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Host response to infection
Refers to the complex physiological and immunological processes the body employs to detect, combat, and eliminate pathogens.
Innate Immunity
The body’s first line of defense, which is rapid, non-specific, and present at birth.
Adaptive Immunity
A slower, specific response that develops over time and provides long-term protection.
Physiological changes
Fever
Inflammation
The host response also involve _____.
Innate Immune Response
The body’s immediate defense mechanism as it responds within minutes to hours of pathogen exposure and does not require prior exposure to the pathogen.
Skin
Mucous Membranes
Chemical defenses
Normal Flora
Physical and Chemical Barriers
Skin
Acts as a physical barrier, preventing pathogen entry. Sweat and sebum contain antimicrobial substances like fatty acids.
Mucous membranes
Line the respiratory, gastrointestinal, and genitourinary tracts, trapping pathogens in mucus and expelling them via cilia or coughing.
Saliva
Tears
Gastric acid
Chemical defenses in innate immune response.
Normal flora
Beneficial microorganisms in the gut, skin, and mucous membranes compete with pathogens for resources, limiting their growth.
Neutrophils
The most abundant white blood cells, rapidly recruited to infection sites engulf and destroy pathogens via phagocytosis.
Macrophages
Found in tissues, they engulf pathogens and debris, and release cytokines to signal other immune cells.
Dendritic Cells
Present pathogens to the adaptive immune system, bridging innate and adaptive immunity.
Natural Killer Cells
Attack virus-infected and cancerous cells by releasing cytotoxic granules.
Mast Cells
Release histamine, contributing to inflammation and recruiting other immune cells.
Inflammation
The hallmark of the innate response, triggered by tissue injury or pathogen invasion.
Vasodilation
Increases blood flow to the infection site, causing redness and warmth.
Redness
Warmth
Swelling
Pain
Loss of function
Local signs of inflammation.
Fever
Fatigue
Elevated WBC count (leukocytosis)
Systemic signs of inflammation.
Increased vascular permeability
Allows immune cells and plasma proteins to reach the site leading to swelling (edema).
Opsonizing pathogens
Marking them for phagocytosis.
Fever
Is a systemic response mediated by pyrogens (e.g., cytokines like IL-1, IL-6).
Adaptive Immune Response
Is slower (days to weeks) but highly specific, targeting the exact pathogen.
Humoral Immunity
Mediated by B lymphocytes (B cells), which produce antibodies (immunoglobulins).
Cellular Immunity
Mediated by T lymphocytes (T cells) and is effective against intracellular pathogens (e.g., viruses, some bacteria like Mycobacterium tuberculosis).
Immunological Memory
The adaptive immune system “remembers” pathogens, allowing a faster and stronger response upon re-exposure.
Incubation Period
Time between pathogen entry and symptom onset. The pathogen replicated but the host may be asymptomatic.
Prodromal Phase
Early, non-specific symptoms wherein the immune system begins responding, but symptoms are vague.
Acute Phase
Peak of symptoms, with full activation of innate and adaptive immunity. Local and systemic signs are prominent.
Convalescent Phase
Symptoms resolve as the immune system clears the pathogen. Tissue repair and recovery occur, but patients may feel fatigued.
Resolution
Complete elimination of the pathogen and return to baseline health.
Complications
Persistent infections, tissue damage, or systemic issues like sepsis.
Systemic Inflammatory Response Syndrome (SIRS)
A widespread inflammatory response triggered by severe infection or other insults (e.g., trauma).
Sepsis
SIRS caused by infection, leading to organ dysfunction.
quick Sequential Organ Failure Assessment
qSOFA score meaning.
Cytokine Storm
Excessive cytokine release leading to severe inflammation and tissue damage.
Fever
Pain
Fatigue
Leukocytosis/Leukopenia
Organ-specific symptoms
Clinical manifestations of infection.
Fever
Indicates immune activation but can lead to dehydration or seizures (in children).
Pain
Often due to inflammation or tissue damage (e.g., sore throat in streptococcal pharyngitis).
Fatigue
Reflects increased metabolic demand and cytokine effects.
Neonates
Immature immune systems increase susceptibility to infections like group B Streptococcus.
Elderly
Reduced immune function and comorbidities increase infection severity (e.g., pneumonia).
Immunocompromised
Patients with HIV, cancer, or transplant recipients are prone to opportunistic infections.
Chronic Illness
Conditions like diabetes impair wound healing and immune responses.