Parallel processing in immune networks

Biology – Quantitative Biology – Cell Behavior

Scientific paper

Rate now

  [ 0.00 ] – not rated yet Voters 0   Comments 0

Details

21 pages, 7 figures

Scientific paper

In this paper we extend our previous investigations on systemic features of the immune system, based on a statistical mechanics approach. In particular, we recently introduced a mean-field spin-glass model for the interaction between helper cells and the effector branches (B and K cells) able to reproduce, as emerging properties, several collective phenomena shown in real immune networks (e.g. the connection between autoimmunity and lymphoproliferative disorders or the breakdown of immunosurveillance by diminishing the amount of helpers in the system). Here, we go beyond the previous fully-connected approximation by introducing dilution in the interactions between helpers and B clones, and show that this makes the former able to orchestrate parallel strategies to fight several pathogens simultaneously. This is an important step forward toward a comprehension of these systems since dilution, which is a biological requisite, results in multitasking capabilities. The latter are indeed the core of the immune system as always multiple attacks are present in a host.

No associations

LandOfFree

Say what you really think

Search LandOfFree.com for scientists and scientific papers. Rate them and share your experience with other people.

Rating

Parallel processing in immune networks does not yet have a rating. At this time, there are no reviews or comments for this scientific paper.

If you have personal experience with Parallel processing in immune networks, we encourage you to share that experience with our LandOfFree.com community. Your opinion is very important and Parallel processing in immune networks will most certainly appreciate the feedback.

Rate now

     

Profile ID: LFWR-SCP-O-291584

  Search
All data on this website is collected from public sources. Our data reflects the most accurate information available at the time of publication.