Literature DB >> 19211156

Myelin basic protein-reactive T cells persist in an inactive state in the bone marrow of Lewis rats that have recovered from autoimmune encephalomyelitis.

Taba Kheradmand1, Norbert A Wolf, Robert H Swanborg.   

Abstract

Lewis rats immunized with guinea pig myelin basic protein residues 68-86 develop acute experimental autoimmune encephalomyelitis and recover. The predominant T cell receptor expressed by the encephalitogenic T cells is TCRBV8S2. They persist in bone marrow many weeks after recovery. CD3 is down-regulated, but >90% express CD4. They fail to proliferate to GPMBP68-86 unless a nitric oxide synthase inhibitor is added to the cultures. Perhaps these are memory T cells that are maintained in a suppressed state in BM by a nitric oxide-dependent mechanism.

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Year:  2009        PMID: 19211156      PMCID: PMC2699580          DOI: 10.1016/j.jneuroim.2009.01.018

Source DB:  PubMed          Journal:  J Neuroimmunol        ISSN: 0165-5728            Impact factor:   3.478


  31 in total

1.  Clinical relapses of multiple sclerosis are associated with 'novel' valleys in natural killer cell functional activity.

Authors:  Lorne F Kastrukoff; Allen Lau; Richard Wee; Daniel Zecchini; Richard White; Donald W Paty
Journal:  J Neuroimmunol       Date:  2003-12       Impact factor: 3.478

Review 2.  T cell receptor signaling: beyond complex complexes.

Authors:  Yanping Huang; Ronald L Wange
Journal:  J Biol Chem       Date:  2004-04-14       Impact factor: 5.157

3.  Evidence for suppressor cells in Lewis rats' experimental allergic encephalomyelitis.

Authors:  D H Adda; E Beraud; R Depieds
Journal:  Eur J Immunol       Date:  1977-09       Impact factor: 5.532

4.  Experimental allergic encephalomyelitis in the Lewis rat: studies on the mechanism of recovery from disease and acquired resistance to reinduction.

Authors:  D O Willenborg
Journal:  J Immunol       Date:  1979-09       Impact factor: 5.422

5.  Experimental allergic encephalomyelitis in Lewis rats: chemical synthesis of disease-inducing determinant.

Authors:  G A Hashim
Journal:  Science       Date:  1977-06-10       Impact factor: 47.728

6.  Inhibition of nitric oxide synthase initiates relapsing remitting experimental autoimmune encephalomyelitis in rats, yet nitric oxide appears to be essential for clinical expression of disease.

Authors:  N C O'Brien; B Charlton; W B Cowden; D O Willenborg
Journal:  J Immunol       Date:  2001-11-15       Impact factor: 5.422

7.  Down-regulation of the T cell receptor CD3 zeta chain in rheumatoid arthritis (RA) and its influence on T cell responsiveness.

Authors:  L Berg; J Rönnelid; L Klareskog; A Bucht
Journal:  Clin Exp Immunol       Date:  2000-04       Impact factor: 4.330

8.  Autoreactive T cells persist in rats protected against experimental autoimmune encephalomyelitis and can be activated through stimulation of innate immunity.

Authors:  Stephanie B Conant; Robert H Swanborg
Journal:  J Immunol       Date:  2004-05-01       Impact factor: 5.422

9.  Characterization of a subset of bone marrow-derived natural killer cells that regulates T cell activation in rats.

Authors:  Taba Kheradmand; Prachi P Trivedi; Norbert A Wolf; Paul C Roberts; Robert H Swanborg
Journal:  J Leukoc Biol       Date:  2008-02-13       Impact factor: 4.962

Review 10.  Experimental autoimmune encephalomyelitis in the rat: lessons in T-cell immunology and autoreactivity.

Authors:  R H Swanborg
Journal:  Immunol Rev       Date:  2001-12       Impact factor: 12.988

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