NCM 112 Module 3 Immunology & Inflammation PDF

Summary

This document provides an introduction to immunology and inflammation, outlining the body's response to foreign agents and organisms. It details white blood cells, lymphocytes, and the different types of immune responses, as well as the process of inflammation.

Full Transcript

NCM 112 | 3rd Year – First Semester (Midterms) Vales, J.B. BSN 3-B  White pulp contains concentrations Module 3: Immunology and Inflammation of lymphocytes....

NCM 112 | 3rd Year – First Semester (Midterms) Vales, J.B. BSN 3-B  White pulp contains concentrations Module 3: Immunology and Inflammation of lymphocytes. Lymph Nodes Introduction  Immunity is the body’s specific  Lymph nodes, which are connected protective response to a foreign by lymph channels and capillaries, agent or organism. are distributed throughout the body.  Immune system functions as the  They remove foreign material from body’s defense mechanism the lymph system before it enters against invasion and allows a the bloodstream. rapid response to foreign  It also serve as centers for immune substances in a specific manner. cell proliferation. White Blood Cells Adaptive Immunity  White blood cells (WBCs)  Acquired (adaptive) immunity involved in immunity are produced usually develops as a result of prior in the bone marrow. exposure to an antigen through immunization (vaccination) or by Two types: contracting a disease, both of which  B lymphocytes (B cells) generate a protective immune  T lymphocytes (T cells) response. Lymphocytes originate from stem cells in the bone marrow. B lymphocytes mature in the bone marrow before entering the bloodstream, whereas T lymphocytes mature in the thymus, where they also differentiate into cells with various functions. Response to Invasion  PHAGOCYTIC IMMUNE Spleen RESPONSE - primarily involves the  Spleen, composed of red and WBCs (granulocytes and white pulp, acts somewhat like a macrophages), which have the filter. ability to ingest foreign particles and  The red pulp is the site where old destroy the invading agent. and injured red blood cells (RBCs)  CELLULAR IMMUNE RESPONSE are destroyed. - also involves the T lymphocytes, which can turn into special cytotoxic NCM 112 | 3rd Year – First Semester (Midterms) Vales, J.B. BSN 3-B (or killer) T cells that can attack the  EFFECTOR CYTOTOXIC T CELLS pathogens. - (killer T cells) attack the antigen  HUMORAL OR ANTIBODY directly by altering the cell IMMUNE RESPONSE - antibody membrane, causing cell lysis response begins with the B (disintegration), and releasing lymphocytes, which can transform cytolytic enzymes and cytokines. themselves into plasma cells that  REGULATORY OR manufacture antibodies. SUPPRESSOR T CELLS - have ANTIBODIES the ability to decrease B-cell production, thereby keeping the  Are large proteins, called immune response at a level that immunoglobulins. is compatible with health (e.g.,  mobilize other components of the sufficient to fight infection immune system to defend against adequately without attacking the the invader. body’s healthy tissues.  MEMORY T CELLS - are responsible for recognizing antigens from previous exposure and mounting an immune response. CELLULAR RESPONSE TO INJURY: INFLAMMATION  is a localized reaction intended to neutralize, control, or eliminate the offending agent to prepare the site for repair. MNEMONICS: GAMED  major function of the natural immune system that is elicited in response to tissue injury or invading organisms. 5 CARDINAL SIGNS OF INFLAMMATION  Pain  Heat TYPES OF T LYMPHOCYTES  Redness  EFFECTOR HELPER T CELLS -  Swelling activated on recognition of antigens  Loss of Function and stimulate the rest of the immune system. When activated, Pathophysiology helper T cells secrete cytokines,  sequence involves changes in the which attract and activate B cells, microcirculation, including cytotoxic T cells, NK cells, vasodilation, increased vascular macrophages, and other cells of the permeability, and leukocytic cellular immune system. infiltration. NCM 112 | 3rd Year – First Semester (Midterms) Vales, J.B. BSN 3-B  As these changes take place, five cardinal signs of inflammation are produced: redness, warmth, swelling, pain, and loss of function.  Vasodilation and an increased rate of blood flow through the microcirculation to the area of tissue damage, Local warmth and redness result.  increase in vascular permeability, plasma fluids leak into the inflamed tissues, producing swelling.  pain that occurs is attributed to the pressure of fluids or swelling on nerve endings AND irritation of nerve endings by chemical mediators.  Loss of function is most likely related to the pain and swelling;  Leukocytes (white blood cells) exit, and migrate to the site of injury to engulf offending organisms and to remove cellular debris.  Fibrinogen in the leaked plasma fluid coagulates, forming fibrin for clot formation, which serves to wall off the injured area and prevent the spread of infection.

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