Fever - The Body's Furnace
- Mechanism: A regulated rise in body temperature orchestrated by the hypothalamus in response to pyrogens. The pathway involves:
- Exogenous pyrogens (e.g., LPS) stimulate immune cells.
- Immune cells release endogenous pyrogens (IL-1, TNF).
- These cytokines increase cyclooxygenase (COX) activity in the hypothalamus.
- This leads to elevated prostaglandin E₂ ($PGE₂$), which raises the thermoregulatory set point.

⭐ High-Yield: NSAIDs (e.g., aspirin) achieve their antipyretic (fever-reducing) effect by inhibiting COX enzymes, thus blocking the synthesis of prostaglandins that elevate the hypothalamic set point.
Acute-Phase Response - Liver's Protein Party
- Systemic reaction to inflammation where pro-inflammatory cytokines (IL-1, IL-6, TNF-α) stimulate hepatic protein synthesis.
- Positive APPs: Plasma concentration ↑ by >25%.
- Negative APPs: Plasma concentration ↓ by >25% to conserve amino acids for positive APP production.
| Protein | Core Function | Trend |
|---|---|---|
| C-Reactive Protein (CRP) | Opsonin; activates complement | ↑ |
| Fibrinogen | Coagulation; basis for ESR | ↑ |
| Hepcidin | ↓ Iron absorption & release | ↑ |
| Ferritin | Binds & sequesters iron | ↑ |
| Serum Amyloid A (SAA) | Recruits immune cells | ↑ |
| Albumin | Maintains oncotic pressure | ↓ |
| Transferrin | Transports iron | ↓ |
📌 Mnemonic (Positive APPs): Can Fierce Hepatocytes Feel Sick? (CRP, Fibrinogen, Hepcidin, Ferritin, SAA)
Leukocytosis & ESR - Cellular Shake-Up
-
Leukocytosis: Systemic inflammation triggers a ↑ in white blood cells.
- Mechanism: Cytokines, primarily IL-1 and TNF, accelerate the release of leukocytes from the bone marrow's post-mitotic pool.
- Neutrophilia with 'Left Shift': A hallmark of acute bacterial infection, characterized by the release of immature neutrophils (e.g., band cells) into the blood.
-
Erythrocyte Sedimentation Rate (ESR): An indirect measure of inflammation.
- Mechanism: ↑ plasma fibrinogen (an acute-phase reactant) coats RBCs, neutralizing their negative surface charge.
- This promotes RBC aggregation into stacks (Rouleaux formation), which sediment faster than individual cells.

⭐ High-Yield: ESR is significantly elevated (>100 mm/hr) in conditions like giant cell arteritis, polymyalgia rheumatica, and multiple myeloma. However, it can be falsely low in sickle cell anemia (due to abnormal RBC shape) and polycythemia.
Sepsis - The Cytokine Storm
-
Pathophysiology: A dysregulated host response to infection, driven by a "cytokine storm" (TNF-α, IL-1, IL-6). This leads to systemic vasodilation, ↑ vascular permeability, and a procoagulant state, potentially causing Disseminated Intravascular Coagulation (DIC).
-
Progression & Definitions:
- SIRS Criteria (≥2): Temp >38°C or <36°C; HR >90; RR >20; WBC >12,000 or <4,000.

⭐ Early septic shock ("warm shock") is characterized by high cardiac output and low systemic vascular resistance (SVR) due to vasodilation. Late-stage "cold shock" involves ↓ cardiac output from myocardial depression.
- Fever: Mediated by IL-1 and TNF which increase PGE₂ in the hypothalamus, raising the temperature set point.
- Leukocytosis: IL-1/TNF stimulate neutrophil release from bone marrow, causing a "left shift".
- Acute-Phase Reactants: Synthesized by the liver (stimulated by IL-6); includes CRP and fibrinogen.
- Elevated ESR: Caused by fibrinogen promoting RBC rouleaux formation.
- Chronic Inflammation Risks: Secondary (AA) amyloidosis from SAA and anemia of chronic disease from hepcidin.
Continue reading on Oncourse
Sign up for free to access the full lesson, plus unlimited questions, flashcards, AI-powered notes, and more.
CONTINUE READING — FREEor get the app