Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Comparative Study
. 2018 Jan;32(1):e22203.
doi: 10.1002/jcla.22203. Epub 2017 Mar 23.

Comparison of commercial methods of immunoblot, ELISA, and chemiluminescent immunoassay for detecting type-specific herpes simplex viruses-1 and -2 IgG

Affiliations
Comparative Study

Comparison of commercial methods of immunoblot, ELISA, and chemiluminescent immunoassay for detecting type-specific herpes simplex viruses-1 and -2 IgG

Fernando de Ory et al. J Clin Lab Anal. 2018 Jan.

Abstract

Background: Serology for type-specific herpes simplex virus (HSV) is based on the use of the respective glycoprotein G (gG).

Methods: Chemiluminescent immunoassay (CLIA; BIO-FLASH® , Biokit, Spain), ELISA (HerpeSelect® , Focus, USA), and immunoblot (IB; Virotech, Germany) for detecting HSV-1- and HSV-2-specific IgG were compared using 384 serum samples received for HSV serology. The samples were classified as positive or negative according to a consensus criterion.

Results: For HSV-1, 262 samples were positive and 118 were negative (four samples were unclassifiable). IB showed agreement, sensitivity, and specificity values of 98.68%, 98.47% and 99.15%, respectively. The corresponding figures for CLIA and ELISA were 98.95%, 99.24% and 98.31%, and 98.16%, 99.62% and 94.92%, respectively. For HSV-2, 106 samples were positive and 278 were negative. Agreement, sensitivity, and specificity of IB were 99.48%, 98.11%, and 100%, respectively. The corresponding figures for CLIA and ELISA were 99.48%, 99.06% and 99.64%, and 98.18%, 99.06% and 97.84%, respectively.

Conclusion: The three methods showed excellent and equivalent performance characteristics for the detection of type-specific IgG to HSV-1 and HSV-2.

Keywords: chemiluminescent immunoassay; enzyme immunoassay; herpes simplex virus type 1; herpes simplex virus type 2; immunoblot.

PubMed Disclaimer

References

    1. Bernstein DI, Bellamy AR, Hook EW III, et al. Epidemiology, clinical presentation, and antibody response to primary infection with herpes simplex virus type 1 and type 2 in young women. Clin Infect Dis. 2013;56:344‐351. - PMC - PubMed
    1. de Ory F, Pachón I, Echevarría JM, Ramírez R. Seroepidemiological study of herpes simplex virus in the female population in the Autonomous Region of Madrid (Spain). Eur J Clin Microbiol Infect Dis. 1999;18:678‐680. - PubMed
    1. Ashley R, Cent A, Maggs V, Nahmias A, Corey L. Inability of enzyme immunoassays to discriminate between infections with herpes simplex types 1 and 2. Ann Intern Med. 1991;115:520‐526. - PubMed
    1. Schmidt NJ, Lennette EH, Magoffin RL. Immunological relationship between herpes simplex and varicella‐zoster viruses demonstrated by complement‐fixation, neutralization and fluorescent antibody tests. J Gen Virol. 1969;4:321‐328. - PubMed
    1. Sánchez‐Martínez D, Schmid DS, Whittington W, et al. Evaluation of a test based on baculovirus‐expressed glycoprotein G for detection of herpes simplex virus type‐specific antibodies. J Infect Dis. 1991;164:1196‐1199. - PubMed

Publication types

MeSH terms

LinkOut - more resources