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dr. edward jenner (1798)
demonstrated protection from smallpox could be generated by transfer of pustular material from cowpox lesion; able to demonstrate CROSS-IMMUNITY
cross-immunity
first demonstrated by edward jenner by transferring material from cowpox to garner immunity for smallpox; exposure to agent produces protection against another agent
louis pasteur (1885)
discovered therapeutic vaccination; first report of live "attenuated" vaccine for rabies
elie metchnikoff (1888)
demonstrated that cells could ingest foreign material -> PHAGOCYTES;
jules bordet (1894)
discovered COMPLEMENT
robert kaus (1897)
discovered PRECIPITIN
emil adolf von behring (1901)
won nobel prize for his work on serum therapy
susumu tonegawa (1987)
awarded nobel prize for his 1978 discovery of genetic principles underlying generation of antibodies with different specificities -> "ANTIBODY DIVERSITY"
1984
year when T CELL RECEPTOR GENES were discovered
karl landsteiner (1930)
studied human blood group antigens and published a book titled "specificity of serologic reactions"
gerald edelman and rodney porter (1972)
demonstrated structure of antibodies; used PAPAIN
niels jerne (1984)
demonstrated immunoregulation
francoise barre-sinoussi and luc montagnier (2008)
awarded nobel prize for their work on HIV
cut by PAPAIN
using this cut cause antibody to separate into THREE fragments
cut by PESIN
using this cut cause antibody to separate into TWO fragments (used by ALFRED NISONOFF)
variolation
practiced by CHINESE; inhalation of pulverized smallpox lesion crust
vaccinia
virus that causes cowpox
variola major
virus that causes smallpox
variola minor
virus that causes alastrim (mild smallpox)
braxton and hicks (1869)
recommended sodium phosphate
hustin (1914)
reported the use of sodium citrate as an anticoagulant solution for transfusions
dr. charles drew (1941)
appointed director of AMERICAN RED CROSS BLOOD BANK (first director)
loutit and mollison (1943)
introduced acid-citrate-dextrose
gibson (1957)
introduced citrate phsophate dextrose
mary mallon
cook who was a carrier of Salmonella typhi infected people garnering the nickname "typhoid mary"
yves lapierre (1985)
developed the gel test
humoral immune system
type of immunity that fights bacteria and viruses in body fluids with antibodies that circulate in blood plasma and lymph, fluids formerly called humors
cellular immune system
destroys host cells infected by viruses and also destroys some parasites and foreign tissues
natural (innate, inborn) immunity
type of immunity characterized as FIRST line of defense; NO memory cells formed; resist infection by NORMALLY present body functions; NON specific; NO prior exposure required
anatomical barrier
FIRST line of defense; keep microorganisms from entering body; consists of skin and mucous membranes and ciliary action (respiratory tract)
internal defense
categorized into cellular mechanism and humoral factors; promote phagocytosis leading to destruction of ofreign cells and organisms; process of inflamation brings cells and humoral factors to area in need of healing
skin and mucous membrane
part of EXTERNAL DEFENSE; has a pH of 5.6 due to presence of lactic acid coming from sweat
urine
part of EXTERNAL DEFENSE; flushing action and its acidity
vagina
part of EXTERNAL DEFENSE; has lactic acid which keeps pH at 5
respiratory tract
part of EXTERNAL DEFENSE; has ciliary action which produce sweeping action
lysozyme
part of HUMORAL FACTORS; cleaves CELL WALL of a class of bacteria (does NOT affect mycoplasma and ureaplasma which are bacteria without cell wall)
stomach acidity
part of HUMORAL FACTORS; has pH as low as 1 due to HCl produced by parietal cells
pepsin
part of HUMORAL FACTORS; digests bacterial surface proteins produced by CHIEF CELLS
lactoferrin
part of HUMORAL FACTORS; binds iron which is essential for microbial growth; produced by CHIEF CELLS
complement proteins
part of HUMORAL FACTORS; leads to destruction of extracellular bacteria
cellular factors
SECOND line of defense; phagocytic cells (neutrophils, macrophages, dendritic cells), cells with inflammatory mediators (basophils, mast cells, eosinophils), natural killer cells
phagocytes
part of CELLULAR FACTORS; type of cell within body capable of engulfing and absorbing bacteria and other small cells and particles; NEUTROPHILS, MACROPHAGE, MONOCYTES
antigen presenting cells
part of CELLULAR FACTORS; present antigenic fragments; dendritic cells, macrophages, B cells with MHC class II
dendritic cells
MOST EFFECTIVE antigen presenting cells (found in skin); capture antigens and deliver them to lymph nodes
langherhans
specialized antigen-presenting cells found on EPIDERMIS
interstitial cells
specialized antigen-presenting cells found in ALL major organs
interdigitating cells
specialized antigen-presenting cells found in SECONDARY LYMPHOID ORGANS and THYMUS
macrophage
part of CELLULAR FACTORS; large white blood cell that removes bacteria, foreign particles, and dead cells
microglial cells
macrophage found in BRAIN
mesangial cells
macrophage found in KIDNEYS
kupffer cells
macrophage found in LIVER
alveolar macrophage
macrophage found in LUNGS
osteoclast
macrophage found in BONES
mast cells
part of CELLULAR FACTORS; resemble basophils; found in connective tissue cells of MESENCHYMAL origin; contains acid phosphatase, alkaline phosphatase, and protease; plays a role in hypersensitivity reactions by binding IgE
eosinophils
part of CELLULAR FACTORS; increased in allergic reactions or parasitic infection; neutralize basophil and mast cell products and kill certain parasites
(1) basophil
(1) part of CELLULAR FACTORS; contains histamine, heparin, eosinophil chemotactic factor-A induce and maintain hypersensitivity reactions
(2) basophil
(2) part of CELLULAR FACTORS; IgE binds readily to basophil cell membranes and granules release constituents when they contact with antigen; granules LACK hydrolytic enzymes
histamine
found in basophils which when released will contract smooth muscle
(1) NK cells
(1) part of CELLULAR FACTORS; mediate cytolytic reactions and kill target cells without prior exposure; LACK specificity -> EARLY defenders against pathogens
(2) NK cells
(2) part of CELLULAR FACTORS; FIRST line of defense against virtually infected and tumor cells; accumulate at maternal-fetal interference -> play essential role in maintaining PREGNANCY
CD 16
CD marker of NK cells; receptor for Fc portion of IgG; NK cells attach and lyse any cells coated with antibody
CD 56
CD marker of NK cells; cytokines produced are INF-y and TNFa and amplify immune response
inhibitory signals
in NK cells, based on recognition of MHC class I (expressed on ALL healthy cells); if NK cells reacts with MHC class I cause inhibtion of natural killing occurs -> receptor for this binding is KILLER CELL Ig-like RECEPTORS
recognition of "missing self"
diseased and cancerous cells lose their ability to produce MHC cells -> NK cells triggered by lack of MHC antigens;
perforins
NK cells granules; pre-forming proteins that polymerize in presence of calcium and form channels in target cell membrane
granzymes
NK cells granules; packets of serine esterase that may enter through channels and mediate cell lysis
phagocytosis
part of HUMORAL FACTORS; physical damage to tissues either by TRAUMA or MICROBIAL MULTIPLICATION, release substances such as activated complement and products of infection to initiate phagocytosis
chemotaxis
stage in phagocytosis; cells are guided to site of injury by chemoattractant substances (C5a); NEUTROPHILS arrive first at site of injury followed by MONOCYTES
chemotaxin
chemotactic substance; chemical messenger that causes migration of cells in a particular direction
positive chemotaxis
movement toward a chemical stimulus
negative chemotaxis
movement of a cell away from a chemical stimulus
adhesion
stage of phagocytosis; receptors of INNATE immunity system recognize PATHOGEN ASSOCIATED MOLECULAR PATTERNS (PAMPS) through PATTERN RECOGNITION RECEPTORS (PRRs)
pathogen associated molecular patterns
molecules associated with groups of pathogen recognized by cells of innate system
toll-like receptors
pattern recognition receptors; each recognize a specific "danger" molecule and are embedded in cellular membranes
toll
protein originally discovered in fruit fly Drosophila; very similar molecules are found on human leukocytes
TLR1
type of toll-like receptor; recognizes LIPOPROTEINS found in MYCOBACTERIA
TLR2
type of toll-like receptor; binds to peptidoglycan in GRAM-POSITIVE BACTERIA
TLR3
type of toll-like receptor; recognizes LIPOPOLYSACCHARIDE in GRAM-NEGATIVE BACTERIA
scavenger receptor
type of toll-like receptor; binds to negatively charged molecules at the surface of microorganisms; recognize anionic receptors
ingestion (engulfment)
stage of phagocytosis; phagocytes engulf and destroy foreign matter through active membrane invagination; bacterium enclosed in phagocytic vacuole or phagosome
S. pneumoniae, H. ingluenzae, N. meningitidis
bacterias with LARGE CAPSULE which inhibits engulfment of phagocytes
diplococcus pneumoniae
inhibit phagocytosis because its capsule is HYDROPHILIC
opsonization
coating of organisms by molecules that speed up phagocytosis; coating of antigens by C3 or IgG
digestion or killing
stage of phagocytosis; granules in phagocyte which contain HYDROLYTIC ENZYMES fuse with phagosome forming PHAGOLYSOSOME
primary (azurophilic) granules
granules in phagocyte containing enzymes (lysozyme and myeloperoxidase)
secondary (specific) granules
granules in phagocyte containign LACTOFERRIN
tertiary granules
granules in phagocyte containing CASPASES
respiratory burst
oxygen-dependent mechanisms; activity of NADPH OXIDASE leads to formation of reactive oxygen species (superoxide anion, hydroxyl radical, hydrogen peroxide, singlet oxygen)
myeloperoxidase mediated system
oxygen-dependent mechanism; hydrogen peroxide kills bacteria in vacuole; production of HYPOCHLORITE which is toxic to bacteria
defensins
oxygen independent mechanism; degrade bacterial cell membrane
nitric oxide
oxygen independent mechanism; produce IFN-y activated macrophage
inflammation
part of HUMORAL FACTOR; result of tissue damage; facilitating phagocytosis; overall reaction of body to injury or invasion by infectious agent
rubor
REDNESS; reddish-blue discoloration of the extremities; indicative of severe peripheral arterial damage in vessels that remain dilated and unable to constrict
dolor
PAIN; result of chemicals released from damaged cells that stimulate nerve endings
calor
HEAT; increased blood flow to inflamed area
tumor
SWELLING; result of fluid accumulating outside blood vessels
functio laesa
LOSS of FUNCTION; result of combination of factors
diapedesis
passage of blood cells through the intact walls of the capillaries, typically accompanying inflammation; movement or squeezing of white blood cells through blood vessel walls
acute phase reactants
increase rapidly due to infection, injury, or trauma causing inflammation; produced by HEPATOCYTES
cytokine storm
overproduction of cytokine caused by SARS-CoV infection causing overproduction of mucus and difficulty in breathing