Overview of The Adaptive Immune System Flashcards

1
Q

What is adaptive immunity?

A
  • The part of the immune system that has enhanced rapidity, potency or specificity as a consequence of previous events (exposure or vaccination).
  • Memory is the key element
  • “Anamnestic response” – not forgetting
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2
Q

Why have adaptive immunity?

A
  • Protection from and defence against pathogens
  • Also role in malignancy surveillance
  • Also linked to damage healing and repair
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3
Q

How do we spot pathogens?

A

• Generic recognisable features – eg TLR – PAMP’s
There’s trouble going on (Their presence is associated with damage)(tissue damage)
• The Danger Hypothesis – co-stimulation – CD28
• Damage-associated molecular pattern molecules (DAMP)
• Seen the pathogen before
• Autoimmunity

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4
Q

What are the main drivers of the adaptive immune response

A

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5
Q

How does the immune system set up a system to recognise things not yet seen?

A

• The “massive array of possibilities” approach

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6
Q

Why do we need effectors?

A
  • The same pathogens often come back and attack again
  • Opportunity to have effectors ready which are specific and potent
  • Some pathogens stick around
  • Need controlling by effectors
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7
Q

Give some examples of T and B cell deficiency’s

A

B cells
• Congenital agammaglobulinaemia
• Common variable immunodeficiency (CVID)
• Novel biologics – Rituximab
T cells
• Severe Combined Immunodeficiency (SCID)
• DiGeorge syndrome -thymic failure
• Acquired – HIV / Chemotherapy / Novel biologics

All create major, often life-threatening clinical problems

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8
Q

Where do lymphocytes fit in the immune response

A

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9
Q

Describe the cells of the innate and adaptive immune system

A

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10
Q

What are the bridging cells between the innate and adaptive immune system?

A

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11
Q

How do we define lymphocytes?

A
•	Morphology:
o	White cell; small, large nucleus
•	Lineage: 
o	T and B cells
•	Location
o	Tissue-resident memory cells (TRM)
o	Marginal zone B cells
•	Differentiation
o	Naïve / memory (central, effector, stem cell memory)
o	Immature / mature or differentiated / senescent
•	Function: What they do 
o	eg Helper / Cytotoxic / Regulatory / Antibody-producing
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12
Q

How can lymphocytes be classified?

A

• Phenotype: What surface markers they express
o Eg CD4, CD8, CD28 … Usually functional receptors–
 not just there for our convenience!
• Specificity
o What target – What Ab produced or epitope recognised (TCR)
• Type of receptor
o Ig class for B cells / αβ vs γδ for T cells
• By what they produce
o TH1 (IL-2, IFN-γ)
o TH2 (IL-4, IL-5, IL-6, IL-10)

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13
Q

How does Adaptive immunity work?

A

Two key features:
• Specificity
• Memory

The pivotal role of clonal selection
• One clone – one specificity
• Progeny can be expanded and retained

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14
Q

Describe clonal selection of the adaptive immune system

A

• Basic tenet – one cell / one specificity
• For B cells – one cell, one Ig
o Defined by their antibody
o May class switch / undergo affinity maturation
o but always the same basic Ig
• For T cells – one cell, one T cell receptor – TCR
o Selection and expansion of that clone ± differentiation
o Retention in “memory” of clonal progeny
• Continued protection
o Continued production of antibody (B cells / Plasma cells)
o More rapid specific secondary responses (B and T cells)

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15
Q

Describe the lineages of T and B cells

A

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16
Q

Describe the structure of a B cell receptor, T cell and antibody

A

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17
Q

Describe MHC class 1 and 2

A

• All cells process their intracellular contents and present on MHC-I
o Recognised by CD8 T cells through their TCR
o Crucial to defence against viruses

• Specialised antigen-presenting cells (APC) process and present peptides in MHC-II
o binds to TCR on CD4 T cells
o Positive selection must bind MHC
o Negative selection must not bind self peptides

18
Q

What happens after T cells have developed in the thymus?

A

• Naïve cells recirculate
o primarily from blood to lymph nodes
• How are they maintained?
• What are the dynamics of memory?

19
Q

Describe B cell repertoire selection

A
•	Positive selection
•	Receptor editing
•	Negative selection
•	Transition to IgM+ IgD+ mature B cell
•	Antigen recognition leads to proliferation/differentiation
•	Activated B cells transform into Plasma cells
o	“Antibody factories”
o	also produce CD27+ memory B cells