tumor immunology Flashcards

1
Q

prevention of development of most tumors through early destruction of abnormal cells

A

immune surveillance

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2
Q

immune system in surveillance

A
  • tumors contain lymphoid infiltrate
  • spontaneous regression of tumors
  • tumors high in neonatal and aged and immunocompromised
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3
Q

what percent are non-tumor cells?

A

20-80%

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4
Q

immune surveillance depends on the type of tumor inducing agent..

A
  • viral
  • chemically induced tumors
  • spontaneous mutations
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5
Q

viral immune surveillance

A

express new viral antigen that become target for immune response

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6
Q

chemically induced tumors immune surveillance

A

highly antigenic by expressing unique antigens

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7
Q

spontaneous mutations immune surveillance

A

deletions and rearrangements lead to tumorigenesis

- difficult to respond to because most of the tumor cells have similar antigens as normal

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8
Q

what is the central paradox of tumor immunology?

A

immunological escape

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9
Q

when does immunological escape occur?

A

balance between factors favoring tumor growth is favored over destruction

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10
Q

Sneak through, not recognize until growth is established

a. tumor kinetics
b. antigenic modulation
c. antigen masking
d. antigen shedding

A

a. tumor kinetics

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11
Q

loss of the determinants leading to removal of target antigens that the immune system’s effectors would recognize

a. tumor kinetics
b. antigenic modulation
c. antigen masking
d. antigen shedding

A

b. antigenic modulation

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12
Q

certain molecules such as sialomucin, bond to membrane masks tumor antigens and prevent recognition

a. tumor kinetics
b. antigenic modulation
c. antigen masking
d. antigen shedding

A

c. antigen masking

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13
Q

circulating soluble tumor associated antigens capable of compromising t chin of antigen binding sites particularly in the tumor microenvironment

a. tumor kinetics
b. antigenic modulation
c. antigen masking
d. antigen shedding

A

d. antigen shedding

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14
Q

inhibition of effective immune response by induction of apoptosis of reactive t cells by generation of suppressive cellular and cytokine environment. failure to generate antigen specific t cells

a. tolerance
b. genetic factors
c. inhibitory factors
d. tumor products

A

a. tolerance

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15
Q

some neoplasm fail to express mhc I antigen. HLA expression is frequently altered in tumors

a. tolerance
b. genetic factors
c. inhibitory factors
d. tumor products

A

b. genetic factors

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16
Q

immune complexes generated by binding of shaded tumor antigens with antibodies could block immune response by binding directly to t cells or binding to th cells and preventing them to recognize the tumors and delivering help to cytotoxic t cells

a. tolerance
b. genetic factors
c. inhibitory factors
d. tumor products

A

c. inhibitory factors

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17
Q

secretory products from tumors capable of inhibiting effective immune functions

a. tolerance
b. genetic factors
c. inhibitory factors
d. tumor products

A

d. tumor products

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18
Q

innate immunity against tumors cells

A
  • NK cells
  • PMNs
  • monocytes/macrophages
  • killer cells
19
Q

Innate immunity against tumors

A

cells can kill tumors spontaneously without prior sensitization

20
Q

Essentially evoked against tumor associated antigens

A

adaptive immune resposne

21
Q

adaptive immune response against tumors cells

A

th cells

cytotoxic cells

22
Q

cytotoxic t cells and tumors

A

recognize tumor antigens in association with MHC products

23
Q

Th cells and tumors

A

after activation produce interleukins which mediate immune response

24
Q

t/f amplification of these responses require an optimal supply of cytokines/interleukins

A

true

25
Q

mechanisms responsible for failure to generate antigen specific t cells

A
  • defects in t cells
  • defects in APCs and antigen presentation
  • defect in microenvironment
26
Q

defects in APCs and antigen presentation

A
  • absence of co-stim molecules

- checkpoint inhibiton

27
Q

when is immunotherapy effective?

A

as adjuvant with conventional therapies

28
Q

facilitates the destruction of hard to treat tumor foci which escapes conventional therapies

A

immunotherapy

29
Q

what should immunotherapy enhance?

A

specific and non-specific host response

30
Q

what should immunotherapy minimize?

A

tumor escape

31
Q

use inactivated tumor cells

A

therapeutic vaccination

32
Q

make tumor cells more immunogenic

A

therapeutic vaccination

33
Q

correction of MHC expression

A

therapeutic vaccination

34
Q

immunization with defined peptide in novel adjuvant to generate cytotoxic t cells

A

therapeutic vaccination

35
Q

recruitment, expansion and target DCs

A

therapeutic vaccination

36
Q

provenge

A

therapeutic vaccination

37
Q

immunization against oncogenic viruses

A

prophylactic vaccination

38
Q

hepatitis b vaccine

A

prophylactic vaccination

39
Q

monoclonal antibodies are used either alone or coupled to drugs, pro-drugs, toxins, cytokines or isotopes

A

passive immunotherapy

40
Q

antibodies inhibit neovascularization

A

avastin

41
Q

limitation to passive immunotherapy

A
  • antibody penetration
  • antibodies bound to other cells
  • antibodies immunogenic
42
Q

nivolumab

A

check point inhibitor

43
Q

when do tumors develop?

A

when surveillance system breaks down or overwhelmed

44
Q

what will be critical for management of malignant disease?

A

adjuvant immunotherapy