CH50 Assay (serum)

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Indications

Reference interval

CH50 Values % of Reference values Interpretation
<100 0-50 Absent or low
100-300 51 to 150 Normal
>300 >150 High

* the CH50 unit is the reciprocal of the dilution of serum that will lyse 50% of the cells in a 1 mL suspension (see Procedure:)

Principle

A test for total complement that involves addition of complement in the presence of Mg+2 & Ca+2 to cause lysis of sheep red blood cells coated with antibody. The amount of hemolysis is evaluated quantitatively & compared with known controls.

The complement system participates in the host immunological defense. Levels of total complement differ from normal levels in certain diseases, genetic deficiencies & other conditions. Thus, determination of total complement levels can be important in the diagnosis & management of these conditions.

Clinical significance

Increases

Decreases

Specimen

Aseptically collect a sample of blood (at least 2 mL) in an empty container, without anti-coagulant. Allow the blood to clot in ice. Separate the serum and store at -50 degrees C until tested. Do not use plasma.

Procedure

Reagents & Equipment:

  • Reference Standard. A reference serum with normal complement levels is required to standardize the assay.
    • EZ Complement Standard, Diamedix Corporation, Catalog No. 789-006 (Store in the lyophilized state, at -20 degrees C), is a reference preparation suitable for standardizing the assay. This standard is prepared from human complement & is stabilized by lyophilization.
    • Reconstitute with 0.3 mL cold (2 - 8 degrees C) distilled water. Swirl gently and refrigerate for 15 - 30 minutes before use. Remove from refrigerator and gently swirl again. Use immediately. Discard unused portion.
  • Diamedix EZ Reader Photometer, Diamedix Corporation Catalog #783-001.

Calibration:

Calibration of the EZ Reader is performed with the reference standard at the time of reading the test results.

See procedure below.

Quality Control:

The reference controls (low positive and high positive) controls are prepared from human complement and are stabilized by lyophilization. Reconstitute with 0.3 mL. cold (2-8 degrees C) distilled water. Swirl gently and refrigerate for 15 - 30 minutes before use. Remove from refrigerator and gently swirl again. Use immediately. Discard unused portion.

A low and a high positive control is run with each batch of CH50 assays. They should be within the range that is printed on the label of each vial used. If not, do not accept the run. The whole assay will have to be repeated. If still out of control, notify the supervisor for further investigation.

General instructions:

  • Set up as many tubes as there are specimens for testing, plus one tube for the reference serum, and one tube for the 'spontaneous lysis' control. The 'Spontaneous Lysis' control is simply one of the EZ Complement tubes containing only the sheep erythrocytes in buffer (no sample). Place test tubes containing the Sensitized Cells in a rack and allow to warm to room temperature (1 hour). Vortex or shake vigorously for 10 seconds to resuspend cells.
  • Remove stopper and transfer 0.005 mL (5ul) of test serum sample, or reference serum, into a tube. Replace stopper & mix immediately by vortexing the tubes. The 'spontaneous lysis' tube should not receive a serum sample, but its contents should also be vortexed.
  • Allow the tubes to stand at room temperature for 60 + 5 minutes. Mix the contents of all of the tubes again by vortexing.
  • Centrifuge the tubes at approximately 1800 rpm for at least 10 minutes.
  • Read the absorbance of the supernates in the EZ Reader Photometer within 15 minutes.

Calculations:

No calculations are required when reading the samples on the EZ reader. When a spectrophotometer other than the EZ reader is used to read the supernate,and results are to be reported out as '% of Reference,' the following calculations are necessary.

Abs of Sample x % value of St'd = % of Reference

Abs of St'd

When results are to be reported out as 'CH50 Units', the following calculations are used.

Absorbance of sample

Absorbance of standard

Reporting Results:

Results can be reported as '% of Reference' or as CH50 Units. When reading the sample on the Diamedix EZ Reader, values that are printed under the 'conc' column on the printer tape are the '% of Reference' values for each sample if the % value of the reference standard is entered when the EZ Reader asks the user to 'Key value of S #1.' If the 'CH50 value' of the reference is entered column will be CH50 units. This lab reports the results out in CH50 units.

Sources of Error:

  • Serum not being properly stored prior to testing.
  • Tubes not being well-mixed prior to & after adding patient serum, & before spinning tubes in centrifuge.
  • Allowing reaction tubes to stand longer or less than 60 minutes, + 5 minutes.
  • Not allowing tubes to spin for at least 10 minutes at 1800 rpm.
  • Waiting longer than 15 minutes to read test after spinning down tubes.
  • Distilled water not being chilled before reconstitution of standard and controls.
  • Not swirling reconstituted controls and standard to dissolve all the lyophilized material on the sides and cap of vials. .

Notes

It is better that not more than 12 tubes be set up per run due to critical timing of assay

More general terms

Additional terms

References

  1. Package Insert, EZ Complement CH50 Assay, Diamedix Corporation, Miami, Fl, 1989
  2. Tietz, Norbert W. Textbook of Clinical Chemistry, The W.B. Saunders Co., p. 579, 1986.
  3. Rose, Noel R. and Freedman, Herman, Manual of Clinical Immunology, 2nd Edition, American Society for Microbiology, pp 166-167, 1980.
  4. Stites, Daniel P., Stobo, John D., Wells, Vivian J., Basic and Clinical Immunology, 6th Edition. Appleton and Lange, pp. 277-278, 1987
  5. Clinical Guide to Laboratory Tests, 3rd ed. Teitz ed., W.B. Saunders, 1995.
  6. 6.0 6.1 6.2 Medical Knowledge Self Assessment Program (MKSAP) 15, American College of Physicians, Philadelphia 2009
    Medical Knowledge Self Assessment Program (MKSAP) 19 Board Basics. An Enhancement to MKSAP19. American College of Physicians, Philadelphia 2022
  7. 7.0 7.1 Interpretation of Diagnostic tests, 8th edition, Wallach J, Lippincott, Williams & Wilkens, Philadelphia, 2007, pg 14
  8. Complement Activity, Total EIA Laboratory Test Directory ARUP: http://www.aruplab.com/guides/ug/tests/0050198.jsp