NAJRAN UNIVERSITY College of Medicine NAJRAN UNIVERSITY College of Medicine Microbiology &Immunology Course Lecture No. 15 Microbiology &Immunology Course.

Slides:



Advertisements
Similar presentations
The lymphatic system and immunity
Advertisements

Chapter15 B cell mediated immune response. B cells mediated immune response Humoral immunity(HI) or antibody mediated immunity: The total immunological.
Chapter 34: The human defence system
Lectures 1 & 2 The immune system Overview
From Blood to Host Defense Host Defense Gregory J. Bagby, Ph.D. Office: 310 (CSRB)
A rough guide to the immune system Dr Adrian Palfreeman Senior Clinical Scientist MRC CTU.
Immunity Chapter 40 Section 2. Lymphatic System.
IMMUNITY.
Copyright © 2013, 2010 by Saunders, an imprint of Elsevier Inc. Chapter 67 Review of the Immune System.
Immune System. System of chemicals, white blood cells, and tissues that protect the body against pathogens (disease causing microorganisms) Immune system.
Lymphocytes and Lymphoid Tissues. Basic Pathway Figure 2-3.
Dental Microbiology #211 IMMUNOLOGY 2006 Lecture 2 The Lymphocytes.
Cytokines Non-antibody proteins acting as mediators between cells, termed: Monokines – mononuclear phagocytes Lymphokines – activated T cells, especially.
Microbiology 204: Cellular and Molecular Immunology Class meets MWF 11-12:30 Lectures are open to auditors Discussions are restricted to those enrolled.
Principles of Immunology Cells of the Immune System 1/26/06 “Those who have health, have hope. Those who have hope have everything.” Arabian proverb.
Immune Cells , Receptors, and Markers. Lymphoid Tissues and Organs.
Immunity : The Immune system plays a role in combating infection, creating inflammation (& consequently heart disease), controlling (or not) cancer and.
Cells of inflammation and Immunity G. Wharfe 2005.
Anatomy and Components of Immune System Components of Immune system.
Part 1 Terry Kotrla, MS, MT(ASCP)BB Unit 3 Immunology and Complement.
Immunity Innate and Adaptive Immunity Cells of the Immune System
Human immune system. By as. E.V. Pokryshko Medical biology, microbiology, virology, immunology department.
1 Chapter 20 Defenses Against Disease: The Immune System.
Specific Resistance = Immunity
Immune System (immunus = to be free) primary defense against disease- causing organisms.
Unit 2 seminar: Adaptive immunity T & B lymphocytes Reminders: -Use references in discussion and be sure to rephrase information in your own words -Evaluate.
Review: Cells of the Immune System Leukocytes – White blood cells Myelocytes –macrophage, neutrophil, eosinophil,basophil Leukocytes – B, T and NK cells.
Bellwork Discuss with your group what you think is happening in the following processes. Why does your body undergo an allergic reaction? Why do some.
Department of Microbiology
The immune response White Blood cell types. Myeloid stem cells Lymphoid cells Pluripotent stem cells (in bone marrow) Monocyte Mast cells Basophils Neutrophils.
IMMUNE SYSTEM OVERVIEW
Lymphoid System T and B Cell Development Prof. Dr. Zahid Shakoor MBBS, Dip. Med. Immunology (UK), Ph D (London) King Saud University.
T-LYMPHOCYTE 1 Lecture 8 Dr. Zahoor. Objectives T-cell Function – Cells mediated immunity Type of T-cells 1. Cytotoxic T-cell – CD8 (Killer T-cell) 2.
Dental Microbiology #211 IMMUNOLOGY Lecture 2. Topics The B and T Lymphocytes Antigen-specific Receptors on B and T cells CD4+ and CD8+ T cells Cytokines.
Chapter 6 Adaptive Immunity “third line of defense”  Develops more slowly  Specific  Memory.
Antigens. Antigen structure of the microorganisms
___________DEFENSES of the HOST: THE IMMUNE RESPONSE
The Immune System Dr. Jena Hamra.
Nada Mohamed Ahmed, MD, MT (ASCP)i. Nada Mohamed Ahmed, MD, MT (ASCP)i.
2nd Year Medicine- IBLS Module May 2008 IBLS Lecture 11 White Blood Cells (Leucocytes)
Overview on Immunology and Introduction to Innate Immunity
Overview of the Immune System. Objectives Purpose of the immune system Cellular basis of immunity Induction of response Effectors of response Ontogeny.
NAJRAN UNIVERSITY College of Medicine NAJRAN UNIVERSITY College of Medicine Microbiology &Immunology Course Lecture No. 17 Microbiology &Immunology Course.
BIOT 307: MOLECULAR IMMUNOLOGY Cells and Organs March 7-9, 2011.
Ch 43 The Body’s Defense. Three lines of Defense: 1. External defenses 2. Internal (phagocytes, inflammation) 3. Specific defense: (lymphocytes) 1 & 2.
Copyright © 2014 Wolters Kluwer Health | Lippincott Williams & Wilkins Chapter 13 Innate and Adaptive Immunity.
Lecture 7 Immunology Cells of adaptive immunity
The Immune System Ch th ed Campbell’s Biology.
Specific Defenses of the Host Adaptive or Specific Immunity.
GENERAL IMMUNOLOGY PHT 324 Dr. Rasheeda Hamid Abdalla Assistant Professor om.
Chapter 43 The Body’s Defenses: The Immune System Innate Immunity Aquired Immunity Cell-Mediated Response Humoral Response Lymphatic tissues.
Cytokines Non-antibody proteins acting as mediators between cells, termed: Monokines – mononuclear phagocytes Lymphokines – activated T cells, especially.
INTRODUCTION TO THE IMMUNE SYSTEM
IMMUNOLOGY AND THE IMMUNE SYSTEM
IMMUNITY ..
T and B Cell Development
GENERAL IMMUNOLOGY PHT 324
Cell-Mediated Immunity
The Lymphatic System Function 1: to return interstitial fluid to blood stream Function 2: to provide working location for immune systemx.
The immune system and the oral cavity
CELL MEDIATED IMMUNITY
Immunity and Immune cells
Ch 43 The Body’s Defense.
Lymphoid system.
The body’s defenders.
Cells & Organs of the immune system Dr. Mohed. Shaker
CELLS INVOLVES IN IMMUNITY UTTARAN MODHUKALYA 1. CONTENT 1. INTRODUCTION 2. HEMATOPOIETIC STEM CELL 3. LYMPHOCYTE CELL 4. MYELOID CELL 5. REFERENCE 6.
Cellular and biochemical mediators of immune response By - (M-PHARM SEM-ii) Dept. of-PHARMACOLOGY.
قسم تقنيات التحليلات المرضية مادة المناعة النظري- المرحلة الثالثة
IMMUNOLOGY AND THE IMMUNE SYSTEM
Presentation transcript:

NAJRAN UNIVERSITY College of Medicine NAJRAN UNIVERSITY College of Medicine Microbiology &Immunology Course Lecture No. 15 Microbiology &Immunology Course Lecture No. 15 By Dr. Ahmed Morad Asaad Associate Professor of Microbiology Dr. Ahmed Morad Asaad Associate Professor of Microbiology

Cells of the immune system ‑ The lymphocyte is the dominant cell of the lymphoid system: Central lymphoid tissues Peripheral lymphoid tissues Bone marrow &Thymus Lymph nodes, spleen, tonsils ‑ The common lymphoid progenitor cell has the potential to differentiate into two lymphocyte populations: ‑ B-lymphocytes ‑ T-lymphocytes: are dependent on the thymus gland for differentiation. -Natural killer (NK) cells: a third population of large granular lymphocytes.

Lymphocyte selection Selection means two processes, 1- in the first B and T cells that respond to the self antigens are eliminated and killed during the embryonic life (Clonal selection). 2- in the second stage the native T lymphocytes will acquire either CD4 or CD8 receptor which is called programming of lymphocytes. T cell selection occurs totally in the thymus while B cell selection occurs first in the bone marrow and then acquiring B Ig receptor occurs in the peripheral lymphoid tissue (tonsils, lymph nodes and spleen).

B-LYMPHOCYTES ‑ These constitute 15 ‑ 30% of the total peripheral lymphocytes. ‑ Are mostly restricted to lymphoid tissues. ‑ Life span is short (5 ‑ 7 days) -On antigen stimulation : B lymphocytes differentiate, proliferate and maturate into plasma cells (large lymphocytes) that synthesize specific immunoglobulins. -Some large lymphocytes can revert to small B lymphocytes called memory cells and are involved in the secondary immune response. -B ‑ cells stimulation requires the cooperation of T ‑ cells and macrophages.

T lymphocytes - They originate also from precursor cells of the bone marrow but maturate in the thymus under the influence of thymic hormones. - Several subsets of the T cells arise during this maturation process; each has a specific function. - These cells have long life span (months or years). - They constitute about 55-75% of the total peripheral lymphocytes. -T lymphocytes are responsible for various immune reactions called "cell mediated immune response".

- T ‑ cell subpopulations express on their surface glycoprotein molecules or receptors, e.g. CD 3, CD 4, CD 8, etc... - All T ‑ cells have CD 3 protein receptors. - Mature T ‑ cells have either CD 4 or CD 8 protein receptors. -T ‑ cells are subdivided into 2 major categories: CD4 T-cells (T helper cells) CD8 T-cells (T cytotoxic and T supressor cells)

CD4 T helper lymphocytes (T H ) - These constitute 65% of peripheral T ‑ cells and predominate in the thymus medulla, tonsils and blood. - T H lymphocytes recognize antigen on the surface of antigen presenting cells (APC). They are the cells affected by the HIV virus (causing AIDS). - T H cells are the principal orchestrators of the immune response, as they are needed for the activation of the major effector cells in the response, i.e. cytotoxic T cells and antibody producing B ‑ cells.

The main functions of T H are: a. They help B ‑ cells to develop into antibody producing plasma cells. b. They help CD 8 T ‑ cytotoxic (T c ) cells to exhibit cytotoxic effects. c. They interact with CD 8 T suppressor T cells to induce suppressor activity. d. They release different soluble factors, i.e. lymphokines that have several stimulatory and proliferative effects on B ‑ cells, T ‑ cells, NK cells and macrophages.

TH0, TH1, TH2 -The virgin, non stimulated T cells termed TH0 after stimulation by specific antigen, T cells secrete stimulatory cytokines as IFN, IL-2, TNF and thus evoke effective CMI, at this stage they are known as TH1. -In some diseases this stage is followed by stage of suppression of these cytokines, T cells in this stage mainly produce inhibitory cytokines IL-10, IL-4, IL-5, IL-9 and are known as TH2. At this stage there is high titre of antibodies e.g. HBV, HCV and tuberculosis.

CD 8 lymphocytes - These predominate in human bone marrow and gut lymphoid tissue. - They constitute 35% of peripheral T ‑ cells. ‑ They include 2 main subpopulations; cytotoxic (T c ) and suppressor (T s ) cells. 1. T c cells recognize antigen. They directly kill virus ‑ infected cells, tumor cells and graft cells.­ 2. T s cells suppress B cell and T ‑ cell activities. They play an important role in regulation of the immune response.

NATURAL KILLER (NK) CELLS ‑ Large granular lymphocytes, lack most surface markers of B and T ‑ cells. ‑ Have spontaneous cytotoxic activity on tumour cells & virus ‑ infected cells. ‑ Their activity is increased by interferon and interleukin 2 (IL ‑ 2). ‑ They have Fc receptors and are also capable of killing antibody coated cells, i.e. antibody dependent cellular cytotoxicity (ADCC).

MACROPHAGES: ‑ They exist: Free in the blood, e.g. monocytes Fixed in tissues, e.g. Kupffer cells of the liver. ‑ Macrophages are activated and attracted to the site of foreign material by the action of different cytokines (including gamma interferon). ‑ Fractions released on complement activation, e.g. C 5a, C 3a also attract macrophages to the site of inflammation.

The main functions of macrophages are: 1. Phagocytosis and opsonization. 2. They are important antigen presenting cells (APC). They ingest foreign material, process it and fragments of antigen are presented. 3. Macrophages may kill antibody coated infected cells or tumor cells (ADCC). 4. They synthesize and secrete: ‑ Soluble mediators called monokines, e.g. interleukin ‑ l (activates T ‑ cell proliferation), interferon, colony stimulating factor (CSF) and tumour necrosis factor (TNF). ‑ Prostaglandins and complement components.

POLYMORPHONUCLEAR NEUTROPHILS : They are phagocytic cells They play a role in the inflammatory reactions. MAST CELLS AND BASOPHILS : They possess receptors for the Fc fragment of IgE. They are involved in type I hypersensitivity (anaphylaxis and atopy) by releasing histamine and other chemical mediators from their granules (i.e. by their degranulation). EOSINOPHILS : -They have anti ‑ parasitic and anti ‑ inflammatory activities. - Their number increases in the circulation in allergic and parasitic diseases.