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114 Cards in this Set

  • Front
  • Back
1st & 2nd Line of Defense
Non-specific
3rd Line of Defense
Specific, results in long term immunity.
Ex. T-Cells, B-Cells, & Antibodies (Ab)
Antigens
Chemical substances, usually a non-self invader
Body recognizes______.
antigenic surface determinants.
Origin of Immune System
Fetus 2mnths after conception; stem cells develope in the bone marrow with variety of stem stem cells.
2 Types: Ex. Erythropoietic- RBC's
Ex. Lymphopoietic- Lymph node site
Dual System of________.
Immunity
CMI ( Cellular Mediated Immunity)
Involves T-cells(advcd. life span, more than half circulating), Lymphokines & Interleukins.
Lymphokines
Protein produced by lymphoblasts; relates to 2nd level, & increases efficiency of phagocytosis.
Interleukins
Produced by WBC's, influences activity of other WBC's.
CMI's are found in 4 Classes of T-Cells:
1. Helper T-Cells
2. Supressor T-Cells
3.Cytotoxic T-Cells (Killer T-Cells)
4. Delayed-hypersensitivity (Memory T-Cells)
Helper T-Cells
Signal to produce more T-cells.
Supressor T-Cells
Reduce production of T-cells.
Cytotoxic T-cells (Killer T-Cells)
Destroy antigens
Delayed- hypersensitivity (Memory T-Cells)
Destroy future,reappearing non-self foreign antigens, resulting in long term immunity.
_____ & ______ aid in B-Cell production & reduction.
Helper T-Cells & Supressor T-Cells
B-Cells remain in ______.
Lymphoid tissue, called plasma cells.
They go through many adaptations; end result is production of antibodies.
Humeral Immunity
Rises from our B cells
Antibody
Globulin groups of protein
Immunoglobulins "aka" ___.
Antibodies
Antibody Structure
(Essay Question)
Antibody Structure
(Essay Question)
Derived from B-cells, part of the humeral immunity & the structure is 4 chains of protein, connected by disulfide bonds. There are contrast regions & variable regions. Constant remains constant & variable changes. The antigen binding site or idiotypic binding site.
5 Groups of Immunoglobulins (Ig)
5 Groups of Immunoglobulins (Ig)
1. IgG- Monomer
2. IgM- Pentamer (Monster/ penta-5)
3. IgA- Dimer (spend your dimes at IGA)
4. IgD- Monomer
5. IgE- Monomer
IgG
Monomer; single sub unit, most abundant. Generally everywhere. Crosses walls of vessels& placenta. Principle component in 2ndary response.
IgM
Pentamer; 5 put together, too large to fit through tissue (a monster) Principle component of primary response & is important in 2ndary response. Has no where to go but in the circulatory system.
IgA
Dimer; Contained in tears, saliva & breastmilk
IgD
Monomer- Don't know what it does. Involved in immune response.
IgE
Monomer; Great role with allergic response. Ellergic
Primary & 2ndary Antibody Response
(Essay Question)
Primary & 2ndary Antibody Response
(Essay Question)
Body will develope antibody to the antigen. 1st exposure to antigen-primary response- IgM arrives first (huge in the circulatory system) followed by IgG. Once IgG experiences that primary, after a variable time interval, the 2ndary exposure to antigen- IgM will still arrive 1st, but IgM will arrive more rapidly and at a higher level of concentration.
Surface determinants
Pathogens can have several antigenic surface determinants. It's a chemaical communication. The body memorizes these determinants & has seen them before.
2 Types of Im
Innate & Aquired
Innate
what you were born with, your genetic make-up.
.
Particular people who don't have innate immunity:
Native Americans- Without innate immunity to small pox.
Polynessians- Without innate immunity to measles
Aquired
after you were born, usually not inherited.
2 groups of Aquired Im
Long term Im & Short term Im
Longterm Im
Naturally active aquired Im. Direct exposure to the disease
Ex. Measles & Mumps
Artificial Aquired Active Im through ____.
vaccination
1st generation vaccines;
3 Groups of Whole cell
Whole cell, Whole Virus, & Whole Toxin
Whole Cell
Killed, inactivated, safer, but could be less effective. Many side effects
Ex. Typhoid Fever
Whole Virus
Ex. Rabies ( Pasteur 1985)
Whole Toxin
Tetanus
Attenuated Vaccinations
Not killed, it's alive, but weakened. Antibody created quickly with more quantity.
Ex. Polio Vaccine (1954)
Sabin- Oral Polio Vaccine ( created 1-2yrs later)
Short term Im
(Part of Essay question)
Naturally aquired Passive Im. Can occur from mother to child via placenta transfer and after birth via breastmilk.
Artificial Aquired Passive Im
Part of Essay Question)
Injected into the body due to exposure to the disease
Gamma globulin
Several types available. Hep. A & Hep. B Must have vaccination for both.
Hepatitus A
(use in essay Q)
Foodborne
Hepatitus B
(Use in Essay Q)
Bloodborne
ISG ( Immune Serum Globulin)
(Essay Q)
Created from horse serum, caused lots of adverse reactions, now usr ISG ( Immune Serum Globulin). Used to treat Hep. A. Is collected from the pool of blood of 1,000 blood donors.
SIG (Specific Immune Globulin)
(Essay Q)
Pooled from serum from convalescing pt's who had the disease. Used to treat Hep. B. Contain higher specific antibodies.
Vaccine
Suspension of Mo's that will induce Im when introduced into the pt. Provides specific Im, defense, & resistance. They are a preventative maintenance, not a cure.
Sub unit Vaccinations
Genetically engineered antigenic protein from the Mo's cell not the whole cell.
Acellular
Using the whole cell, Using antigenic fragments of the cell.
Anti-idiotypic
Harmless. Antigen from Mo that mimics an antibody.
Serology
Branch of Immunology & deals with in vitro testing.
In Vitro
Remove blood into a test tube for diagnostic testing. Antibody/antigenic properties. If there's surface determinants, then you've been exposed. Test can reveal what has invaded you and how to treat it.
5 Different groups of Serilogical Testing Methods
1. Agglutination Tests
2. Percipitation Tests
3. Complement Fixation
4. Immunoflourescence
5. Immunoassays
Agglutintation Tests
Will show visible clumping.
1. Measure antibody level
2. Looking for highest dilution that gives antibody reaction
Looking for high titer levels. Titer tests can tell if you have had the disease or vaccine.
Percipitation Tests
Will show bands
Complement Fixation
Looking for Lysin
Immunoflourescence
Uses dye, Flourochrome
Immunoassays
2 groups: RIA & ELISA
Radioimmunoassay (RIA)
Radioactive labeling
Enzyme Linked Immuno Sorbent (ELISA)
Uses enzymes and dyes to detect antibody complexes.
Immunopathology
Study of disease associated with accesses or difficiencies with the immune response.
2 Groups of Antigens
Exogenous & Endogenous
Exogenous
Outside the body. Ex. Pollen
Endogenous
Inside the body from self tissue called autoimmunities.
Gell & Coombs hypersensitivity
Classification of allergic responses
Allergys
Exaggerated immune response to an allergen(substance that promotes or provokes an allergic response)
Type 1
After 2nd contact, specific B(lymphocyte)-Cells react within 30min or less with the allergen. Invades IgE & histamine. Is immediate. 2 varriations based on local & astymic.
Atrophy
Local & chronic
Ex. Pollen allergy (Hay fever)
Anaphylaxis
Systemic & acute, explosive.
Ex. Anaphylactic shock(airway obstruction)
Epinephrine
Antihistamine
Type 2
Antibody mediated. After 2nd contact with specific B-Cells. Is within hrs or days. Involves IgG, IgM, & Compliment.
Ex. Type & cross-match.
Hymolitic disease of a newborn.Rh factors of mom(-) and baby(+) don't match. Mom's body sees the baby Rh(+) as an invader and wants to destroy it.
RhoGam
Gamuglobulate given with 1st pregnancy to moms with an (-) Rh factor at 24wks, to prevent any issues.
Type 3
After 2nd contact with specific B-cells, reacts within hrs or days and involves IgG,IgA, IgM & complement. Immune complex is trapped & causes chronic inflammation.
2 Types of syndromes: Systemic- Serum Sickness
Local- Arthus reaction
Autoimmunities
Non-self molecule auto antigenis the unrecognized self tissue & would form T-cells that are synthesized to antibodies. Antibodies are produced to unrecognized auto antigens.
Ex. SLE- Systemic Lupus Erythematosus
RA- Rheumatoid Arthritis
Type 4
T-Cell mediated; Cytotoxin T-cells react with in 1 to many days or months. Response to self tissue or transplanted tissue.
Self tissue response
delayed allergic response
Tuberculin test, Transplanted tissue
Host would reject the transplant
Graft
time frame within 2 weeks(14 days), body will reject the graft.
Graft vs. Host disease
Graft begins to reject,
bone marrow transplant- rejection can occur from 3mnths to 10mnths
Tissue typing
Major histocompatibility complex (MHC) or known as Human Leukocyte Antigen Complex (HLA)- Identify pt. tissue and type the tissue
Transplantation tissue grfts has______ &______.
Privileged tissue & Privileged Sites
Privileged tissue
Tissue safe from rejection
ex. pig valves
Privileged sites
Sites where antibodies do not circulate.
Ex. Cornea & Brain
4 Basic Types of Grafts
1. Autograph
2. Isograft
3. Allograft
4. Xenograft
Autograph
Burn victims (face, ears) remove skin off same person from a large surface area. Some MHC
Isograft
Balanced, from identified twin(don't tissue type). If older, affected by disease or health MHC can change.
Allograft
Most common type. Individuals of same species. Does require tissue type testing. Human to human. Will need immunosupressives.
Ex. Ayclosparin A, Steroid, Prednisone
Xenograft
Graft between 2 different species, Organs from animal. Can be temporary. Artificial as well.
2 Groups of Immunodificiency Diseases
1. Primary
2. Secondary
Primary
Disease that is genetic. Born with it. B-cell defect (Ab) lacks the body to produce antibodies.
Ex. Agammaglobulinemia (deficit of B-cells)
Di George Syndrome- (Deficit in T-cells) With out a Thymus.
B & T-Cell deficit- No immune system at all. Fatal without transplant or live in a speacial facility.
Secondary
Aquired after birth. Damage to the immune system.
Ex. Aids ( Aquired immunodificiency Syndrome)- T-Helper cells are the main target. Cause opportunistic infections, & cancer.
Tumor
New growth of abnormal cells, caused by mytosis gone wild.
Types of Tumors
Benign, Malignant, Metstasize
Local
Considered Benign
Malignant
Cancerous
Mestastasize
Goes Systemic
Neoplasm
Another name for cancer
Oncology
Medical specialty regarding the study of cancer
Theory for Cancer
Basic Mechanism Theory of Transformation of cancer.
Oncogene
Cancer gene
Anti Oncogene
The tumor suppressing gene & regulates tumor suppression & the protein oncogene.
Proto- oncogene
Regulates start of mytosis
Genetic disruption occurs
Oncogene takes control, over-riding the stop of mytosis, resulting in immortalization.
Immortalization
Non-stop cell division of new growth of a tumor(abnormak cells) , and then goes systemic.
Genetic disruptions (systemic)
How viruses play in this: Some viruses cause cancer. There are DNA & RNA viruses NOT BOTH!!
RNA ( Retroviruses)
Some contain an enzyme called revostranscriptase, & uses it to synthesize it's nucleic acid in the host.
Ex. T-cell leukemia
DNA Virus
HPV ( Human Papillomavirus)- May cause cervical cancer
Immune Surveillance
Patrolling cells for particular abnormal cells. After locating them they will begin to destroy abnormal cells, unless we have antigen modulation. ( can shed determinants)
3 Types of Abnormal cells
Cytotoxic T-Cells
NK's ( Natural Killers)
LAK ( Lymphokine Activated Killers)
Essay 1. Compare & Contrast Primary & Secondary Antibody Response. Draw and explain drawing.
Body will develope antibody to the antigen. 1st exposure to antigen-primary response- IgM arrives first (huge in the circulatory system) followed by IgG. Once IgG experiences that primary, after a variable time interval, the 2ndary exposure to antigen- Ig
Body will develope antibody to the antigen. 1st exposure to antigen-primary response- IgM arrives first (huge in the circulatory system) followed by IgG. Once IgG experiences that primary, after a variable time interval, the 2ndary exposure to antigen- IgM will still arrive 1st, but IgM will arrive more rapidly and at a higher level of concentration
Essay2.
Draw, Label & Explain antibody structure and include discussion on all immunoglobulin classes. (monomer, variable, Constant)
Derived from B-cells, part of the humeral immunity & the structure is 4 chains of protein, connected by disulfide bonds. There are contrast regions & variable regions. Constant remains constant & variable changes. The antigen binding site or idiotypic bin
Derived from B-cells, part of the humeral immunity & the structure is 4 chains of protein, connected by disulfide bonds. There are contrast regions & variable regions. Constant remains constant & variable changes. The antigen binding site or idiotypic binding site.
5 Groups of Immunoglobulins (Ig)

1. IgG- Monomer;single sub unit, most abundant. Generally everywhere. Crosses walls of vessels& placenta. Principle component in 2ndary response.

2. IgM- Pentamer (Monster/ penta-5) 5 put together, too large to fit through tissue (a monster) Principle component of primary response & is important in 2ndary response. Has no where to go but in the circulatory system.

3. IgA- Dimer (spend your dimes at IGA) Contained in tears, saliva & breastmilk

4. IgD- Monomer; Don't know what it does. Involved in immune response.

5. IgE- Monomer;
Great role with allergic response. Ellergic
Essay 3.
List format, the basic mechanism of transfer theory of cancer.
Oncogene - Cancer gene

Anti-oncogene - The tumor suppressing gene & regulates tumor suppression & the protein oncogene.

Proto- oncogene- Regulates start of mytosis

Genetic disruption occurs; Oncogene takes control, over-riding the stop of mytosis, resulting in immortalization.

Immortalization - Non-stop cell division of new growth of a tumor(abnormak cells) , and then goes systemic.

There are DNA & RNA viruses NOT BOTH!!

RNA ( Retroviruses) - Some contain an enzyme called revostranscriptase, & uses it to synthesize it's nucleic acid in the host.
Ex. T-cell leukemia

DNA Virus - HPV ( Human Papillomavirus)- May cause cervical cancer


Genetic disruptions (systemic)
Essay 4.
Passive Immunity in regard to artificially aquired passive immunity as discussed in lecture. ( Hep. A,B,C, SIG, treatment)
Longterm Im- Naturally active aquired Im. Direct exposure to the disease
Ex. Measles & Mumps

Artificial Aquired Active Im through vaccination
1st generation vaccines; 3 Groups of Whole cell

Whole Cell -Killed, inactivated, safer, but could be less effective. Many side effects Ex. Typhoid Fever

Whole Virus- Ex. Rabies ( Pasteur 1985)

Whole Toxin- Tetanus

Naturally aquired Passive Im. Can occur from mother to child via placenta transfer and after birth via breastmilk

Artificial Aquired Passive Im- Injected into the body due to exposure to the disease

ISG ( Immune Serum Globulin) Created from horse serum, caused lots of adverse reactions, now usr ISG ( Immune
Serum Globulin). Used to treat Hep. A. Is collected from the pool of blood of 1,000 blood donors.

SIG (Specific Immune Globulin) Pooled from serum from convalescing pt's who had the disease. Used to treat Hep. B. Contain higher specific antibodies.