Crossref journal-article
Oxford University Press (OUP)
The Journal of Immunology (286)
Abstract

Abstract Lewis x Buffalo F1 rat lymphocytes express both forms of the allelic marker RT7.1 (Lewis) and RT7.2 (Buffalo). We generated myelin basic protein (MBP)-specific encephalitogenic F1 T helper cell lines and adoptively transferred them into naive irradiated Lewis recipients, which enabled us to detect and isolate donor T cells (with RT7.2) within the recipients. The spinal cord and cerebrospinal fluid (CSF) were highly enriched for the donor T cells compared with the blood and spleen. The donor cell number peaked on the first day of disease in the spinal cord and CSF and decreased as the disease progressed. A high percentage of the donor T cells isolated from the spinal cord were positive for the T helper cell activation marker OX-40, whereas a (lower) percentage of CSF donor cells expressed OX-40. Donor cells isolated from blood or spleen were negative for OX-40 expression. In contrast, the IL-2 receptor (CD25) was positive on all the transferred T cells in all tissue sites examined. Cell-sorting experiments showed that the MBP-specific donor cells were enriched for IFN-gamma, IL-2, TNF-alpha, and IL-3 mRNA when compared with the host-recruited spinal cord cells, whereas similar amounts of IL-10 mRNA were produced by both populations. Lymphokine mRNA production was also enriched in donor T cells isolated from the spinal cord compared with donor T cells isolated from the spleen. The spinal cord donor cells produced higher levels of IL-2, IFN-gamma, and IL-3 mRNA, whereas similar amounts of IL-10 and TNF-alpha mRNA were produced from donor cells isolated from the spleen and the spinal cord. Our data suggest that the amount/percentage, activation state, and enhanced lymphokine production at the site of inflammation are all important factors in determining the autoimmune potential of Ag-specific effector T helper cells.

Bibliography

Weinberg, A. D., Wallin, J. J., Jones, R. E., Sullivan, T. J., Bourdette, D. N., Vandenbark, A. A., & Offner, H. (1994). Target organ-specific up-regulation of the MRC OX-40 marker and selective production of Th1 lymphokine mRNA by encephalitogenic T helper cells isolated from the spinal cord of rats with experimental autoimmune encephalomyelitis. The Journal of Immunology, 152(9), 4712–4721.

Authors 7
  1. A D Weinberg (first)
  2. J J Wallin (additional)
  3. R E Jones (additional)
  4. T J Sullivan (additional)
  5. D N Bourdette (additional)
  6. A A Vandenbark (additional)
  7. H Offner (additional)
References 0 Referenced 79

None

Dates
Type When
Created 2 years, 8 months ago (Dec. 31, 2022, 5:59 a.m.)
Deposited 5 months ago (March 31, 2025, 12:43 p.m.)
Indexed 2 months, 2 weeks ago (June 21, 2025, 12:30 a.m.)
Issued 31 years, 4 months ago (May 1, 1994)
Published 31 years, 4 months ago (May 1, 1994)
Published Online 31 years, 4 months ago (May 1, 1994)
Published Print 31 years, 4 months ago (May 1, 1994)
Funders 0

None

@article{Weinberg_1994, title={Target organ-specific up-regulation of the MRC OX-40 marker and selective production of Th1 lymphokine mRNA by encephalitogenic T helper cells isolated from the spinal cord of rats with experimental autoimmune encephalomyelitis.}, volume={152}, ISSN={1550-6606}, url={http://dx.doi.org/10.4049/jimmunol.152.9.4712}, DOI={10.4049/jimmunol.152.9.4712}, number={9}, journal={The Journal of Immunology}, publisher={Oxford University Press (OUP)}, author={Weinberg, A D and Wallin, J J and Jones, R E and Sullivan, T J and Bourdette, D N and Vandenbark, A A and Offner, H}, year={1994}, month=may, pages={4712–4721} }