Immune system part 2 Flashcards
Immune response: timeline
First barrier: physical and chemical (innate immune response)
Second barrier: cells innate immune response, phagocytic and NK cells (non specific, does not induce memory)
Third barrier: cells acquired immune response (specific, induces immune memory, long lasting immunity)
name the cells involved in innate immunity
basophil, eosinophil and neutrophils
mast cells
natural killer cells
name the cells involved in adaptive immunity
macrophages and dendritic cells
b cells and t cells
how are nt cells activated
Interferon attacks the virus directly and also makes the MHC less efficient
Decrease of MHC I tips NK cells to destroy the infected cell. NK are non specific, they are lymphocyte after all but they do not need priming in the same way that T cells or B cell need.
how are macrophages, and neutrophils that phagocyte activated
Virus produces protein that the cells expose in the MHC I and this activates cells from the innate immune response such as macrophages, and neutrophils that phagocyte the infected cell or cause cellular destruction and they phagocyte the “left overs”. These also trigger the activation of maturation of T cells as macrophages are also APC.
How are Cytotoxic T cell and helper T cells activated?
Virus produces protein that the cells expose and Cytotoxic T cell attacks the marked cell which are displaying viral proteins with cytokines and other enzymes such as perforins that make holes in the cells, leading to apoptosis (death – self destruction)
When recognized by a CD4+ cell, this cell does not kill the infected cell but activates other pathways such as Bcell activation
Innate immune response
Non specific and quick
Physical barriers (skin, mucous membranes)
Chemical barriers (saliva, gastric enzymes, skin gland secretions, tears, flora, mucociliar system in airways, milk, urine, mucus)
Cellular “barrier” made of phagocytic antigen presenting cells (APCs): neutrophils, macrophages, dendritic cells, monocytes, natural killer cells (NK) –> inflammatory response
APCs inform B and T cells to start adaptative (specific, long lasting) immunity
Inflammatory response, including the complement
Inflammatory response
Rapid mechanism of response to tissue damage, injury or infection, which ends with healing or death of tissue
Reaction of tissues to an irritant as a hypersensitivity response
Inflammation prevents the spread of infection and speeds up healing, alerts the immune system but it might be detrimental to the animal!!
The signs…
PRISH = pain, redness, immobility, swelling, heat
Made by chemical signalling cascades that lead to the production or involve the production of inflammatory cytokines
Histamine, bradykinin, PG, IL-6, TNF-⍺, IL-1 are some examples of substances that lead to non-specific local (swelling and exudate) or systemic (fever) reactions
Some of these substances also attract cells from the immune system that will phagocyte pathogens and infected cells
A good example is the formation of pus (dead tissues, neutrophils that have phagocyted pathogens and dead pathogens)
Tumour necrosis factor (TNF)
Prostaglandins (PG)
Interleucin (IL)
Examples of innate immunity
Dendritic cells in the skin
Mucociliary system in the respiratory system
In GIT, saliva and gastric acids (HCl)
Physical barriers: skin, mucous membranes
Neutrophils and macrophages phagocyting pathogens
Cellular lysis by T cytotoxic cells and NK cells
Complement activation that leads to pathogen lysis
Adaptative immune response
Specific, long lasting, slower to kick in and with memory (except colostrum)
Cellular (T cells) and humoural (B cells producing antibodies)
Memory (B memory cells)
Adaptative immune response: Active
Cellular and humoral immune responses from immune system
Generates memory, duration of memory variable
Cell mediated Immunity – T cells
. Humoural Immunity – B cells
Cell mediated Immunity – T cells
(thymus gland)
T cells when activated will turn into:
Cytotoxic T cells (CD8+) kills the cell and any cell with the same antigen!
T helpers:
Th1: amplify number of T cells and NK/macrophages
Th2: activate B cells
Humoural Immunity – B cells
(antibody production)
B cells would trigger formation of antibodies:
Neutralising the pathogen
Marking it leading to opsonisation (by macrophages)
Activate the complement
B cells could also create “memory” B cells (plasma cells), super creators of antibodies
Adaptative response: Passive
Antibodies produced by a mother that are passed to a puppy via colostrum (antibody-rich first milk produced)
Antibodies produced by another animal and given to a sick animal (e.g., administration of tetanus antitoxin)
They do not induce immunity memory
It is essential that neonates receive colostrum within the first 24 hours of life because in some species the intestinal barrier closes at 48h not letting any Ig through! Remember this when doing a C section in dogs and assisting newborns in other species!
Artificial” active adaptative immunity
Vaccination
Moderna and Pfizer-BioTech: mRNA
Oxford-AstraZeneca spike protein B dsDNA vaccine
Different “protection”, “efficacy” and preservation conditions