Transcript PPT 2003

LECTURE 4
The Magic of Antigen
Presentation
Feng Zhang (Ph.D)
Office：Biological Building Room 402
Email：[email protected]
CLASS I MHC MOLECULES
CLASS I I MHC MOLECULES
ANTIGEN PRESENTATION BY CLASS I
MHC MOLECULES
• the MHC I billboards advertise a “sampling”of all the proteins that
are being made inside a cell.
• Almost every cell in the human body expresses class I molecules
on its surface, although the number of molecules varies from cell
to cell.
• Killer T cells (also called cytotoxic lymphocytes or CTLs) inspect
the protein fragments displayed by class I MHC molecules.
• Consequently, almost every cell is an “open book” that can be
checked by CTLs to determine whether it has been invaded by a
virus or other parasite and should be destroyed.
• Importantly, after they have been on the surface for a short while,
the MHC billboards are replaced by new ones – so the class I MHC
display is kept current.
ANTIGEN PRESENTATION BY CLASS I I
MHC MOLECULES
ANTIGEN PRESENTING CELLS
Activated dendritic cells
• Dendritic cells can initiate the immune response
by activating virgin T cells.
• TLRs （ Toll-like receptors ） recognize general
characteristics of classes of invaders – not just a
single invader.
• The second important characteristic of the
patterns which TLRs recognize is that they
represent structural features which are so
important to the pathogen that they cannot
easily be altered by mutation to avoid detection.
Traveling dendritic cells
• It is its ability to “travel when
activated” that makes the
dendritic antigen presenting
cell so special.
• By the time it reaches a
lymph node, the mature
dendritic cell has everything
it needs to activate virgin T
cells: high levels of class I and
class II MHC molecules
loaded with the appropriate
peptides, and plenty of B7
proteins.
• Dendritic cells take a “snapshot” of what is happening on the
“front lines,” and carry this image to a lymph node – the place
where virgin T cells congregate. There the traveling dendritic cells
activate those virgin T cells whose T cell receptors recognize the
invader that is “in the picture.”
• Dendritic antigen presenting cells are sentinel cells that “sample”
antigens out in the tissues. If there is an invasion, DCs become
activated and travel to nearby lymph nodes. There they initiate
the adaptive immune response by presenting antigen collected at
the battle scene to virgin T cells.
• Activated DCs are short-lived, and the rapid turnover of these
cells insures that the “pictures” they bring to a lymph node are
continuously updated.
• The number of dendritic cells dispatched from the tissues and the
number of replacement dendritic cells recruited will depend on
the severity of the attack. Consequently, the immune system is
able to mount a response that is proportional to the danger posed
by the invasion.
Activated macrophages
• Dendritic antigen presenting cells don’t kill,
and macrophages don’t travel.
• Mature dendritic cells activate virgin T cells,
and activated macrophages mainly function
to re-stimulate experienced T cells.
Activated B cells
NON-CLASSICAL MHC MOLECULES
AND LIPID PRESENTATION
• CD1 family of proteins
• The CD1, nonclassical MHC molecules have
evolved grooves which are designed to bind
lipids.
• CD1 presentation of lipids to killer T cells
THE LOGIC OF CLASS I
MHC PRESENTATION
• One reason for class I presentation is to focus the attention of
killer T cells on infected cells, not on viruses and other pathogens
that are outside our cells in blood and tissues
• It would be extremely dangerous to have unpresented antigen
signal T cell killing.
• Most proteins made in a pathogen-infected cell remain inside the
cell, and never make their way to the cell surface. So without class
I display, many pathogen infected cells would go undetected. In
fact, part of the magic of the class I MHC display is that, in
principle, every protein of an invading pathogen can be chopped
up and displayed by class I MHC molecules for killer T cells to view.
• When a protein is chopped up into short pieces and presented by
class I MHC molecules, epitopes cannot be hidden from killer T
cells.
THE LOGIC OF CLASS I I
MHC PRESENTATION
• Antigen presenting cells only present antigen
efficiently when a battle is going on, and helper
T cells are educated not to react to our own
proteins. Consequently, both the helper T cell
and the antigen presenting cell must “agree”
that there has been an invasion before a helper
T cell can be activated. By requiring that helper T
cells only recognize presented antigen, Mother
Nature guarantees that the decision to deploy
the deadly adaptive immune system is not made
by a single cell.
MHC PROTEINS AND ORGAN
TRANSPLANTS
• “major histocompatibility complex”or MHC
• the MHC molecules are responsible for
immediate rejection of transplanted organs.
• the diversity of MHC molecules, which is so
important in protecting us from new invaders,
creates a real problem for organ
transplantation.
SUMMARY
THOUGHT QUESTIONS
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1. Mother Nature uses “fail-safe technology” to prevent inappropriate activation of
the immune system. Can you give several examples of this strategy?
2. Give several reasons why antigen presentation by class I MHC molecules is
important for the function of the adaptive immune system.
3. Why does antigen presentation by class II MHC molecules make good sense?
4. Describe the different roles that activated dendritic cells, activated macrophages,
and activated B cells playin the presentation of antigen during the course of an
infection.
5. During their lifetimes, dendritic antigen presenting cells can be “samplers,”
“travelers,” and “presenters.” Describe what DCs are doing during each of these
three stages.
6. Some peptides are presented more efficiently than others. What factors
influence the efficiency of presentation by class I and class II MHC molecules?
• 1， 造物主利用“自动保险”技术来防止免疫系统的不
恰当激活，你能就此策略举出几个例子吗？
• 2， 请就MHCⅠ类分子介导的抗原提呈对获得性没有系
统功能具有重要作用，给出几个解释理由。
• 3， MHCⅡ类分子介导的抗原提呈具有什么重要意义？
• 4， 请阐述在感染过程中，活化的树突状细胞、活化的
巨噬细胞以及活化的B细胞分别在抗原提呈中发挥的不
同作用。
• 5， 在其生命周期中，树突状抗原提呈细胞经历了“取
样者（samplers）”、“旅行者（travelers）”、和“提
呈者（presenters）”三个时相，请分别阐述树突状细
胞在各个阶段都有哪些活动表现。
• 6， 与同类分子相比较，某些多肽能更有效地被提呈，
请问影响MHCⅠ类和 Ⅱ类分子提呈效率的因素有哪些？