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Title: Sept15_lecture8a_immunology


1
Lecture 8Immunology and disease how vertebrate
immunity works
2
Today
  • Lymphocytes
  • How does the right lymphocyte arise?
  • Lymphocyte receptor diversity
  • Clonal selection
  • Different types of T-cells
  • Architecture of immunity
  • Origins of adaptive immunity (next time)

3
Lymphocytes
Lymphocytes, like wasps, are genetically
programmed for exploration, but each of them
seems to be permitted a different, solitary idea.
They roam through the tissues, sensing and
monitoring. Since there are so many of them,
they can make collective guesses at almost
anything antigenic on the surface of the earth,
but they must do their work one notion at a time.
They carry specific information in the surface
receptors, presented in the form of a question
is there, anywhere out there, my particular
molecular configuration? Lewis Thomas, 1974
4
Lymphocytes
  • The phenomena of antibody formation,
    immunological memory, and the success of vaccines
    were well known before 1900
  • It wasnt until the 1950s that it became clear
    that they were all due to lymphocytes
  • Lymphocytes make up about a third of the white
    blood cells and are very different from other
    leukocytes like phagocytes
  • They are very long lived (years/decades)
  • They recirculate from blood to tissues and back
    again

5
Lymphocytes
  • Each endlessly searches for its unique target
  • When a new pathogen appears somewhere in the
    body, only one or a few out of the millions and
    millions of lymphocytes will be able to recognize
    it
  • (Think Holmes and Moriarty)

6
Lymphocytes
  • To increase the chance of seeing its nemesis,
    there are special locations where pathogens and
    lymphocytes are likely to meet
  • These are the lymphoid organs, most importantly
    the lymph nodes (or glands)
  • When you have swollen glands, say in your throat,
    theres a lot going on
  • Lymphocytes recognizing the invading virus or
    bacteria home in to do battle

7
Lymphocytes
  • Unless it takes extraordinary precautions, a
    pathogen cannot avoid coming into contact with
    the right lymphocyte sooner or later
  • That marks the beginning of the end for most
    invaders
  • At this point, via antibody production (B-cells)
    and/or various killing devices mediated
    (T-cells), the lymphocytes wage all out war on
    the pathogen
  • What is meant by the right lymphocyte?
  • How does a lymphocyte get to be right?
  • How many sorts of lymphocyte are there?

8
The right lymphocyte
  • By right were talking about receptors
  • Protein molecules on the surface of the
    lymphocytes that can bind tightly to suitably
    shapes molecules (think lock/key or cinderellas
    slipper and foot)
  • Slipper receptor
  • Foot some tiny portion of the pathogen
    (epitope)
  • Sort of similar to phagocytes, but with a crucial
    difference
  • What?

9
Phagocyte
Lymphocytes
  • Each lymphocyte carries thousands of copies of a
    single receptor
  • It can recognize only one single shape, unique to
    that lymphocyte
  • The cells of innate immunity (like phagocytes)
    carry many different types of receptor
  • All phagocytes carry the same set of 15 or more
    receptors of PAMPs

10
The right lymphocyte
  • Paul Ehrlich (1854-1915)
  • Put forward the fundamental immunological idea of
    unique receptors on cells in 1890!
  • 70 years before it was confirmed
  • He thought the bonds would be chemical but they
    turned out to be physical--just like a slipper
    and foot.
  • The indefatigable industry shown by Ehrlich
    throughout his life, his kindness and modesty,
    his lifelong habit of eating little and smoking
    incessantly 25 strong cigars a day, a box of
    which he frequently carried under one armhave
    been vividly described.

11
The right lymphocyte
  • The lymphocyte type of recognition is often
    referred to as specificity (specific immunity
    and so on)
  • To refer to the phagocyte type of innate immunity
    as non-specific is a bit unfair since they can
    distinguish perfectly well between most pathogens
    and normal body cells
  • Thats actually more than lymphocytes can do
    they have no way of knowing if the shape they
    bind to is part of a pathogen, a harmless
    symbiont, or one of the bodys own cells
  • It is shape-directed millions of shapes,
    millions of receptors
  • So, where does the diversity come from?

12
Lymphocyte receptor diversity
  • Humans have about 30,000 genes, so theres
    clearly not one gene for each of the tens of
    millions of different receptors on our T-cells
  • Instead we have a combination of three things
  • Receptors (at least B-cell ones) are composed of
    two protein chains, each different

13
Lymphocyte receptor diversity
  • Each chain is built of multiple segments that are
    combined by specially controlled recombination
    (somatic recombination)
  • Heavy chains have three regions that affect
    recognition (receptor binding), variable (V),
    diversity (D), and joining (J)
  • Light chains have only V and J regions
  • In humans there are about 100 different V genes,
    12 D genes, and 4 J genes

14
Lymphocyte receptor diversity
  • Each progenitor of a B-cell clone undergoes
    somatic recombination that brings together a
    V-D-J combination for the heavy chain
  • There are 100X12X4 4,800 V-D-J combinations
  • Similar recombination events lead to the light
    chain
  • How many possible light chain combinations are
    there?
  • And heavy plus light chain combinations?

15
Lymphocyte receptor diversity
  • 4,800 V-D-J combinations for the heavy chain
  • 400 V-J combination for the light chain
  • 1,920,000 different B-cell receptors (aka
    immunoglobulins, aka antibodies)
  • Plus there are random DNA bases added between
    segments, so the possible diversity is pretty
    much infinite
  • There are lymphocytes with around 100 million
    specificities floating around inside each of us

16
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18
Lymphocyte receptor diversity
  • 3. Finally, the six areas of the genes that code
    for the parts of the receptor that do the
    recognizing can undergo further small changes due
    to mutations within individual lymphocytes
  • The V-D-J shuffle will be different for each
    lymphocyte, and is then locked in for that
    lymphocyte
  • The glass slipper doesnt changemuch. But it
    changes a bit through somatic hypermutation
    (Haldanes idea)
  • Somatic recombination gives a combinatorial pool
    of diversity which is then fine tuned

19
Lymphocyte receptor diversity
  • Upon infection, one of the clones generated by
    VDJ recombination of might fit a pathogen epitope
    like Cinderellas slipper
  • This stimulates amplification of that clone
  • The new generation of clones increase their
    mutation rate at recognition site
  • This creates slight variation in the clone
    population, and variants with tighter binding are
    stimulated to divide more rapidly affinity
    maturation
  • Remind you of anything?

20
Lymphocyte receptor diversity
21
Clonal selection
  • The process that underlies lymphocyte specificity
    and differentiation is akin to natural selection
  • only those lymphocytes that encounter an antigen
    to which their receptor binds will be activated
    to proliferate and differentiate into effector
    cells
  • This selective mechanisms was first proposed in
    the 1950s by the Australian biologist Frank
    MacFarlane Burnet
  • at a time when nothing was known about
    lymphocyte receptors, or even that lymphocytes
    were important

22
Clonal selection
  • It wasnt until the 1960s that James Gowans
    removed lymphocytes from rats and noticed that
    their adaptive immunity disappeared
  • Peter Medawar removed the last conceptual problem
    in the 1950s by showing how the problem of immune
    responses to self is solved
  • How?

23
Clonal selection
  • Exposure to foreign tissues during embryonic
    development of mice caused them to become
    tolerent of those tissues later (I.e. no immune
    response)
  • Led to the idea that developing lymphocytes that
    are potentially self-reactive are removed before
    they can mature clonal deletion
  • these sorts of experiments are why we call MHC
    MHC
  • (major histocompatibility complex)

24
Figure 1-15
25
Figure 1-14 part 1 of 2
26
Figure 1-14 part 2 of 2
27
Clonal selection
  • The proliferation of lymphocytes after clonal
    selection leads to immunological memory
  • After a lymphocyte is activated, it takes 4-5
    days of proliferation before clonal expansion is
    complete
  • Thats why adaptive responses occur only after a
    delay of several days
  • After this primary response, some
    antigen-specific cells persist and lead to a more
    rapid and effective secondary response, and
    lasting immunity immunological memory

28
Clonal selection, adaptive immunity, and
diversity generation
  • The proliferation of lymphocytes after clonal
    selection leads to immunological memory (and
    vaccines)

29
Types of lymphocytes
  • B-cells produce immunoglobulins, molecules
    produced by adaptive immunity to dispose of
    particular threats
  • Antibody immunoglobulin free-floating B-cell
    receptor.
  • B-cells main job is to produce humoral immunity,
    to neutralize pathogens floating anywhere outside
    of cells (extracellular)
  • Thats enough about them
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