Session 3: Immune System Flashcards

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1
Q

What are nonspecific defences (innate immunity)?

A

First line of defense is intact skin, and mucous membranes and their secretions. Second line of defense is phagocytic white blood cells (which engulf foreign materials like bacteria), inflammation and fever, and antimicrobial substances (substances that kill microbes). Nonspecific defenses are present before any exposure to pathogens and are effective from the time of birth.

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2
Q

What are specific defense mechanism (adaptive/acquired immunity)?

A

Specific defence mechanisms are the third line of defense: specialized lymphocytes (B-cells and T-cells) and antibodies. Specific mechanisms develop after exposure to microbes, toxins, or other foreign substances.

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3
Q

Describe the first line of defence (skin).

A

The skin provides a physical barrier to the entry of pathogens and is rarely penetrated by microorganisms. Harmless microbes live on the skin, making it difficult for others to colonise - natural microflora of intact skin inhibits the growth of most pathogenic microbes. The skin continuously sheds old skin cells which can physically remove microbes. The skin also produces chemical secretions, which inhibit the growth of bacteria and fungi. If microorganisms enter the body (get past the skin) they face a range of other defences: the lining of the respiratory, urinary, reproductive, and gastrointestinal tracts have sticky mucus that traps microorganisms and expels them using cilia.

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4
Q

Describe the second line of defence.

A

A range of non-specific cellular and chemical defences inside the body inhibit or destroy pathogens. Non-specific defences react to the presence of any foreign body, regardless of its nature. White blood cells are involved in most of these responses.

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5
Q

Describe blood clotting.

A

When tissue is wounded, the blood quickly coagulates to prevent further blood loss and maintain the integrity of the circulatory system. A tear or puncture of a blood vessel initiates clotting in order to prevent blood loss and invasion of bacteria. Clot formation is triggered by the release of clotting factors from damaged cells. A hardened clot forms a scab which acts as a barrier against the entry of pathogens. Injury to the lining of a blood vessel exposes collagen fibres to the blood. Platelets stick to the collagen fibres. Platelet releases chemicals that make the surrounding platelets sticky. Platelets clump together, the platelet plug forms an emergency protection against blood loss. A fibrin clot reinforces the seal by trapping blood cells. The clot eventually dries to form a scab.

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6
Q

Describe phagocytes and the phagocytosis process

A

Phagocytes are white blood cells that ingest microbes by phagocytosis and dispose of them, there are three types: granulocytes (including neutrophils), monocytes, and lympocytes. Detection: phagocyte locates harmful microbes via their chemical signature (chemotaxis). The microbes stick to receptors on the phagocyte’s surface. Ingestion: The phagocyte wraps pseudopodia around the bacteria, engulfing them. Phagosome forms: A phagosome (phagocytic vesicle) is formed, enclosing the bacteria within a membrane. Fusion with lysosome: phagosome fuses with a lysosome (containing powerful enzymes that can destroy the bacteria). Digestion: The bacteria are broken down by enzymes into their chemical constituents. Discharge: indigestible material is discharged from the phagocyte.

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7
Q

Describe monocytes (type of phagocyte).

A

Monocytes are the largest type of immune cell, they circulate in the blood and move quickly to the site of infection. They differentiate into macrophages in body tissues and dendritic cells. Macrophages engulf cellular debris and pathogens, and help stimulate lymphocytes and other immune cells. They are able to replace their lysosomes and are thought to have a much longer active life to destroy multiple pathogens. Dendritic cells act as messengers between the innate and adaptive immune system, sampling cellular structures and presenting antigen fragments to lymphocytes in order to help develop longer term immunity.

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8
Q

Describe neutrophils.

A

Neutrophils are the most abundant type of phagocyte. They are unable to renew their lysosomes and die after having phagocytosed a few pathogens. The accumulated dead neutrophils forms the majority of pus).

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9
Q

What are three types of leukocytes?

A

Basophils - involved in the inflammation response by releasing histamine and heparin. Eosinophil - discharge destructive enzymes, often in response to parasitic infections. Mast cell – very similar role to basophils (store histamine and heparin), also involved in allergy and anaphylaxis.

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10
Q

What are natural killer cells?

A

Type of cellular innate defence: Natural Killer Cells circulate through the body and detect abnormal cells. They are a type of lymphocyte that release chemicals leading to cell death, inhibiting the spread of virally infected or cancerous cells. They are not adaptive and do not keep memory of pathogenic cell, they destroy any potential threats they come across.

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11
Q

What are the functions of inflammation?

A

To destroy the cause of the infection and remove it and its products from the body. If this fails, to limit the effects on the body by confining the infection to a small area. To replace or repair tissue damaged by the infection by improving blood flow. Inflammation can be either local or systemic (throughout the body).

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12
Q

What is the process of inflammation?

A

Bacteria enter, a blood clot forms, and chemicals are released by damaged cells (e.g. histamines and prostaglandins) which attract phagocytes to the infection. Blood vessels increase in diameter and permeability in the area of damage. This increases blood flow to the area and allows defensive substances to leak into tissue spaces. Phagocytes reach the damaged area within one hour of injury, they squeeze between cells of blood vessel walls to enter the region and destroy invading microbes. An abscess starts to form after a few days. This collection of dead phagocytes, damaged tissue and various body fluids is called pus. Functioning cells or supporting connective tissue cells create new tissue to replace dead or damaged cells.

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13
Q

Describe inflammatory responses.

A

The inflammatory response, pain, redness, heat, and swelling, is brought about by molecules released upon infection injury. Mast cells and basophils release histamine, which triggers blood vessels to dilate and become more permeable, which causes fluids to collect around an injury to dilute toxins. This causes swelling. They also produce heparin which acts as an anticoagulant, preventing the formation or extension of clots. Prostaglandins increase blood flow and can cause pain. Activated macrophages and neutrophils release cytokines, signalling molecules that enhance the immune response. The temperature of the tissues may rise, which can kill temperature-sensitive microbes.

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14
Q

What is the function of fever?

A

Fever is a systemic inflammatory response triggered by pyrogens released by macrophages and by toxins from pathogens. Fever is a defense mechanism that can destroy many types of microbes. Fever also helps fight viral infections by increasing interferon production, proteins that are produced by the body’s cells as a defensive response to viruses. While high fevers can be dangerous, some doctors recommend letting low fevers run their course without taking aspirin or ibuprofen.

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15
Q

Describe antimicrobial peptides and proteins.

A

Peptides and proteins function in innate defence by attacking pathogens or impeding their reproduction. Interferon proteins provide innate defence, interfering with viruses and helping activate macrophages. About 30 proteins make up the complement system, which causes lysis of invading cells and helps trigger inflammation.

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16
Q

What is a complement system?

A

About 30 plasma proteins circulating in the blood make up the complement system. There are tag microbes for phagocytosis (opsonization) where microbes are “tagged” so that phagocytes know to kill them. There is activation of macrophages and neutrophils (inflammation) which fight and engulf foreign material. And proteins make a complex that forms a hole in bacterial cell membranes. Fluid rushes into the bacteria, causing lysis (the cell bursts).

17
Q

What are the two main components to adaptive immunity?

A

Humoral immunity and cell-mediated immunity. The two components work separately and together to protect us from disease.

18
Q

Describe humoral immunity.

A

Humoral immunity involves B -Lymphocytes that produce antibodies and help defend against extracellular pathogens. B-lymphocytes (also called B-cells) originate and mature in the bone marrow of the long bones (e.g. the femur) and migrate to the lymphatic tissue, such as the spleen and lymph nodes. B-cells defend against bacteria and viruses outside the cell and toxins produced by bacteria (free antigens). Each B-cell can produce antibodies against only one specific antigen. A mature B-cell may carry as many as 100,000 antibody molecules embedded in its surface membrane.

19
Q

What are antigens?

A

Antigens are foreign substances that cause the formation of antibodies. Antigens include Cell surface proteins, potentially damaging microbes and their toxins, and substances such as pollen and flea and dust mite faeces.

20
Q

What are antibodies?

A

Antibodies (also called immunoglobulins) are proteins made in response to antigens. Antibodies recognize and bind to antigens. Antibodies are highly specific and can help destroy antigens. Each antibody has at least two sites that can bind to an antigen. Antibodies help identify antigens for destruction

21
Q

Describe the inactivation of antigens?

A

Neutralisation: bacterial toxins and viruses are bound by antibodies and neutralised. Clumping: particulate antigens, such as bacterial cells, are stuck together in clumps. Precipitation: soluble antigens are stuck together to form precipitates. Phagocytosis is enhanced by these three processes.

22
Q

Describe B-Cell Differentiation.

A

B-cells differentiate into plasma cells and memory cells. Plasma cells secrete antibodies against specific antigens. Each plasma cell has a lifespan of only a few days but can produce about 2000 antibody molecules per second. Memory cells are long-lived and reside in the lymph nodes and provide future immunity. When these cells reencounter the same antigen (even many years after the initial infection), they rapidly differentiate into antibody-producing plasma cells.

23
Q

What is clonal selection?

A

When a B-cell encounters its antigen, it responds by producing many clones with the same antibody. This is called clonal selection because the antigen selects the B-cells that will clone. This enables a rapid response to a wide range of antigens

24
Q

Describe cell mediated immunity.

A

Cell-mediated immunity involves T-lymphocytes that defend against irregular cells (foreign, infected, or cancerous). T-lymphocytes (also called T-cells) originate in the bone marrow of the long bones (e.g. the femur) and mature after passing through the thymus (located above the heart over the trachea). T-cells provide cellular immunity against Intracellular bacteria and viruses, protozoa, fungi, flatworms, roundworms, and tumour cells and transplanted foreign tissue.

25
Q

What are the types of T-cells?

A

Helper T cells express the CD4+ receptor and help activate cytotoxic T-cells, B-cells, and other immune cells. Cytotoxic T cells express the CD8+ receptor and remove pathogens and infected host cells. T regulatory cells express the CD4+ receptor and another receptor, called CD25. T regulatory cells have a role in regulating or suppressing other cells in the immune system, controlling the immune response to self and foreign particles (antigens), and helping prevent autoimmune disease

26
Q

Describe distinguishing self from non-self.

A

The immune system has the capacity to distinguish between body cells (‘self’) and foreign materials (‘non-self’). Your cells possess unique surface molecules called major histocompatibility complex molecules (MHC). MHC Class I function as identification tags that the immune system recognises (self). Surface markers that are not recognised (non-self) can stimulate an immune response (E.g. bacteria, viral, parasitic, foreign cell markers). Some immune cells possess MHC Class II molecules that can “present” antigens from previously destroyed pathogens to Helper T-Cells to further stimulate the immune response. Some pathogens have developed the ability to mutate so that the MHC recognises the cell as a normal tissue cell and not as a foreign cell.

27
Q

Describe T-cell activation.

A

CD4+ cells can become activated Helper T Cells by antigenic fragments that are processed and presented bound to MHC II molecules by antigen-presenting cells (APCs) such as macrophages and dendritic cells. They then activate other immune cells. CD8+ cells engage antigen-embedded MHC I molecules on irregular cells ( e.g. virus-infected or cancerous cells) and are stimulated to become cytotoxic T cells, which directly kill infected cells by apoptosis and emit cytokines to amplify the immune response.

28
Q

Describe the first line of defence:

A

Tears, saliva, nasal secretions and breast milk contain antimicrobial properties including lysozymes and phospholipases (enzymes), and Gastric secretions have a low pH

29
Q

What is inflammation?

A

Inflammation is a beneficial, defensive response triggered by damage to the body’s tissues by physical agents (e.g. sharp objects), microbial infection, or chemical agents. Inflammation is usually characterized by four symptoms: pain, redness, heat, and swelling

30
Q

Describe the activation process of a T-cell that occurs in the dendrite.

A

A pathogen or extracellular antigen is phagocytized by an antigen-presenting cell (often a dendritic cell) and placed into a vesicle. Ingested pathogens are digested by lysosomes to extract their antigens. The antigens then bind with MHC proteins that enter the vesicle. Then, the MHC proteins, now carrying antigens, are released from the vesicle and travel to the outer surface of the cell membrane. The dendritic cell is now presenting antigens, which will activate T cells that bind with the MHC proteins.

31
Q

Describe T cell activation for Helper T cells.

A

When a CD4+ helper T cell binds to the MHC ll-antigen complex on an antigen-presenting cell, both the antigen-presenting cell and the T-cell release cytokines. In response to the cytokines, the T cell clones itself. The cloned T cells produce different cytokines that activate B-cells and CD8+ cells. Then, when a CD8+ cytotoxic cell interacts with the MHC l epitome complex on an infected cell, it produces granzymes and perforins. The perforins form pores in the plasma membrane. Granzymes enter the cell and break down proteins, lysing the cell.