Response to Infection

Communicable diseases: are usually caused by micro-organisms, can be transmitted from one person to another

Pathogens

  • disease causing organisms

  • defence against pathogens can be specific or non-specific

  • non-specific a generalised response against all pathogens, infections or injuries

  • specific work against selected pathogens

Bacteria: are microscopic living organisms, usually one-celled, that can be found everywhere

  • they can be dangerous, such as when they cause infection, or beneficial, as in the process of fermentation (such as in wine) and that of decomposition.

  • pathogenic bacteria may enter the body in many ways, such as through the mouth or through cuts in the skin

  • they invade the body and are able to multiply. if they multiply sufficiently they can cause an infection

  • the infection may be caused by the microbes themselves, or by poisons called toxins that they produce

Cell Structure

Function

Capsule

Protect the cell

Cell wall

Protect the cell and gives the cell its shape

Plasma membrane

Controls movement in and out of cell

Cytoplasm

(cell content between nuclear and cell membrane)

Includes organelles and cytosol.

Where life activities occur.

DNA

Genetic instructions

Plasmid

Circular DNA capable of

self - replication

Flagellum (tail like structure)

Allows movement


Viruses

  • are 10-100 times smaller than bacteria

  • are able to multiply only within the living cells of a host and therefore tend to target specific tissues (cells) in the host

  • the ‘flu’ virus will lock onto a target cell in the respiratory system and dock onto the cell surface. they then enter the cell

  • once they’re in the cell they use it like a factory; they take it over and make it produce thousands, or millions, of new copies of the virus, which come streaming out of the cell

  • they infect other cells to make more viruses, or they escape from the body and infect a new victim

  • taking over a cell can kill the host cell which has a consequence for us because it might damage the mucosa (the lining of your airway). this means you get inflammation.

Cell Structure

Function

Spike proteins

For attachment to specific cell receptors

Envelop

Protective outer layer

Protein coat

Surrounds the genetic material

DNA

Genetic instructions


Transmission of Pathogens

  • Transmission by contact through direct or indirect means

  • Ingestion of contaminated food or drink

  • Transfer of bodily fluids

  • Airborne transmission

  • Infection by droplets

  • Transmission by vectors

Three lines of defence

  1. Keep microbes out of the body

  2. Non-specific attack on microbes

  3. Specific attack on microbes

Skin

  • Barrier; prevents entry of micro-organisms. Large amounts of bacteria live on skin → occupying bacteria makes it difficult for new (pathogenic) establishments

  • Sebum (oily secretion) → substances which kill some pathogenic bacteria

  • Sweat → salts and fatty acids prevent growth of many micro-organisms, lysozyme kills bacteria

Mucous Membranes

Hair

Cilia

  • found in the respiratory tract

Acids

  • found in stomach, vagina and sweat

Lysozyme

  • found in tears, saliva, sweat, nasal secretions, tissue fluid.

  • enzyme → kills bacteria

Cerumen

Flushing action

  • occurs in urine flowing through urethra; tears, sweat, saliva

  • cleansing action → prevents bacterial growth/travel through ducts/tracts

Protective reflexes

Sneezing

  • Stimulus of irritation of walls of nasal cavity

  • Forceful expulsion of air from lungs

Coughing

Vomiting

  • Stimulus of psychological; excessive stretching of stomach; bacterial toxins

  • Muscles of abdomen and diaphragm contract

  • Stomach contents expelled

Diarrhoea

  • Stimulus of irritation of small/large intestines by bacteria/virus/protozoans

  • Increased peristalsis to quickly remove irritant

  • Material spends less time in intestine → faeces watery

2nd Line of Defense

  • Fever (elevation of body temperature). Increases production of killer T cells, increases metabolic rate which speeds up tissue repair, increases heart rate/blood flow which enables lymphocytes to reach sites of infection faster, creates a non-optimum temperature that kills pathogens


Specific Defences: Recognises foreign molecules and acts to inactivate or destroy them. If it fails, diseases may occur. Three important aspects: acts against specific pathogens or foreign substances, not restricted to initial infection site, recognises and launches stronger attack on previous encountered pathogen

Antigens: Any substance capable of causing a specific immune response e.g. proteins, carbohydrates, lipids, whole microbes, flagellae, cell walls, virus, cell structures from other individuals, pollen grain, egg white

Self-Antigens: Human cells have many surface proteins, our immune cells do not attack our own proteins. Our cells in another person’s body can trigger an immune response.

Non-Self-Antigens: Materials recognised by the immune system as not belonging to the organism. Stimulate an immune response.

Two types of specific immunity

→ Humoral or antibody mediated (B cells): Involves B-cell production of antibodies that bind antigens resulting in either neutralization, lysis or phagocytosis

  • Antibodies: Specialised protein produced in response to a non-self-antigen. Protein group called immunoglobulins (Ig)

  • Antigen-Antibody Complex: Specific antibody attaches to specific antigen. Result in destruction/inactivation of the antigen

  • Agglutination: The clumping together of microorganisms or of blood cells due to a reaction between substances on the surfaces of the cells and antibodies in the surroundings.

  • Humoral response: A macrophage engulfs a pathogen. Macrophages presents the pathogen to a helper T call and B-cell. Helper T cell secretes cytokines which activates the specific B cell to enlarge and divide through mitosis producing clones of themselves. B cell proliferates and differentiate into plasma cells which makes specific antibody for invading antigen/pathogen. Some clones of B cells become memory cells. Memory cells remain to increase immune response when reinfection occurs. Memory cells respond faster to re-exposure to the antigen.

  • First exposure to antigen is the primary response. It takes time for B cells to differentiate into plasma cells and then build up antibody levels. Re-exposure response is the secondary response. Memory cells respond much faster.

  • All antibodies combine with the antigen for which they are specific. Antibodies may:

    • Combine with bacterial/viral/toxins/enzymes and inhibit them

    • Bind to viruses to prevent cell entry

    • Coat bacteria for easier phagocytosis

    • Cause agglutination of foreign particles

    • Make substances insoluble and hence easier to phagocytose


    → Cell mediated (T cells): Involves T-cell recognition of abnormal antigens on the surface of host cells (indicating viral infection or tumorigenic change) and the killing of infected cells.

B and T cells are both produced by bone marrow. B cells mature in the bones. T cells mature in the thymus gland


T cells

  • One T cell is specific to one antigen

  • May be stimulated by cytokines during Humoral immunity

  • Intercellular infection of non-self antigen stimulates T cells

  • Killer T cell, Helper T cell, Suppressor T cell, Memory T cell


Cell Mediated Response