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Cancer & the Immune System
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Cancer & the Immune System
 Assigned Reading
 Content Outline
 Performance Objectives
– Key terms
– Key Concepts
 Short Answer Questions
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Assigned Reading
 Janis Kuby’s Immunology 4th Ed
Chapter: 22 pp 539-561
 Janis Kuby’s Immunology 3rd Ed
Chapter: 24 pp 573-596
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4
2/21/2024
Content Outline
 Origins & Terms
 Malignant Transformation
 Tumours of the Immune System
 Tumour Antigens
 TATAs on human melanomas
 Immune Response to Tumours
 Tumour Evasion of Immune Response
 Cancer Immunotherapy
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Origins & Terms
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2/21/2024
Benign vs malignant
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Distribution of Cancer
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2/21/2024
Growth of Breast Cancer
Diameter
of
Tumour
(mm)
Tumour Cell doubling
Tumour visible by X rays
Tumour first palpable
Death of Patient
108cells
109cells
1012cells
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Altered Growth Properties
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Localized Benign Tumour
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Tumour Invasion of Basal
Lamina
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Metastasizes to Other Sites
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2/21/2024
Tumour Antigens
 Tumour specific Antigens
– chemically induced
– virally induced
 Tumour associated antigens
– oncofetal tumour antigens
– oncogene proteins
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2/21/2024
TSTA vs TATA
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Radio labelled anti CEA
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Genes
for TSTAs
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Malignant Transformation
 Oncogenes
 Induction of cell proliferation
 Inhibition of cell proliferation
 Regulation of apoptosis
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Tumour
Induction
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Induction of Tumours
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Tumours of the Immune
System
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2/21/2024
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2/21/2024
TATAs on human melanomas
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2/21/2024
TATAs on human melanomas
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2/21/2024
Immunity to Polyoma virus(1)
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Immunity to Polyoma virus(2)
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Immunity to Polyoma virus (3)
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Immunity to Polyoma Virus (4)
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Immune Response to
Tumours
 NK cells & macrophages
 Immune surveillance theory
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2/21/2024
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Tumour Evasion of Immune
Response
 Immunologic enhancement
 Modulation of tumour antigens
 Reduce MHC-I
 No co-stimulatory signal
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Tumor Escape
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Cancer Immunotherapy
 Modify Co-stimulatory signal
 Enhance APC activity
 Cytokine therapy
 MABs
 Tumour cell vaccines
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2/21/2024
Cancers Treatable by Bone
Marrow Transplants
Allogenic/syngenic
Transplant
– Breast cancer
– aplastic anemia
– leukemia
– ALL
– CML
– Myeolodysplasia
– multiple myeloma
– Non- Hodgkin’s lymphoma
– Hodgkin’s disease
Autologous Transplants
– Leukemia
– AML
– ALL
– Multiple Myeloma
– Non Hodgkin’s lymphoma
– Hodkin’s disease
– Solid tumours
– Breast
– ovarian
– testicular
– Neuroblastoma
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Transfect co stimulartory
signal
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Transfect with GM-CSF
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Lak cells & IL-2
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2/21/2024
Mabs to B cell Lymphoma
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Tumour Cell Vaccine
Immune Response to MCA or PV
Transplant killed cells of
MCA induced sarcoma
A
 Challenge with
Sarcoma A- No Growth
 Challenge with
Sarcoma B- growth
Transplant killed cells of
Polyoma Virus induced
sarcoma A
 Challenge with sarcoma
A no growth
 challenge with sarcoma
B no growth
 SV40 induced sarcoma
C- growth
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2/21/2024
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2/21/2024
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50
2/21/2024
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2/21/2024
Performance Objectives
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2/21/2024
Key Terms
 antibody dependent cell mediated
cytotoxicity (ADCC), benign tumour,
cancer,
 carcinogens, proto oncogens, immune
surveillance, Specific immunotherapy,
 non specific immunotherapy,
immunotoxins,Lymphokine activated
killer cell(LAK),
53
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2/21/2024
 neoplasm, oncofetal antigens, oncogens,
tumour, tumour associated antigens,
 tumour associated transplantation
antigens, tumour specific antigens,
 tumour specific transplantation
antigens
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2/21/2024
Key Concepts
 Differentiate between a benign tumour and a
malignant tumour.
 Describe the concept of immunosurveillance
 Describe the different ways that tumours can
camouflage themselves to evade immune
defenses,
 Discuss the advantages of immunotherapy
over other forms of cancer therapy.
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55
2/21/2024
 Distinguish between specific and nonspecific
immunotherapy with the use of specific
examples.
 Describe immunotoxins.
 Describe the development of humanized
antibodies to tumour antigens
 Evalulate the contribution of T cells, NK cells,
Macrophages, and B cells to tumour
immunity.
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2/21/2024
 Distinguish between tumour specific
transplantation antigens and tumour
assoicated transplantation antigens.
 Describe oncofetal antigens.
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2/21/2024
Short Answer Questions
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2/21/2024
 Explain how some cancer cells that can
make TGF-beta are immunosuppressive.
 Tumours and transplants are similar to one
another,yet very different. Explain this
observation in the context of what the
immune system recognizes and the result of
this recognition.
 The qualities of proliferation and
differentiation are essentially all that
distinguishes a normal cell from a cancer
cell. Explain.
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2/21/2024
 Describe an experiment using mice that
proves that the immune system provides
immunity against tumours.
 Distinguish between tumour-specific
transplantation antigens (TSTA) and tumour
associated transplantation antigens (TATA).
 Design an experiment to show Tumour
associated Transplantation Antigens (TATA).
 What is the main difference separating cell
surface antigens from chemically induced and
virually induced cancers?
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60
2/21/2024
 Speculate on why this difference leads to
difficulty in designing anticancer vaccines.
 What are oncofetal antigens? Are they
important in tumour immunity? Why?
 What is immune surveillance?
 All evidence for immune surveillance is
indirect. Speculate on how you could get
direct evidence.
61
61
2/21/2024
 What immune cells play a role in tumour
rejection? Briefly describe how each
accomplishes this task. Include such things as
cytokines, perforins, ADCC etc.
 Cancers camouflage themselves to evade
antitumour defenses. Pick three possible
forms of camouflage that you think are most
important, describe them and state why you
think they are most important.
 What are immunotoxins?
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2/21/2024
 Surgery, radiation and chemotherapy
are the methods most widely used to
treat cancer patients. What are the
problems with this regimen, and how
could immunotherapy overcome these
problems.
 Distinguish between specific and
nonspecific immunotherapy.

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The Immunology of Tumor in rats Lecture.ppt

Editor's Notes

  1. Transfection with Granulocyte-monocyte colony sttimulationg factor ene will increase the amount of CM-CSF and allw recovery of the immune response
  2. Cancers were inducedwith either MCA or polymoa virus and killed cells from the induced tumours were injected into syngenic animals which were then challenged with live cells from the indicated tour lines The absence of tumour growth after the live challenge indicates that the immune response induced by tumour antigens on the killed cells provide protection against the live cells MCA = methyl cholanthrene