The Immune Response Flashcards

1
Q

Latent Phase (aka: lag or inductive)

A

After initial exposure to an immunogen it is the period of time before Ab can be detected

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2
Q

Exponential Phase (aka: logarithmic)

A

Ab begins and rate of production increases resulting in exponential increase in Ab concentration

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3
Q

Steady State

A

Peak Ab concentration

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4
Q

Decay (aka: decline)

A

Decline in Abs followed by a time when a small amount of Ab can be detected

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5
Q

Secondary Response (aka: memory)

A

After initial exposure to Ag

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6
Q

How does 2ndary response compare to primary?

A
Faster - Shorter lag time
Higher rates of Ab synthesis 
Higher peak of Ab
Longer persistent response
Predominance of IgG
Higher affinity to Ab
Requires less Ag
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7
Q

B-cells

A

Express surface Ig

Each only allowed to express a SINGLE variable region

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8
Q

What is repertoire?

A

The total population of B-cells make up the repertoire of Ab specificities

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9
Q

How are Ags seen

A

Seen by B-cells–> and those cells with COMPLEMENTARY Ig sequence will respond

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10
Q

How are T-cells involved in this process?

A

They aid in BC proliferation

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11
Q

Clonal Expansion

A

A single BC can produce up to 1000 daughter cells in 10 days

  • As immune response continues there is an increase in affinity of Ab produced
  • Class switching occurs (IgM–>IgG)
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12
Q

How can increase affinity be explained?

A

As a selective expansion of those clones w/ the highest affinity to Ag
-As [Ag] drops only those clones w/ the highest affinity will be stimulated

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13
Q

Helper T-cells - CD4+

A

Recognize diff set of Ags than BCs

Most Ags it reacts to are proteins or peptides

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14
Q

How do TCs react with Ag

A

React with Ag on the surface of the APC and in response to Ag (with MHC) and co-stimulatory molecules
-TCs proliferate and produce factors that stimulate BCs

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15
Q

How do BCs respond to TCs

A
  • Many daughter BCs will react to TC derived factors and differentiate into plasma cells
  • Other TC factors involved in switching IgM production to IgG
  • Some of the daughter cells wont differentiate and will become memory cells
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16
Q

T-independent Ags

A
  • Not all immunogens require TC help to produce an immune response
  • Generally polymorphic molecules having a large # of repeating subunits that can cross link to Ig on BC
  • Others are polyclonal activators of BCs (usually provided by TCs) through TLR
17
Q

APCs

A

Initiate interaction w/ Ag by endocytosis or phagocytosis

18
Q

How can this be enhanced?

A

Interaction w/ complement
Pre-existing Ab
With specific receptors that recognize pathogens

19
Q

APC after uptake of Ag

A

Is followed by Ag-processing - where Ag is digested
and
Ag presentation - Ag is deposited on the surface of the presenting cell
This is a HIGHLY immunogenic form of Ag

20
Q

How is Ag presented

A

As MHC/Ag complex

21
Q

What do lymphocytes respond to?

A

To Ag that is presented w/ self MHC

22
Q

Apart from Ag processing, what must APCs provide?

A

Co-stimulatory signal

  • cell surface Ags are considered CRITICAL for an immune response
  • ->most imp CD28 (on TC)-B7(on APC)
23
Q

Does presentation of Ag w/o co-stimulation produce immune response?

A

NO

24
Q

A APC must …

A

1- take up and process Ag
2- have MHC C2 Ag on its surface
3- present Ag w/ MHC C2 Ag
4- provide co-stimulatory signal (B7)

25
Q

B-cells are capable of …

A

1- processing Ag
2- expressing MHC C2 Ag
3- expressing co-stimulators

26
Q

What is a toxin?

A

Proteins that will kill you
-no amount that wont
-will not induce immune response
If you somehow survive - you are NOT immune and STILL need vaccine

27
Q

What is a toxoid?

A

Chemically modified protein that will induce immune response

-antigenitically same as toxin, but wont kill you

28
Q

Hepten Carrier

A

Hepten seen by BC

Carrier seen by TC