Listeria Antibody, CF

Test Code

LSTAB

Alias/See Also

LAB13736

CPT Codes
86609

Preferred Specimen

1 mL serum collected in a red-top tube

Minimum Volume

0.5 mL

Transport Temperature

Room temperature

Specimen Stability

Room temperature: 7 days Refrigerated: 14 days Frozen: 30
days

Methodology

Complement Fixation (CF)
This test was developed and its analytical performance characteristics have been determined by Quest Diagnostics. It has not been cleared or approved by FDA. This assay has been validated pursuant to the CLIA regulations and is used for clinical purposes.

FDA Status
This test was developed and its analytical performance characteristics have been determined by Quest Diagnostics. It has not been cleared or approved by the U.S. Food and Drug Administration. This assay has been validated pursuant to the CLIA regulations and is used for clinical purposes.

Setup Schedule

Tues-Sat a.m.

Report Available

1-5 days

Reference Range

<1:8

Clinical Significance

This test uses complement fixation to detect antibodies to Listeria monocytogenes in serum and may be helpful in diagnosing encephalitis caused by L monocytogenes [1]. Listeriosis is mainly diagnosed by isolation of L monocytogenes; serologic tests for listeriosis are not recommended, because of their low sensitivity and specificity [2].

Listeriosis is the third-leading cause of death from eating contaminated food. Each year in the United States, approximately 1,600 people are diagnosed with listeriosis and 260 die of the condition [2]. Infected pregnant women usually have mild flu-like symptoms. However, by crossing the placenta and infecting fetuses, Listeria can cause fetal loss or newborn death in up to a quarter of cases [2,3]. Other groups at high risk of developing serious disease secondary to Listeria infection include elderly and immunocompromised individuals.

Listeria infection is mainly diagnosed by isolation of L monocytogenes from a normally sterile site. Detecting Listeria antibodies with complement fixation in serum and/or cerebrospinal fluid may be helpful for diagnosing encephalitis caused by L monocytogenes [1]. Because of their low sensitivity and specificity, serologic tests are inadequate for diagnosing listeriosis and thus are generally not recommended [2-4].

The results of this test should be interpreted in the context of pertinent clinical history and physical examination findings.

References
1. Miller JM, et al. Clin Infect Dis. 2018;67(6):813-816.
2. Center for Disease Control and Prevention. Listeria (Listeriosis). Accessed January 26, 2022. https://www.cdc.gov/listeria/technical.html
3. Wellinghausen N. Toxoplasma. In: Carroll KC, et al, eds. Manual of Clinical Microbiology. 12th ed. ASM Press; 2019. https://www.clinmicronow.org/doi/full/10.1128/9781683670438.MCM.ch28_1
4. Gellin BG, Broome CV. Listeriosis. JAMA. 1989;261(9):1313-1320.

Performing Laboratory
Quest Diagnostics Infectious Disease, Inc. 33608 Ortega Highway, Bldg B-West Wing San Juan Capistrano, CA 92675-2042

Last Updated: February 17, 2023

The CPT Codes provided in this document are based on AMA guidelines and are for informational purposes only. CPT coding is the sole responsibility of the billing party. Please direct any questions regarding coding to the payor being billed. Any Profile/panel component may be ordered separately. Reflex tests are performed at an additional charge.