Volume 32, Issue 5 pp. 651-657
Original Article
Full Access

HTLV-I-specific cytotoxic T lymphocytes in the cerebrospinal fluid of patients with HTLV-I-associated neurological disease

Dr. Steven Jacobson PhD

Corresponding Author

Dr. Steven Jacobson PhD

Neuroimmunology Branch, National Institutes of Health, Bethesda

NIH/NINDS, Building 10, Room 5B-16, Bethesda, MD 20892Search for more papers by this author
Dale E. McFarlin MD

Dale E. McFarlin MD

Neuroimmunology Branch, National Institutes of Health, Bethesda

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Susan Robinson BS

Susan Robinson BS

Neuroimmunology Branch, National Institutes of Health, Bethesda

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Rhonda Voskuhl MD

Rhonda Voskuhl MD

Neuroimmunology Branch, National Institutes of Health, Bethesda

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Roland Martin MD

Roland Martin MD

Neuroimmunology Branch, National Institutes of Health, Bethesda

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Alfred Brewah MS

Alfred Brewah MS

MedImmune Inc, Gaithersburg, MD

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Amy J. Newell BS

Amy J. Newell BS

MedImmune Inc, Gaithersburg, MD

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Scott Koenig PhD, MD

Scott Koenig PhD, MD

MedImmune Inc, Gaithersburg, MD

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First published: November 1992
Citations: 63

Abstract

Recently, it has been shown that in patients with human T-cell lymphotropic virus type I (HTLV-I)–associated neurological disease, high levels of HTLV-I–specific cytotoxic T lymphocytes (CTLs) could be detected in the peripheral blood. These CTLs predominantly recognized products of the pX region of HTLV-I, had a CD8+ phenotype, and were human leukocyte class I restricted. Moreover, these responses were not detected in asymptomatic, HTLV-I–seropositive individuals. This implied a role for these CTLs in the pathogenesis of the neurological disorder associated with HTLV-I. We have extended these observations by demonstrating HTLV-I–specific CTLs directly from lymphocytes obtained from the cerebrospinal fluid of patients with HTLV-I–associated myelopathy/tropical spastic parapare-sis. Uncultured cerebrospinal fluid lymphocytes were used directly as effectors on a variety of targets expressing HTLV-I. These cells were lysed in a virus-specific and HLA class I-restricted manner. Moreover, the cerebrospinal fluid lymphocytes were sorted into purified CD8+ populations, cloned by limiting dilution, and assayed for CTL activity. An exceedingly high proportion of these resultant lines were shown to be cytolytic and precursor frequency analysis indicated that as many as 1 in 500 cells were HTLV-I–specific CTLs. The majority of these CTL lines recognized HTLV-I gene products encoded within the pX region of HTLV-I. The significance of these HTLV-I–specific CTLs in the central nervous system of patients with HTLV-I–associated neurological disease is discussed with regard to the potential role of CTLs in the pathogenesis of this disease.

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