Evaluation of total immunoglobulin G and subclass antibodies in an enzyme-linked immunosorbent assay for serodiagnosis of human amebic liver abscess

Author:

Janwan Penchom12,Sadaow Lakkhana34,Rodpai Rutchanee34,Yamasaki Hiroshi56,Luvira Vor7,Sukeepaisarnjaroen Wattana8,Kitkhuandee Amnat7,Paonariang Krisada7,Sanpool Oranuch34,Boonroumkaew Patcharaporn34,Thanchomnang Tongjit49,Mita Toshihiro6,Intapan Pewpan M.34,Maleewong Wanchai34

Affiliation:

1. Department of Medical Technology, School of Allied Health Sciences, Walailak University, Nakhon Si Thammarat, Thailand

2. Hematology and Transfusion Science Research Center, Walailak University, Nakhon Si Thammarat, Thailand

3. Department of Parasitology, Faculty of Medicine, Khon Kaen University, Khon Kaen, Thailand

4. Mekong Health Science Research Institute, Khon Kaen University, Khon Kaen, Thailand

5. Department of Parasitology, National Institute of Infectious Diseases, Tokyo, Japan

6. Department of Tropical Medicine and Parasitology, Juntendo University School of Medicine, Tokyo, Japan

7. Department of Surgery, Faculty of Medicine, Khon Kaen University, Khon Kaen, Thailand

8. Department of Medicine, Faculty of Medicine, Khon Kaen University, Khon Kaen, Thailand

9. Faculty of Medicine, Mahasarakham University, Maha Sarakham, Thailand

Abstract

Background Amebic liver abscess (ALA) caused by Entamoeba histolytica is usually diagnosed based on its clinical symptoms, medical imaging abnormalities of the liver, and serological tests, the most common being the enzyme-linked immunosorbent assay (ELISA). For more than three decades, no investigation has evaluated the diagnostic performance of immunoglobulin G (IgG) subclasses in the serodiagnosis of ALA. Herein, we assessed the efficiencies of anti-amebic IgG and IgG subclasses for diagnosing ALA. Methods A serological ELISA-based test was performed to assess its diagnostic performance using a total of 330 serum samples from ALA patients (n = 14), healthy individuals (n = 40), and patients with other diseases (n = 276). Results ELISA targeting the total IgG antibody to E. histolytica antigen exhibited 100% sensitivity 95% CI [76.8–100.0] and 97.8% specificity 95% CI [95.5–99.1], whereas the assay targeting IgG1 showed the same sensitivity (100% 95% CI [76.8–100.0]) and a slightly higher specificity (99.1% 95% CI [97.3–99.8]). The other IgG subclasses (IgG2, IgG3, and IgG4) displayed a lower sensitivity and specificity. The sensitivity and specificity did not significantly differ between tests measuring total IgG and IgG1 (Exact McNemar’s test; p > 0.05), with a concordance of 98.2%, represented by a Cohen’s kappa of 0.83 (p < 0.001), indicating almost perfect agreement. Conclusion ELISA targeting IgG1 can provide valuable information to clinicians in differentiating ALA from other parasitic diseases, cancers, cirrhosis, and viral hepatitis. However, enzyme-conjugated anti-human total IgG is cheaper than anti-human IgG subclasses. Therefore, we suggest that total IgG-based ELISA is sufficient for the routine serodiagnosis of human ALA and possibly other clinical manifestations of invasive amebiasis.

Funder

National Science, Research and Innovation Fund, Thailand

Khon Kaen University, Research and Graduate Studies Affairs

Faculty of Medicine, Khon Kaen University

Publisher

PeerJ

Subject

General Agricultural and Biological Sciences,General Biochemistry, Genetics and Molecular Biology,General Medicine,General Neuroscience

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