@CO2, if lexitu is going to answer it in depth then I won't bother, but from a purely biochemical standpoint I presume it's related to decreased ATP production from the TCA cycle (and thus reduced CO2 production)
i'm getting annoying but i got another question.
I am having trouble finding a solid description on the process of cell mediated immunity, there seems to be some discrepancies between text books such as heinemann and other texts. heinemann says that a naive t cell will recognise an antigen on the mhc 1 marker on the antigen displaying cell. the t cell will then develop and proliferate into t cytotoxic cells and t helper cells. The t helper cells then release cytokines (interleukin-1) to activate natural killer cells. Cytotoxic cells and natural killer cells then directly kill virus infected cell. Other texts say that a t helper cell recognises the antigen, rather than a naive t cell.
Which is correct?
A naive T cell will recognise an antigen on MHC (MHC1=CD4, MHC2=CD8). This will cause proliferation and differentiation. CD4 cells will become T helper (Th) cells and CD8 cells will become cytotoxic T lymphocytes (CTLs).
Th cells will produce multiple cytokines, some of which will activate NK cells. NK cells do not absolutely require activation, they can have effects without T cell help. CTLs and NK cells will then target intracellular pathogens (NK cells are predominantly for antiviral functions, CTLs can target all many of intracellular pathogens).
The confusion may stem from the fact that a naive T cell can be either a Th cell or a CTL. By the time they reach the periphery and encounter Ag, they've already determined whether or not they will become Th or CTLs. As such, sometimes people say "naive cells encounter Ag" and sometimes they say "T Helper cells encouter Ag".
Our uni lecturer taught that naive T cells are activated by antigens, which causes them to specialise and proliferate.
fwiw, Ag signalling isn't enough for specialisation, they need cytokine stimulation as well