We present a network model that incorporates: 1) symmetric idiotypic interactions,
2) an explicit affinity parameter (matrix), 3) external (i.e., non idiotypic)
antigens, 4) idiotypic stimulation at low population densities, and 5) idiotypic suppression
at high densities. Such an idiotypic network of two clones has three stable
states: a virgin state, i.e., an equilibrium between the normal influx and turnover
of cells, and two immune states (one for each clone), which are maintained by idiotypic
interactions. In its immune state, a clone suppresses its idiotypic partner and
immediately rejects antigen. Introduction of antigen into the virgin state causes
a state switch to the corresponding immune state: antigens are thus remembered,
i.e., the network displays memory. This symmetric network cannot account for suppression
of proliferating clones. Clones that proliferate suppress their anti-idiotypic
"suppressors" long before these have grown large enough to become suppressive.
This is a consequence of symmetry: asymmetric versions of our model do account
for suppression. We here assume that proliferation precedes suppression; if the reverse
is assumed (i.e., suppression), the model cannot account for either memory
or suppression. We conclude that the model incorporating proliferation before suppression
is superior. We next analyse 50-dimensional (50-D) networks of this same model. The network connectance crucially determines the behavior of the network.
Only weakly connected networks know a 50-D virgin state in which all clones are
in a "resting" state. Switching behavior only occurs in weakly connected systems.
The stability of the respective states reached by the systems first decreases, but
later increases when connectance increases. Most importantly, highly connected
systems are highly unresponsive, i.e., most clones are suppressed; hence, most antigens
expand progressively. We conclude that only weakly connected networks have,
immunologically, reasonable behavior.
[1]
Jerne Nk.
Towards a network theory of the immune system.
,
1974
.
[2]
K. Rajewsky,et al.
Induction of T and B cell immunity by anti‐idiotypic antibody
,
1975,
European journal of immunology.
[3]
J. Hiernaux,et al.
Some remarks on the stability of the idiotypic network.
,
1977,
Immunochemistry.
[4]
M Seghers,et al.
A qualitative study of an idiotypic cyclic network.
,
1979,
Journal of theoretical biology.
[5]
G W Hoffmann,et al.
On network theory and H-2 restriction.
,
1980,
Contemporary topics in immunobiology.
[6]
J. Kearney,et al.
Structural and biological properties of a monoclonal auto-anti-(anti-idiotype) antibody
,
1982,
Nature.
[7]
G W Hoffmann,et al.
Qualitative dynamics of a network model of regulation of the immune system: a rationale for the IgM to IgG switch.
,
1982,
Journal of Theoretical Biology.
[8]
M. Simon,et al.
Network Regulation among T Cells: Qualitative and Quantitative Studies on Suppression in the Non‐Immune State
,
1984,
Immunological reviews.
[9]
N. K. Jerne,et al.
Idiotypic Networks and Other Preconceived Ideas
,
1984,
Immunological reviews.
[10]
A. Coutinho,et al.
Reactions among IgM antibodies derived from normal, neonatal mice
,
1984,
European journal of immunology.
[11]
J. Kearney,et al.
In vivo suppression of perinatal multispecific B cells results in a distortion of the adult B cell repertoire
,
1986,
European journal of immunology.
[12]
A. Coutinho,et al.
Long‐lived B cells: mitogen reactivity as a tool for studying their life‐spans
,
1987,
European journal of immunology.