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Lymphatic System and Immune Response Overview

The document summarizes key aspects of the lymphatic system and immune response. It describes how the lymphatic system picks up fluid leaked from blood vessels and returns it to the blood while also transporting white blood cells. It then discusses the structure and function of lymphatic vessels, lymph nodes, and other lymphoid organs like the spleen, thymus, tonsils, and Peyer's patches. Finally, it provides an overview of the innate and adaptive immune response, focusing on lymphocytes, macrophages, humoral immunity, and the roles of antibodies and immunoglobulins.

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Louise Mica Lee
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0% found this document useful (0 votes)
40 views12 pages

Lymphatic System and Immune Response Overview

The document summarizes key aspects of the lymphatic system and immune response. It describes how the lymphatic system picks up fluid leaked from blood vessels and returns it to the blood while also transporting white blood cells. It then discusses the structure and function of lymphatic vessels, lymph nodes, and other lymphoid organs like the spleen, thymus, tonsils, and Peyer's patches. Finally, it provides an overview of the innate and adaptive immune response, focusing on lymphocytes, macrophages, humoral immunity, and the roles of antibodies and immunoglobulins.

Uploaded by

Louise Mica Lee
Copyright
© All Rights Reserved
We take content rights seriously. If you suspect this is your content, claim it here.
Available Formats
Download as DOCX, PDF, TXT or read online on Scribd

MODULE 5

1|Page
Lymphatic system
 Picks up fluid leaked from blood vessels and returns it to blood, disposes of
debris in the lymphatic stream, houses white blood cells involved in immunity

Lymphatic vessels
 It forms an elaborate drainage system that picks up
this excess tissue fluid which is called the lymph
 it is also called lymphatics, form a one-way system,
and lymph flows only to the heart
 It forms an elaborate drainage system that picks up
this excess tissue fluid which is called the lymph
 it is also called lymphatics, form a one-way system,
and lymph flows only to the heart
 Lymph capillaries weave between the tissue cells
and blood capillaries in the loose connective tissues of the body and absorb the
leaked fluid.

2|Page
 Lymphatic collecting vessels are larger lymphatic vessels which transports lymph
from lymphatic capillaries to the venous system through one of the largest ducts
in the thoracic regions

Lymph nodes
 It help to protect the body by removing foreign material such as bacteria and
tumor cells from lymphatic stream and by producing lymphocytes that function in
the immune response.

 Within the lymph nodes are macrophages which engulf and destroy bacteria,
viruses, and other foreign substances.
 Collection of lymphocytes are also located in the lymph nodes and respond to
foreign substances
 The center (germinal centers) enlarge when specific lymphocytes are generating
daughter cells called plasma cells which release antibodies.
 Phagocytic macrophages are located in the central medulla.

3|Page
Other lymphoid organs
SPLEEN
 Is a soft, blood rich organ that filters blood.
 It filters and cleanses blood of bacteria, viruses and other debris
 Provides a site for lymphocyte proliferation and immune response
 Destroy worn out red blood cells and return some of their breakdown products to
the liver.

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Thymus gland
 Functions at peak levels only during youth
 It produces hormone- thymosin – that
function in the programming of certain
lymphocytes so they can carry out their
protective roles in the body.

TONSILS
 small masses of lymphoid tissue that ring
the pharynx
 They trap and remove any bacteria or other
foreign pathogens entering the throat

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Peyer’s patches
 Found in the walls of intestine
 It prevent bacteria from penetrating the intestine
 Is part of collection of small lymphoid tissues –MALT (mucosa-associated
Lymphatic Tissue) which acts as sentinel to protect the upper respiratory
and digestive tracts from the attack of pathogens.

Body defenses
INNATE BODY DEFENSES
 Also called the non-specific defense system
 It refers to the mechanical barriers that cover the body surface and to the cells
and chemicals that act to protect the body from pathogens such as:
o Surface membrane barrier
* Intact skin
* The acidic pH of the skin secretions inhibits bacterial growth.
Sebum that contains chemicals that are toxic to the bacteria.
Vaginal secretions of adults in females
* The stomach mucosa secretes hydrochloric acid and protein
digesting enzymes
* Saliva and lacrimal fluid contains lysozyme
* Sticky mucus traps many microorganisms that enter Digestive and
Respiratory
o Internal defenses: cells and chemicals
* phagocytes (e.g. macrophage or neutrophil) that engulfs foreign
particles
* Natural killer cells which is consider the “police” the body in the
lymph, are unique group of lymphocytes that can lyse and kill
cancer cells and virus infected body cells .
o Inflammatory response: Is a non specific response that is triggered
whenever body tissues are injured. The four most common indicators of
inflammatory are redness, swelling, heat and pain.
o Antimicrobial proteins: Enhances the innate defenses either by attacking
microorganisms directly or by hindering their ability to reproduce.
* The most important of these is Complement protein and Interferon

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 Complement: group of plasma proteins that lyses
microorganisms, enhances phagocytosis by
opsonization and intensifies inflammatory response
 Interferon: protein released by virus infected cells that
protect uninfected tissue cells from viral takeover,
mobilize immune system
o Fever : Or abnormally high body temperature, is a systemic response to
invading microorganisms. It is regulated by a part of hypothalamus.
ADAPTIVE BODY DEFENSES
 IMMUNE RESPONSE: it involves tremendously increased internal nonspecific
defenses and provides protection that is carefully targeted against specific
antigens
 Sometimes referred as the third line of defense
 Three important aspects of adaptive defenses:
o It is antigen specific- it recognizes and acts against particular pathogens
o It is systemic- immunity is not restricted to initial site of infection
o It has memory- it recognizes and mounts even stronger attacks on
previously encountered pathogens
 The crucial cell of the adaptive system are lymphocytes and macrophages.
 Lymphocytes exist in two “flavors”:
o The B lymphocytes or B cells which produce antibodies
o The T lymphocytes or T cells oversee the humoral immunity- non-antibody-
producing lymphocytes that constitute the cell-mediated arm of the
adaptive defense system
Lymphocyte
 Originates from hematocytoblast
 T cells arise from lymphocytes that migrate to thymus where they undergo
maturation process for 2 to 3 days directed by thymosin
 B cells develop immunocompetence in bone marrow but is less is known about
the factors that regulate B cell maturation

Macrophages
 widely distributed in lymphoid organs and connective tissues
 Arise from monocytes formed in the bone marrow

7|Page
 The major role is to engulf foreign particles and rid them from the area.
 they also present the fragments of those antigens like signal flags on their own
surface where they can be recognized by immuno-competent T cells.
 They also secrete cytokines proteins that is important in the immune response.

Humoral (antibody-mediated) immune response


 Is provided by antibodies present in the body’s “humors” or fluids.
 An immunocompetent but as yet immature B lymphocyte is stimulated to
complete its development when antigens bind to its surface receptors.
 This binding event sensitizes or activates, the lymphocyte to switch on and
undergo clonal section
 The lymphocytes begins to grow and then multiplies rapidly to form an army of
cells all exactly like itself and bearing the same antigen specific receptors
 The resulting family of identical cells descended from the same ancestor cell is
called a clone, and clone formation is the primary humoral response to that
antigen
 Most of the B cell clone members, or descendants become plasma cells.
 B cell clone members that do not become plasma cells become long-lived memory
cells capable of responding to the same antigen. It is responsible for the
immunologic memory. This later immune responses called secondary humoral
response, are produced much faster, are more prolonged and more effective

Active and passive humoral immunity


 Active Immunity
- Is naturally acquired during bacterial and viral infection
- Artificially acquired through vaccine
- two benefits from vaccines:
- They spare us most of the signs and symptoms of the disease that would
otherwise occur during the primary response
- The weakened antigens are still able to stimulate antibody production and
promote immunological memory
 passive immunity
- It is conferred naturally on fetus when the mother’s antibodies cross the placenta
and enter the fetal circulation and after birth during breastfeeding.

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- Is artificially conferred when one receives immune serum or gamma globulin
- Gamma globulin is commonly administered after exposure to hepatitis. Other
immune sera are used to treat poisonous snake bites, botulism, rabies and
tetanus

Antibodies
 Also referred to as immunoglobulins, constitute the gamma globulin part of blood
proteins
 Are soluble proteins secreted by a activated B cells or by their plasma-cell
offspring in response to antigen.
 Immunoglobin Classes
 IgD
- Virtually always attached to B cell
- Believed to be cell surface receptor of immunocompetent B cell
- Important in activation of B cell
 IgM
- Attached to B cell; free plasma
- When bound to the B cell membrane, serves as antigen receptor,
first Ig released to plasma cells during primary response
- Fixes complement

9|Page
 IgG
- Most abundant antibody in plasma
- Main antibody of both primary and secondary responses, crosses
placenta and provides passive immunity to fetus.
- Fixes complement
 IgE
- Secreted by plasma cells in skin, mucosae of GI and respiratory
tract and tonsils
- Binds to mast cells and basophils, and triggers release of histamine
and other chemicals that mediate inflammation and certain allergic
response

Antibody function
 Complement
- Is the chief antibody ammunition
- It is fixed during innate defenses.
- It is activated very efficiently when it binds to antibodies attached to
cellular targets.
 Neutralization
- Occurs when antibodies bind to specific site on bacterial exotoxins or on
virus that can cause cell injury

10 | P a g e
 Agglutination
-the process causes clumping of the foreign cells
- This type of antigen-antibody reaction occurs when mismatched blood is
transfused
 Precipitation
- when the cross-linking reaction involves soluble antigenic molecules, the
resulting antigen-antibody complexes are so large that they may become
insoluble and settle out of solution.
Cellular (cell mediated) immune response
 When lymphocytes themselves defend the body
 Immunocompetent T cells are activated to form a clone by binding with a
recognized antigen
 T cells are not able to bind with free antigens instead the antigens must be
presented by a macrophage and double recognition must occur.
 A macrophage engulf an antigen and process it internally.

Different classes of T cell clones


 Cytotoxic (Killer) T cells
- Cells that specialize in killing virus infected, cancer or foreign graft cells
 Helper T cells
- T cells that act as the directors or managers of the immune system
 Regulatory T cells
- Formerly called the suppressor T cells
- Releases chemicals that suppress the body activity of both T and B cells

11 | P a g e
- They are vital in winding down and finally stopping the immune response after
an antigen has successfully inactivated
 Memory Cells
- Provide the immunological memory for each antigen encountered and enable the
body to respond quickly to subsequent invasion.

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Common questions

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B cells and T cells serve distinct but complementary roles in the adaptive immune system. B cells are primarily responsible for humoral immunity. They recognize antigens via surface receptors, undergo clonal expansion, and differentiate into plasma cells that secrete antibodies specific to those antigens. These antibodies neutralize pathogens and mark them for destruction. T cells, on the other hand, are responsible for cell-mediated immunity. They cannot bind free antigens; instead, they require antigen presentation by other cells. T cells further differentiate into helper T cells, which assist in activating B cells and cytotoxic T cells, and cytotoxic T cells, which directly kill infected or cancerous cells. The collaboration between B cells and T cells ensures a comprehensive immune response, where B cells handle circulating pathogens and T cells address intracellular infections .

Innate and adaptive immune defenses differ fundamentally in their components and mechanisms. Innate immunity, the body's first line of defense, involves non-specific barriers and cells, such as skin, mucous membranes, phagocytes (e.g., macrophages), and natural killer cells. It provides an immediate, albeit general, defense against pathogens through mechanisms like physical barriers, inflammation, and antimicrobial proteins. In contrast, adaptive immunity is antigen-specific, comprising B and T lymphocytes that recognize and target specific antigens. It operates through humoral (antibody-mediated) and cell-mediated responses, has memory for enhanced response upon re-exposure, and involves complex processes such as antigen presentation and clonal expansion. Both systems work in concert to protect the body, with innate immunity providing initial containment and adaptive immunity ensuring long-term and targeted pathogen clearance .

The thymus gland produces the hormone thymosin, which is crucial for the maturation and differentiation of T lymphocytes. During youth, the thymus is particularly active, ensuring that immature T lymphocytes develop immunocompetence, or the ability to recognize specific antigens. This process allows T cells to carry out their vital regulatory and cytotoxic roles in the immune response. The significant activity of the thymus in youth is essential for establishing a robust immune system and effective adaptive immunity .

Peyer's patches are integral components of the immune surveillance system in the intestines, forming part of the mucosa-associated lymphoid tissue (MALT). They act as sentinel structures that monitor intestinal bacteria populations and prevent pathogenic bacteria from breaching the intestinal wall. This is accomplished by educating immune cells to respond to pathogens present in the gut, thereby maintaining intestinal immune balance and preventing infections. Their position along the intestinal wall allows for the efficient sampling of antigens and pathogens, contributing to the systemic production of immune responses and mucosal immunity .

The spleen complements the functions of lymph nodes by filtering blood instead of lymph, where it removes old and damaged blood cells and pathogens, and provides a site for immune cell activation and proliferation. Unique to the spleen is its ability to recycle breakdown products of red blood cells to the liver and its role in filtering and cleansing the blood, thereby providing a systemic level of immune defense against blood-borne pathogens .

Lymph capillaries play a crucial role in maintaining fluid balance in tissues by absorbing excess fluid, known as lymph, that leaks from blood vessels into the surrounding tissues. This prevents tissue swelling and maintains fluid equilibrium. The lymphatic system, beginning with these capillaries, forms a one-way network that channels lymph toward the heart, ensuring that fluid is returned to the bloodstream and not accumulated in the tissue, thus preventing edema .

Clonal selection is a critical process in the humoral immune response where an immunocompetent B lymphocyte encounters and binds to its specific antigen via surface receptors. This binding event activates the lymphocyte and initiates clonal expansion, where the cell proliferates to form a clone of identical cells equipped with antigen-specific receptors. Most of these cells differentiate into plasma cells, which secrete antibodies targeting the antigen, while others become memory cells providing long-term immunity. Clonal selection ensures a tailored and amplified immune response, allowing for effective antigen neutralization and long-lasting immunological memory .

Lymph nodes serve a dual role in the immune response by filtering harmful substances from the lymph and housing lymphocytes that contribute to the immune response. Structurally, lymph nodes contain germinal centers, where lymphocytes proliferate and produce antibodies, macrophages that engulf pathogens, and a medullary region where phagocytic activity occurs. This architecture efficiently enables lymph nodes to trap foreign materials such as bacteria and tumor cells and coordinate an immune response through lymphocyte activation and antibody production .

Passive immunity is conferred through the transfer of antibodies from one individual to another, providing immediate but temporary protection. This transfer can occur naturally, such as the transfer of maternal antibodies to the fetus through the placenta or to infants through breastfeeding. Artificially, it can be conferred via the administration of immune serum or gamma globulin, often used in instances requiring immediate protection, like after exposure to hepatitis, snake bites, or toxins like botulism, rabies, and tetanus. This type of immunity is crucial in providing rapid defense without the time required for the development of an active immune response .

Antibodies neutralize pathogens through mechanisms such as precipitation and agglutination. In precipitation, antibodies cross-link soluble antigens, forming large complexes that become insoluble and precipitate out of solution, facilitating removal by phagocytosis. In agglutination, antibodies cause clumping of cellular antigens, such as bacteria or mismatched blood cells, enhancing their phagocytosis and clearance from the bloodstream. These mechanisms prevent the spread of pathogens, enhance phagocytic removal, and provide a targeted immune response, reducing the likelihood of pathogen evasion and persistence .

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