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Immunology
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Immunology the science that encompassesthe body's defense mechanically.
Immune system a defense system developedin vertebrates.
Protection against pathogenic microbes andcancer.
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The Nature of Disease
Pathogenic Organisms Genetic Disorders Toxic Chemicals Other Environmental Factors Physical Damage to Organs
Nutritional Disorders
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Types of Pathogenic Organisms
Viruses Bacteria Protozoan Fungi
Animal Parasites
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Mechanisms of Diseaseby Pathogens
Utilization of host nutritionalresources
Physical damage to host tissues Production of toxic substances Chromosomal and gene damage Body cells behave abnormally
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Immune response has 2 interrelated activities: Recognition- between 2 foreign pathogens
-Discriminate between self and foreign
Response- Effector response
- Memory response
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Immunity State of protection from infectiousdiseases.
Immune response reaction of the bodyagainst foreign antigen.
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Types of immunity
Innate immunity (Native immunity)Resistance by virtue of genetic and constitutional make
up Specific Non-specific species Racial Individual
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Species immunity-eg: humans unsusceptible to plantpathogens and many animal pathogens
Racial immunity-eg: resistance of algerian sheep to
anthrax.People of negroid origin susceptible to TB than
caucasians
Individual immunity- eg:factors like age, hormonalinfluence, nutrition e tc
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Defensive barriers
Anatomic barriers Physiologic barrier
Endocytic and phagocytic barrier Inflamatory barrier
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Skin acts as barrier to microbes and viruses- sweat has a low pH- sebaceous glands
Mucus traps foreign particles
Tears Saliva
Anatomic barriers
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Body Coverings: The Skin
sebaceousglands
sweat gland
epidermis
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Body Coverings:Mucous Membranes
mucus
cilia
columnarepithelium
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Temperature pH Oxygen tension Gastric acidity Soluble proteins like:
- Lysozyme- hydrolytic enzyme in mucous secretions,can cleave PG layer
- Interferon- proteins produced by virus infected
cells, can bind to nearby cells and inducegeneralised antiviral state- Complements- group of serum proteins that
circulate in a inactive proenzyme state which can be
activated to destroy pathogens
Physiologic barriers
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Endocytic and Phagocytic barriers
Endocytosis- Process of internalization of macromolecules. By formation of endocyticvesicles by the PM.
Endocytosis occurs through Pinocytosis orreceptor mediated endocytosis.
Pinocytosis- internalization through non-specific
membrane invaginations Receptor mediated endocytosis- selective
internalization by binding to membrane receptors
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After internalization- endoytic vesicles fuseand are delivered to endosomes
In endosomes macromolecules are lysed bylysosymes from golgi complex in to smallerproducts like peptides, sugars, nucleotides etc
This is called the endosomal processingpathway.
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Phagocytosis- ingestion of particulate matterincluding whole pathogenic microorganism.
PM expands around the particulate materialto form a large vesicle called phagosome 10-20 times larger than the endocytic vesicle.
Only specialised cells can phagocytose eg
Monocytes, Neutrophils, Macrophages Phagosome fuse with lysozome and ingested
material is digested
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Nonspecific Phagocytosis
Neutrophils
MonocytesEosinophils
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Mechanism of Phagocytosis
Macrophage
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Lymphatic System
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Inflamatory barrier
Tissue damage caused by a wound or invasionof a pathogenic microorganism induces aInflammatory Response.
3 main events occur: Vasodilation Increased capillary permeability Influx of phagocytic cells
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Vasodilation:
Increase in the diameter of blood vessels due toconstriction of blood vessels that carry bloodaway from the affected area- results inengorgement of the capillary network
Cause Erythema- tissue redness
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Increase in capillary permeability:
Influx of fluids from engorged capillaries intotissues.
This fluid is called Exudate causes Edema tissue swelling
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Influx of phagocytic cells:Capillary permeability facilitate migration of WBCs
from capillary to tissues.
Emigration of phagocytes involve a complex seriesof events including cellular adherence -(Margination ) to endothelial wall
-emigration between capillary endothelial cells intotissues DIAPEDESIS or EXTRAVASATION
- Migration through tissue to site of response-Chemotaxis.
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Phagocytic cells accumulate and phagocytosebacteria , release lytic enzymes that candamage nearby healthy cells .
Accumulation of dead cells, digested materialand fluid form a substance called PUS
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Inflammatory Response
Histamine &prostaglandinsreleased
Capillaries dilateClotting begins
Chemotacticfactors attractphagocytic cells
Phagocytesconsumepathogens & cell
debris
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Acquired Immunity
Active Immunity
- Naturally-Acquired Active Immunity
- Artificially-Acquired Active Immunity
Passive Immunity
- Naturally-Acquired Passive Immunity- Artificially-Acquired Passive Immunity
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Active Immunity
Resistance developed as a result of antigenicstimulus
Active functioning of Immune system Synthesis of antibodies Production of immunologically active cells
Long lasting associated with immunologicalmemory.
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Artificial active immunity: resistance induced by vaccines Vaccines are preparations of live or killed microorganisms
or their products used for immunisation Eg: Bacterial vaccines:
Live- BCGkilled- TAB
Viral vaccines:Live- OPV
Killed- salk for polioBacterial products- toxoids for diphtheria and tetanus
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Live vaccines- initiate infection withoutcausing injury or disease.
Immunity similar to natural infection. Lasts for several years, boosters
recommended Administration can be oral or parenteral
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Killed vaccines less immunogenic Protection for short period Administration repeatedly, atleast 2 doses for
immunity, primary dose and booster dose.
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Passive immunity
Resistance transmitted to a recipient in aready made form.
Recepients immune system plays no activerole
No antigenic stimulus, preformed antibodiesare administered
Protection immediate Immunity for days or weeks
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Natural passive immunity:
Resistance transferred from mother to baby,through placenta in humans, and in animalsthrough colostrum.
Human colostrum is rich in IgA.
Human foetus acquires ability to syntiesizeantibodies from 20 th week of life.
Maternal antibodies give passive protection
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Artificial passive immunity:Transferred by administration of antibodies.
Agents used- hyperimmune sera of animal or humanorigin.
Eg antitetanus serum ATS
Tetanus toxoids are injected to horse, blood iscollected and serum separated , antibodies areconcentrated and purified.
Administration- subcutaneous for prophylaxis, IV fortreatment.
Passive immunisation- provides immedaite andtemporary protection in a non immune host.
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Types of AcquiredImmunity
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The production of antibodies against aspecific disease by the immune system.
Naturally acquired through disease Artificially acquired through vaccination
Vaccines include inactivated toxins, killedmicrobes, parts of microbes, and viable but
weakened microbes. Active immunity is usually permanent
Active Immunity
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A vaccinated person has a secondaryresponse based on memory cells when
encountering the specific pathogen. Routine immunization against infectious
diseases such as measles and whoopingcough, and has led to the eradication of smallpox, a viral disease.
Unfortunately, not all infectious agents areeasily managed by vaccination.
HIV vaccine in the works
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Passive Immunity - Protectionagainst disease through antibodies
produced by another human beingor animal. Effective, but temporary Ex. Maternal antibodiesColostrum.
Passive Immunity
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Passive immunity can be transferredartificially by injecting antibodies from an
animal that is already immune to a diseaseinto another animal. Rabies treatment: injection with antibodies
against rabies virus that are both passiveimmunizations (the immediate fight) and activeimmunizations (longer term defense).