chapter 11 - specific resistance to infection Flashcards

1
Q

what is a macrophage

A
  • type of WBC, involved in specific and nonspecific defence
  • large phagocytic cells (phagocytosis)
  • alert immune system to presence of foreign material
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2
Q

what is specific defence

A
  • directed towards a particular pathogen
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3
Q

what is the immune system / response

A
  • system: composed of different types of cells that occur in most organs
  • response: cells react to produce immune response, homeostatic mechanism (antibody / cell mediated)
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4
Q

what is homeostasis

A
  • maintenance of a relatively constant internal environment

- fluctuations in the external environment

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5
Q

what is an antigen

A
  • substance capable of causing an immune response (specific)

- large molecule, could be a protein, carbohydrate, fat, nucleic acid, whole / part of bacteria

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6
Q

what are self and non self antigens

A
  • S: substances produced by a persons own body, do not trigger an immune response
  • NS: foreign substances that trigger an immune response
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7
Q

what is an antibody

A
  • specialised protein that is produced in response to a non self antigen
  • belong to a group of proteins called immunoglobulin (lg)
  • many different types (lgA, lgD, lgE, lgM, lgG)
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8
Q

what is antibody mediated response

A
  • produces and releases antibodies into blood / lymph, provides resistance / attack invading agents
    1. B cell remains in lymphoid tissue until activated / sensitised by an antigen.
    2. one type of B cell is sensitised, enlarges and divides
    3. clones of B cell are formed
    4. most B cells become plasma cells and secrete antibodies (circulate body), these combine to form antigen-antibody complex
    5. some B cells become memory cells, spread to bodies tissues, allow response to occur more rapidly if there is a second antigen exposure
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9
Q

what are the different exposures to the same antigen

A
  • 1: primary response, takes several days for large amounts of antibodies to accumulate
  • 1.5: secrete antibodies = increased antibodies in blood, peak is reached and decline occurs, memory cells remain
  • 2: secondary response, much faster, plasma cells form straight from memory cells, antibody levels in blood increase
  • 2.5: most of the time the antigen doesn’t cause illness due to such fast detection
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10
Q

what are the functions of antibodies

A
  • inactivate: foreign enzyme by inhibiting reaction with other cells / compounds
  • bind to surface: of viruses and prevent them from entering cells
  • coat bacteria: more easily consumed by macrophages
  • agglutination: cause clumping
  • dissolve organisms
  • make insoluble: by reacting with soluble substances (more easily consumed)
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11
Q

what is cell mediated response

A
  • provides resistance to intercellular phase of bacterial / viral infections (those pathogens that specialise in invading / replicating in host cells, e.g HIV)
  • provide resistance fungi and parasites, rejection of transplants, fights cancer cells
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12
Q

what is a B cell

A
  • type of lymphocyte, produced in bone marrow, incorporated in lymphoid tissue
  • capable of responding to a specific antigen
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13
Q

what is a T cell

A
  • type of lymphocyte, produced in bone marrow and mature in thymus, incorporated in lymphoid tissue
  • capable of responding to a specific antigen
  • become activated after B cells encounter antigen and they travel to nearest lymph node to present to T cells
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14
Q

process of cell mediated response

A
  • same division process as antibody mediated response
  • instead of producing plasma and memory cells, produce killer, helper and suppressor T cells (migrate to area with increased antigens)
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15
Q

what are the types of T cells

A
  • killer: attach themselves to invading cell and secrete substance that destroys antigen
  • helper: secrete substances that; cause lymphocytes to become sensitised (intensifies IR), attract macrophages (intensify phagocytic activity of macrophages)
  • suppressor: act when immune system becomes too excessive / when infection is gone, release substance that inhibits b and T cell activity (slows / stops immune system)
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16
Q

what are lymphocytes

A
  • type of WBC (20-30%), involved in specific and non specific defence, produced in bone marrow and lymphoid tissue
  • move around blood / enter tissue or lymph
  • types: B cells and T cells
17
Q

what is immunity

A
  • resistance to infection by invading micro-organisms
18
Q

what is passive immunity

A
  • acquires antibodies from mother or injection
  • natural (maternal): antibodies enter blood stream across placenta / breast milk, short term immunity, no specific immune response, no memory cells
  • artificial: antibodies enter blood stream via injection, short term immunity, no specific immunity, memory cells, no symptoms
19
Q

what is active immunity

A
  • acquires antigen via infection or injection
  • natural (infection): ability to manufacture antibodies results from pathogen entering body, person has symptoms, specific immune response, long term immunity, memory cells produced
  • artificial: antigen given via a vaccine injection, specific immune response, long term immunity, memory cells, no symptoms
20
Q

what is immunisation

A
  • programming the immune system so that the body can respond rapidly to infecting microorganisms, can occur naturally/ artificially
  • naturally immunised: against chicken pox, mumps, measles, diphtheria
21
Q

what are vaccinations

A
  • artificial introduction of antigens or pathogenic substances so that antibodies are produced
22
Q

what are the types of vaccines

A
  • living attenuated: live microorganisms of reduced virulence, antibodies, lasts longer
  • dead: dead microorganisms, short
  • toxoids: inactivated toxins produced by bacteria
  • sub unit: fragment of microorganism
23
Q

what is recombinant DNA

A
  • altering the DNA in the microorganism so that it is less virulent
  • inserting DNA from pathogen into harmless bacteria to produce antigens, vaccination of harmless bacteria = immunity
  • increases immunity, decreases number of deaths
24
Q

what are the types of vaccine delivery

A
  • injection: via syringe (most common)
  • oral: sweet syrup / lumps of sugar (polio vaccine), not in aus
  • new: fine spray into nostrils (USA), skin patches (self administered), vaccines in food (difficult to control dose)
25
Q

what is herd immunity

A
  • reducing the chance of disease in susceptible individuals, increasing immunity in population
  • depends on high proportion of population being immunised (less chance of disease being transmitted)
  • problem: incidence of disease declines, people become complacent and decide risk of getting disease is less than that of side effects, outbreak can occur
26
Q

what age is suggested for first vaccine / what are booster shots

A
  • after 2 months (baby has antibodies from mother which will remove antigen in vaccine)
  • BS: first does of vaccine doesn’t activate enough b-cells / memory cells, booster shots activate more
  • -> timing needs to be correct (antibodies can eliminate vaccine before more B cells are activated), period of 2 months in between is required
27
Q

what are the risks of vaccines

A
  • allergic reaction: not from vaccine but the medium it was cultured in (influenza -> made in fertilised eggs -> allergic to egg protein will react) (hepatitis b -> made with yeast)
  • isolation: of just one virus from tissue used to culture medium is impossible (cross species disease introduction)
  • preservatives: used to make vaccines -> can affect nervous system or other health problems
28
Q

what are some ethical concerns of vaccines

A
  • manufacture: viruses require a host, concerns about treatment of animals and humans (tissue aborted from human foetuses, influenza is cultured in chicken embryos)
  • testing: developed countries often produce them (education standees are low, not informed of risks = exploitation), animals (mice, other mammals, birds, amphibians, fish) (sacrifice animals for science)
  • decisions: parents need to weigh up risks / be well informed (for themselves and children)
  • -> HPV vaccine: HPV is an STI that causes genital warts and cervical cancer, most effective on girls yet to have sex (11-12), many believe this is too young (promote promiscuous behaviour), others believe it will prevent serious illness later in life and have no effect on sexual behaviour
29
Q

what are the factors affecting participation with vaccines

A
  • economic: in Australia most immunisations are free (government rebate), may not have access, can’t afford them (low average income), assistance of WHO
  • social: poor education regarding risks / benefits, education of women / mothers, Internet sites with misinformation, ethical / religious beliefs, day care centres is now mandatory, peer pressure, medical risks (allergies)
  • cultural: family history / background of receiving vaccinations, animal / embryo testing, traditional / alternative medicine, recommended not to by practitioners
30
Q

what are antibiotics

A
  • drugs produced from microorganisms / fungi used to fight infections of / inhibit growth of bacteria
  • antigen specific, cannot treat viral infections
  • bacteriostatic: stop bacteria from producing / disrupts protein synthesis (streptomycin)
  • bactericidal: kill bacteria by changing structure of cell wall / membrane or disrupting the action of essential enzymes (penicillin and cephalosporin)
31
Q

what is antibiotic resistance

A
  • high number of bacteria (few resistant to antibiotic) -> antibiotics kills infection causing bacteria / good bacteria that protects body from infection -> resistant bacteria now have preferred conditions to grow, thrive and take over -> bacteria can even transfer drug resistance to other bacteria
  • overcoming problem: reviving antibiotics by using them in a combination with other substances, to genetically engineer bacteria to disable antibiotic- resistant gene
32
Q

what are antivirals

A
  • act on virals, killing virus means killing the host cells

- solution: identify viral proteins / design chemicals to disable virus (so it never enters the host)

33
Q

how will routine vaccinations decrease the risk of disease of a specific pathogen

A
  • immunisation of individual via active immunity leads to antibody / memory cells
  • on second exposure no symptoms will be produced
  • leads to herd immunity as there are fewer potential sufferers and it is more difficult for disease to spread
  • reduced number of unaffected carriers
  • programmed immune system to produce antibodies against pathogen