UNIT 3 Flashcards

1
Q

belong to the host
○ Can be a tolerogen since it belongs to the
host

A

autoantigens

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2
Q

from other members of the host’s
species

A

alloantigens

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3
Q

from other species

A

heteroantigens

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4
Q

hetero ags that exist in
unrelated plants or animals but are either identical or closely-related in structure so that ab to one can
cross react w/ ag of the other.

A

heterophile antigens

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5
Q

antigens that can be tolerated by the
immune system; it could be an autoantigen
(self-antigen)

A

tolerogen

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6
Q

Substance administered with an immunogen that
increases and hastens the immune response

A

adjuvants

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7
Q

Ag capable of stimulating the IR

A

immunogens

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8
Q

Are antigens that can be recognized and should be
reacted by immune system, eliciting a response

A

immunogens

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9
Q

Generation of immune
response against an immunogen

A

immunogenecity

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10
Q

All immunogens are antigen; but not all antigens are
immunogen

A

TRUE

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11
Q

best immunogens

A

proteins

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12
Q

Present in the pathogen

A

PAMP

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13
Q

This is the pattern recognized by
PRR and deemed foreign, eliciting
response

A

PAMP

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14
Q

This recognizes damaged patterns
and considers it foreign therefore
removed from the immune system

A

DAMP

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15
Q

the ability of the APR to
degrade the antigen to smaller pieces;
smaller pieces are easier to lyse

A

degradability

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16
Q

antigen still remains present in the APR until
communicated with T Cell (must remain
stable to be detected by T cell pag pinasa ni
APR)

A

stability

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17
Q

MHC Class I

A

TC

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18
Q

MHC Class II

A

TH

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19
Q

CD8+ / All nucleated cell / red
cell

A

MHC Class 1

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20
Q

APC (dendritic, Macrophage /
Monocyte, B cell)

A

MHC Class 2

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21
Q

Any cell which utilizes MHC______ communicates with T cytotoxic or T suppressor cells

A

Class I

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22
Q

but in certain times,
specially _______ there is a chance
for them to use class 1 molecules.

A

dendritic cells

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23
Q

is the most potent
APC because it effectively uses
both Class II (CD4+ T helper) and
Class I (CD8+ T8 cytotoxic) MHC

A

DC

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24
Q

small substances that are
non-immunogenic in itself.
Complexed to larger molecule (carriers) to be
immunogenic

A

HAPTENS

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25
Q

It requires a carrier protein for them to be an
immunogen and be recognized by the immune system

A

TRUE

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26
Q

most potent APR during
inflammation and can increase up to 100-1000x

A

CRP

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27
Q

Cutting; breaks down/maps out the effects
of neutrophil (eats and becomes destroyed
(frustrated phagocytosis) → leaves kalat →
_______cleans it

A

a1 antitrypsin

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28
Q

Should create lysis
○ Attach to the cell surface of the antigen
acting as an opsonin (C4, C1 etc)

A

complement proteins

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29
Q

Should create lysis
○ Attach to the cell surface of the antigen
acting as an opsonin (C4, C1 etc)

A

complement proteins

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30
Q

Needed for digestion of cholesterol, Accumulates in the cytoplasm of
the macrophage → lead to
nonfunctional macrophage, hence it should be removed from the cytoplasm by

A

serum amyloid A

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31
Q

Binds to free hemoglobin (in the form of ferrous)

A

haptoglobin

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32
Q

Binds to copper
Translates iron so that the ferric state would
bind to the transferrin and then go to the
bone marrow (Ferrous to Ferric)

A

ceruloplasmin

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33
Q

Antigens that induce tolerance

A

tolerogens

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34
Q

________are tolerogens; not attacked by your
immune system because they are known to your
immune system
Type A given to Type B
○ To the donor (Type A) - A antigen is a
tolerogen
○ To the recipient (Type B) - A antigen now
becomes an immunogen

A

BLOOD TYPES

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35
Q

small portion of the antigen is recognized by its
corresponding receptor

A

epitopes

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36
Q

Recognized both linear and conformational
epitopes present on the surface of an
immunogen

A

B CELLS

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37
Q

is most effective
in extracellular infection; anything
in the blood/tissues, the B cell
attaches and recognizes it

A

HUMORAL

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38
Q

Recognized epitope only as a part of the
complex formed with MHC on the surface of
antigen-presenting cells.
■ Only a specific confirmation of the
epitope can be recognized
■ Can only recognize simpler
epitopes = Linear

A

T CELLS

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39
Q

Binds to antigens

A

B CELLS

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40
Q

Protein,
polysaccharides,
lipids

A

b cells

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41
Q

Binds antigenic
peptides bound to
MHC

A

t cells

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42
Q

Internal linear
peptides produced
by antigen
processing

A

t cells

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43
Q

Accessible,
sequential or
nonsequential

A

b cells

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44
Q

Main goal: make the antigen stable (protector); like a
capsule

A

ADJUVANTS

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45
Q

For it to now melt easily, main use is on
vaccine since external forces can affect the
vaccine
○ Each vaccine has its own

A

adjuvant

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46
Q

Capable of releasing porphyrin and granzymes

A

effector t cytotoxic

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47
Q

pro-inflammatory; goal is to kill intracellular
pathogen

A

th1

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48
Q

Releases Cytokines needed to enhance action against intracellular pathogens

A

th1

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49
Q

anti-inflammatory; to calm (secretes _____

A

th2

IL4
IL5
TGF-BETA
IL 10

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50
Q

class switching of
immunoglobulins

A

IL4 AND IL5

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51
Q

IgM ⟶ IgE

A

IL4

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52
Q

IgM IgG ⟶ IgA

A

IL5

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53
Q

anti-inflammatory
cytokine
● Its effect is to calm
overstimulated T-cells.

A

TGF BETA

TH2

54
Q

Tells/signals your body to produce
antibody
■ Without this interleukin, your B cell will not function properly

55
Q

pro-inflammatory; increased phagocytic
function of the cell (macrophage)
○ Hastens the activity of phagocytes
Needed against extracellular infection such
as fungal infection.

56
Q

anti-inflammatory
○ Releases IL10 and TGF-Beta

A

t-regulator

57
Q

In order for the T cells to recognize an antigen, it
should be processed and broken down into

58
Q

bound to the MHC molecules of APCs

59
Q

To consider a protein it should contain ______ peptide chains

60
Q

produced by many cells
including antigen presenting cells to cut the
protein into smaller pieces

A

proteasomes

61
Q

Only receives the antigen

62
Q

one that recognizes
the MHC molecule at a specific domain

63
Q

When CD4 + MHC, it
causes the TCR to receive the antigen:

A

primary/first signal

64
Q

Co-stimulatory receptors or molecules.

A

secondary signals/co-stimulatory

65
Q

Rule of thumb: both primary and secondary must be
present for an immune response to be present

66
Q

Given that it has antigen, it will activate T
cell and become an effector to do its function; naive T
cell just sleeps

A

activation

67
Q

Immunogenicity

A

co-stimulation

68
Q

Infections

A

no co-stimulation

69
Q

Graft Acceptance

A

no co-stimulation

70
Q

Graft rejection

A

co-stimulation

71
Q

Self tolerance
Malignancy
No response

A

no co-stimulation

72
Q

allergy

A

co-stimulation

73
Q

Discovered as a genetic locus that determines
acceptance or rejection of tissue grafts exchanged
between persons

74
Q

are polymorphic and its alleles are
co-dominantly expressed

75
Q

Derives from the research on transplantation that
started in the mid-20th century.

These are studies which provided insights on the rules
governing the acceptance or rejection of tissues

A

histocompatibility

76
Q

It is also necessary for control of cellular interaction of
immune cells
Production of certain serum proteins

77
Q

Are cell surface markers that allow immune cells to
distinguish “self” from “non-self.

A

Human leukocyte antigens

78
Q

Markers which can be found within (cytoplasm) and on (trying to present an
antigen to the T cell or it has already
presented the antigen

79
Q

HLA antigens are prominent in ______
along with IgD and MHC

80
Q

These antigens were first described on white blood
cells (leukocytes) and are coded for by genes in the
MHC located on chromosome

81
Q

products were identified as responsible for
graft rejection

82
Q

The term “HLA” was coined by______ because
these were first defined by discovering an antibody
response to circulating WBCs.

A

JEAN DAUSSET

83
Q

named according to the product
expressed by the gene locus (capital letter) and the
allele (number)

A

CAPS - GENE LOCUS
NUMBER- ALLELE

84
Q

Combination of inherited HLA alleles

85
Q

2 KEY FUNCTIONS OF MHC IN ANTIGEN PRESENTATION

A
  1. to selectively bind to peptides
  2. to present peptides on the surface of the host cell to a t cell with a correct t cell receptor
86
Q

Transplantation Antigens
Serologically Detected Membrane Antigens
Cellular Target Antigens for Cell
Mediated Lympholysis

A

CLASS 1 - A,B,C,E,F,G,H,X

87
Q

I -region leukocyte antigen
T and B cell interaction
Immune Response
Mixed Leukocyte Reaction
Tumor Virus Susceptibility
Peptide Transport
Generation of Cytosolic Proteins

A

Class II - DP DQ DR
DM DN DO

88
Q

Serum Protein Molecules
Complement Levels, Cytokines and Proteins

A

Class III - C’
Components,
cytochrome p450, 21
hydroxylases and
TNF

89
Q

do not respond to host cells in the absence of
foreign peptide
________focus on responding to infected cells but
cannot respond to host cells that are uninfected

90
Q

● CD8+ T cell responds to peptide plus self-MHC

91
Q

CD4+ T cell responds to peptide plus self-MHC

92
Q

The chains that MHC Class I has is _______
also has an independent protein which is the
_________

A

alpha 1 to 3 chains

beta-2-microglobulin

93
Q

binding site in class 1

94
Q

coded by chromosome 15
○ just added to the MHC molecule represented
by alpha domains

A

b2 microglobulin

95
Q

alpha 1
alpha 2
beta 1
beta 2

A

CLASS 2 MHC

96
Q

binding site of class 2

97
Q

Designated as E, F, and G

A

non classical class 1 mhc antigens

98
Q

All ________ are not expressed on the cell surfaces
and do not function in antigen recognition but has
other role in immune response

99
Q

are expressed on fetal trophoblast cells
during the 1st trimester of pregnancy.

A

G ANTIGENS

100
Q

It helps ensure tolerance for the fetus by
protecting placental tissue from the action of
NK cells

A

G ANTIGENS

101
Q

molecules involved in loading
peptides onto class Il molecules

102
Q

controls antigen binding

103
Q

function remains unknown

104
Q

ARE NOT ASSOCIATED WITH CELL
MEMBRANE SURFACES

105
Q

molecules that bind peptides (8-11 amino
acid long) (Stevens & Miller, 2017) derived from
proteins catabolized in the cytoplasm

A

CLASS 1

8-11

106
Q

are transported into the
endoplasmic reticulum where they interact
with newly synthesized MHC Class I
Beta-2-microglobulin chains

107
Q

Smaller peptides are presented by Class

A

CLASS 1 SMALLER

108
Q

molecules longer are for Class

A

CLASS 2 LONGER

109
Q

In the cytoplasm they meets with the Class I
molecule, they will then be presented in
surface via

A

exocytosis

110
Q

Molecules that are found in nearly every nucleated cell
surface

A

CLASS 1 NUCLEATED

111
Q

These are molecules that interacts with peptides
(12-17 aa long; Stevens) derived from proteins taken
into cells and catabolized in acid vesicles in APCs.

A

CLASS 2

12-17

112
Q

Protein is from the outside (aka exogenous)

A

CLASS 2 EXOGENOUS

113
Q

As it enters the APC, it is already in antigen protein form
■ It processes exogenous antigens to the T-helper cells (CD4)

A

CLASS 2 CD4 TH EXO

114
Q

endogenous for _____(doon
ginawa sa loob)
● Presents to Tc

A

CLASS 1 CD8 TC ENDO

115
Q

Made intracellularly by viruses,
tumors, intracellular pathogens
● They aim to multiply in
the cell
■ Bypass to produce protein inside

116
Q

Takes up exogenous antigens
Dendritic cells and macrophages eat it

117
Q

Consist of 2 non-covalently bound
polypeptide chains that are encoded by
separate genes in the MHC complex.

A

major class 2

118
Q

Are heterodimers because they contain 2 different
chains

A

major class 2

119
Q

expressed at the
highest levels; accounts ~ ½ of all class II
MHC molecules on a cell.

120
Q

molecules -found in the shortest

121
Q
  • Both are polygenic and are highly
    polymorphic in nature
  • They bind to peptides
  • Expressed coordinately and
    codominantly
122
Q

can only respond to antigens
when antigens are combined with MC molecules.

123
Q

Synthesized in the RER

124
Q

88-kd membrane-bound molecule in
the ER keeping the a chains partially folded while it is
waiting to bind with the B2-microglobulin.

125
Q

also bind to a chain that is still unpaired with
ß2-microglobulin.

126
Q

Once a chain is bound with ß2-macroglobulin, ______will be released, chaperones
________will join the complex and help
on stabilizing the MHC molecule for peptide binding

A

calnexin and erp57

calreticulin and tapasin

127
Q

stabilization until it
reaches the peptides being presented to it
by transporter proteins (TAP)

A

chaperones

128
Q

will cut it into smaller pieces/peptides
which will be transported by TAP

A

proteasomes

129
Q

transporter proteins of peptide to MHC molecule

130
Q

Class II molecules are synthesized in the ER and
associate with the protein:

A

Ii INVARIANT CHAIN

131
Q

serves as a chaperone to direct
the aB heterodimer to an endosomal, acidic
protein–processing location

A

Ii INVARIANT CHAIN