𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Effects of oral tolerance induction by myelin basic protein on Vβ8+ lewis rat T cells

✍ Scribed by Shari Goldman-Brezinski; Xiang-Ming Zhang; Dr. Ellen Heber-Katz; Keith Brezinski; Ingrid Gienapp; Karen Cox; Caroline Whitacre


Publisher
John Wiley and Sons
Year
1998
Tongue
English
Weight
148 KB
Volume
51
Category
Article
ISSN
0360-4012

No coin nor oath required. For personal study only.

✦ Synopsis


Encephalitogenic T cells from Lewis rats use a restricted T cell receptor (TCR) gene combination, Vbeta8.2 and Valpha2. The oral administration of myelin basic protein (MBP) to Lewis rats prior to encephalitogenic challenge results in a marked inhibition of clinical neurologic signs of encephalitis, reduced central nervous system pathology, suppressed T cell reactivity to MBP, and decreased serum anti-MBP antibody responses. The present study determined the TCR Vbeta8 gene usage in rats rendered orally tolerant to MBP as compared with vehicle-fed or unfed controls. Total RNA was extracted from lymph node cells (LNC), Northern blots run, and hybridizations performed using a rat beta chain V region probe positive for Vbeta8.2. The results indicate that feeding MBP results in a decrease in Vbeta8+ TCR RNA expression in lymph nodes draining the site of encephalitogenic challenge. T cell proliferation was reduced in LNC of tolerized rats relative to control rats. No change in the Vbeta8+ TCR RNA expression or MBP reactivity was observed in the mesenteric lymph nodes (MLN) of vehicle-fed or MBP-fed rats, although an increase in cell number was found in the MLN of both groups. These results suggest that the mechanisms of orally induced tolerance involve local clonal deletion or migration of Vbeta8+ T cells, of which MBP-specific T cells are a part.


📜 SIMILAR VOLUMES


Usage of vβ3.3 T-cell receptor by myelin
✍ Andrew Chan; Ralf Gold; Gerhard Giegerich; Thomas Herrmann; Stefan Jung; Klaus V 📂 Article 📅 1999 🏛 John Wiley and Sons 🌐 English ⚖ 470 KB 👁 1 views

T-cell receptor (TCR) ␤-chain usage in experimental autoimmune encephalomyelitis (EAE) seems to be much more heterogeneous than previously assumed even for a single autoantigen in an inbred animal strain. Owing to the lack of suitable antibodies, this has been demonstrated only at the RNA level so f