Immunology 4: Tumour immunology and immunology of cancer Flashcards

1
Q

Recall the 4 points used for evidence that the immune system surveys for tumour presence

A
  1. Small tumours found at autopsy 2. Disease-free melanoma patients donating tissue 3. Increased cancer risk in the immunosuppresion 4. Men have higher risk of dying from cancer - women mount stronger responses
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2
Q

Summarise the basis of immune-surveillance for malignancy

A

Tumour cell apoptosis –> antigen release –> APC action T cells activated “tumour-infiltrating lymphocytes” (TILs) proliferate an enter bloodstream Cancer cell apoptosis

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3
Q

Describe the selection pressure that is induced by the immune response to tumours

A

Good immune response to tumour cells by TILs favours cells that have a mutation that allows them to “hide” from immune system

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4
Q

Describe the function of PD1-PDL1 interactions

A

Repeat exposure to an Ag causes T cell to express PD1 Tumour cell responds by upregulating PDL1 PD-1-PDL1 interactions decrease the T cell response

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5
Q

How might the T cell response be boosted as an immune therapy for cancer?

A

PD1-PDL1 interaction blockade

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6
Q

Recall the cell types involved in the innate response to a tumour

A

NKSc DCs Macrophages

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7
Q

Recall 2 problems with the body’s immune surveillance for tumours

A
  1. It takes a little while for the local inflammation in the tumour to be sufficient to produce a danger signal that provides costimulation for the adaptive immune response 2. Antigenic differences between tumour and self proteins may be very subtle
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8
Q

Explain 2 ways in which immune responses to tumours have some similarities with those to virus infected cells

A
  1. T cells can “see” inside cells and recognise TSAs 2. MHC displays contents of cell for surveillance
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9
Q

What is a tumour-associated antigen?

A

Derived from a normal cellular protein Aberrantly expressed To recognise, tolerance must be overcome

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10
Q

Recall 5 examples of TAAs

A

PSA HER2 MAGE (melanoma) MUC-1 (many) CEA (should be foetal, expressed in tumours)

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11
Q

How might the tyrosinase enzyme be used in cancer immunotherapy

A

It generally develops poor self-tolerance It is expressed in many melanomas Can direct immune response against it

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12
Q

What are the 2 potential pitfalls of using TAAs in tumour immunotherapy?

A

AI responses to normal tissues Development of tolerance

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13
Q

Which proteins produced by HPV are oncogenes?

A

E6 and E7

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14
Q

Recall a malignancy that is associated with immune suppression following transplant

A

EBV+ lymphoma

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15
Q

Recall a malignancy that is associated with HIV

A

HHV8+ kaposi sarcoma

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16
Q

Recall an example of using “naked” monoclonal antibodies in cancer therapy

A

Herceptin

17
Q

Describe the conjugated monoclonal antibodies used in cancer therapy

A

Antibody conjugated to cytotoxic drug

18
Q

Describe the bi-specific monoclonal antibodies used in cancer therapy and give an example of how this might work

A

GM to combine 2 specifities Eg combining B and T cell specificity - used as a drug against B cell malignancy - drug crosslinks the T and B cells

19
Q

What is the main drawback of monoclonal antibody therapy?

A

Cost

20
Q

What is the only approved vaccination for cancer so far?

A

Advanced prostate cancer

21
Q

Describe how the anti-prostate cancer vaccination works

A

Remove patient’s WBCs Stimulate them with a fusion protein between PAP and GM-CSF DC maturation stimulated PAP-specific T cell response stimulated

22
Q

What is the aim of immune-checkpoint blockade in cancer therapy?

A

Reduces the regulatory effect of existing T cell responses (eg tRegs)

23
Q

Recall and describe the pathways targeted by immune-checkpoint blockade

A

CTLA-4: expressed on activated tRegs, binds costimulatory molecules for APCs PD-1: expressed on activated T cells, binds PDL1 to reduce T cell response (perhaps panopto this)