"Walter and Eliza Hall
Institute researchers have defined for the first time how the size of
the immune response is controlled, using mathematical models to predict
how powerfully immune cells respond to infection and disease." according to Phys.Org.
The finding, published today in the journal Science, has implications for our understanding of how harmful or beneficial immune responses can be manipulated for better health.
The research team used mathematics and computer modeling to
understand how complex signaling impacts the size of the response by key
infection-fighting immune cells
called T cells. The team included Ms Julia Marchingo, Dr Andrey Kan, Dr
Susanne Heinzel and Professor Phil Hodgkin from the Walter and Eliza
Hall Institute, and Professor Ken Duffy from the National University of
Ireland, Maynooth.
T cells are important for launching specific immune responses against invading microbes, as well as eliminating some cancer cells.
Errors in the control of T cells can lead to harmful 'autoimmune'
responses that attack the body's own tissues, the underlying cause of
diseases including type 1 diabetes and rheumatoid arthritis.
The team combined laboratory data with mathematical models to clarify
how different external signals impact on T cell proliferation, Ms
Marchingo said. "The more times T cells divide, the more powerfully they
can fight their target," she said. "For example, if T cells are
responding to a vaccine, more division can produce a better protective
immune response.
"The outcome of our research is that, for the first time, we are able
to predict the size of an immune response, such as the response to flu
virus, based on the sum of the signals received by the flu-responsive T
cells."
Read more...
Additional resources
"Antigen affinity, costimulation, and cytokine inputs sum linearly to amplify T cell expansion," by J.M. Marchingo et al. Science, 2014.
www.sciencemag.org/lookup/doi/… 1126/science.1260044
Source: Phys.Org