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.
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
-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
-chain TCR transcripts by nonpalindromic adaptor (NPA)-PCR-V
-specific PCR. TCR transcripts from only five V
families (V
13, V
3, V
17, V
8, and V
20) were detected in
CSF. The amplified products were combined, cloned, and sequenced.
Sequence analysis revealed in the CSF substantial proportions of
identical
-chain of TCR transcripts, demonstrating oligoclonal
populations of T cells. Seventeen of 35 (48%) transcripts were 100%
identical, demonstrating a major V
13.3 D
2.1 J
1.3 clonal
expansion. Six of 35 (17%) transcripts were also 100% identical,
revealing a second V
13 clonal expansion (V
13.1 D
2.1 J
1.2).
Clonal expansions were also found within the V
3 family (transcript
V
3.1 D
2.1 J
1.5 accounted for 5 of 35 transcripts [14%]) and
within the V
20 family (transcript V
20.1 D
1.1 J
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 V
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.
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