IMMUNOLOGY
Bios 328
a textbook-based study of immunology
Spring 2003
http://www.lehigh.edu/~sk08/Courses/Bios328/mainpage.htm
Immunogen, antigen, epitope, hapten
•Immunogen: a stimulus that
produces a humoral or cell-
mediated immune response
•Antigen: any substance that
binds specifically to an antibody or
a T-cell receptor
Immunogen, antigen, epitope, hapten
•All immunogens are antigens but
not all antigens are immunogens
•Some very small molecules
called haptens can bind to Ab’s
or TCR’s but they cannot initiate
an immune response…
Immunogen, antigen, epitope, hapten
•Immunogen: a stimulus that produces a
humoral or cell-mediated immune response
•Antigen: any substance that binds
specifically to an antibody or a T-cell receptor
•Epitope: the portion of an antigen that is
recognized and bound by an Ab or TCR/MHC
complex (aka antigenic determinant)
•Hapten: a low molecular weight molecule that
can be made immunogenic by conjugation to a
suitable carrier
Immunogen, antigen, epitope, hapten
• Paratope…
• Paratope: “The site in the variable (V)
domain of an antibody or T-cell receptor
that binds to an epitope on an antigen
The key event…
The basis of immunogenicity…
•Foreignness
•Molecular size
•Chemical composition and
heterogeneity
•Degradability
The key event…
A processed antigen in an MHC is seen
by a TCR.
The TCR asks the MHC, “Are you me?”
and receives an affirmative answer, “Yes.”
The TCR asks the processed antigen,
“Are you me?” and receives the negative
answer, “No!”
Thus, the processed antigen is seen as
“not-self,” i. e., “foreign.”
The key event…
A processed antigen in an MHC is seen by a TCR. This
“viewing” occurs in the ternary complex.
The TCR asks the MHC, “Are you me?” and receives an affirmative
answer, “Yes.” Here the TCR looks at the MHC
histotope.
The TCR asks the processed antigen, “Are you me?” and receives
the negative answer, “No!” Here the TCR uses its
paratope and looks at the epitope.
The key event…
A processed antigen in an MHC is seen by a TCR.
The TCR asks the MHC, “Are you me?” and receives an affirmative
answer, “Yes.”
The TCR asks the processed antigen, “Are you me?” and receives
the negative answer, “No!”
But what if the TCR asks the processed antigen,
“Are you me?” and receives the answer, “Yes.” TCR’s
which can see “self” are eliminated in a process called
clonal deletion.
Clonal deletion assures that TCR’s don’t see “self.”
The basis of immunogenicity…
•Foreignness
•Molecular size
•Chemical composition and
heterogeneity
•Degradability
Experimental systems…
Epitopes for B-cells versus T-cells
By examining myoglobin one can see that the Ag’s seen by B-
cells and T-cells are different. B-cells see a continuous or
discontinuous series of amino acids; by some circumstance,
amino acid residue 109 has never been a part of an epitope for
any monoclonal antibody; yet residue 109 is always part of the
processed antigen seen by a TCR.
Presentation of processed antigen…
Presentation of processed antigen…
There are two general classes of antigens
Exogenous (external)
Endogenous (internal)
There are two general classes of antigens
Exogenous: presented by Antigen
Presenting Cells (APC’s). These are
macrophages, B-cells, and some
dendritic cells
Endogenous: typically peptides derived
from any protein; an infected cell
displays “not-self” proteins and is, thus, an
“altered self cell”
There are two general classes of antigens
Exogenous: these antigens are
presented in MHC-II; they are seen
by T-cells with a TCR and an
associated protein called CD4
Endogenous: these antigens are
presented by MHC-I; they are seen
by T-cells with a TCR and an
associated protein called CD8
There are two classes of T-cells
TH have CD4 which interacts with
MHC-II; thus, CD4+
T-cells are
“MHC-II restricted.”
TH cells are “helper cells” that send
signals (via cytokines and surface
proteins) to other cells of the immune
system. The TH cells function as the
“brain” of the immune system.
There are two classes of T-cells
TC have CD8 which interacts with
MHC-I; thus, CD8+
T-cells are “MHC-
I restricted.”
TC cells become cytotoxic T
lymphocytes (CTL’s) which attack
“altered self-cells (e. g., infected
cells.) “Altered self-cells” are also
called “target cells.” They are the
targets for the CTL’s cytotoxicity.
Experimental systems…
viz. “haptens”
Hapten: a low molecular-weight
molecule that can be made immunogenic
by conjugation to a suitable carrier…
Haptens…
Haptens…
Summary…
• Immunogen
• Antigen
• Epitope
• Hapten
• Foreignness
• Molecular size
• Chemical compo-
sition and
heterogeneity
• Degradability
Experimental systems…
viz. “adjuvants”
Adjuvants: A substance that non-
specifically enhances the immune
response to an antigen
•Prolong the presence of the antigen
•Enhance production of “co-stimulatory” signals
•Induce granuloma formation (i.e., an accumulation of
macrophages)
•Non-specifically stimulate lymphocytes

Immunogen, antiiiigen, epitope, hapten.ppt

  • 1.
    IMMUNOLOGY Bios 328 a textbook-basedstudy of immunology Spring 2003 http://www.lehigh.edu/~sk08/Courses/Bios328/mainpage.htm
  • 2.
    Immunogen, antigen, epitope,hapten •Immunogen: a stimulus that produces a humoral or cell- mediated immune response •Antigen: any substance that binds specifically to an antibody or a T-cell receptor
  • 3.
    Immunogen, antigen, epitope,hapten •All immunogens are antigens but not all antigens are immunogens •Some very small molecules called haptens can bind to Ab’s or TCR’s but they cannot initiate an immune response…
  • 4.
    Immunogen, antigen, epitope,hapten •Immunogen: a stimulus that produces a humoral or cell-mediated immune response •Antigen: any substance that binds specifically to an antibody or a T-cell receptor •Epitope: the portion of an antigen that is recognized and bound by an Ab or TCR/MHC complex (aka antigenic determinant) •Hapten: a low molecular weight molecule that can be made immunogenic by conjugation to a suitable carrier
  • 5.
    Immunogen, antigen, epitope,hapten • Paratope… • Paratope: “The site in the variable (V) domain of an antibody or T-cell receptor that binds to an epitope on an antigen
  • 6.
  • 7.
    The basis ofimmunogenicity… •Foreignness •Molecular size •Chemical composition and heterogeneity •Degradability
  • 8.
    The key event… Aprocessed antigen in an MHC is seen by a TCR. The TCR asks the MHC, “Are you me?” and receives an affirmative answer, “Yes.” The TCR asks the processed antigen, “Are you me?” and receives the negative answer, “No!” Thus, the processed antigen is seen as “not-self,” i. e., “foreign.”
  • 9.
    The key event… Aprocessed antigen in an MHC is seen by a TCR. This “viewing” occurs in the ternary complex. The TCR asks the MHC, “Are you me?” and receives an affirmative answer, “Yes.” Here the TCR looks at the MHC histotope. The TCR asks the processed antigen, “Are you me?” and receives the negative answer, “No!” Here the TCR uses its paratope and looks at the epitope.
  • 10.
    The key event… Aprocessed antigen in an MHC is seen by a TCR. The TCR asks the MHC, “Are you me?” and receives an affirmative answer, “Yes.” The TCR asks the processed antigen, “Are you me?” and receives the negative answer, “No!” But what if the TCR asks the processed antigen, “Are you me?” and receives the answer, “Yes.” TCR’s which can see “self” are eliminated in a process called clonal deletion. Clonal deletion assures that TCR’s don’t see “self.”
  • 12.
    The basis ofimmunogenicity… •Foreignness •Molecular size •Chemical composition and heterogeneity •Degradability
  • 15.
  • 16.
    Epitopes for B-cellsversus T-cells By examining myoglobin one can see that the Ag’s seen by B- cells and T-cells are different. B-cells see a continuous or discontinuous series of amino acids; by some circumstance, amino acid residue 109 has never been a part of an epitope for any monoclonal antibody; yet residue 109 is always part of the processed antigen seen by a TCR.
  • 17.
  • 18.
  • 19.
    There are twogeneral classes of antigens Exogenous (external) Endogenous (internal)
  • 20.
    There are twogeneral classes of antigens Exogenous: presented by Antigen Presenting Cells (APC’s). These are macrophages, B-cells, and some dendritic cells Endogenous: typically peptides derived from any protein; an infected cell displays “not-self” proteins and is, thus, an “altered self cell”
  • 21.
    There are twogeneral classes of antigens Exogenous: these antigens are presented in MHC-II; they are seen by T-cells with a TCR and an associated protein called CD4 Endogenous: these antigens are presented by MHC-I; they are seen by T-cells with a TCR and an associated protein called CD8
  • 22.
    There are twoclasses of T-cells TH have CD4 which interacts with MHC-II; thus, CD4+ T-cells are “MHC-II restricted.” TH cells are “helper cells” that send signals (via cytokines and surface proteins) to other cells of the immune system. The TH cells function as the “brain” of the immune system.
  • 23.
    There are twoclasses of T-cells TC have CD8 which interacts with MHC-I; thus, CD8+ T-cells are “MHC- I restricted.” TC cells become cytotoxic T lymphocytes (CTL’s) which attack “altered self-cells (e. g., infected cells.) “Altered self-cells” are also called “target cells.” They are the targets for the CTL’s cytotoxicity.
  • 24.
    Experimental systems… viz. “haptens” Hapten:a low molecular-weight molecule that can be made immunogenic by conjugation to a suitable carrier…
  • 25.
  • 26.
  • 27.
    Summary… • Immunogen • Antigen •Epitope • Hapten • Foreignness • Molecular size • Chemical compo- sition and heterogeneity • Degradability
  • 28.
    Experimental systems… viz. “adjuvants” Adjuvants:A substance that non- specifically enhances the immune response to an antigen •Prolong the presence of the antigen •Enhance production of “co-stimulatory” signals •Induce granuloma formation (i.e., an accumulation of macrophages) •Non-specifically stimulate lymphocytes