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3 lines of defense 1st line
physical/chemical barriers (skin, mucous, microbiota). 2nd line: innate immunity (phagocytes, inflammation, complement, fever). 3rd line: adaptive immunity (T/B cells, antibodies, memory).
Blood cell types & origin
All blood cells come from bone marrow. RBCs = O2 transport. Platelets = clotting. WBCs = immune defense: neutrophils (phagocytes), eosinophils (parasites), basophils/mast cells (histamine), macrophages (phagocytosis), lymphocytes (B/T/NK cells).
Cell communication
Immune cells communicate via cytokines, chemokines, receptors to coordinate response.
Sensor system signals
PAMPs detect microbes (LPS, flagellin). DAMPs detect host cell damage. Both trigger immune activation.
Phagocytosis
Engulf & digest microbes. Done by neutrophils, macrophages, dendritic cells.
Inflammation
Response to infection/injury. Steps: vasodilation → permeability ↑ → phagocytes recruited → tissue repair. Purpose: contain infection & heal.
Complement & MAC Complement
opsonizes pathogens, triggers inflammation, forms MAC to lyse bacteria.
Interferons
Antiviral proteins that warn nearby cells after viral infection.
Why adaptive immunity is specific
Uses specific antigen receptors. Main cells: B cells & T cells.
B cells make antibodies → attack extracellular microbes.
T cells kill infected or abnormal cells directly.
Produces & activates immune cells. Primary: bone marrow, thymus. Secondary: lymph nodes, spleen, MALT, tonsils.
Antibodies bind specific antigen epitopes via variable region.
IgG = most abundant, long-term. IgM = first made. IgA = mucosal. IgE = allergies/parasites. IgD = B cell receptor.
B cell binds antigen + T cell help → plasma cells & memory B cells.
Recognize antigen on MHC → helper T cells (activate others) & cytotoxic T cells (kill infected cells) + memory T cells.
Primary = slow, symptoms. Secondary = fast & strong due to memory, fewer symptoms.
Kill virus-infected & cancer cells without prior exposure.
Antigen recognized → helper T cells activate → B cells make antibodies → cytotoxic T cells kill infected cells → memory cells formed.
Entry → adhesion → invasion → immune evasion (capsules, antigen changes, toxins) → damage.
Helpful microbes on skin, GI, respiratory, urogenital systems. Built through birth, environment, diet.
= microbe multiplies. Disease = symptoms. Signs = measurable (fever). Symptoms = felt (pain).
Ability to cause disease. Stages: incubation → prodromal → illness → decline → recovery.
Entry → adhesion → colonization → invasion → damage.
Capsules, hide inside cells, toxin production, immune suppression. Damage from toxins & immune response.
Yes — infection without symptoms if immune control is strong.
Droplets, feces, urine, blood, skin, sexual fluids → transmission to new hosts.
Study of disease distribution, causes, and spread in populations.
Communicable spreads between people. Non-communicable does not (tetanus, food poisoning).
Track incidence, prevalence, mortality, attack rates to measure spread & severity.
Reservoir → portal of exit → transmission → portal of entry → susceptible host.
Where pathogen lives: humans, animals, soil, water.
Direct contact, droplets, airborne, vectors, contaminated food/water, fomites.
Pathogen traits, host immunity, population density, environment, sanitation, behavior.