seven days, scFv protein was presented to the regional lymph nodes cells. Moreover, we showed that the DCs transfected with scFv were capable of efficiently activating proliferation of total lymph node cells and inducing a decrease in lung infection. Therefore, our results suggested that the use of scFv-transfected DCs may be a promising therapy in the paracoccidioidomycosis (PCM) model
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