Defense Against Pathogens
Overview of Immunity
Vertebrates have both innate (nonspecific) and adaptive (specific) immune defenses that work together to protect against pathogens by distinguishing self from non-self.
Innate Immunity
Innate Immunity: First line of defense, consisting of:
Physical barriers: Skin, mucus.
Antimicrobial substances: Lysozyme, antimicrobial peptides.
Immune cells: Phagocytic blood cells such as macrophages and neutrophils.
Mechanisms: Rapid response to pathogens using pattern recognition receptors (PRRs) that recognize pathogen-associated molecular patterns (PAMPs).
Non-adaptive features: These defenses are classified as non-adaptive because they do not improve with repeated exposure to pathogens and recognize broad classes of pathogens rather than specific antigens.
Skin and Mucosal Barriers
Skin: The largest organ contributing to defense with:
Acidic pH (3-5) inhibiting pathogen growth.
Secretion of lysozyme and antimicrobial peptides.
Normal flora preemptively outcompetes incoming pathogens.
Mucosal Surfaces: Lines the digestive, respiratory, and urogenital tracts, traps pathogens in mucus, and includes lysozyme in saliva and acidic secretions in the stomach.
Phagocytes in Innate Immunity
Phagocytic cells help eliminate pathogens:
Macrophages: Large cells engulfing pathogens and debris.
Neutrophils: Most abundant, primary responders at infection sites, effective at generating reactive oxygen species.
Natural Killer (NK) Cells: Attack infected or cancerous cells, inducing apoptosis.
Adaptive Immunity
Characterized by specificity, diversity, memory, and the ability to distinguish self from non-self:
Humoral immunity (B cells): Produce antibodies upon recognizing specific antigens.
Cell-mediated immunity (T cells): Specialize in killing infected cells or regulating other immune responses.
Major Characteristics of Adaptive Immunity:
Specificity: Responds to particular pathogens.
Diversity: Can recognize a vast number of antigens.
Memory: Faster response upon re-exposure due to memory cells.
Self/non-self discrimination: Distinguishes between body’s own cells and foreign cells.
Molecules in Adaptive Immunity
Epitope: Small part of an antigen that is recognized by the immune system.
Antigen: A substance that triggers an immune response, derived from pathogens or foreign bodies.
MHC (Major Histocompatibility Complex): Proteins on cell surfaces that present antigen fragments to T cells.
Antibody: Proteins produced by B cells composed of two light chains and two heavy chains; facilitates pathogen neutralization.
Cytokines: Signaling molecules that regulate immune responses, originating from various immune cells.
Immune Cells in Adaptive Immunity
Macrophage: Originates from monocytes; role in engulfing pathogens and presenting antigens.
Natural Killer Cells: Derived from lymphoid progenitor cells; role in targeting infected/cancerous cells.
Mast Cells: Found in tissues; release histamine and play a role in allergic responses.
B-cells: Mature in bone marrow; responsible for producing antibodies and memory cells.
T-cells: Mature in thymus; cytotoxic T-cells kill infected cells while helper T-cells regulate immune responses.
Distinguishing Immune Responses
Antigen-Presenting Cells (APCs): Capture and present antigens to T cells to activate them.
B-cells: When activated, differentiate into plasma cells that secrete antibodies.
Plasma Cells: B-cell derivatives that produce antibodies.
Helper T-cells: Assist in activating B-cells and cytotoxic T-cells.
Cytotoxic T-cells: Kill infected or abnormal cells.
Immunization and Types of Immunity
Active Immunity: Developed through exposure to pathogens or vaccines; triggers long-term immune response.
Passive Immunity: Acquired through maternal antibodies or administration of antibodies; provides temporary protection.
Mechanism of Immunization: Involves introducing non-pathogenic antigens to stimulate the adaptive immune response, leading to immunity.
Allergies and Autoimmune Diseases
Allergies: Result from inappropriate immune responses to harmless allergens, mediated by IgE.
Autoimmune Diseases: Occur when the immune system fails to recognize self-tissues, leading to attacks on the body’s own cells.
HIV and the Immune System
HIV Interaction: Targets CD4+ T cells, leading to AIDS which compromises immune response.
Vaccine Challenge: Difficulty lies in the virus's rapid mutation rate and its ability to evade the immune system.