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Clinical and Diagnostic Laboratory Immunology, September 2001, p. 984-992, Vol. 8, No. 5
1071-412X/01/$04.00+0   DOI: 10.1128/CDLI.8.5.984-992.2001
Copyright © 2001, American Society for Microbiology. All rights reserved.

Presence of Oligoclonal T Cells in Cerebrospinal Fluid of a Child with Multiphasic Disseminated Encephalomyelitis following Hepatitis A Virus Infection

Emilia L. Oleszak,1,* Wan Lu Lin,2 Agustin Legido,3,4 Joseph Melvin,3,4 Huntley Hardison,3,4 Brad E. Hoffman,2 Christos D. Katsetos,2,3,4,5 and Chris D. Platsoucas2

Department of Anatomy and Cell Biology, Fels Institute for Cancer Research and Molecular Biology,1 and Department of Microbiology and Immunology,2 Temple University School of Medicine, Philadelphia, Pennsylvania 19140; and Department of Pediatrics, MCP Hahnemann University,3 and Section of Neurology,4 Department of Pathology and Laboratory Medicine,5 St. Christopher's Hospital for Children, Philadelphia, Pennsylvania 19134

Received 20 November 2000/Returned for modification 26 February 2001/Accepted 22 June 2001

We have investigated the clonality of beta -chain T-cell receptor (TCR) transcripts from the cerebrospinal fluid (CSF) and peripheral blood from a 7-year old child who developed a multiphasic disseminated encephalomyelitis following an infection with hepatitis A virus. We amplified beta -chain TCR transcripts by nonpalindromic adaptor (NPA)-PCR-Vbeta -specific PCR. TCR transcripts from only five Vbeta families (Vbeta 13, Vbeta 3, Vbeta 17, Vbeta 8, and Vbeta 20) were detected in CSF. The amplified products were combined, cloned, and sequenced. Sequence analysis revealed in the CSF substantial proportions of identical beta -chain of TCR transcripts, demonstrating oligoclonal populations of T cells. Seventeen of 35 (48%) transcripts were 100% identical, demonstrating a major Vbeta 13.3 Dbeta 2.1 Jbeta 1.3 clonal expansion. Six of 35 (17%) transcripts were also 100% identical, revealing a second Vbeta 13 clonal expansion (Vbeta 13.1 Dbeta 2.1 Jbeta 1.2). Clonal expansions were also found within the Vbeta 3 family (transcript Vbeta 3.1 Dbeta 2.1 Jbeta 1.5 accounted for 5 of 35 transcripts [14%]) and within the Vbeta 20 family (transcript Vbeta 20.1 Dbeta 1.1 Jbeta 2.4 accounted for 3 of 35 transcripts [8%]). These results demonstrate the presence of T-cell oligoclonal expansions in the CSF of this patient following infection with hepatitis A virus. Analysis of the CDR3 motifs revealed that two of the clonally expanded T-cell clones exhibited substantial homology to myelin basic protein-reactive T-cell clones. In contrast, all Vbeta TCR families were expressed in peripheral blood lymphocytes. Oligoclonal expansions of T cells were not detected in the peripheral blood of this patient. It remains to be determined whether these clonally expanded T cells are specific for hepatitis A viral antigen(s) or host central nervous system antigen(s) and whether molecular mimicry between hepatitis A viral protein and a host protein is responsible for demyelinating disease in this patient.


* Corresponding author. Mailing address: Department of Anatomy and Cell Biology, Fels Institute for Cancer Research and Molecular Biology, Temple University School of Medicine, 3307 North Broad St., Philadelphia, PA 19140. Phone: (215) 707-7657. Fax: (215) 829-1320. E-mail: eoleszak{at}astro.temple.edu.


Clinical and Diagnostic Laboratory Immunology, September 2001, p. 984-992, Vol. 8, No. 5
1071-412X/01/$04.00+0   DOI: 10.1128/CDLI.8.5.984-992.2001
Copyright © 2001, American Society for Microbiology. All rights reserved.



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