Innate Immunity Responses

BIO 230 Lecture Notes - Big Innate Immunity Responses to Infection and Bridging from Innate to Adaptive Immunity

Learning Objectives

  • Vocabulary:

    • Granuloma: A walled-off pocket of infection that contains dead cells and pathogens, often surrounded by white blood cells.

    • Pyrogen: Substances that induce fever by causing an increase in the body temperature.

    • Immune Specificity: The ability of the immune system to target specific pathogens.

    • Immune Memory: The capacity of the immune system to remember past infections and respond more effectively upon re-exposure.

    • Antigen: Any particle, molecule, or cellular component that can trigger an adaptive immune response.

    • Epitope: A small, three-dimensional shape that is characteristic for antigens and is the specific part recognized by antibodies.

    • Hapten: A small molecule that, when combined with a larger carrier such as a protein, can elicit an immune response.

    • Adjuvant: A substance that enhances the body's immune response to an antigen.

    • Antibody Variable Region: The part of the antibody where antigen binding occurs, allowing for the specificity of the antibody to various antigens.

  • Outline how innate immunity can fail in fighting infections and describe how granulomas transition from an immune problem to a broader health issue.

  • Briefly describe the pathway from immune stimulus to bodily fever.

  • Identify the two primary characteristics of the adaptive immune system.

  • Characterize the relationship between antigens and epitopes.

  • Reading Material: OpenStax Chapter 17.4 and 18.1.

Concept Map of the Immune System

  • Innate Immunity

    • Physical, Mechanical, and Microbiome Barrier Functions.

    • Non-specific Cells (Granulocytes and Agranulocytes).

    • Signals and Inflammation (Chemical Signals and Fever).

  • Bridge to Adaptive Immunity.

Chronic Inflammation

  • Acute Inflammation:

    • Sometimes fails to clear pathogens or particles from the target site, leading to chronic inflammation.

    • Chronic inflammation can manifest as granulomas, which are essentially pockets of infection.

    • Granulomas consist of dead cells and pathogens, and they are particularly significant in tuberculosis infections.

    • The same mechanism of chronic inflammation is seen in cirrhosis, where scar tissue forms in the liver over time.

Pathogens and Phagocytosis

  • Co-opting Mechanisms:

    • Certain pathogens exploit phagocytosis for their survival, such as Leishmania tropica, which causes cutaneous leishmaniasis.

    • Massive granulomas develop in the skin to contain this parasite in susceptible individuals.

    • Listeria monocytogenes can escape from phagocytes (through listerolysin O) due to its ability to break out from amoebae in its natural environment.

    • HIV uses macrophages for entry into the body by utilizing phagocytosis.

  • Questioning Phagocytosis Failure: What happens if phagocytosis does not clear the infection?

System-Wide Signals in the Immune Response

  • Chemical Signals:

    • These signals can travel beyond the local environment, often initiating a cascade of responses.

    • The immune system amplifies its response, leading to the attraction of varied leukocytes and lymphocytes to the site of infection and nearby lymph nodes.

    • This chemotactic process may also contribute to homeostatic mechanisms necessary for hematopoiesis.

    • This amplification is a crucial aspect of bridging innate responses to adaptive immunity.

Fever Induction

  • Exogenous Pyrogens:

    • Substances like LPS provoke strong chemical responses from leukocytes, leading to the generation and diffusion of endogenous pyrogens.

    • This cascade promotes the production of prostaglandins, which are targeted by NSAIDs to reduce fever.

    • If endogenous pyrogens reach the hypothalamus, fever is induced.

Benefits of Fever

  1. **Impact on Pathogens: **

    • Elevated body temperatures inhibit bacteria by pushing them away from optimal growth temperatures, causing slower growth.

    • Heat increases vulnerability of pathogens to stress, including iron deprivation and exposure to complement proteins.

  2. Enhanced Immune Cell Function:

    • Neutrophils and macrophages move more rapidly in elevated temperatures.

    • Phagocytic activity increases, leading to more effective pathogen clearance.

    • Enzymes in granulocytes and lymphocytes function more effectively during fever.

    • The intensity of tissue antiviral responses increases, and dying damaged cells deprive invading pathogens of resources.

Overview of the Lymphatic System

  • Lymphatic Vessels:

    • Form a one-way system that conducts lymph from tissues back to the circulatory system.

  • Composition of Lymph:

    • It consists of a liquid similar to blood plasma and arises from fluid leaked from blood vessels into surrounding tissues.

Adaptive Immunity

  • Overview:

    • A major flaw in innate immunity is its static response, which does not adapt when pathogens evolve to evade defenses.

    • The adaptive immune response provides specificity for unique pathogens and adapts to new challenges (

    • It recognizes unique molecular structures characterized by microbes.

    • The hallmark of adaptive immunity is memory, allowing for a heightened response upon subsequent exposures to the same pathogens.

    • B cells and T cells serve as the primary effectors in adaptive immunity.

Specificity: Antigens and Epitopes

  • Definition of Antigens:

    • Any particle, molecule, or cellular component capable of triggering an adaptive immune response.

  • Definition of Epitopes:

    • Small three-dimensional shapes that are characteristic of antigens and are the specific sites recognized by antibodies.

Memory in the Immune Response

  • Primary vs Secondary Responses:

    • The secondary immune response is characterized by enhanced amplification of immune function, marking the strength of the adaptive immune response upon re-exposure to the same pathogen.