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Lecture # 9
Cells, tissues and organs
that monitor body surfaces
and internal fluid
compartments;
 react to (+) potentially
harmful antigenic substances
(infectious microorganisms,
viral entities, toxins, foreign
cells and tissues, & normaL
cells that transformed into
cancer cells)
recognized as ("non-self“).
- Organs in which immune
cells undergo maturation,
and/or differentiation, and
proliferation.
 Bone marrow and Thymus
 Sites of immune cell maturation and
differentiation.
 Tissues in which lymphocytes are generated
and differentiate into mature naïve B cells
and T cells.
 Cells here do not come into contact with an
antigen.
Primary site of
hematopoiesis.
Immune cells arise from
progenitors in the bone
marrow.
Site for B cell maturation.
Lect. 11   lymphatic tissues
Bone Marrow
 Rearrangement of genes that encode the B
cell receptor that will recognize foreign
antigen, but not foreign molecules.
 B cell receptor – membrane
immunoglobulins
 Screening process – self-reactive B cells
are eliminated
 Naïve, mature B cells (functional): released
in the bone marrow.
 seed the peripheral lymphoid tissues
 circulate in immunosurveillance
Lect. 11   lymphatic tissues
Thymus
 Flat, bilobed organ
situated above the heart
and below the thyroid
gland.
 Encapsulated organ
It increases in size until
it reaches its peak
development during
adolescence.
Becomes smaller with
age.
A
B
Lect. 11   lymphatic tissues
Lect. 11   lymphatic tissues
Pre-T cells from the bone
marrow migrate to the
cortex to undergo
maturation.
The thymus is where T
cells are "educated" to
distinguish self from
nonself.
 Construction of T cell receptor (TCR) - gene
rearrangement (a random process).
 Thymic Selection: a screening process
 only the T cells with TCRs that can recognize
antigens (TCRs beneficial to the host) will survive
and mature.
 Mature T cells leave the thymic medulla,
enter the blood stream.
 Seed the secondary lymphoid tissues
 circulate in immunosurveillance.
Table 1. Approximate Percentage of B and T Lymphocytes in
Lymphoid Organs (Junquiera et al., 2005)
Lymphoid
Organ
T Lymphocytes, (%) B Lymphocytes, (%)
Thymus 100 0
Bone marrow 10 90
Spleen 45 55
Blood 75 35
Lymph nodes, spleen,
tonsils, Peyer’s
patches, MALT, and
cutaneous
immune system
Exposure to antigens
initiates immune
responses in the
secondary lymphoid
tissues.
 Secondary lymphoid tissues provide a place
where lymphocytes can talk to each other,
and to other cells.
 They provide an environment for antigen
focusing, where lymphocytes can 'study' an
antigen, and sharpen up the immune
response by clonal expansion and affinity
maturation.
 They provide a home for lymphocytes, where
they can be available when they're needed.
LYMPH NODES
Small encapsulated
structures located at
the junction of the main
lymphatic tracts.
Serve as central
collecting points for
lymph fluid from
adjacent tissues; mainly
functions for filtration.
BONE
MARROW
APPENDIX
THYMUS
BRONCHUS
ASSOCIATED
LYMPHOID
TISSUE
TONSIL
Axillary node
Intercostal node
SPLEEN
PEYER’S PATCHES
Lumbar node
Iliac node
Inguinal node
Cervical node
LYMPH NODES
Filtering function - to
trap antigens and cells
containing antigen that
flow into them via
afferent lymphatics.
To provide a site for
clonal expansion of
lymphoid cells recruited
from the millions of
cells that enter and
leave via various routes.
Lymph fluid
 fluids and low-molecular-weight solutes
drained from the tissues (by passing out of
blood vessel walls and into the interstitial
spaces between cells).
 flowing through thin-walled lymphatic
vessels.
Afferent lymphatic vessel: the
entrance of lymph fluid which contains
the antigens and cells
Efferent lymphatic vessel: where
drained lymph fluid along with
lymphocytes exit; connected with
the thoracic duct and venous
system.
Subcapsular sinus – lined with macrophages where
antigen processing takes place.
Node: cortex, paracortex and medulla
Lect. 11   lymphatic tissues
 Cortex – mostly B cells
 Paracortex – mostly T cells; APCs; HEV (high
endothelial venules)
 Interfollicular region – T cells; APCs
 Medulla – less densely populated area but
contains some T cells, B cells and macrophages.
 Primary follicles – small rounded masses of
cells which are inactive due to absence of
antigenic stimulation. Contains mature,
resting B cells
 B cells that are not yet stimulated by an antigen
 Secondary follicles – larger masses or follicles
containing germinal centers generated
during an encounter with antigens carried by
the lymph.
 B cells are stimulated / activated by antigens
• a mass of activated B
cells
• site where B cells
proliferate and
differentiate into plasma
cells.
Plasma cell-release
antibodies
Lymphocyte
B cell
Plasma cell
SS – subcapsular space
T – trabecula
Lect. 11   lymphatic tissues
Lect. 11   lymphatic tissues
 the largest secondary lymphoid organ
 located in the upper left quadrant of the
abdomen just below the diaphragm
 a large discriminating filter
 filters out old and damaged cells and foreign
antigens from the blood
Lect. 11   lymphatic tissues
 makes up more than one-half of the total
volume;
 its function is the destruction of old red
blood cells – by splenic macrophages
 blood flows from the arterioles into the
red pulp and exits through the splenic
vein
 red matrix; composed of sinusoids and
splenic cords of cells (cords of Billroth);
vascular areas
Lect. 11   lymphatic tissues
 contains the lymphoid tissue
 arranged around arterioles in a periarterial
lymphatic sheath (PALS)
 with lymphoid follicles attached; PALS and
lymphoid follicles are surrounded by a
marginal zone.
Lect. 11   lymphatic tissues
 Periarterial lymphatic sheath (PALS)
• Contains primarily T cells; also macrophages,
plasma cells and granulocytes.
• Lymphocytes enter and leave this area by
means of the many capillary branches that
connect to the arterioles
 White marginal zone
• contains dendritic cells and macrophages; CD+4
T cells and B cells
 MALT (mucosa-associated lymphoid tissue)
1. GALT – gut-associated lymphoid tissue
 Peyer’s patches
2. BALT – bronchus-associated
lymphoid tissue
 Tonsils
Exhibit primary and secondary
lymphoid nodules
 consist of diffusely distributed lymphoid cells
and follicles that underlie all regions coated
with mucosa.
 has similar immune tissue components as the
lymph nodes and spleen.
 the main difference of MALT: immune tissue
components are not encapsulated; scattered
diffusely.
Lect. 11   lymphatic tissues
- involved in defense against pathogens that may be colonizing the gut.
Esophagus
 Payer’s patches: represents a specialized
type of MALT; form larger aggregates of
lymphoid nodules (colon, appendix, ileum)
Notice the germinal center where B-cells proliferate. These are a
major source of antibody production.
 small masses of macrophages and lymphoid
tissue found in the mucous membrane lining
of the oral and pharyngeal cavities
 Function: to respond to pathogens entering
the respiratory and
alimentary tracts
Palatine
tonsil
GC- Germinal center
The pharyngeal tonsil is distinguished from the palatine by the
presence of pseudostratified columnar epithelium (arrows).
 Cutaneous-associated lymphoid tissue
 Immune cells present in the epidermis and
dermis of the skin
 Activated Keratinocytes – produce a number
molecules that play an important role in host
defenses
 Langerhan’s cells – APC’s in the skin
 T cells – uniquely positioned to combat any
antigens that enter through the skin

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Lect. 11 lymphatic tissues

  • 2. Cells, tissues and organs that monitor body surfaces and internal fluid compartments;  react to (+) potentially harmful antigenic substances (infectious microorganisms, viral entities, toxins, foreign cells and tissues, & normaL cells that transformed into cancer cells) recognized as ("non-self“).
  • 3. - Organs in which immune cells undergo maturation, and/or differentiation, and proliferation.
  • 4.  Bone marrow and Thymus  Sites of immune cell maturation and differentiation.  Tissues in which lymphocytes are generated and differentiate into mature naïve B cells and T cells.  Cells here do not come into contact with an antigen.
  • 5. Primary site of hematopoiesis. Immune cells arise from progenitors in the bone marrow. Site for B cell maturation.
  • 7. Bone Marrow  Rearrangement of genes that encode the B cell receptor that will recognize foreign antigen, but not foreign molecules.  B cell receptor – membrane immunoglobulins  Screening process – self-reactive B cells are eliminated  Naïve, mature B cells (functional): released in the bone marrow.  seed the peripheral lymphoid tissues  circulate in immunosurveillance
  • 9. Thymus  Flat, bilobed organ situated above the heart and below the thyroid gland.  Encapsulated organ
  • 10. It increases in size until it reaches its peak development during adolescence. Becomes smaller with age. A B
  • 13. Pre-T cells from the bone marrow migrate to the cortex to undergo maturation. The thymus is where T cells are "educated" to distinguish self from nonself.
  • 14.  Construction of T cell receptor (TCR) - gene rearrangement (a random process).  Thymic Selection: a screening process  only the T cells with TCRs that can recognize antigens (TCRs beneficial to the host) will survive and mature.  Mature T cells leave the thymic medulla, enter the blood stream.  Seed the secondary lymphoid tissues  circulate in immunosurveillance.
  • 15. Table 1. Approximate Percentage of B and T Lymphocytes in Lymphoid Organs (Junquiera et al., 2005) Lymphoid Organ T Lymphocytes, (%) B Lymphocytes, (%) Thymus 100 0 Bone marrow 10 90 Spleen 45 55 Blood 75 35
  • 16. Lymph nodes, spleen, tonsils, Peyer’s patches, MALT, and cutaneous immune system Exposure to antigens initiates immune responses in the secondary lymphoid tissues.
  • 17.  Secondary lymphoid tissues provide a place where lymphocytes can talk to each other, and to other cells.  They provide an environment for antigen focusing, where lymphocytes can 'study' an antigen, and sharpen up the immune response by clonal expansion and affinity maturation.  They provide a home for lymphocytes, where they can be available when they're needed.
  • 18. LYMPH NODES Small encapsulated structures located at the junction of the main lymphatic tracts. Serve as central collecting points for lymph fluid from adjacent tissues; mainly functions for filtration. BONE MARROW APPENDIX THYMUS BRONCHUS ASSOCIATED LYMPHOID TISSUE TONSIL Axillary node Intercostal node SPLEEN PEYER’S PATCHES Lumbar node Iliac node Inguinal node Cervical node
  • 19. LYMPH NODES Filtering function - to trap antigens and cells containing antigen that flow into them via afferent lymphatics. To provide a site for clonal expansion of lymphoid cells recruited from the millions of cells that enter and leave via various routes.
  • 20. Lymph fluid  fluids and low-molecular-weight solutes drained from the tissues (by passing out of blood vessel walls and into the interstitial spaces between cells).  flowing through thin-walled lymphatic vessels.
  • 21. Afferent lymphatic vessel: the entrance of lymph fluid which contains the antigens and cells Efferent lymphatic vessel: where drained lymph fluid along with lymphocytes exit; connected with the thoracic duct and venous system. Subcapsular sinus – lined with macrophages where antigen processing takes place. Node: cortex, paracortex and medulla
  • 23.  Cortex – mostly B cells  Paracortex – mostly T cells; APCs; HEV (high endothelial venules)  Interfollicular region – T cells; APCs  Medulla – less densely populated area but contains some T cells, B cells and macrophages.
  • 24.  Primary follicles – small rounded masses of cells which are inactive due to absence of antigenic stimulation. Contains mature, resting B cells  B cells that are not yet stimulated by an antigen  Secondary follicles – larger masses or follicles containing germinal centers generated during an encounter with antigens carried by the lymph.  B cells are stimulated / activated by antigens
  • 25. • a mass of activated B cells • site where B cells proliferate and differentiate into plasma cells. Plasma cell-release antibodies Lymphocyte B cell Plasma cell
  • 26. SS – subcapsular space T – trabecula
  • 29.  the largest secondary lymphoid organ  located in the upper left quadrant of the abdomen just below the diaphragm  a large discriminating filter  filters out old and damaged cells and foreign antigens from the blood
  • 31.  makes up more than one-half of the total volume;  its function is the destruction of old red blood cells – by splenic macrophages  blood flows from the arterioles into the red pulp and exits through the splenic vein  red matrix; composed of sinusoids and splenic cords of cells (cords of Billroth); vascular areas
  • 33.  contains the lymphoid tissue  arranged around arterioles in a periarterial lymphatic sheath (PALS)  with lymphoid follicles attached; PALS and lymphoid follicles are surrounded by a marginal zone.
  • 35.  Periarterial lymphatic sheath (PALS) • Contains primarily T cells; also macrophages, plasma cells and granulocytes. • Lymphocytes enter and leave this area by means of the many capillary branches that connect to the arterioles  White marginal zone • contains dendritic cells and macrophages; CD+4 T cells and B cells
  • 36.  MALT (mucosa-associated lymphoid tissue) 1. GALT – gut-associated lymphoid tissue  Peyer’s patches 2. BALT – bronchus-associated lymphoid tissue  Tonsils Exhibit primary and secondary lymphoid nodules
  • 37.  consist of diffusely distributed lymphoid cells and follicles that underlie all regions coated with mucosa.  has similar immune tissue components as the lymph nodes and spleen.  the main difference of MALT: immune tissue components are not encapsulated; scattered diffusely.
  • 39. - involved in defense against pathogens that may be colonizing the gut. Esophagus
  • 40.  Payer’s patches: represents a specialized type of MALT; form larger aggregates of lymphoid nodules (colon, appendix, ileum)
  • 41. Notice the germinal center where B-cells proliferate. These are a major source of antibody production.
  • 42.  small masses of macrophages and lymphoid tissue found in the mucous membrane lining of the oral and pharyngeal cavities  Function: to respond to pathogens entering the respiratory and alimentary tracts Palatine tonsil
  • 44. The pharyngeal tonsil is distinguished from the palatine by the presence of pseudostratified columnar epithelium (arrows).
  • 45.  Cutaneous-associated lymphoid tissue  Immune cells present in the epidermis and dermis of the skin  Activated Keratinocytes – produce a number molecules that play an important role in host defenses  Langerhan’s cells – APC’s in the skin  T cells – uniquely positioned to combat any antigens that enter through the skin