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Test Code MMRV MMRV Immune Status Profile, Serum

Reporting Name

MMRV Immune Status Profile, S

Useful For

Determination of 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


Specimen Required


Preferred: Serum gel

Acceptable: Red top

Specimen Volume: 1 mL

Specimen Minimum Volume

0.4 mL

Specimen Stability Information

Specimen Type Temperature Time Special Container
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



Vaccinated: Positive (≥1.0 AI)

Unvaccinated: Negative (≤0.7 AI)

Reference values apply to all ages

CPT Code Information

86735-Mumps virus antibody, IgG

86762-Rubella antibodies, IgG

86765-Measles (rubeola) antibodies, IgG

86787-Varicella-Zoster antibody, IgG

LOINC Code Information

Test ID Test Order Name Order LOINC Value
MMRV MMRV Immune Status Profile, S In Process


Result ID Test Result Name Result LOINC Value
VZG Varicella-Zoster Ab, IgG, S 15410-4
RBG Rubella Ab, IgG, S 40667-8
MUMG Mumps Ab, IgG, S 6476-6
ROG Measles (Rubeola) Ab, IgG, S 35275-7
DEXG3 Measles IgG Antibody Index 5244-9
DEXG2 Rubella IgG Antibody Index 52986-7
DEXG5 Mumps IgG Antibody Index 25418-5
DEXG4 Varicella IgG Antibody Index 5403-1

Reject Due To

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

Method Name

Multiplex Flow Immunoassay (MFI)


If not ordering electronically, complete, print, and send a Microbiology Test Request (T244) with the specimen.

Test Classification

This test has been cleared or approved by the U.S. Food and Drug Administration and is used per manufacturer's instructions. Performance characteristics were verified by Mayo Clinic in a manner consistent with CLIA requirements.