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Order Code LABMMRVM Measles, Mumps, Rubella, and Varicella (MMRV) Immune Status Profile, Serum

Important Note

This test provides qualitative and quantitative results.

If qualitative results are only needed, please order: MEASLES, MUMPS, RUBELLA & VARICELLA ZOSTER IMMUNE STATUS [LABMMRV]

Additional Codes

Mayo Test Code: MMRV
EPIC Test Code: LABMMRVM

Reporting Name

MMRV Immune Status Profile, S

Useful For

Determining immune status of individuals to measles, mumps, rubella, and varicella-zoster viruses (VZV)

 

Documentation of previous infection with measles, mumps, rubella, or VZV in an individual without a previous record of immunization to these viruses

Profile Information

Test ID Reporting Name Available Separately Always Performed
ROPG Measles (Rubeola) Ab, IgG, S Yes Yes
MPPG Mumps Ab, IgG, S Yes Yes
RBPG Rubella Ab, IgG, S Yes Yes
VZPG Varicella-Zoster Ab, IgG, S Yes Yes

Performing Laboratory

Mayo Clinic Laboratories in Rochester

Specimen Type

Serum


Specimen Required


Supplies: Sarstedt Aliquot Tube 5 mL (T914)

Collection Container/Tube:

Preferred: Serum gel

Acceptable: Red top

Submission Instructions: Plastic vial

Specimen Volume: 1 mL

Collection Instructions: Centrifuge and aliquot serum into a plastic vial.


Specimen Minimum Volume

0.4 mL

Specimen Stability Information

Specimen Type Temperature Time
Serum Refrigerated (preferred) 14 days
  Frozen  14 days

Reference Values

MEASLES, MUMPS and VARICELLA:

Vaccinated: Positive (≥1.1 AI)

Unvaccinated: Negative (≤0.8 AI)

Reference values apply to all ages

 

RUBELLA:

Vaccinated: Positive (≥1.0 AI)

Unvaccinated: Negative (≤0.7 AI)

Reference values apply to all ages

CPT Code Information

86735

86762

86765

86787

Ridgeview Laboratory Note:

This test provider QUANTITATIVE results along with the qualitative results.

Method Description

The BioPlex 2200 MMRV IgG kit uses multiplex flow immunoassay technology, which allows for the detection and identification of many different antibodies in a single tube. Four different populations of dyed beads are coated with antigens to identify the presence of IgG-class antibodies associated with measles, mumps, rubella, and varicella-zoster. The patient sample, sample diluent, and bead set reagent are mixed together in a reaction vessel and then incubated at 37° C. After a wash cycle, anti-human IgG antibody conjugated to phycoerythrin (PE) is added to the dyed beads, and this mixture is incubated at 37° C. Excess conjugate is removed during a wash cycle, and the beads are resuspended in wash buffer. The bead mixture next passes through the detector, and the identity of the beads is determined by the fluorescence of the dyes. The amount of antibody captured by the antigen on the bead is determined by the fluorescence of the attached PE. Raw data is calculated in relative fluorescence intensity.

 

Three additional dyed beads, an internal standard bead, a serum verification bead, and a reagent blank bead are present in each reaction mixture to verify detector response, the addition of serum to the reaction vessel, and the absence of significant non-specific binding in serum.(Package insert: BioPlex 2200 System MMRV IgG. Bio-Rad Laboratories; 02/2019)

Reject Due To

Gross hemolysis Reject
Gross lipemia Reject
Gross icterus Reject
Heat-inactivated specimen Reject

Method Name

Multiplex Flow Immunoassay (MFI)

Forms

If not ordering electronically, complete, print, and send Infectious Disease Serology Test Request (T916) with the specimen.

Day(s) Performed

Monday through Friday