Abstract |
A causal role of IL-4 (Th2) production for recovery in experimental allergic neuritis (EAN) was indicated by experiments where Th1-like autoreactive cell populations, taken from the induction phase of the disease, were deviated to extensive secretion of IL-4 in a selective fashion, by ex vivo stimulation with autoantigen in the presence of IL-4. The deviated cells were adoptively transferred to EAN rats at a time just prior to the onset of clinical signs. This treatment ameliorated EAN compared with sham treatment. This therapeutic approach, with generation of autoreactive IL-4-secreting cells ex vivo followed by subsequent adoptive transfer, may become a new selective treatment of organ-specific autoimmune diseases since, in contrast to previous attempts, it is done in a physiological and technically easy way.
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Authors | C Ekerfelt, C Dahle, R Weissert, M Kvarnström, T Olsson, J Ernerudh |
Journal | Clinical and experimental immunology
(Clin Exp Immunol)
Vol. 123
Issue 1
Pg. 112-8
(Jan 2001)
ISSN: 0009-9104 [Print] England |
PMID | 11168007
(Publication Type: Journal Article)
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Chemical References |
- Cytokines
- Epitopes, T-Lymphocyte
- Myelin P2 Protein
- Peptide Fragments
- Recombinant Proteins
- myelin P2 peptide SP26
- Interleukin-4
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Topics |
- Adoptive Transfer
(methods)
- Animals
- Cytokines
(metabolism)
- Epitopes, T-Lymphocyte
(immunology, toxicity)
- Interleukin-4
(biosynthesis, genetics, pharmacology)
- Lymph Nodes
(cytology, immunology, metabolism)
- Lymphocyte Transfusion
- Male
- Myelin P2 Protein
(immunology, toxicity)
- Neuritis, Autoimmune, Experimental
(immunology, metabolism, prevention & control)
- Peptide Fragments
(immunology, toxicity)
- Rats
- Rats, Inbred Lew
- Recombinant Proteins
(pharmacology)
- T-Lymphocyte Subsets
(immunology, metabolism, transplantation)
- Th2 Cells
(immunology, metabolism, transplantation)
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