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Immune Recognition
PRRs
Mammals detect microbe‑specific, conserved structures—PAMPs such as nucleic acids and microbial cell‑wall components—using LRR‑based PRRs on the surface, in endosomes, and in the cytosol, which trigger strong activating and pro‑inflammatory responses
TLRs and NOD1 drive
Proinflammatory cytokines through NF-kB
Viral sensors drive
Interferon production
Inflammasome forming NLRs give
sensitive, near binary, very proinflammatory signal
NLRs recognize
PAMPs and DAMPs
Innate Receptors
PRRs, LRR motifs
Adaptive
Ig superfamily, two chains
Antibodies
two identical heavy and two identical light chains; variable domains bind antigen, constant domains give structure. the variable loops that recognize ligand
Ig domain
antiparallel beta sheets, disulfide stabilized, very stable
BCR binds directly
TCR sees short peptides on MHC. Both use co-receptors for signaling
Hallmarks of Adaptive immunity
Specificity and Memory
Antigen Binding are mediated by
Variable Domains
Antibodies are
homodimers of heterodimers
BCR Binds
directly
Cells that drive adaptive immunity
Lymphocytes (B and T cells)
Lymphocytes recognize antigen with what?
Diversified antigen receptors
Adaptive immunity is driven by
Rare B and T cells that are very specific for small pieces of antigens (epitopes)
rare antigen specific lymphocytes that are activated
clonally expand
B cells generate
antibodies
T cells generate
Cytokines and mediate cytotoxicity
Ig superfamily
proteins are built from repeating Ig domains
Antigen receptor’s CDR mediate
antigen recognition
B Cell receptors ___ recognize pathogens
Directly
T cell receptors recognize
pieces of pathogens present on MHC Molecules
B and T cells use ___ to transduce signals
co-receptors
B cell antigen receptors are secreted as ___ that share the antigen binding properties of BCR
Soluble antibodies
Antibodies come in ___ with specialized effector functions
B and T cells can both recognize ___ but not usually the same ____