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C-Reactive Protein (CRP) Test: Rapid Biomarker for Acute Inflammation
Clinical Laboratory & Diagnostics Aug 14, 2026 · 6 min read

C-Reactive Protein (CRP) Test: Rapid Biomarker for Acute Inflammation

Explore the CRP latex agglutination test. A highly sensitive acute-phase reactant used to promptly detect inflammation, tissue injury, and assess response to treatments.

1. Abstract & Brief Introduction

The C-Reactive Protein (CRP) test measures the level of CRP, an acute-phase protein synthesized by the liver in response to interleukin-6 (IL-6) during inflammation. CRP levels rise rapidly within hours of tissue injury, infection, or inflammation, making it a highly sensitive but non-specific biomarker.

2. Test Objectives

  • Detect the presence of acute inflammation or tissue injury.
  • Differentiate between bacterial infections (markedly elevated) and viral infections (mildly elevated or normal).
  • Monitor disease activity in chronic inflammatory conditions (e.g., Rheumatoid Arthritis, Lupus).
  • Evaluate the response to antibiotic or anti-inflammatory therapy.

3. Method Principle (Latex Agglutination / Immunoturbidimetry)

The manual qualitative/semi-quantitative method uses Latex Agglutination:
Polystyrene latex particles coated with anti-human CRP antibodies are mixed with the patient's serum. If CRP is present in the serum at levels above the detection limit (usually 6 mg/L), the antigen-antibody reaction causes the latex particles to clump together (macroscopic agglutination).

Note: Automated labs use Immunoturbidimetry, where the formation of antigen-antibody complexes increases the turbidity of the sample, measured photometrically.

4. Laboratory Equipment

Glass slide with black background (Agglutination slide)
Mechanical rotator (set at 100 rpm) or manual rocking
Disposable applicator sticks
Precision pipettes (20 µL, 50 µL)

5. Reagents & Solutions

  • CRP Latex Reagent (Latex particles coated with anti-CRP).
  • Positive Control Serum.
  • Negative Control Serum.
  • Normal Saline (for serial dilutions in semi-quantitative testing).

6. Sample & Pre-analytical Protocol

Parameter Details & Protocol
SpecimenSerum.
ContainerPlain tube (red top) or SST (yellow top).
StabilityStable for up to 8 days at 2-8°C, or 3 months at -20°C.
InterferencesExtreme lipemia, heavy hemolysis, or high rheumatoid factor (RF) levels may cause false positives.

7. Complete Step-by-Step Procedure

Step Action & Execution
Step 1Bring all reagents and the patient's serum to room temperature.
Step 2Place 50 µL (or one drop) of the patient's serum in a designated circle on the agglutination slide.
Step 3Place 50 µL of Positive Control and 50 µL of Negative Control in separate circles.
Step 4Gently mix the CRP Latex Reagent vial and add 50 µL (one drop) to each circle next to the serum/controls.
Step 5Using a clean applicator stick for each circle, mix the latex and serum well and spread over the entire area of the circle.
Step 6Rock the slide gently manually or place on a mechanical rotator at 100 rpm for exactly 2 minutes.
Step 7Observe immediately for macroscopic clumping (agglutination) under a strong light source.

8. Result Interpretation

Finding Clinical Significance
Agglutination observed within 2 minutesPositive (CRP level > 6 mg/L). Indicates acute inflammation.
No agglutination observedNegative (CRP level < 6 mg/L).
Prozone EffectIn cases of extremely high CRP, agglutination may be falsely negative (requires dilution).

9. Reference Ranges

Parameter Normal Range
Qualitative TestNegative (< 6 mg/L)
Quantitative (Automated)< 5 mg/L or < 0.5 mg/dL (depending on lab units)
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Mohammad Sulieman Ibrahim

Full Stack Developer & Writer

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