Order Code LABMMRVM Measles, Mumps, Rubella, and Varicella (MMRV) Immune Status Profile, Serum
Additional Codes
Mayo Test Code: MMRV
EPIC Test Code: LABMMRVM
Reporting Name
MMRV Immune Status Profile, SUseful 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

Specimen Type
SerumSpecimen 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
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