immune system p.II Flashcards

1
Q

humoral (antibody mediated) IR

A

when B cells encounter antigens they produce:

primary response (initial encounter)
secondary response (can be years later)
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2
Q

primary humoral response

A

maturation of B lymphocytes with first encounter of antigens causes lymphocyte to do clonal selection

this process is PHR

antigens on B cellsare IgD/IgM antibodies

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3
Q

clonal reponse

A

lymphocyte grows + multiplies to form family of clone cells

most cloned cells become plasma cells

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4
Q

new clones plasma cells

A

after lag period plasma cells produce same highly specific antibodies at enormous rate to destroy antigens (2000 antibodies/second)

lasts about 4-5 days then dies out
antibody levels in blood peak at 10 days and then decline

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5
Q

secondary immune response

A

B cell clone members that do not become plasma cells + become memory cells that can respond later

much faster, prolonged, more effective because it is in works for a long time

2-3 days antibodies peak and levels remain high for weeks

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6
Q

active immunity

A

B cells encounter antigens + produce antibodies

IR is same whether natural/artificial

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7
Q

active naturally acquired

A

during bacteria/viral infections,get symptoms of disease and suffer

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8
Q

active artificially acquired

A

when vaccines are administered, which have dead/weakenedpathogens

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9
Q

vaccines

A

spared signs/symptoms of disease in primary response

weakened antigens still stimulate antibody production + immunological memory (booster shots may be needed)

protect against pneumonia, smallpox, polio, tetanus, diphtheria, measels

serious childhood diseases have been eradicated due to immunization programs

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10
Q

passive immunity

A

when antibodies are obtained from someone else

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11
Q

passive natural

A

from mother to fetus through placenta where antibodies enter fetal circulation + during breastfeeding

baby is protected for several months after birth

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12
Q

passive artificial

A

from immune serum/gamma globulin

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13
Q

gamma globulin

A

used to increase immunity after disease
used after hepatitis, as antivenom, botulism,rabies, tetanus bc these can kill before active immunity works

provide protection immediately, for 2-3 weeks then body takes over

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14
Q

2 months

A

DPt, tetanus, OPV

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15
Q

4 months

A

DPT, OPV

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16
Q

6 months

A

DPT, OPV for some

17
Q

12-15 months

A

DPT, OPV, MMR

18
Q

18 months

A

HbCV (flu)

19
Q

4-6 years

A

DPT, OPV

20
Q

11-13 years

A

MMR

21
Q

14-16 years, every 10 yrs

A

Td booster

22
Q

antibodies

A

immunoglobulins
soluble proteins secreted by B cells (plasma cells) in response to antigens
carried in blood plasma and make up gamma globulin part of blood proteins

23
Q

antibody structure

A

formed in response to many antigens

have similar basic anatomy,grouped in Ig classes

24
Q

basic structure

A

4 looping amino acid chain linked by disulfide bonds

2 identical amino acid heavy H chains w/ 400 amino acids each, have flexible hinge region at middles

2 other identical amino acid chains light L chains, half as long

25
Q

chain loops

A

disulfide bonds between amino acids in same chain but about 60-70 apart which causes loop spaces

4 chains make antibody molecule w/ 2 identical halves w/ heavy + light chains, x/y shaped

26
Q

each antibody

A

one variable V region at end and larger constant C region at other end

variable change w/ type of antibodies but constant stays almost the same

variable regions of heavy+ light in each form antigen-binding site to fit specific antigen

has 2 antigen binding regions

27
Q

functions of antibody chains

A
  1. determine type of antibody formed (class)
  2. how antibody class carries out immuneroles
  3. cell types/chemicals the antibody can bind w/
28
Q

antibody classes

A

have slightly different roles

five major classes

29
Q

IgM

A

can fix complement

present in monomer + pentamer

30
Q

IgA

A

found mainly in mucus, saliva, sweat, intestinal juice, milk
limited amounts in plasma
prevents attachment of pathogen to epithelial cells

31
Q

IgD

A

important in activation of B cell

always attached to external surface of B cell, works as antigen receptor

32
Q

IgG

A

can cross placental barrier for passive immunity
abundant and diverse in plasma
protects against viruses,
bacteria, toxins
main antibody of secondary and late primary

33
Q

IgE

A

involved in allergies
secreted by plasma,mucosae of GI + resp. tract, + tonsils

attracts to mast cells + basophils
release histamine when triggered by antigen

34
Q

antibody function

A

antibodies act tag antigens for destruction
number of antigen-antibody complexes which can be crosslinked into big networks

  1. precipitation
  2. complement fixation
  3. agglutination
  4. neutralization
35
Q

complement fixation

A

used against cellular antigens (bacteria, mismatched RBCs)

antibodies bind to antigens of foreigncells, trigger events that lyse foreign cells + release molecules to enhance inflammatory process + promote phagocytosis

36
Q

neutralization

A

used against bacterial exotoxins released by bacteria or on viruses that cause cell injury

antibodies bind to specfic sites on invader, which loses its toxic effect, destroyed by phagocytes

37
Q

agglutination

A

antigen-antibody complex causes clumping of foreign cells
done mostly by IgM w/ 10 antigen-binding sites
used for blood typing

immobilized, easier to phagocytize

38
Q

precipitation

A

antigen-antibody complexes involve soluble antigenic molecules

complexes become so large that they become insoluble and settle

immobilized, easier to phagocytize