STUDY OF IMMUNITY. NON-SPECIFIC RESISTANCE

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Presentation transcript:

STUDY OF IMMUNITY. NON-SPECIFIC RESISTANCE Immunity. Types of immunity Innate immunity. Mechanism of innate immunity

IMMUNITY The resistance offered by the host to the harmful effect of pathogenic microbial infection is called immunity. Immunity against infectious diseases is of different types.

IMMUNITY INNATE ACQUIRED ADAPTIVE Non specific Specific Passive Active Natural Artificial

INNATE IMMUNITY This is basic immunity, which may be genetically passed on from one generation to other generation It does not depend on prior contacts with microorganisms It may be non-specific when it indicates a degree of resistance to all infection It is specific when it shows resistance to particular pathogens

The differences between Non-specific Immunity and Specific Immunity Response is antigen-independent Response is antigen-dependent There is immediate maximal response There is a lag time between exposure and maximal response Not antigen-specific Antigen-specific Exposure results in no immunologic memory Exposure results in immunologic memory

INNATE IMMUNITY Species immunity: Individuals of same species show uniform pattern of susceptibility to different bacterial infection. Racial immunity: Within a species different races show differences in susceptibility to infection. Individual immunity: Individual in population shows variation in their response to microbial infections. Factors influencing level of innate immunity in an individual are: age; hormonal influence; nutrition.

DEFENSE MECHANISMS OF BODY Epithelial surfaces: the intact skin and mucous membrane covering the body confers on it considerable protection against bacteria. They provide mechanical barrier. They also provide bactericidal secretions. Tissue defenses: If barrier of body is overcome by the organisms, a number of factors in normal tissue and body fluid, play their role.

Tissue factor may be divided into: Humoral factors - the body fluids and organized tissues of human organism naturally contain a variety of antimicrobial agent that kill or inhibit the growth of microbes. The sources and activities of a variety of host antimicrobial substances are summarized in the next slide Cellular factors

Lactoferrin and transferrin Humoral factors Substance Common Sources Chemical Composition Activity Lysozyme Serum, saliva, sweat, tears Protein Bacterial cell lysis Complement Serum Protein-carbohydrate lipoprotein complex Cell death or lysis of bacteria; participates in inflammation Basic proteins and polypeptides (histones,lysins and other cationic proteins, tissue polypeptides)  Serum or organized tissues Proteins or basic peptides Disruption of bacterial plasma membrane Lactoferrin and transferrin Body secretions, serum, organized tissue spaces  Glycoprotein Inhibit microbial growth by binding iron Peroxidase Saliva, tissues, cells (neutrophils) Act with peroxide to cause lethal oxidations of cells Fibronectin Serum and mucosal surfaces Clearance of bacteria (opsonization) Interferons Virus-infected cells, lymphocytes Resistance to virus infections  Interleukins Macrophages, lymphocytes Cause fever; promote activation of immune system

MICROBIAL ANTAGONISM This refers to the protection of the surfaces afforded by an intact normal flora in a healthy organism E.coli bacteria (yellow) in the gut are part of the normal intestinal flora of humans

Phagocyte attacks bacteria Phagocytosis: Natural defense against invasion of blood and tissue by bacteria or others foreign particles are mediated by phagocytic cell which ingest and destroy them

PHAGOCYTOSIS CELLS MAY BE: Microphages, e.g. polymorphonuclear leucocytes. Macrophages: histocytes, fixed reticuloendothelial cells; monocytes. Phagocytosis, a phagocyte (blue) engulfing a yeast cell (yellow)

The process of phagocytosis consist of: The first phase involves the approach of the phagocyte to the microbe by means of positive hemotaxis In the second phase absorption of the microorganism on the surface of the phagocyte take place The third phase is characterized by submergence of the microbe into the phagocyte In the fourth phase intracellular digestion of the engulfed microbes by the phagocytosis take place

Phagocytosis by a Macrophage

The neutrophils can form Neutrophil Extracellular Traps (NETs) The neutrophils can form Neutrophil Extracellular Traps (NETs). Once triggered, the cells undergo a novel program leading to their death. While they perish, the cells release the content of their nuclei. The nucleic acid, mingled with bactericidal enzymes, forms a lethal network outside the cell. Invading bacteria and pathogenic fungi get caught and killed in the NETs

Neutrophil granulocytes have trapped Shigella bacteria in NETs (Neutrophil Extracellular Traps)

Cilia: The ciliary escalator propels trapped particles out of the respiratory tract Cilia in the trachea rhythmically beating

NON-SPECIFIC IMMUNITY Inflammation: Tissue injury or irritation initiated by entry of bacteria or of other irritant leads to inflammation Fever: It is natural defense mechanism. It may actually destroy the infecting organism. Fever stimulates the production of interferon and helps in recovery from virus infections

COMPLEMENT SYSTEM Complement can be considered as part of the constitutive host defense mechanisms because of its role in inflammation and phagocytosis. Complement is well known for its ability to react with wide variety of antigen antibody combination to produce important physiological results. At present complement is known to have 9 distinct components (C1-C9), making a total of 20 proteins.

Important physiological effects of complement system The destruction of erythrocytes as well as other tissue cells. The initiation of inflammatory changes. The lysis of bacteria cells. Enhancement of phagocytosis involving some opsonized particles.

Two ways of Complement’s activation Cell membrane Classical pathway Alternative pathway Damage of membrane Kinin activation С1 С4 С2 С3 С5-С9 Phagocytosis Virus neutrali-zation Immune adherence Increasing of per-meability of vessels Virus neutrali-zation Producing of MAC

Complement Fixation Y Methodology Ag No Ag Ag mixed with test serum to be assayed for Ab Standard amount of complement is added Erythrocytes coated with Abs is added Amount of erythrocyte lysis is determined Ag No Ag Ag Y Patient’s serum Ag Y