Recognises lipid and carbs – lipoproteins, glycolipids, on gram
positive bacterial cell wall
"TLR2:TLR2" - homodimerization of TLR2, meaning that two TLR2
molecules pair up to form a functional receptor complex.
Ligands: peptidoglycan, lipoteichoic acid (LTA), and
mycobacterial lipoprotein from mycobacteria.
TLR1:TLR2
triacylated lipoproteins, M tuberculosis
TLR2:TLR6
diacylated lipoproteins and LTA.
TLR2:Dectin 1 - cooperative interaction between TLR2 and Dectin 1,
Beta-glucans, components of yeast cell walls.
These different pairings of TLR2 with either itself or with other
receptors like TLR1, TLR6, or Dectin 1 allow the immune system to
detect a wide range of microbial components.
TLR 4
Recognises LPS form gram negative bacteria
Also taxol (anti-tumour agent), HMBG1 (released by dying cells),
fibrinogen
May contribute to sepsis (hyperinflammatory response) – mice with
TLR4 knock out resistant to disease
TLR 5, 10
TLR 5 – flagellin from gram positive and gram negative bacteria
9 – viral dna, bacterial dna with unmethylated CpG motif
All induce the type 1 IFN response – viral infection
Role of TLR in infectious disease
Autosomal recessive IRAK-4 deficiency: This deficiency leads to
a condition where patients' cells do not respond to ligands for TLR1-
6 and TLR9, nor do they respond well to the cytokines IL-1 and IL-
18. This results in a poor cytokine response when stimulated with
whole bacteria. IRAK-4 (Interleukin-1 Receptor-Associated Kinase 4)
is a kinase that plays an essential role in the TLR signaling pathway.
Increased susceptibility to infections: Patients with IRAK-4
deficiency are particularly susceptible to a narrow spectrum of
infections, especially from bacteria like Streptococcus
pneumoniae and Staphylococcus aureus, which are common
in early childhood.
Similar phenotype with MyD88 deficiency: Individuals
with a deficiency in MyD88 (Myeloid differentiation primary
response 88), another crucial adaptor protein in TLR signaling,
exhibit a similar susceptibility to infections, including those
caused by Pseudomonas aeruginosa.
Thus, it is not because of alterations to TLR/IRK signalling pathway
that lead to resistance to many microorganisms as an alternative
way can restore the function
Mtb is spread by aerosol droplets which are inhaled into the
alveoli of the lungs
Alveolar macrophages phagocytose mycobacteria through
receptors
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