Ordering Recommendation

Use to detect increased complement activation in complement-related diseases. May also be used to aid in monitoring the effectiveness of anticomplement therapies such as eculizumab.

New York DOH Approval Status

This test is New York state approved.

Specimen Required

Patient Preparation
Collect

Pink (K2EDTA), Tan (K2EDTA), Royal blue (K2EDTA), or Lavender (EDTA).

Specimen Preparation

Separate plasma within 2 hours (1 hour is preferable) by centrifugation ~2700 rpm (1300 100 g) for 10 minutes. Transfer plasma (minimum 0.5 mL) to an ARUP standard transport tube and freeze immediately.

Storage/Transport Temperature

CRITICAL FROZEN. Separate specimens must be submitted when multiple tests are ordered.

Unacceptable Conditions

Nonfrozen specimens. Specimens exposed to repeated freeze/thaw cycles. Grossly hemolyzed, lipemic, and icteric specimens. Serum samples. Heparinized and lithium samples.

Remarks
Stability

Ambient: Unacceptable; Refrigerated: Unacceptable; Frozen: 30 days

Methodology

Quantitative Enzyme-Linked Immunosorbent Assay (ELISA)

Performed

Sun, Wed

Reported

2-12 days

Reference Interval

Test Number
Components
Reference Interval
  C5b9 Soluble Terminal Complement Complex Less than or equal to 260 ng/mL

Interpretive Data

Elevated soluble C5b-9 (SC5b-9) levels indicate recent or ongoing activation of the complement system, while normal or reduced levels suggest no excessive activation. High SC5b-9 concentrations are associated with transplant-associated thrombotic microangiopathy (TA-TMA), a complication of hematopoietic stem cell transplants. Increased SC5b-9 may also occur in various conditions involving primary or secondary complement activation, such as immune-complex disease, infection, atypical hemolytic uremic syndrome, and C3 glomerulopathies. Due to a low specificity for SC5b-9 testing, results should be interpreted in combination with other clinical and laboratory evidence of disease activity. Plasma SC5b-9 levels may be used to monitor the efficacy of complement inhibitor drugs, as elevated levels suggest insufficient complement blockage to effectively prevent the formation of the terminal attack complex.

Compliance Category

Laboratory Developed Test (LDT)

Note

Hotline History

N/A

CPT Codes

86160

Components

Component Test Code* Component Chart Name LOINC
3017917 C5b9 Soluble Terminal Complement Complex 93244-2
* Component test codes cannot be used to order tests. The information provided here is not sufficient for interface builds; for a complete test mix, please click the sidebar link to access the Interface Map.

Aliases

  • MAC
  • Membrane attack complex
  • SC5b9
  • sMAC
  • Soluble membrane attack complex
  • Soluble terminal complement complex
  • TCC
  • Terminal activation product
  • Terminal complex
SC5b-9