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By
Ashwani Kesarwani
M.Sc IInd sem
Presentation on
cancer immunology &
cancer
immunotherapy
Introduction
CANCER IMMUNOLOGY-
It is the study of interaction between immune
system & cancer cell (also called Tumors or
malignancies).
• TUMOR- Cells that continue to replicate, fail
to differentiate into specialized cells, and
become immortal.
MalignantBenign
,
Types of Cancer
Carcinoma: arising from epithelial tissue, such as
glands, breast, skin, and linings of the urogenital,
digestive, and respiratory systems.
Sarcoma: solid tumors of muscles, bone, and
cartilage that arise from the mesoderm connective
tissue.
Leukemia: disease of bone marrow causing
excessive production of leukocytes.
Lymphoma: diseases of the lymph nodes and
spleen that cause excessive production of
lymphocytes.
ONCOGENES
A gene that has the potential to cause cancer.
Oncogenes may also be found in normal cells.
The cellular ones (c-onc) in contrast to the viral
ones (v-onc) are called “PROTO-
ONCOGENES”
A proto-oncogene is a normal gene that can
become an oncogene due to mutation or
increased expression.
60-100 different proto-oncogenes have been
identified.
.
Functional classification of cancer
associated genes
GENES THAT REGULATE
PROGRAMMED CELL
DEATH.
Eg- bcl-2 etc.
TUMOR-SUPRESSOR
GENES, INHIBITORS OF
CELLULAR
PROLIFERATION.
Eg- p53 etc.
GENES THAT INDUCE
CELLULAR
PROLIFERATION.
Eg- sis, fms, erbB,
neu etc.
Conversion of Proto-oncogenes to oncogenes
Tumor Antigens
Cell-surface protein present on the surface
of tumor cells that can-mediate immune
response.
Some are found only on tumor cells;
others are also found on normal cells.
TUMOR ANTIGENS
Tumor-associated
transplantation antigens
(TATAs)
Tumor-specific
transplantation antigens
(TSTAs)
Tumor-Specific Antigens
Unique to tumor cells and do not occur on
normal cells in the body.
These are identified on tumors, induced with
chemical or physical carcinogens and on some
virally induced tumors.
CHEMICALLY OR PHYSICALLY INDUCED
TUMOR ANTIGENS-
Methylcholanthrene and
ultraviolet light
Chemical-induced tumors
(Methylcholanthrene)
Virally induced tumor antigens
Virally induced tumors express tumor antigens
shared by all tumors induced by the same virus.
When syngeneic mice are injected with killed
cells from a particular SV40 or polyoma-
induced tumor, the recipients are protected
against subsequent challenge with live cells
from any SV40 or polyoma-induced tumors.
Likewise, when lymphocytes are transferred
from mice with a virus-induced tumor into
normal syngeneic recipients, the recipients
reject subsequent transplants of all syngeneic
tumors induced by the same virus.
Virally induced Tumor antigens
.
Animal models to show the potential value of
virally induced tumor antigens
In one experiment, mice immunized with a
preparation of genetically engineered polyoma
virus tumor antigen were shown to be immune to
subsequent injections of live polyoma-induced
tumor cells.
In another experiment, mice were immunized
with a vaccinia-virus vaccine engineered with
the gene encoding the polyoma-tumor antigen.
These mice also developed immunity, rejecting
later injections of live polyoma-induced tumor
cells.
TUMOR-ASSOCIATED ANTIGENS
These tumor associated transplantation
antigens may be proteins usually
expressed only on fetal cells but not on
normal adult cells.
They may be proteins expressed at low
levels by normal cells but at much higher
levels by tumor cells.
Example- transferrin growth factor,
designated p97 (aid in transport of iron
into cells).
Oncofetal tumor antigen
Found not only on cancerous cells but
also on normal fetal cells.
Appear only in embryonic development,
before the immune system acquires
immunocompetence.
If appear late in cancer cells, they are
recognized as non-self and induce an
immunologic response.
Example- Alpha-fetoprotein (AFP) &
carcinoembrionic antigen(CEA).
Examples of tumor antigens
IMMUNE RESPONSE TO TUMORS
Tumor antigens can be shown to induce
both humoral and cell-mediated immune
responses that result In the destruction of the
tumor cell.
[1] Role of Cytotoxic T Lymphocytes (CTL)
Tumour antigens associate with MHC class I molecule on
surface of tumours.
CTL recognise tumour cells with MHC class I.
Bind to them and release TNF- - toxicity to tumour cell -
tumour cell killing.
.
[2] Natural Killer Cells (NK Cells)
Capable of lysing a wide variety of tumour cells.
NK cells recognise this and attack the tumour
cell “Antibody-Dependent Cell-Mediated
Cytotoxicity” (ADCC)
NK cells release TNF- & NK cytotoxic factor.
[3] Macrophages
Activated macrophages secrete lytic enzymes.
Also secrete TNF-.
Secrete nitric oxide (potential antitumour
effects).
IMMUNE SURVEILLANCE THEORY
First conceptualized in the early 1900s by Paul
Ehrlich.
Cancer cells frequently arise in the body but are
recognized as foreign and eliminated by the
immune system.
The basic concept of the immune surveillance
theory— Malignant tumors arise only if the
immune system is somehow impaired or if the
tumor cells lose their immunogenicity, enabling
them to escape immune surveillance.
Cancer immunotherapy
Use of immune system to reject
cancer.
Several types of Cancer
immunotherapy in current use
are-
.
.
tumor CTL
CD28
tumor
B7
No killing
No T cell
activation
Killing
T cell
activation
Manipulation of co-stimulatory signals
CTL
TCR
MHC class I Ag
Systemic Cytokine Therapy for Tumors
.
Use of LAK cells + IL-2 to treat cancer
Isolate lymphocytes
from blood
lymphocytes
+IL-2 for
3 days
IL-2
LAK
cells
melanoma
LAK- lymphokine activated killer cells
Treatment of Melanoma with
LAK cells +IL-2
.
.
Before After
.
.
Use of tumor-infiltrating lymphocytes + IL-2
to treat cancer
surgical removal
of cancer nodule
tumor
T cell
+IL-2
IL-2
Treatment of melanoma and renal cell carcinoma
lymphodepletion
.
.
Fig-Treatment of Melanomas with TIL + IL-2
Before After
Fig-Treatment of B-cell lymphoma with monoclonal antibody
specific for idiotypic determinants on the cancer cells
Monoclonal antibodies
.
Cancer vaccines
SUMMARY
Tumor antigens are recognized by immune
system
Immune response mainly mediated by CTL,
NK cells and macrophages
Immunotherapy aims at activating the
patient’s own immune system to fight the
tumor.
References
Kuby immunology (4th edition), Richard
A. Goldsby, Thomas J. Kindt, Barbara A.
Osborne.
Cellular & molecular immunology (5th
edition), Abdul K. Abbas, Andrew H.
Lichtman.
Immunology (6th edition), Ivan Roitt,
Jonathan Brostoff, David Male.
Ashwani
Ashwani

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Ashwani

  • 1.
  • 2. . .. By Ashwani Kesarwani M.Sc IInd sem Presentation on cancer immunology & cancer immunotherapy
  • 3. Introduction CANCER IMMUNOLOGY- It is the study of interaction between immune system & cancer cell (also called Tumors or malignancies). • TUMOR- Cells that continue to replicate, fail to differentiate into specialized cells, and become immortal. MalignantBenign
  • 4. ,
  • 5. Types of Cancer Carcinoma: arising from epithelial tissue, such as glands, breast, skin, and linings of the urogenital, digestive, and respiratory systems. Sarcoma: solid tumors of muscles, bone, and cartilage that arise from the mesoderm connective tissue. Leukemia: disease of bone marrow causing excessive production of leukocytes. Lymphoma: diseases of the lymph nodes and spleen that cause excessive production of lymphocytes.
  • 6. ONCOGENES A gene that has the potential to cause cancer. Oncogenes may also be found in normal cells. The cellular ones (c-onc) in contrast to the viral ones (v-onc) are called “PROTO- ONCOGENES” A proto-oncogene is a normal gene that can become an oncogene due to mutation or increased expression. 60-100 different proto-oncogenes have been identified.
  • 7. . Functional classification of cancer associated genes GENES THAT REGULATE PROGRAMMED CELL DEATH. Eg- bcl-2 etc. TUMOR-SUPRESSOR GENES, INHIBITORS OF CELLULAR PROLIFERATION. Eg- p53 etc. GENES THAT INDUCE CELLULAR PROLIFERATION. Eg- sis, fms, erbB, neu etc.
  • 9. Tumor Antigens Cell-surface protein present on the surface of tumor cells that can-mediate immune response. Some are found only on tumor cells; others are also found on normal cells. TUMOR ANTIGENS Tumor-associated transplantation antigens (TATAs) Tumor-specific transplantation antigens (TSTAs)
  • 10. Tumor-Specific Antigens Unique to tumor cells and do not occur on normal cells in the body. These are identified on tumors, induced with chemical or physical carcinogens and on some virally induced tumors. CHEMICALLY OR PHYSICALLY INDUCED TUMOR ANTIGENS- Methylcholanthrene and ultraviolet light
  • 12. Virally induced tumor antigens Virally induced tumors express tumor antigens shared by all tumors induced by the same virus. When syngeneic mice are injected with killed cells from a particular SV40 or polyoma- induced tumor, the recipients are protected against subsequent challenge with live cells from any SV40 or polyoma-induced tumors. Likewise, when lymphocytes are transferred from mice with a virus-induced tumor into normal syngeneic recipients, the recipients reject subsequent transplants of all syngeneic tumors induced by the same virus.
  • 13. Virally induced Tumor antigens .
  • 14. Animal models to show the potential value of virally induced tumor antigens In one experiment, mice immunized with a preparation of genetically engineered polyoma virus tumor antigen were shown to be immune to subsequent injections of live polyoma-induced tumor cells. In another experiment, mice were immunized with a vaccinia-virus vaccine engineered with the gene encoding the polyoma-tumor antigen. These mice also developed immunity, rejecting later injections of live polyoma-induced tumor cells.
  • 15. TUMOR-ASSOCIATED ANTIGENS These tumor associated transplantation antigens may be proteins usually expressed only on fetal cells but not on normal adult cells. They may be proteins expressed at low levels by normal cells but at much higher levels by tumor cells. Example- transferrin growth factor, designated p97 (aid in transport of iron into cells).
  • 16. Oncofetal tumor antigen Found not only on cancerous cells but also on normal fetal cells. Appear only in embryonic development, before the immune system acquires immunocompetence. If appear late in cancer cells, they are recognized as non-self and induce an immunologic response. Example- Alpha-fetoprotein (AFP) & carcinoembrionic antigen(CEA).
  • 17. Examples of tumor antigens
  • 18. IMMUNE RESPONSE TO TUMORS Tumor antigens can be shown to induce both humoral and cell-mediated immune responses that result In the destruction of the tumor cell. [1] Role of Cytotoxic T Lymphocytes (CTL) Tumour antigens associate with MHC class I molecule on surface of tumours. CTL recognise tumour cells with MHC class I. Bind to them and release TNF- - toxicity to tumour cell - tumour cell killing.
  • 19. . [2] Natural Killer Cells (NK Cells) Capable of lysing a wide variety of tumour cells. NK cells recognise this and attack the tumour cell “Antibody-Dependent Cell-Mediated Cytotoxicity” (ADCC) NK cells release TNF- & NK cytotoxic factor. [3] Macrophages Activated macrophages secrete lytic enzymes. Also secrete TNF-. Secrete nitric oxide (potential antitumour effects).
  • 20. IMMUNE SURVEILLANCE THEORY First conceptualized in the early 1900s by Paul Ehrlich. Cancer cells frequently arise in the body but are recognized as foreign and eliminated by the immune system. The basic concept of the immune surveillance theory— Malignant tumors arise only if the immune system is somehow impaired or if the tumor cells lose their immunogenicity, enabling them to escape immune surveillance.
  • 21. Cancer immunotherapy Use of immune system to reject cancer. Several types of Cancer immunotherapy in current use are-
  • 22. . . tumor CTL CD28 tumor B7 No killing No T cell activation Killing T cell activation Manipulation of co-stimulatory signals CTL TCR MHC class I Ag
  • 24. . Use of LAK cells + IL-2 to treat cancer Isolate lymphocytes from blood lymphocytes +IL-2 for 3 days IL-2 LAK cells melanoma LAK- lymphokine activated killer cells
  • 25. Treatment of Melanoma with LAK cells +IL-2 . . Before After
  • 26. . . Use of tumor-infiltrating lymphocytes + IL-2 to treat cancer surgical removal of cancer nodule tumor T cell +IL-2 IL-2 Treatment of melanoma and renal cell carcinoma lymphodepletion
  • 27. . . Fig-Treatment of Melanomas with TIL + IL-2 Before After
  • 28. Fig-Treatment of B-cell lymphoma with monoclonal antibody specific for idiotypic determinants on the cancer cells
  • 31. SUMMARY Tumor antigens are recognized by immune system Immune response mainly mediated by CTL, NK cells and macrophages Immunotherapy aims at activating the patient’s own immune system to fight the tumor.
  • 32. References Kuby immunology (4th edition), Richard A. Goldsby, Thomas J. Kindt, Barbara A. Osborne. Cellular & molecular immunology (5th edition), Abdul K. Abbas, Andrew H. Lichtman. Immunology (6th edition), Ivan Roitt, Jonathan Brostoff, David Male.