Immunology Flashcards
Primary lymphoid organs
Bone marrow
Thymus
Secondary lymphoid organs
Lymph nodes
Exists prior to infection
Responds rapidly
Innate immunity
Adaptive immunity
Develops after exposure
Remembers antigens
Mounts specific response
Leukocytes
Neutrophils
Monocytes
Lymphocytes
Tissue resident sentinel cells
Dendritic cells
Macrophages
Mast cells
Secrete cytokines & inflammatory mediators
Cytokines
Pro-inflammatory proteins
Released by dendritic cells, macrophages & mast cells
Bind to receptors on venule endothelial cells
Pus
Bacteria killed by neutrophils
DNA extruded by neutrophils
Apoptotic neutrophils
Adhesion molecules
On luminal endothelium
E-selectin - low affinity, binds to E-selectin ligand & slows
ICAM-1 - high affinity, binds to integrins (e.g., LFA-1) & arrests
Origins of macrophages
Tissue resident - embryonic precursors
Monocyte-differentiated - bone marrow-derived monocytes
Defensins
Small, positively charged peptides
on skin in sweat, saliva & other secretions
with broad-spectrum antimicrobial activity against bacteria, fungi & some viruses
by disrupting cell membranes
Epithelial cells
Provide physical barrier
Produce defensins, cytokines & chemokines
Sentinel cell that detects viruses & releases type 1 interferons
Plasmacytoid dendritic cell (pDC)
Type 1 interferons are cytokines produced by
pDCs
Trigger neighboring cells to synthesize protective proteins which induce antiviral state
Antiviral state triggers
proteins that bind to dsRNA
which activates
further anti-viral signaling
expression of apoptosis genes & RNase that degrades some viral RNAs
Pathogen-associated molecular patterns (PAMPs) are molecules common on
pathogens but not on vertebrate cells
Lipo polysaccharide (LPS)
A PAMP expressed on many gram-negative bacteria
Pattern recognition receptors (PRRs)
bind to PAMPs & activate immune response
Toll-like receptors recognize & bind to
PAMPs
Bacteria PAMPs
(Recognized by pattern recognition receptors)
LPS
Flagellin
Peptidoglycan
Teichoic acids
Virus PAMPs
(Recognized by pattern recognition receptors)
Single-stranded RNA
Double-stranded RNA
Double-stranded DNA
PRR signaling leads to production of
cytokines such as Type 1 IFNs, IL-1 & TNF-a
Viral PAMPs bind to
Endosomal TLRs
Bacterial PAMPs bind to
Cell membrane TLRs
TLRs induce proinflammatory cytokine transcription by activating
NF Kappa B
Endosomal TLRs activate
Type 1 interferon
Opsonin that coats bacteria
Also plays a role in activating cleavage of C5
C3b
C9 is a protein that forms
a pore (MAC) which kills bacteria by punching holes in membranes
Antibodies (e.g., IgM & IgG) bind to
microbes
Agglutinins & Natural antibodies (IgM & IgG)
Agglutinate (clump/immobilize) microbes & fix/activate complement
C3 cleavage pathways
Spontaneous/alternative - microbial surface activates
Antibodies/classical - C1q binds Ab on microbe
Lectin - agglutinins recognize carbohydrates & bind to microbe
All 3 complement pathways activate C3 to produce
C3a - inflammation
C3b - opsonization to induce phagocytosis
Lysis
C9 pore
Membrane attack complex (MAC)
Complement system defends against bacteria via
- inflammation
- lysis
- opsonization
Adaptive immunity is comprised of 2 connected systems
Humoral immunity - B cells (type of lymphocyte) produce plasma cells which produce antibodies that protect against microbes outside of cells
Cell-mediated immunity - T cells produce Helper T cells which activate other immune cells & Cytotoxic T cells which kill infected cells
4 ways antibodies work
Neutralization
Opsonization
Complement fixation (porous)
Antibody-dependent cellular cytotoxicity (viral)
Antibodies are tetramers composed of
2 heavy peptide chains
2 light peptide chains
Each chain has 3 fingers projecting from variable region forming antigen binding site
Antibody classes
IgG - most common
IgA - in gut, protease resistant, dimer
IgM - low affinity, high avidity, pentamer
IgD - in blood
IgE - allergy & helminths
Fc portion of antibody is on
Heavy chain
Bound to complement
or
Recognized by receptors in phagocytes or natural killer cells
Receptors on neutrophils, NK cells & macrophages
Antibody isotypes that require J chains
IgA (dimer)
IgM (pentamer)
Ig cause disease by
Binding to self-antigens
Or
Depositing antibody-antigen immune complexes in vessel walls
Then
Complement fixation (lyse)
Opsonization (phagocytosis)
Neutralization (blocks function)
Inflammation (self or microbial antigen on epithelial cell)
B cell receptors recognize
any antigen
T cell receptors recognize
1 antigen
Clonal selection
Process of microbial antigen finding its specific lymphocyte receptor
Lymphocyte proliferation after clonal selection
Clonal expansion
B cells mature in
Bone marrow
T cells mature in
Thymus
Granulocytes include
Neutrophils, basophils & eosinophils
Stage of development in which B cells first express immunoglobulin (IgG) heavy chains
Pre-B cell
Transmembrane proteins that bind to peptides & display them to T cells
MHC (major histocompatibility complex)
Cytotoxic T cells (CTLs) express CD8 on surface and release
granules that induce apoptosis in infected cells
V, D & J segments make up
Antibody & T cell receptor genes
Genetic shuffling process that generates receptor diversity
VDJ recombination
Immune repertoire created by
Combinatorial & junctional diversity
Portion of antibody light chain protein that contains antigen binding site
N-terminus, which contains the variable region
Naive T cells undergo activation in lymph nodes to become
Effector T cells
CD4+ cells are also known as
Helper T cells
Co-receptor expressed by helper T cells
CD4+