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LYMPHATIC SYSTEM AND IMMUNITY

This page will provide information to understand the function of the lymphatic system and our body's immune process.  There are also extensive links for further research.  Because of our impaired  lymph system, those of us with lymphedema should be informed as to how we fight and/or resist infections and why we are so susceptible to them. 

Pat O'Connor

June 18, 2008

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Table of Contents

The Lymphatic System | Immunity | General Defenses | Specific Defenses

Antibody-mediated Immunity | Blood Types, Rh, and Antibodies

Organ Transplants and Antibodies | Allergies and Disorders of the Immune System

The Lymphatic System

The lymphatic system is composed of lymph vessels, lymph nodes, and organs. The functions of this system include the absorption of excess fluid and its return to the blood stream, absorption of fat (in the villi of the small intestine) and the immune system function.

Lymph vessels are closely associated with the circulatory system vessels. Larger lymph vessels are similar to veins. Lymph capillaries are scatted throughout the body. Contraction of skeletal muscle causes movement of the lymph fluid through valves.

Lymph organs include the bone marrow, lymph nodes, spleen, and thymus. Bone marrow contains tissue that produces lymphocytes. B-lymphocytes (B-cells) mature in the bone marrow. T-lymphocytes (T-cells) mature in the thymus gland. Other blood cells such as monocytes and leukocytes are produced in the bone marrow. Lymph nodes are areas of concentrated lymphocytes and macrophages along the lymphatic veins. The spleen is similar to the lymph node except that it is larger and filled with blood. The spleen serves as a reservoir for blood, and filters or purifies the blood and lymph fluid that flows through it. If the spleen is damaged or removed, the individual is more susceptible to infections. The thymus secretes a hormone, thymosin, that causes pre-T-cells to mature (in the thymus) into T-cells.

Immunity

Immunity is the body's capability to repel foreign substances and cells. The nonspecific responses are the first line of defense. Highly specific responses are the second line of defense and are tailored to an individual threat. The immune response includes both specific and nonspecific components. Nonspecific responses block the entry and spread of disease-causing agents. Antibody-mediated and cell-mediated responses are two types of specific response. The immune system is associated with defense against disease-causing agents, problems in transplants and blood transfusions, and diseases resulting from over-reaction (autoimmune, allergies) and under-reaction (AIDS).

General Defenses


Barriers to entry are the skin and mucous membranes. The skin is a passive barrier to infectious agents such as bacteria and viruses. The organisms living on the skin surface are unable to penetrate the layers of dead skin at the surface. Tears and saliva secrete enzymes that breakdown bacterial cell walls. Skin glands secrete chemicals that retard the growth of bacteria. Mucus membranes lining the respiratory, digestive, urinary, and reproductive tracts secrete mucus that forms another barrier. Physical barriers are the first line of defense.

When microorganisms penetrate skin or epithelium lining respiratory, digestive, or urinary tracts, inflammation results. Damaged cells release chemical signals such as histamine that increase capillary blood flow into the affected area (causing the areas to become heated and reddened). The heat makes the environment unfavorable for microbes, promotes healing, raises mobility of white blood cells, and increases the metabolic rate of nearby cells. Capillaries pass fluid into interstitial areas, causing the infected/injured area to swell. Clotting factors trigger formation of many small blood clots. Finally, monocytes (a type of white blood cell) clean up dead microbes, cells, and debris.

The inflammatory response is often strong enough to stop the spread of disease-causing agents such as viruses, bacteria, and fungi. The response begins with the release of chemical signals and ends with cleanup by monocytes. If this is not enough to stop the invaders, the complement system and immune response act.

Protective proteins that are produced in the liver include the complement system of proteins. The complement system proteins bind to a bacterium and open pores in its membrane through which fluids and salt move, swelling and bursting the cell.

The complement system directly kills microbes, supplements inflammatory response, and works with the immune response. It complements the actions of the immune system. Complement proteins are made in the liver and become active in a sequence (C1 activates C2, etc.). The final five proteins form a membrane-attack complex (MAC) that embeds itself into the plasma membrane of the attacker. Salts enter the invader, facilitating water to cross the membrane, swelling and bursting the microbe. Complement also functions in the immune response by tagging the outer surface of invaders for attack by phagocytes.


The complement system of proteins and their functioning. Image from Purves et al., Life: The Science of Biology, 4th Edition, by Sinauer Associates (www.sinauer.com) and WH Freeman (www.whfreeman.com), used with permission.

Interferon is a species-specific chemical produced by cells that are viral attack. It alerts nearby cells to prepare for a virus. The cells that have been contacted by interferon resist all viral attacks.

Specific Defenses

The immune system also generates specific responses to specific invaders.

The immune system is more effective than the nonspecific methods, and has a memory component that improves response time when an invader of the same type (or species) is again encountered.

Immunity results from the production of antibodies specific to a given antigen (antibody-generators, located on the surface of an invader). Antibodies bind to the antigens on invaders and kill or inactivate them in several ways. Most antibodies are themselves proteins or are a mix of protein and polysaccharides. Antigens can be any molecule that causes antibody production.

Lymphocytes

White blood cells known as lymphocytes arise from by mitosis of stem cells in the bone marrow. Some lymphocytes migrate to the thymus and become T cells that circulate in the blood and are associated with the lymph nodes and spleen. B cells remain in the bone marrow and develop before moving into the circulatory and lymph systems. B cells produce antibodies.

Antibody-mediated (humoral immunity)

Antibody mediated (humoral) immunity is regulated by B cells and the antibodies they produce. Cell-mediated immunity is controlled by T cells. Antibody-mediated reactions defend against invading viruses and bacteria. Cell-mediated immunity concerns cells in the body that have been infected by viruses and bacteria, protect against parasites, fungi, and protozoans, and also kill cancerous body cells.

Antibody-mediated Immunity | Back to Top
Stages in this process are:

antigen detection
activation of helper T cells
antibody production by B cells
Each stage is directed by a specific cell type.

Macrophages

Macrophages are white blood cells that continually search for foreign (nonself) antigenic molecules, viruses, or microbes. When found, the macrophages engulfs and destroys them. Small fragments of the antigen are displayed on the outer surface of the macrophage plasma membrane.

Helper T Cells

Helper T cells are macrophages that become activated when they encounter the antigens now displayed on the macrophage surface. Activated T cells identify and activate B cells.

B Cells

B cells divide, forming plasma cells and B memory cells. Plasma cells make and release between 2000 and 20,000 antibody molecules per second into the blood for the next four or five days. B memory cells live for months or years, and are part of the immune memory system.

Antibodies

Antibodies bind to specific antigens in a lock-and-key fashion, forming an antigen-antibody complex. Antibodies are a type of protein molecule known as immunoglobulins. There are five classes of immunoglobulins: IgG, IgA, IgD, IgE, and IgM.

The five classes of Ig antibodies. Image from Purves et al., Life: The Science of Biology, 4th Edition, by Sinauer Associates (www.sinauer.com) and WH Freeman (www.whfreeman.com), used with permission.

Antibodies are Y-shaped molecules composed of two identical long polypeptide (Heavy or H chains) and two identical short polypeptides (Light or L chains). Function of antibodies includes:

Recognition and binding to antigens
Inactivation of the antigen

A unique antigenic determinant recognizes and binds to a site on the antigen, leading to the destruction of the antigen in several ways. The ends of the Y are the antigen-combining site that is different for each antigen. Click here to learn more about the different classes of antibodies.

Helper T Cells

Helper T cells activate B cells that produce antibodies. Supressor T cells slow down and stop the immune response of B and T cells, serving as an off switch for the immune system. Cytotoxic (or killer) T cells destroy body cells infected with a virus or bacteria. Memory T cells remain in the body awaiting the reintroduction of the antigen.

A cell infected with a virus will display viral antigens on its plasma membrane. Killer T cells recognize the viral antigens and attach to that cell's plasma membrane. The T cells secrete proteins that punch holes in the infected cell's plasma membrane. The infected cell's cytoplasm leaks out, the cell dies, and is removed by phagocytes. Killer T cells may also bind to cells of transplanted organs.

The immune system is the major component of this defense. Lymphocytes, monocytes, lymph organs, and lymph vessels make up the system. The immune system is able to distinguish self from non-self. Antigens are chemicals on the surface of a cell. All cells have these. The immune system checks cells and identifies them as "self" or "non-self". Antibodies are proteins produced by certain lymphocytes in response to a specific antigen. B-lymphocytes and T-lymphocytes produce the antibodies. B-lymphocytes become plasma cells which then generate antibodies. T-lymphocytes attack cells which bear antigens they recognize. They also mediate the immune response.

The immune system and memory of infections

Secondary immunity, the resistance to certain diseases after having had them once, results from production of Memory B and T cells during the first exposure to the antigen. A second exposure to the same antigen produces a more massive and faster response. The secondary response is the basis for vaccination.

Vaccination

Vaccination is a term derived from the Latin vacca (cow, after the cowpox material used by Edward Jenner in the first vaccination). A vaccine stimulates the antibody production and formation of memory cells without causing of the disease. Vaccines are made from killed pathogens or weakened strains that cause antibody production but not the disease. Recombinant DNA techniques can now be used to develop even safer vaccines.

The immune system can develop long-term immunity to some diseases. Man can use this to develop vaccines, which produce induced immunity. Active immunity develops after an illness or vaccine. Vaccines are weakened (or killed) viruses or bacteria that prompt the development of antibodies. Application of biotechnology allows development of vaccines that are the protein (antigen) which in no way can cause the disease. Passive immunity is the type of immunity when the individual is given antibodies to combat a specific disease. Passive immunity is short-lived.

Blood Types, Rh, and Antibodies

There are 30 or more known antigens on the surface of blood cells. These form the blood groups or blood types. In a transfusion, the blood groups of the recipient and donor must be matched. If improperly matched, the recipient's immune system will produce antibodies causing clotting of the transfused cells, blocking circulation through capillaries and producing serious or even fatal results.

ABO blood types are determined by a gene, I (for isoagglutinin). There are three alleles, IA, IB and IO. Proteins produced by the A and B alleles are antigenic. Individuals with blood type A have the A antigen on the surface of their red blood cells, and antibodies to type B blood in their plasma. People with blood type B have the B antigen on their blood cells and antibodies against type A in their plasma. Individuals with type AB blood produce have antigens for A and B on their cell surfaces and no antibodies for either blood type A or B in their plasma. Type O individuals have no antigens on their red blood cells but antigens to both A and B are in their plasma.

People with type AB blood can receive blood of any type. Those with type O blood can donate to anyone. If a transfusion is made between an incompatible donor and recipient, the recipient's blood will undergo a cascade of events. Reaction of antigens on cells and antibodies in plasma will produce clumping that clogs capillaries, other cells burst, releasing hemoglobin that can crystallize in the kidney and lead to kidney failure.

The Rh (for the rhesus monkey in which it was discovered) blood group is made up of those Rh positive (Rh+) individuals who can make the Rh antigen and those Rh negative (Rh-) who cannot.

Hemolytic disease of the newborn (HDN) results from Rh incompatibility between an Rh- mother and Rh+ fetus. Rh+ blood from the fetus enters the mother's system during birth, causing her to produce Rh antibodies. The first child is usually not affected, however subsequent Rh+ fetuses will cause a massive secondary reaction of the maternal immune system. To prevent HDN, Rh- mothers are given an Rh antibody during the first pregnancy with an Rh+ fetus and all subsequent Rh+ fetuses.

Organ Transplants and Antibodies

Success of organ transplants and skin grafts requires a matching of histocompatibility antigens that occur on all cells in the body. Chromosome 6 contains a cluster of genes known as the human leukocyte antigen complex (HLA) that are critical to the outcome of such procedures. The array of HLA alleles on either copy of our chromosome 6 is known as a haplotype.

The large number of alleles involved mean no two individuals, even in a family, will have the same identical haplotype. Identical twins have a 100% HLA match. The best matches are going to occur within a family. The preference order for transplants is identical twin > sibling > parent > unrelated donor. Chances of an unrelated donor matching the recipient range between 1 in 100,000-200,000. Matches across racial or ethnic lines are often more difficult. When HLA types are matched survival of transplanted organs dramatically increases.

Allergies and Disorders of the Immune System

The immune system can overreact, causing allergies or autoimmune diseases. Likewise, a suppressed, absent, or destroyed immune system can also result in disease and death.

Allergies result from immune system hypersensitivity to weak antigens that do not cause an immune response in most people. Allergens, substances that cause allergies, include dust, molds, pollen, cat dander, certain foods, and some medicines (such as penicillin). Up to 10% of the US population suffer from at least one allergy.

After exposure to an allergen, some people make IgE antibodies as well as B and T memory cells. Subsequent exposure to the same allergen causes a massive secondary immune response that releases plenty of IgE antibodies. These bind to mast cells found usually in connective tissues surrounding blood vessels. Mast cells then release histamine, which starts the inflammatory response. In some individuals the histamine release causes life-threatening anaphylaxis or anaphylactic shock.

The immune system usually distinguishes "self" from "nonself". The immune system learns the difference between cells of the body and foreign invaders. Autoimmune diseases result when the immune system attacks and destroys cells and tissues of the body. Juvenile diabetes, Grave's disease, Multiple sclerosis, Systemic lupus erythematosus, and Rheumatoid arthritis are some of the autoimmune diseases.

Myasthenia gravis (MG) is a muscle weakness caused by destruction of muscle-nerve connections. Multiple sclerosis (MS) is caused by antibodies attacking the myelin of nerve cells. Systemic lupus erythematosis (SLE) has the person forming a series of antibodies to their own tissues, such as kidneys (the leading cause of death in SLE patients) and the DNA in their own cellular nuclei. In systemic lupus erythematosus (SLE), the immune system attacks connective tissues and major organs of the body. Rheumatoid Arthritis; sufferers have damage to their joints. Some evidence supports Type I diabetes as an auto immune disease. Juvenile diabetes results from the destruction of insulin-producing cells in the pancreas.

Immunodeficiency diseases result from the lack or failure of one or more parts of the immune system. Affected individuals are susceptible to diseases that normally would not bother most people. Genetic disorders, Hodgkin's disease, cancer chemotherapy, and radiation therapy can cause immunodeficiency diseases.

Severe Combined Immunodeficiency (SCID) results from a complete absence of the cell-mediated and antibody-mediated immune responses. Affected individuals suffer from a series of seemingly minor infections and usually die at an early age. A small group suffering from adenosine deaminase (ADA) deficiency, a type of SCID, are undergoing gene therapy to provide them with normal copies of the defective gene.

Acquired Immunodeficiency Syndrome (AIDS) is currently receiving the most attention among the immunodeficiency diseases. AIDS is a collection of disorders resulting from the destruction of T cells by the Human Immunodeficiency Virus (HIV), a retrovirus. When HIV replicates in the human T cells, it buds from the T cell plasma membrane encased in a coat derived from the T cell plasma membrane. HIV selectively infects and kills T4 helper cells. The viral RNA is converted into DNA by the enzyme reverse transcriptase; this DNA can become incorporated into a human chromosome for months or years.

When the infected T cell is needed in the immune response, the viral genes are activated and the virus replicates, killing the infected cell and producing a new round on T4 cell infection. Gradually the number of T4 cells, the master on switch for the immune system, decline. The immune response grows less powerful, eventually failing. Premature death results from a series of rare diseases (such as fungal pneumonia and Kaposi's sarcoma, a rare cancer) that overwhelm the body and its compromised immune system.

Text ©1992, 1994, 1997, 1998, 2000, 2001, by M.J. Farabee, all rights reserved.

Use for educational purposes is encouraged


http://www.emc.maricopa.edu/faculty/farabee/BIOBK/BioBookIMMUN.html

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The Immune System

The Body's First Line of Defense
The immune system is a complex of organs--highly specialized cells and even a circulatory system separate from blood vessels--all of which work together to clear infection from the body.

The organs of the immune system, positioned throughout the body, are called lymphoid organs. The word "lymph" in Greek means a pure, clear stream--an appropriate description considering its appearance and purpose.

 
Diagram: Lymphatic vessels
Lymphatic vessels form a circulatory system that operates in close partnership with blood circulation.
Lymphatic vessels and lymph nodes are the parts of the special circulatory system that carries lymph, a transparent fluid containing white blood cells, chiefly lymphocytes.

 
Lymph bathes the tissues of the body, and the lymphatic vessels collect and move it eventually back into the blood circulation. Lymph nodes dot the network of lymphatic vessels and provide meeting grounds for the immune system cells that defend against invaders. The spleen, at the upper left of the abdomen, is also a staging ground and a place where immune system cells confront foreign microbes.  
Diagram: Immune system organs
Organs and tissues of the immune system dot the body in a protective network of barriers to infection.

Pockets of lymphoid tissue are in many other locations throughout the body, such as the bone marrow and thymus. Tonsils, adenoids, Peyer's patches, and the appendix are also lymphoid tissues.

Both immune cells and foreign molecules enter the lymph nodes via blood vessels or lymphatic vessels. All immune cells exit the lymphatic system and eventually return to the bloodstream. Once in the bloodstream, lymphocytes are transported to tissues throughout the body, where they act as sentries on the lookout for foreign antigens.

How the Immune System Works
Cells that will grow into the many types of more specialized cells that circulate throughout the immune system are produced in the bone marrow. This nutrient-rich, spongy tissue is found in the center shafts of certain long, flat bones of the body, such as the bones of the pelvis. The cells most relevant for understanding vaccines are the lymphocytes, numbering close to one trillion.

The two major classes of lymphocytes are B cells, which grow to maturity in the bone marrow, and T cells, which mature in the thymus, high in the chest behind the breastbone.

B cells produce antibodies that circulate in the blood and lymph streams and attach to foreign antigens to mark them for destruction by other immune cells.

B cells are part of what is known as antibody-mediated or humoral immunity, so called because the antibodies circulate in blood and lymph, which the ancient Greeks called, the body's "humors."

 
B cells

B cells become plasma cells, which produce antibodies when a foreign antigen triggers the immune response.

Certain T cells, which also patrol the blood and lymph for foreign invaders, can do more than mark the antigens; they attack and destroy diseased cells they recognize as foreign. T lymphocytes are responsible for cell-mediated immunity (or cellular immunity). T cells also orchestrate, regulate and coordinate the overall immune response. T cells depend on unique cell surface molecules called the major histocompatibility complex (MHC) to help them recognize antigen fragments.
Antigens
Antibodies produced by cells of the immune system recognize foreign antigens and mark them for destruction.
Antibodies

The antibodies that B cells produce are basic templates with a special region that is highly specific to target a given antigen. Much like a car coming off a production line, the antibody's frame remains constant, but through chemical and cellular messages, the immune system selects a green sedan, a red convertible or a white truck to combat this particular invader.

However, in contrast to cars, the variety of antibodies is very large. Different antibodies are destined for different purposes. Some coat the foreign invaders to make them attractive to the circulating scavenger cells, phagocytes, that will engulf an unwelcome microbe.

When some antibodies combine with antigens, they activate a cascade of nine proteins, known as complement, that have been circulating in inactive form in the blood. Complement forms a partnership with antibodies, once they have reacted with antigen, to help destroy foreign invaders and remove them from the body. Still other types of antibodies block viruses from entering cells.

T Cells
T cells have two major roles in immune defense. Regulatory T cells are essential for orchestrating the response of an elaborate system of different types of immune cells.

 

Helper T cells, for example, also known as CD4 positive T cells (CD4+ T cells), alert B cells to start making antibodies; they also can activate other T cells and immune system scavenger cells called macrophages and influence which type of antibody is produced.

Certain T cells, called CD8 positive T cells (CD8+ T cells), can become killer cells that attack and destroy infected cells. The killer T cells are also called cytotoxic T cells or CTLs (cytotoxic lymphocytes).

T cells
T lymphocytes become CD4+ or helper T cells, or they can become CD8+ cells, which in turn can become killer T cells, also called cytotoxic T cells.

Immune system process
Activation of helper T cells

Activation_T cells

After it engulfs and processes an antigen, the macrophage displays the antigen fragments combined with a Class II MHC protein on the macrophage cell surface. The antigen-protein combination attracts a helper T cell, and promotes its activation.

Activation of cytotoxic T cells

Activation

After a macrophage engulfs and processes an antigen, the macrophage displays the antigen fragments combined with a Class I MHC protein on the macrophage cell surface. A receptor on a circulating, resting cytotoxic T cell recognizes the antigen-protein complex and binds to it. The binding process and a helper T cell activate the cytotoxic T cell so that it can attack and destroy the diseased cell.

Activation of B cells to make antibody

Activation of B Cells to make antibody

A B cell uses one of its receptors to bind to its matching antigen, which the B cell engulfs and processes. The B cell then displays a piece of the antigen, bound to a Class II MHC protein, on the cell surface. This whole complex then binds to an activated helper T cell. This binding process stimulates the transformation of the B cell into an antibody-secreting plasma cell.

*Link no longer available - from The National Institutes of health

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Regional lymphatic immunity in melanoma.

Nov 2011

Grotz TE, Mansfield AS, Jakub JW, Markovic SN.

Source

aDivision of Surgery bDivision of Hematology/Department of Internal Medicine cDepartment of Oncology at Mayo Clinic, Rochester, Minnesota, USA.

Abstract

Melanoma is an immunogenic tumor that has developed methods to successfully evade immune recognition, while paradoxically spreading through the lymphatic system. Increasing evidence supports that melanoma-derived factors suppress regional immunity within the host. At a very early stage, melanoma communicates with the tumor-draining lymph nodes, and prepares them for seeding of metastatic disease by stimulating lymphangiogenesis and downregulation of the sentinel lymph node immunity well before the malignant cells arrive. Investigations have demonstrated that the induction of suppressor cells, peripheral tolerance, and a less tumor-responsive Th2 cytokine environment may provide a hospitable environment for subsequent lymphatic metastasis. Patients with early-stage disease may benefit from the restoration of the regional immune function to a level that controls the progression of residual occult metastases and ensures a durable clinical response. Herein we provide a succinct summary of the current progress in this field in order to guide future investigations. 

Melanoma Research

http://journals.lww.com/melanomresearch/pages/articleviewer.aspx?year=9000&issue=00000&article=99814&type=abstract

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Cell Mediated Immunity

http://www.cehs.siu.edu/fix/medmicro/cmir.htm

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The Immune System
National Institute of Allergy and Infectious Diseases

http://www.niaid.nih.gov/topics/immuneSystem/pages/whatisimmunesystem.aspx
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The Lymphatic System and Body Defenses

http://www.isu.edu/departments/PTA/HO111/Lymph_Sys_Immunity_student_03.doc

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What are some of the terms we need to know to understand immune function?

http://www.healthandage.com/html/min/afar/content/other9_2.htm


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Organ: Immune system

http://www.niaid.nih.gov/final/immun/immun.htm

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Primary Immunodeficiency: Complex Genetic Disorders?

http://www.clinchem.org/cgi/content/full/53/2/159

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Lymphatic System Problems

Dr. Mo Lerner

http://www.dimensionsmagazine.com/dimtext/lerner/drmo74.html


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The Lymphatic System

SIGBIO

http://www.acm.uiuc.edu/sigbio/project/updated-lymphatic/lymph1.html


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Thoracic Duct

http://www.acm.uiuc.edu/sigbio/project/updated-lymphatic/lymph2.html


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Lymph Nodes

http://www.acm.uiuc.edu/sigbio/project/updated-lymphatic/lymph3.html


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Bone Marrow

http://www.acm.uiuc.edu/sigbio/project/updated-lymphatic/lymph4.html


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Thymus

http://www.acm.uiuc.edu/sigbio/project/updated-lymphatic/lymph5.html


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Spleen

http://www.acm.uiuc.edu/sigbio/project/updated-lymphatic/lymph6.html


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Lymph Nodes, A Closer Look

http://www.acm.uiuc.edu/sigbio/project/updated-lymphatic/lymph7.html


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Cell Mediated and Humoral Immunity

http://www.acm.uiuc.edu/sigbio/project/updated-lymphatic/lymph8.html

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Advocates for Lymphedema

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Pat O'Connor

Lymphedema People / Advocates for Lymphedema

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Lymphedema People - Support Groups

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Children with Lymphedema

The time has come for families, parents, caregivers to have a support group of their own. Support group for parents, families and caregivers of chilren with lymphedema. Sharing information on coping, diagnosis, treatment and prognosis. Sponsored by Lymphedema People.

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Lipedema Lipodema Lipoedema

No matter how you spell it, this is another very little understood and totally frustrating conditions out there. This will be a support group for those suffering with lipedema/lipodema. A place for information, sharing experiences, exploring treatment options and coping.

Come join, be a part of the family!

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MEN WITH LYMPHEDEMA

If you are a man with lymphedema; a man with a loved one with lymphedema who you are trying to help and understand come join us and discover what it is to be the master instead of the sufferer of lymphedema.

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All About Lymphangiectasia

Support group for parents, patients, children who suffer from all forms of lymphangiectasia. This condition is caused by dilation of the lymphatics. It can affect the intestinal tract, lungs and other critical body areas.

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Lymphatic Disorders Support Group @ Yahoo Groups

While we have a number of support groups for lymphedema... there is nothing out there for other lymphatic disorders. Because we have one of the most comprehensive information sites on all lymphatic disorders, I thought perhaps, it is time that one be offered.

DISCRIPTION

Information and support for rare and unusual disorders affecting the lymph system. Includes lymphangiomas, lymphatic malformations, telangiectasia, hennekam's syndrome, distichiasis, Figueroa
syndrome, ptosis syndrome, plus many more. Extensive database of information available through sister site Lymphedema People.

http://health.groups.yahoo.com/group/lymphaticdisorders/

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Lymphedema People New Wiki Pages

Have you seen our new “Wiki” pages yet?  Listed below are just a sample of the more than 140 pages now listed in our Wiki section. We are also working on hundred more.  Come and take a stroll! 

Lymphedema Glossary 

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Lymphedema 

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Arm Lymphedema  

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Leg Lymphedema 

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Acute Lymphedema 

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The Lymphedema Diet 

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Exercises for Lymphedema  

http://www.lymphedemapeople.com/wiki/doku.php?id=exercises_for_lymphedema 

Diuretics are not for Lymphedema 

http://www.lymphedemapeople.com/wiki/doku.php?id=diuretics_are_not_for_lymphedema 

Lymphedema People Online Support Groups 

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Lipedema 

http://www.lymphedemapeople.com/wiki/doku.php?id=lipedema 

Treatment 

http://www.lymphedemapeople.com/wiki/doku.php?id=treatment 

Lymphedema and Pain Management 

http://www.lymphedemapeople.com/wiki/doku.php?id=lymphedema_and_pain_management 

Manual Lymphatic Drainage (MLD) and Complex Decongestive Therapy (CDT)

http://www.lymphedemapeople.com/wiki/doku.php?id=manual_lymphatic_drainage_mld_complex_decongestive_therapy_cdt 

Infections Associated with Lymphedema 

http://www.lymphedemapeople.com/wiki/doku.php?id=infections_associated_with_lymphedema 

How to Treat a Lymphedema Wound 

http://www.lymphedemapeople.com/wiki/doku.php?id=how_to_treat_a_lymphedema_wound 

Fungal Infections Associated with Lymphe dema 

http://www.lymphedemapeople.com/wiki/doku.php?id=fungal_infections_associated_with_lymphedema 

Lymphedema in Children 

http://www.lymphedemapeople.com/wiki/doku.php?id=lymphedema_in_children 

Lymphoscintigraphy 

http://www.lymphedemapeople.com/wiki/doku.php?id=lymphoscintigraphy 

Magnetic Resonance Imaging 

http://www.lymphedemapeople.com/wiki/doku.php?id=magnetic_resonance_imaging 

Extraperitoneal para-aortic lymph node dissection (EPLND) 

http://www.lymphedemapeople.com/wiki/doku.php?id=extraperitoneal_para-aortic_lymph_node_dissection_eplnd 

Axillary node biopsy 

http://www.lymphedemapeople.com/wiki/doku.php?id=axillary_node_biopsy

Sentinel Node Biopsy 

http://www.lymphedemapeople.com/wiki/doku.php?id=sentinel_node_biopsy

Small Needle Biopsy - Fine Needle Aspiration 

http://www.lymphedemapeople.com/wiki/doku.php?id=small_needle_biopsy 

Magnetic Resonance Imaging 

http://www.lymphedemapeople.com/wiki/doku.php?id=magnetic_resonance_imaging 

Lymphedema Gene FOXC2

 http://www.lymphedemapeople.com/wiki/doku.php?id=lymphedema_gene_foxc2

 Lymphedema Gene VEGFC

http://www.lymphedemapeople.com/wiki/doku.php?id=lymphedema_gene_vegfc

 Lymphedema Gene SOX18

 http://www.lymphedemapeople.com/wiki/doku.php?id=lymphedema_gene_sox18

 Lymphedema and Pregnancy

http://www.lymphedemapeople.com/wiki/doku.php?id=lymphedema_and_pregnancy

Home page: Lymphedema People

http://www.lymphedemapeople.com

Page Updated: Dec. 29, 2011