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The study of our protection from and response to foreign invading organisms and altered host cells.
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The study of organisms that are immune to all influence.
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The study of hereditary differences in illnesses.
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The study of our brain and the neurological impact of diseases on the human mind.
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Research suggests that microbes in this area of the body activate the immune system to help the immune system proliferate.
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Gut.
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Liver.
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Kidney
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Esophagus.
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Even when a person is not sick, they still have viruses and bacteria inside them.
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An increase in the strength of the immune system is always a good thing.
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In the ideal balance of immune system and pathogens,
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The immune system and the pathogens are equally weighted.
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The pathogens in the body outweigh the strength of the immune system.
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The strength of the immune system outweighs the pathogens in the body.
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The immune system is a three-tiered system. The first is [blank_start]intrinsic/physiological barriers[blank_end]. The second is the [blank_start]innate immunity response[blank_end]. Lastly, the body relies on [blank_start]acquired immunity[blank_end].
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intrinsic/physiological barriers
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innate immunity response
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acquired immunity
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innate immunity response
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intrinsic/physiological barriers
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acquired immunity
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acquired immunity
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intrinsic/physiological barriers
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innate immunity response
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Consider the following differences between immunity responses.
Speed (how long does it take to respond?)
Innate: [blank_start]Immediate/hours.[blank_end]
Adaptive: [blank_start]A few days.[blank_end]
Immunological Memory (does it remember viruses it has already faced?)
Innate: [blank_start]Does not possess.[blank_end]
Adaptive: [blank_start]Can remember viruses.[blank_end]
Specificity (What viruses will it deal with?)
Innate: [blank_start]One cell recognizes many pathogens.[blank_end]
Adaptive: [blank_start]One cell recognizes one pathogen.[blank_end]
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Immediate/hours.
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A few days.
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A few days.
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Immediate/hours.
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Does not possess.
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Can remember viruses.
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Can remember viruses.
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Does not possess.
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One cell recognizes many pathogens.
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One cell recognizes one pathogen.
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One cell recognizes one pathogen.
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One cell recognizes many pathogens.
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Match the description to the proper disease or condition.
[blank_start]Impetigo[blank_end] - A disease caused by too much proliferation of bacteria already inside us.
[blank_start]E Coli 0157[blank_end] - A virulent strain of a virus commonly found in the human body.
[blank_start]HIV[blank_end] - Causes a reduction in the immune system.
[blank_start]Autoimmune disease[blank_end] - When the immune system loses sensitivity between host cells and foreign cells, and so attacks the body.
[blank_start]Sepsis[blank_end] - When the immune system triggers violently against a disease, causing inflammation throughout the body.
[blank_start]Cytokine storm[blank_end] - A immune system reaction to disease that, in the lungs, can lead to a potentially lethal excess of liquids.
[blank_start]Rotavirus[blank_end] - a virus most common in youths that uses the low pH of the stomach to its advantage.
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Impetigo
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E Coli 0157
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HIV
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Autoimmune disease
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Sepsis
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Cytokine storm
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Rotavirus
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Streptococcus, a disease in the throat, can be confirmed with the using the following antibody function:
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Neutralization.
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Agglutination.
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Precipitation.
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Complement Activation.
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Vaccinations help the immune system by enhancing this portion of immunity:
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There are multiple functions of antibodies that allow them to deal with foreign cells.
[blank_start]Neutralization[blank_end] is the process wherein Ab 'neutralizes' toxins by binding to them so they cannot activate.
[blank_start]Agglutination[blank_end] creates a complex of cells.
[blank_start]Precipitation[blank_end] involves creating complexes of free molecules.
[blank_start]Complement activation[blank_end] occurs when antibodies bind to antigens and create a hole in them.
[blank_start]Opsonization[blank_end] involves antibodies binding to the pathogen, inciting macrophages to surround and destroy them.
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Opsonization
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Complement activation
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Precipitation
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Agglutination
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Neutralization
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Antigens are produced by plasma in response to a pathogen and can respond specifically to that pathogen.
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An antibody is comprised of the following parts:
(check all that apply)
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In neutralization, A-B toxins have an active, virulent part and a binding part. To prevent these toxins from doing damage, the antibodies:
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Bind to the binding part, preventing it from binding to host cells.
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Attaching to the virulent part and monitoring its actions so it can signal microphages if the virus attaches to a host.
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Surrounding the virulent part and breaking it off from the binding receptor.
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Attacking the binding port, destroying it so the toxin cannot attach to host cells.
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Approximately how many cells do we have specific to each antigen when not infected?
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In response to our body not having enough cells to fend off all diseases at all times, we use a process called Clonal Selection. In Clonal Selection,
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Antigen-specific cells multiply only when they come in contact with their antigen.
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Upon the entrance of a foreign entity to the body, all antibodies begin cloning themselves.
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Antibodies attach to antigens and prevent them from cloning themselves.
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The entire human body clones itself, abandoning its previous, diseased form for a newer, healthier body.
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When dealing with streptococcus in the throat, the immune system will create many antibodies. These antibodies can cause a problem after the infection in an autoimmune disease called Rheumatic fever, which targets:
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The heart.
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The liver.
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The kidney.
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The brain.
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Comparatively to the first exposure of a pathogen, the secondary immune response is:
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In the lymph node, naïve B cells produce two different types of cells when they encounter an antigen. The [blank_start]plasma cells[blank_end] produced excrete antibodies to deal with the infection. The [blank_start]memory cells[blank_end] produced last for a long time, and prepare the body should it be re-infected with the same pathogen.
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plasma cells
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memory cells
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naïve B cells
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antibody cells
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memory cells
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rememberos
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plasma cells
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super-immunity cells
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The body has two cellular events in response to antigens. In the primary reponse, the cells produced are [blank_start]IgM[blank_end] cells. In the secondary response, the cells produced are [blank_start]IgG[blank_end] cells.
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IgM
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strong
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antigen
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IgG
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long
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EgG
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Order the steps in the antibody production process.
[blank_start]5.[blank_end] In response to the antigen protein, the naïve B cell begins reproducing, creating IgM plasma cells and memory cells.
[blank_start]8.[blank_end] IgG memory cells remain in the body, preparing the body for a second infection.
[blank_start]2.[blank_end] Proteins on the surface of the pathogen enter the lymphatic system.
[blank_start]3.[blank_end] Proteins from the surface of the antigen enter the lymph nodes.
[blank_start]6.[blank_end] Plasma cells excrete antibodies to deal with the antigen.
[blank_start]4.[blank_end] The proteins encounter a naïve B cell that reacts to them.
[blank_start]7.[blank_end] As antibodies deal with the infection, some cells mutate into IgG cells.
[blank_start]1.[blank_end] The body is infected with a disease, and pathogens enter the system.
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A large concentration of B cells are housed:
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In passive immunization, the body's antibody concentration:
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Is highest right after injection.
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Is highest one year after injection.
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remains stable over time.
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increases over time.
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Taking the bus, what type of immunity are you most likely to get?
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Passive, Natural.
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Passive, Artificial.
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Active, Natural.
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Active, Artificial.
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Serum is a term for:
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Blood cells.
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Plasma.
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Infection.
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Immunization.
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Injecting the body with thousands of antibodies.
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Triggering passive immunity.
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Triggering active immunity by use of antigens, stimulating the body to defend itself.
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Wrapping around the body's cells, protecting them from infection.
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In passive immunization, B Cells produce memory cells to protect the body from future infection.
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Variolation is an inoculation for small pox that originated from China in approximately ~2000 BC. This was done by:
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Collecting small-pox patients in the same room.
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Sniffing smallpox crust.
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Using parts of the pathogen in foods to boost immunity.
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Massaging smallpox cream on the skin.
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In 1796, Edward Jenner was looking at smallpox as a disease. To do so, he observed this group of people, who were frequently immune to smallpox.
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Milkmaids.
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Orphans.
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Aristocrats.
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Florists.
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The vaccine for Rota Virus was taken out of the market after a brief period of time because the vaccine was assumed to occasionally cause:
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Intussusception, wherein the intestine folds into itself.
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Polio, which can cause paralysis.
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Pertussis, or whooping cough.
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Mumps, a condition that causes bumps on the skin.
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Match the viruses to the years their vaccines were created.
1796: [blank_start]Smallpox[blank_end]
1855: [blank_start]Rabies[blank_end]
1920: [blank_start]Diptheria, Tetanus[blank_end]
1930: [blank_start]Pertussis[blank_end]
1950: [blank_start]Polio[blank_end]
1960: [blank_start]Mumps, measles, rubella virus[blank_end]
1990: [blank_start]Hepatitis B[blank_end]
2000: [blank_start]Rota virus, HPV[blank_end]
Frage 32
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Vaccination in a portion of the population providing protection to unprotected individuals.
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A specific type of immunity seen in herd animals, specifically buffalo.
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Fewer people being immunized than unimmunized.
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A type of immune response generated by herds of sick people gathering together.
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People refusing to vaccinate their children is a major problem in the development of herd immunity.
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In terms of attenuated organisms, 'live' means:
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Attenuation of a virus is a process in which:
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Viruses are forced to adapt into less virulent forms, making them less dangerous for humans.
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The virus is neutralized.
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The virus is strengthened through concentration in one species.
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The virus is pitted against other viruses, where they combat in a battle-royale-esque scenario until only the strongest virus is left alive.
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A common host when attenuating viruses for humans is:
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Chicken eggs.
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Bats.
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Babies.
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Rats.
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Varicella zoster is another name for this infection:
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Shingles.
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HIV.
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Polio.
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Pertussis.
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A danger with live attenuated vaccines is called back mutation. These are:
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The virus reverting back to a more virulent form.
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The virus occasionally eating through the back of your cells, destroying them.
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The attenuated virus acting as back-up and exacerbating a different disease.
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The virus backing out of the regular part of the system that it usually affects and focusing on a new, less prepared area in the body.
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Kill vaccines work by:
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Eliminating viral ability to replicate and infectivity without compromising antigenicity.
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Dissolving the entire virus, taking apart the shell and chemically destroying the nucleus.
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Chemically activating with the shell, opening it up for the immune system to deal with the inside.
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Killing the body's cells so the virus has nothing to do.
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In more recent years, small fragment vaccines have been created through cloning using yeast/bacterial cells to make proteins. In the past, proteins were gathered by:
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Extracting the blood plasma of of patients.
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Removing and de-shelling viruses from patients.
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Eating specific, protein-rich foods.
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Eating bats.
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Which are types of artificial vaccination strategies? (Check all that apply)
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Match the type of vaccination to its process:
[blank_start]Live attenuated vaccines[blank_end] - 'weakened down' forms of disease that are less dangerous for humans, and replicate.
[blank_start]Kill vaccines[blank_end] - Vaccines that inactivate the viruses by destroying the insides of them, leaving the shell.
[blank_start]Small Fragments[blank_end] - Purified subunit vaccines created from fractionation of the original disease.
[blank_start]Bacterial Exotoxins[blank_end] - Destroys the active side of A-B toxins, creating toxoids - inactive toxins with binding ports.
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Live attenuated vaccines
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Kill vaccines
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Small Fragments
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Bacterial Exotoxins
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Placental transfer can give us IgG cells, and breastfeeding can give us IgA cells. These types of immunization are examples of:
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Passive, natural immunization.
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Passive, artificial immunization.
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Active, natural immunization.
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Active, artificial immunization.
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For greatest levels of immunity 5 years into the future, you would want active instead of passive acquired immunity.
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Botulism is dangerous for the body in moderate quantities, and is extremely dangerous for infants. This said, it still has uses. In small doses, botulism is used in botox. This is because:
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Botulism releases muscles, alleviating wrinkles.
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Botulism constricts muscles, firming skin.
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Botulism has numbing qualities that prevent pain in the process.
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Botulism reinvigorates cells.
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If on a camping trip someone was to be bitten by a bat with rabies, these are the steps that should be taken to care for the injury: (check all that apply)
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Licking the wound clean.
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Washing the wound with soap and water.
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Rubbing alcohol over the wound.
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Getting treated with antibodies against rabies as soon as possible.
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Rubbing grass in the wound.
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Apply a tourniquet and amputate as soon as possible.
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When a baby is at risk getting Hepatitis B from their mother, the CDC recommends applying H-BIG (passively delivered antibody) and three doses of the Hep B vaccine at 0 months, 1-2 months and 6 months. When given this treatment, this many kids are Hepatitis B-free for life:
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19/20 kids.
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99/100 kids.
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1/2 kids.
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1/20 kids.