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Types of tumor antigens recognized by T cells
Immune mechanisms of tumor rejection
How tumors evade immune responses?
Novel therapeutic approaches (immunotherapies)
Types of tumor antigens recognized by T cells
Immune mechanisms of tumor rejection
How tumors evade immune responses?
Novel therapeutic approaches (immunotherapies)
Types of Tumor antigens
Tumor-associatedantigens
(TAAs)
Tumor-specificantigens
(TSAs)
Tumor-associated
antigens
•expressed also on normal cells .
•normal cellular constituents but aberrant or
dysregulated in tumors .
Tumor-specific
antigens
•expressed on tumor cells but not on normal
cells .
•individually unique or shared.
Tumor reactive CTLs lines from cancer patients
Relevant peptide antigens .
CD4Tcell lines for tumor antigens .
 SEREX (serological analysis of recombinant c DNAexpression)
humoral immune responses in tumor patients Using antibodies present patient’s serum .
1- Abnormally expressed but unmutated cellular
proteins :
• Normal cellular proteins that are either
overexpressed or whose expression is normally
limited to particular tissues or stages of
development but is dysregulated in tumor cells.
• This aberrant expression may be enough to
elicit such responses.
• e.g. Self protein that are expressed only in
embryonic tissues may not induce tolerance in
adults .
2- Products of mutated self genes :
• Intrinsic genomic instability of many cancers .
• Tumor antigens may be produced by randomly
mutated genes whose products are not related
to the malignant phenotype .
• Class I MHC pathway
• Wide variety of genes may be mutated in tumor
cells.
3- Oncogenes and mutated tumor suppressor genes :
• Differ from normal cellular proteins .
• Class I MHC pathway
• Mutated Ras , Bcr/Abl fusion protein are two
examples of oncogenes.
• Mutated p53 is an example of mutated tumor
expressed gene .
4- Antigens of Oncogenic viruses :
• The products of oncogenic virus: function as
tumor antigens and elicit specific T cell
responses
• Virus-encoded protein antigens are found in the
nucleus, cytoplasm or plasmamembrnare of the
tumor cells.
• most immunogenic tumor antigens.
• shared by all tumors induced by the same type
of virus
4- Antigens of Oncogenic viruses :
DNA viruses RNA viruses
4- Antigens of Oncogenic viruses :
• EBV: B cell lymphomas, nasopharyngeal
carcinoma
• HPV : cervical carcinoma
• Popovaviruse and adenovirus
• HPV vaccine for cervical cancer in women
• Vaccination against Hepatitis B virus
RNA viruses
4- Antigens of Oncogenic viruses :
• Human T cell lymphotropic virus 1 (HTLV-1)
• Adult T cell leukemia/lymphoma (ATL)
DNA viruses
5- oncofetal antigens:
• Proteins expressed at high levels in cancer cells and in normal developing fetal but not
adult tissues
• Silent during development, derepressed with malignant transformation
• Increased in tissues and in the circulation in various inflammatory conditions
• Markers for tumor diagnosis
• Small quantities even in normal tissues .
α-fetoprotein (AFP)
Carcinoembryonic antigen (CEA:CD66)
Oncofetal antigens
6- Tissue-specific differentiation antigens :
• Tumors may express molecules that are present only on the normal cells of origin and not
on cells from other tissues
• Melanoma antigens : targets of CTLs (Tyrosinase)
• Lymphomas :CD10 and CD20
Tumors infiltrated with lymphocytes show less chance to survive than coated
tumors .
Lymphocytes proliferation in lymph nodes in some tumors point to an immune
response
tumors of those who take immune suppressors
Regression of some tumors spontaneously “lymphoma ,mylanoma”
High ratio of tumors of neonatals and olders who have weak immune reactions
studies have focused on the antitumor response of CTLs
because most tumors express class I Major
Histocompatibility Complex (MHC) antigens and not
MHC class II antigens.
Antitumor immunity
results from both:
Macrophage/Dendritic cell attack or antigen
presentation
CD8 cell-mediated cytotoxicity
Antibody dependent cell mediated cytotoxicity
(ADCC)
Natural killer cells


NK
cell
Target cell
(infected or
cancerous)
Perforin and
enzymeskiller
activating
receptor


γ
Immune responses often fail to check tumor growth, because these responses
are ineffective or because tumors evolve to evade immune attack
The immune system faces a daunting challenge if it has to be effective against malignant
tumors because:
Immune responses must kill all tumor cells and tumors
grow rapidly. Often, the growth simply outstrips immune
defenses.
Immune responses against tumors may be weak because
many tumor antigens are weakly immunogenic, perhaps
because they differ only slightly from self-antigens.
Growing tumors also develop mechanisms for evading
immune responses.
Evasion of Immune Responses by Tumors:
 Loss of T cell recognition:
 Antigen loss variants
 Loss of TAPs and other molecules involved in antigen processing
 Stop expressing class ∣ MHC molecules
Explanations for why tumor cells that have lost HLA
class I are not destroyed by NK cells ?
Evasion of Immune Responses by Tumors:
loss or down-regulation of NKG2D ligands expression
lack of stimulatory cytokines and secretion of
immunosuppressant cytokines
producing the matrix metalloproteinase 9, which results
in ICAM-1 shedding and resistance to NK cell killing
 Tumor antigens may be inaccessible to the immune system:
 Antigen masking:
 The cell surface antigens :

Glycocalyx molecule
(sialic acid-
containing
mucopolysaccharide
s)
Evasion of Immune Responses by Tumors:
Tumor may engage molecules that inhibit immune
response:
 Involvement of PD-L1 , CTLA-4
Secreted products of tumor cells may suppress anti-
tumor immune response:
 TGF-β, secreted in large quantities by many tumors that Inhibits the proliferation
and effector functions of lymphocytes and macrophages
Evasion of Immune Responses by Tumors:
Evasion of Immune Responses by Tumors:
Tumor-associated macrophages (TAMs):
Evasion of Immune Responses by Tumors:
 Regulatory T cells: may suppress T cell responses to
tumors:
A population of T cells that regulate the activation or effector
functions of other T cells and may be necessary to maintain
tolerance to self antigens.
Regulatory T cells express 𝐂𝐃𝟒+
and CD25
Depletion of regulatory T cells in tumor-bearing mouse enhances
anti-tumor immunity and reduces tumor growth
 Regulatory T cells:
 the Fas counter attack :
is the use of immune system to reject cancer .
What about Chemotherapy?
Types of Cancer
Immunotherapy
Naked mAbs
Conjugated mAbs :
Radiolabelled
Chemolabelled
Immunotoxin
Types of Cancer
Immunotherapy
Types of Cancer
Immunotherapy
• Therapeutic cancer vaccines trigger the immune system to
recognize and attack certain markers, or antigens, present on or in
cancer cells .
• Unlike traditional vaccines, which help to prevent disease,
therapeutic cancer vaccines treat disease that is already there .
• Cancer vaccines often require additional substances called
adjuvants for optimal effectiveness .
Cancer Vaccines :
 Antigen vaccines
 Dendritic cell vaccines
 DNA vaccines .
Types of Cancer
Immunotherapy
Types of Cancer
Immunotherapy
•
•
•
Types of Cancer
Immunotherapy
Cytokines are messenger molecules that help control
the growth and activity of immune system cells
interleukins (IL) help immune cells grow and divide
more quickly
interferons (IFN) boost the ability of certain immune
cells to attack cancer cells
Immune response against tumors
Immune response against tumors

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Immune response against tumors

  • 1.
  • 2.
  • 3. Types of tumor antigens recognized by T cells Immune mechanisms of tumor rejection How tumors evade immune responses? Novel therapeutic approaches (immunotherapies)
  • 4. Types of tumor antigens recognized by T cells Immune mechanisms of tumor rejection How tumors evade immune responses? Novel therapeutic approaches (immunotherapies)
  • 5. Types of Tumor antigens Tumor-associatedantigens (TAAs) Tumor-specificantigens (TSAs)
  • 6. Tumor-associated antigens •expressed also on normal cells . •normal cellular constituents but aberrant or dysregulated in tumors . Tumor-specific antigens •expressed on tumor cells but not on normal cells . •individually unique or shared.
  • 7. Tumor reactive CTLs lines from cancer patients Relevant peptide antigens . CD4Tcell lines for tumor antigens .  SEREX (serological analysis of recombinant c DNAexpression) humoral immune responses in tumor patients Using antibodies present patient’s serum .
  • 8.
  • 9. 1- Abnormally expressed but unmutated cellular proteins : • Normal cellular proteins that are either overexpressed or whose expression is normally limited to particular tissues or stages of development but is dysregulated in tumor cells. • This aberrant expression may be enough to elicit such responses. • e.g. Self protein that are expressed only in embryonic tissues may not induce tolerance in adults .
  • 10. 2- Products of mutated self genes : • Intrinsic genomic instability of many cancers . • Tumor antigens may be produced by randomly mutated genes whose products are not related to the malignant phenotype . • Class I MHC pathway • Wide variety of genes may be mutated in tumor cells.
  • 11. 3- Oncogenes and mutated tumor suppressor genes : • Differ from normal cellular proteins . • Class I MHC pathway • Mutated Ras , Bcr/Abl fusion protein are two examples of oncogenes. • Mutated p53 is an example of mutated tumor expressed gene .
  • 12. 4- Antigens of Oncogenic viruses : • The products of oncogenic virus: function as tumor antigens and elicit specific T cell responses • Virus-encoded protein antigens are found in the nucleus, cytoplasm or plasmamembrnare of the tumor cells. • most immunogenic tumor antigens. • shared by all tumors induced by the same type of virus
  • 13. 4- Antigens of Oncogenic viruses : DNA viruses RNA viruses
  • 14. 4- Antigens of Oncogenic viruses : • EBV: B cell lymphomas, nasopharyngeal carcinoma • HPV : cervical carcinoma • Popovaviruse and adenovirus • HPV vaccine for cervical cancer in women • Vaccination against Hepatitis B virus RNA viruses
  • 15. 4- Antigens of Oncogenic viruses : • Human T cell lymphotropic virus 1 (HTLV-1) • Adult T cell leukemia/lymphoma (ATL) DNA viruses
  • 16. 5- oncofetal antigens: • Proteins expressed at high levels in cancer cells and in normal developing fetal but not adult tissues • Silent during development, derepressed with malignant transformation • Increased in tissues and in the circulation in various inflammatory conditions • Markers for tumor diagnosis • Small quantities even in normal tissues . α-fetoprotein (AFP) Carcinoembryonic antigen (CEA:CD66) Oncofetal antigens
  • 17. 6- Tissue-specific differentiation antigens : • Tumors may express molecules that are present only on the normal cells of origin and not on cells from other tissues • Melanoma antigens : targets of CTLs (Tyrosinase) • Lymphomas :CD10 and CD20
  • 18.
  • 19. Tumors infiltrated with lymphocytes show less chance to survive than coated tumors . Lymphocytes proliferation in lymph nodes in some tumors point to an immune response tumors of those who take immune suppressors Regression of some tumors spontaneously “lymphoma ,mylanoma” High ratio of tumors of neonatals and olders who have weak immune reactions
  • 20.
  • 21. studies have focused on the antitumor response of CTLs because most tumors express class I Major Histocompatibility Complex (MHC) antigens and not MHC class II antigens. Antitumor immunity results from both:
  • 22. Macrophage/Dendritic cell attack or antigen presentation CD8 cell-mediated cytotoxicity Antibody dependent cell mediated cytotoxicity (ADCC) Natural killer cells
  • 23.
  • 24.
  • 25.
  • 26.
  • 27.   NK cell Target cell (infected or cancerous) Perforin and enzymeskiller activating receptor
  • 29.
  • 30. Immune responses often fail to check tumor growth, because these responses are ineffective or because tumors evolve to evade immune attack The immune system faces a daunting challenge if it has to be effective against malignant tumors because: Immune responses must kill all tumor cells and tumors grow rapidly. Often, the growth simply outstrips immune defenses. Immune responses against tumors may be weak because many tumor antigens are weakly immunogenic, perhaps because they differ only slightly from self-antigens. Growing tumors also develop mechanisms for evading immune responses.
  • 31.
  • 32. Evasion of Immune Responses by Tumors:  Loss of T cell recognition:  Antigen loss variants  Loss of TAPs and other molecules involved in antigen processing  Stop expressing class ∣ MHC molecules
  • 33. Explanations for why tumor cells that have lost HLA class I are not destroyed by NK cells ? Evasion of Immune Responses by Tumors: loss or down-regulation of NKG2D ligands expression lack of stimulatory cytokines and secretion of immunosuppressant cytokines producing the matrix metalloproteinase 9, which results in ICAM-1 shedding and resistance to NK cell killing
  • 34.  Tumor antigens may be inaccessible to the immune system:  Antigen masking:  The cell surface antigens :  Glycocalyx molecule (sialic acid- containing mucopolysaccharide s) Evasion of Immune Responses by Tumors:
  • 35. Tumor may engage molecules that inhibit immune response:  Involvement of PD-L1 , CTLA-4 Secreted products of tumor cells may suppress anti- tumor immune response:  TGF-β, secreted in large quantities by many tumors that Inhibits the proliferation and effector functions of lymphocytes and macrophages Evasion of Immune Responses by Tumors:
  • 36. Evasion of Immune Responses by Tumors: Tumor-associated macrophages (TAMs):
  • 37. Evasion of Immune Responses by Tumors:  Regulatory T cells: may suppress T cell responses to tumors: A population of T cells that regulate the activation or effector functions of other T cells and may be necessary to maintain tolerance to self antigens. Regulatory T cells express 𝐂𝐃𝟒+ and CD25 Depletion of regulatory T cells in tumor-bearing mouse enhances anti-tumor immunity and reduces tumor growth
  • 39.  the Fas counter attack :
  • 40.
  • 41. is the use of immune system to reject cancer . What about Chemotherapy?
  • 43. Naked mAbs Conjugated mAbs : Radiolabelled Chemolabelled Immunotoxin
  • 44.
  • 46.
  • 48. • Therapeutic cancer vaccines trigger the immune system to recognize and attack certain markers, or antigens, present on or in cancer cells . • Unlike traditional vaccines, which help to prevent disease, therapeutic cancer vaccines treat disease that is already there . • Cancer vaccines often require additional substances called adjuvants for optimal effectiveness .
  • 49. Cancer Vaccines :  Antigen vaccines  Dendritic cell vaccines  DNA vaccines .
  • 50.
  • 51.
  • 52.
  • 53.
  • 55.
  • 57.
  • 59.
  • 60.
  • 62. Cytokines are messenger molecules that help control the growth and activity of immune system cells interleukins (IL) help immune cells grow and divide more quickly interferons (IFN) boost the ability of certain immune cells to attack cancer cells