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Clinical and Diagnostic Laboratory Immunology, May 1999, p. 383-387, Vol. 6, No. 3
1071-412X/99/$04.00+0
Copyright © 1999, American Society for Microbiology. All rights reserved.

Preparation of Recombinant Human Monoclonal Antibody Fab Fragments Specific for Entamoeba histolytica

Hiroshi Tachibana,1,* Xun-Jia Cheng,1 Katsuomi Watanabe,1 Masataka Takekoshi,2 Fumiko Maeda,2 Satoshi Aotsuka,3 Yoshimasa Kaneda,1 Tsutomu Takeuchi,4 and Seiji Ihara2

Departments of Infectious Diseases1 and Molecular Life Science,2 Tokai University School of Medicine, Isehara, Kanagawa 259-1193, Tokyo Research Center, Nisshinbo Industries, Inc., Nishiarai Sakaecho, Adachi-ku, Tokyo 123-8585,3 and Department of Tropical Medicine and Parasitology, School of Medicine, Keio University, Shinanomachi, Shinjuku-ku, Tokyo 160-8582,4 Japan

Received 12 October 1998/Returned for modification 28 December 1998/Accepted 10 February 1999

Genes coding for human antibody Fab fragments specific for Entamoeba histolytica were cloned and expressed in Escherichia coli. Lymphocytes were separated from the peripheral blood of a patient with an amebic liver abscess. Poly(A)+ RNA was isolated from the lymphocytes, and then genes coding for the light chain and Fd region of the heavy chain were amplified by a reverse transcriptase PCR. The amplified DNA fragments were ligated with a plasmid vector and were introduced into Escherichia coli. Three thousand colonies were screened for the production of antibodies to E. histolytica HM-1:IMSS by an indirect fluorescence-antibody (IFA) test. Lysates from five Escherichia coli clones were positive. Analysis of the DNA sequences of the five clones showed that three of the five heavy-chain sequences and four of the five light-chain sequences differed from each other. When the reactivities of the Escherichia coli lysates to nine reference strains of E. histolytica were examined by the IFA test, three Fab fragments with different DNA sequences were found to react with all nine strains and another Fab fragment was found to react with seven strains. None of the four human monoclonal antibody Fab fragments reacted with Entamoeba dispar reference strains or with other enteric protozoan parasites. These results indicate that the bacterial expression system reported here is effective for the production of human monoclonal antibodies specific for E. histolytica. The recombinant human monoclonal antibody Fab fragments may be applicable for distinguishing E. histolytica from E. dispar and for use in the serodiagnosis of amebiasis.

* Corresponding author. Mailing address: Department of Infectious Diseases, Tokai University School of Medicine, Bohseidai, Isehara, Kanagawa 259-1193, Japan. Phone: 81 (463) 93-1121. Fax: 81 (463) 95-5450. E-mail: htachiba{at}is.icc.u-tokai.ac.jp.

Clinical and Diagnostic Laboratory Immunology, May 1999, p. 383-387, Vol. 6, No. 3
1071-412X/99/$04.00+0
Copyright © 1999, American Society for Microbiology. All rights reserved.


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  • Tachibana, H., Watanabe, K., Cheng, X.-J., Tsukamoto, H., Kaneda, Y., Takeuchi, T., Ihara, S., Petri, W. A. Jr. (2003). VH3 Gene Usage in Neutralizing Human Antibodies Specific for the Entamoeba histolytica Gal/GalNAc Lectin Heavy Subunit. Infect. Immun. 71: 4313-4319 [Abstract] [Full Text]  
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