✦ LIBER ✦

The basis of autoimmunity in MRL-lpr/lpr mice: a role for self Ia-reactive T cells

✍ Scribed by Yvonne J. Rosenberg; Alfred D. Steinberg; Thomas J. Santoro

Publisher: Elsevier Science
Year: 1984
Tongue: English
Weight: 467 KB
Volume: 5
Category: Article
ISSN: 0167-5699
DOI: 10.1016/0167-5699(84)90166-x

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

The lymphoproliferating cells of MRL-lpr

The lymphoproliferating cells of MRL-lpr/lpr mice are a polyclonal population that bear the T lymphocyte receptor for antigen

✍ David A. Nemazee; Suzanne Studer; Michael Steinmetz; Zlatko Dembić; Michael Kief 📂 Article 📅 1985 🏛 John Wiley and Sons 🌐 English ⚖ 610 KB

The expansion of a CD4+ T cell populatio

The expansion of a CD4+ T cell population bearing a distinctive β chain in MRL lpr/lpr mice suggests a role for the fas protein in peripheral T cell selection

✍ Philippe Musette; Christophe Pannetier; Gabriel Gachelin; Philippe Kourilsky 📂 Article 📅 1994 🏛 John Wiley and Sons 🌐 English ⚖ 623 KB

T cell recognition and therapeutic effec

T cell recognition and therapeutic effect of a phosphorylated synthetic peptide of the 70K snRNP protein administered in MRL/lpr mice

✍ Fanny Monneaux; José Manuel Lozano; Manuel E. Patarroyo; Jean-Paul Briand; Sylvi 📂 Article 📅 2003 🏛 John Wiley and Sons 🌐 English ⚖ 244 KB 👁 1 views

## Abstract Modifications of self antigens that occur during apoptosis might be involved in the generation of neo‐antigens, which can break tolerance and induce autoimmunity. We have previously identifiedan epitope at residues 131–151 of the U1‐70K snRNP protein, recognized by IgG antibodies and CD

A specific intercellular pathway of apop

A specific intercellular pathway of apoptotic cell death is defective in the mature peripheral T cells of autoimmune lpr and gld mice

✍ Illona Gillette-Ferguson; Charles L. Sidman 📂 Article 📅 1994 🏛 John Wiley and Sons 🌐 English ⚖ 540 KB

T cells of staphylococcal enterotoxin B-

T cells of staphylococcal enterotoxin B-tolerized autoimmune MRL-lpr/lpr mice require co-stimulation through the B7-CD28/CTLA-4 pathway for activation and can be reanergized in vivo by stimulation of the T cell receptor in the absence of this co-stimulatory signal

✍ Tong Zhou; Casey Weaver; Peter S. Linsley; John D. Mountz 📂 Article 📅 1994 🏛 John Wiley and Sons 🌐 English ⚖ 811 KB