immunology 5 Flashcards
Toll Like Receptors (TLR) that recognize bacteria
1, 2, 4, 5, 6, 9
toll like receptors (TLR) that recognize viruses
3, 7, 8, 9
common features of adaptive immune response to pathogens
intracellular pathogens-Th1-mediated activation of cytotoxin T cells; cell mediated immunity
extracellular pathogen-Th2-mediated activation of humoral immunity
immune response to viruses
innate-type I interferons signals through JAK/STAT pathways to exert antiviral functions
humoral mediated by antibodies-block viral entry, stimulate phagocytosis, activate complement for lysis of virus infected cells and mediated ADCC to kill virus infected cells
cell-mediated-cytoxic T cells kill virus infected cells anf T helper cells activate macrophages
immune response to bacteria
innate-recognition by PRR and cytokine release, complement activation, inflammation and phagocytosis
adaptive to extracellular-humoral-neutralization (IgA and IgG), opsonization (IgM better than IgG) complement activation, phagocytosis and ADCC less important
adaptive to intracellular-cell-mediated-Th1 cells activate macrophages and enable killing and destruction by cytotoxic T cells and NK cells
evasion of immune response
Viruses
RNA virus-antigenic variation
DNA virus-besides antigenic variation, express immunoregulatory genes that block interferon signaling
bacteria
evasion of innate-interfere with TLR signaling, resistance to antibacterial peptides, block phagocytosis, if intracellular bacteria interfere with phagosome maturation and or escape phagosome
evasion of adaptive-antigenic variation and secrete proteases to destroy antibodies or cytokines
parasites
organisms that live in/on host and gets nutrients from the host or at the expense of the host
protozoa-single celled intracellular or extracellular
helminths-multicellular and extracellular
arthropods-multicellular and extracellular
immune response to protozoa
innate mechanism similar to bacteria and virus
mutual adaptation and species-specific infection is important
stimulate both cell mediated and humoral response
humoral-antibodies opsonize parasites in blood and tissue
cell mediated is important for intracellular protozoa
extracellular protozoa
similar response to bacteria
Th22 responses are important-macrophages produce IL-22
recruitment of neutrophils-oxidative damage to pathogens
intracellular protozoa
intracellular location protects organisms from immune detection
some actively penetrate cells
Th1 responses are important
recruitment of cytotoxic T cells
immune evasion-protozoa
parasite-induced immunosuppression
reduced antigenicity of encysted protozoan
antigenic variation
infection more common in immunosuppressed host
adverse consequences
immune response to protozoa may result in hypersensitivity
type 1: trichomoniasis infection that causes local irritation of genital tract
type II: parasite antigens bind to host erythrocytes
type III: immune complex formation in visceral leishmaniasis
immune response to helminths
mostly Th2 adaptive response
effectiveness of response depends on
genetic susceptibility
host age, gender and overall health
site of infection
parasite burden
helminth species
larvae and adults trigger Th2 response-attacked by eosinophils and basophils
adults worms are expelled from mucosal surface IgE binding
similar clinical signs to type I hypersensitivity-eosinophilia, edema, asthma and urticaria
thick cuticle or tegument
Th2 effector cells are important in destroying migration larvae-eosinophils and macrophages release Th2 cytokines-cuticle damage
innate immune cells and Th2 cells secrete IL-4, 5 and 13
eosinophils have FC receptors and bind to opsonized worms
IgE dependent eosinophil mediated response important for larval response
immune evasion-helminths
migrating larvae are very good at immune evasion
innate immunity-neutrophil inhibitors, surface antioxidants and inference with complement
adaptive immunity-reduced antigenicity over time, antigenic variation and interference with antigen processing
imunosuppresion
common feature of parasitized animals
parasites produce immunosuppressive molecules
redirection of T cell response-produce Il-10 which is immunosuppressive