Cancer Immunology
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Transcript Cancer Immunology
Tumor Immunology (II):
Cancer Immunotherapy
Masoud H. Manjili
Department of Microbiology & Immunology
Goodwin Research Building-286
(804) 828-8779
Learning Objective
Learn how to harness the immune system to
kill tumors: immunotherapy
Cancer Immunotherapy
How to kill tumors without killing normal cells?
To induce an immune response against the
tumor that would discriminate between the
tumor and normal cells:
Adaptive immunity
Tumor antigens
Tumor
Specific Antigens (TSA)
Are only found on tumors
As a result of point mutations or gene rearrangement
derive from viral antigens
Tumor Associated Antigens (TAA)
Found on both normal and tumor cells, but are overexpressed
on cancer cells
Developmental antigens which become derepressed. (CEA)
Differentiation antigens are tissue specific
Altered modification of a protein could be an antigen
Tumor antigens
Tumor antigens
Immunotherapy
Adoptive T cell therapy (AIT)
Passive immunotherapy using antibodies
Active-specific immunotherapy by using
vaccines
AIT + IL-2
against
melanoma
AIT + IL-2 against melanoma
Before
After
Transfer tumor-specific T cell receptor
genes using retroviral vectors into
patients’ T cell before AIT
AIT for B cell lymphoma
Passive immunotherapy
Passive immunotherapy
Passive immunotherapy: mAbs
Herceptin: anti-HER-2/neu in breast
cancer patients
Rituximab: anti-CD20 in patients with
non-Hodgkin’s lymphoma
Bevacizumab: anti-VEGF in patients with
advanced colorectal cancer
Limitations: clearance by soluble Ags, antigenic variation of
the tumor, inefficient killing or penetration into the tumor
mass
Passive immunotherapy:
immunotoxins
Anti-CD22 Ab fused to a fragment of
Pseudomonas toxin in patients with B-cell
leukemia (hairy-cell leukemia)
Passive immunotherapy: druglinked antibodies
Anti-CD20 antibodies linked to a
radioisotope yttrium-90 in patients with
refractory B-cell lymphoma
Antibody-directed enzyme/pro-drug
therapy (ADEPT): Antibodies linked to
an enzyme that metabolizes a nontoxic
pro-drug to the active cytotoxic drug
Vaccination: cross presentation of
tumor antigens by APCs
T cell activation
T cell killer function
Signal I
T cells
Tumor
Signal II
Vaccination
Cell-based vaccines using irradiated
tumors with adjuvants such as BCG
Peptide- and protein-based vaccines
DNA vaccines
Vaccination: increase
immunogenicity of tumor cells
Vaccination
HPV vaccine for the prevention of
cervical cancer
Oncophage (gp96): a tumor-derived heat
shock protein vaccine against kidney
cancer and melanoma
Vaccination: Oncophage
Summary
Manipulation of tumors for the expression of
new antigens is a promising approach for the
induction of anti-tumor immune responses
Vaccines may be effective against residual
tumors but AIT and passive immunotherapy
have potentials for the treatment of primary
tumors
Suggested Reading
Janeway’s Immunobiology, 7th edition: Chapter
15; Pgs. 672-678