fifth lecture notes
Immunity Overview
Innate Immunity
Basic Characteristics
First line of defense against pathogens.
Utilizes physical barriers (skin, mucous membranes).
Involves innate immune responses that are not pathogen-specific.
Cell Types
Eosinophils: Break down multicellular parasites, discharge destructive enzymes.
Natural Killer (NK) Cells: Detect abnormal surface proteins in virus-infected or cancerous cells, leading to cell death via chemical release.
Lymphatic System
Distributes lymph, aiding in the immune response.
Lymph Nodes: Reservoir for macrophages and dendritic cells that engulf pathogens from lymph.
Interaction of dendritic cells with lymphocytes triggers adaptive immunity.
Antimicrobial Peptides and Proteins
Produced in response to pathogens, acting similarly to insect antimicrobial peptides.
Interferons: Proteins secreted by virus-infected cells to inhibit viral replication in nearby cells.
Complement System: Composed of approximately 30 proteins; activates in response to pathogens to promote cell lysis and inflammation.
Inflammatory Response
Characteristics of Inflammation
Triggered by injury or infection; results in swelling, redness, and pain.
Histamine: Released by mast cells, causing blood vessels to dilate and become permeable, allowing immune cells to enter tissues.
Phagocytic Activity
Activated macrophages and neutrophils release cytokines, promoting blood flow and attracting more immune cells.
Accumulation of pus, consisting of dead pathogens and immune cells, indicates localized immune response.
Systemic Response
Severe infection can lead to heightened systemic inflammatory responses, potentially resulting in conditions such as septic shock.
Evasion of Innate Immunity by Pathogens
Pathogen Mechanisms
Some pathogens, like Streptococcus pneumoniae, have outer capsules that hinder recognition by the immune system.
Opportunistic pathogens can resist lysosomal breakdown and replicate within host cells.
Adaptive Immunity
Characteristics
Unique to vertebrates; provides specific recognition and response to pathogens.
Involves B and T lymphocytes which mature from bone marrow-derived stem cells.
Antigens
Any substance that elicits a response from B or T cells; typically large molecules (proteins or polysaccharides).
Epitopes: The specific parts of antigens that are recognized by antibodies or receptors on B and T cells.
B and T Cell Recognition
B cell receptors (BCRs) recognize intact antigens; T cell receptors (TCRs) recognize antigen fragments presented by MHC molecules.
B Cell Activation
Binding of antigen to BCR leads to B cell activation, proliferation, and differentiation into plasma cells that secrete antibodies.
T Cell Activation
Requires interaction with antigen-presenting cells displaying antigen-MHC complexes; helper T cells stimulate both B cells and cytotoxic T cells.
Clonal Selection and Immunological Memory
Clonal Selection
Upon activation, B and T cells proliferate into clones of cells specific to the recognized antigen.
Memory Cells
Some cloned cells become long-lived memory cells, enabling faster and stronger responses upon re-exposure to the same antigen.
Humoral vs. Cell-Mediated Immune Responses
Humoral Response
Mediated by antibodies secreted by plasma cells; operates in bodily fluids.
Functions include neutralization of toxins and pathogens, opsonization, and activation of complement systems.
Cell-Mediated Response
Involves cytotoxic T cells that kill infected host cells; effective against intracellular pathogens.
Immunization
Provides long-term protection through immunological memory against specific pathogens due to prior exposure or vaccination.
Active vs. Passive Immunity
Active Immunity: Generated by the host’s immune response to infection or vaccination.
Passive Immunity: Provides short-term protection (e.g., antibodies transferred from mother to fetus).
Monoclonal vs. Polyclonal Antibodies
Monoclonal Antibodies: Identical and specific to one epitope; produced from a single B cell clone.
Polyclonal Antibodies: Mixture from multiple B cell clones, recognizing different epitopes.
Transfer and Rejection of Tissues
Tissue and organ transplants involve MHC recognition, leading to potential immune rejection.
Immune Regulation and Disorders
Hyperactive Responses / Allergies: Exaggerated immune responses to harmless antigens, mediated by IgE antibodies.
Autoimmune Diseases: Occur when the immune system erroneously targets the body's own tissues, as seen in conditions like lupus and rheumatoid arthritis.
Immunodeficiency: Can be congenital or acquired, leading to increased susceptibility to infections.
Pathogen Adaptations
Pathogens develop mechanisms like antigenic variation and latency to evade immune detection.
Antigenic Variation: Changes in surface proteins to avoid immune response; e.g., the influenza virus's constant mutation.
Latency: Ability of some viruses to enter a dormant state, avoiding immune recognition.
Conclusion
Understanding the immune system's innate and adaptive components is crucial for developing treatments and vaccines, and combating infectious diseases, autoimmune disorders, and immunodeficiencies.