The JI
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     
 


This Article
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Right arrow Citation Map
Services
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Kennedy, M. K.
Right arrow Articles by Miller, S. D.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Kennedy, M. K.
Right arrow Articles by Miller, S. D.

The Journal of Immunology, Vol 141, Issue 9 2986-2993, Copyright © 1988 by American Association of Immunologists


ARTICLES

Specific immune regulation of chronic-relapsing experimental allergic encephalomyelitis in mice

MK Kennedy, MC Dal Canto, JL Trotter and SD Miller
Department of Microbiology-Immunology, Northwestern University Medical School, Chicago, IL 60611.

These studies were designed to examine immunologic means of regulating the clinical course of murine chronic-relapsing experimental allergic encephalomyelitis (R-EAE). We asked whether induction of specific immune tolerance to the major CNS myelin proteins, myelin basic protein (MBP) and proteolipid protein (PLP), could inhibit the development of R- EAE. Neuroantigen-specific tolerance was induced in SJL/J mice in a dose-dependent manner by the i.v. injection of mouse spinal cord homogenate-coupled syngeneic splenocytes (MSCH-SP) on day -7 relative to immunization on days 0 and +7. Sham-tolerized controls developed significant MBP- and PLP-specific DTH responses before the onset of clinical R-EAE. In contrast, MSCH-SP tolerized mice exhibited a dramatically reduced incidence of clinical and histologic signs of disease which correlated with the failure to develop MBP- and PLP- specific DTH responses. In 10 separate experiments, 118/149 (79%) of control mice, but only 22/137 (16%) of tolerized mice developed clinical R-EAE. Tolerance took time to develop and lasted at least 4 wk as mice injected with Ag-coupled splenocytes on day -1 relative to immunization remained susceptible to R-EAE, whereas mice injected on days -7, -14, or -28 were resistant. Tolerance induction required neuroantigens as injection of splenocytes coupled with a syngeneic mouse kidney homogenate failed to significantly alter the incidence of R-EAE or the development of neuroantigen-specific DTH responses. Thus, induction of R-EAE can be specifically and significantly regulated after the i.v. injection of splenocytes coupled with a crude, heterogeneous mixture of neuroantigens (i.e. MSCH).


This article has been cited by other articles:


Home page
J. Immunol.Home page
H. Zhang, J. R. Podojil, X. Luo, and S. D. Miller
Intrinsic and Induced Regulation of the Age-Associated Onset of Spontaneous Experimental Autoimmune Encephalomyelitis
J. Immunol., October 1, 2008; 181(7): 4638 - 4647.
[Abstract] [Full Text] [PDF]


Home page
J. Immunol.Home page
H. Li, G.-X. Zhang, Y. Chen, H. Xu, D. C. Fitzgerald, Z. Zhao, and A. Rostami
CD11c+CD11b+ Dendritic Cells Play an Important Role in Intravenous Tolerance and the Suppression of Experimental Autoimmune Encephalomyelitis
J. Immunol., August 15, 2008; 181(4): 2483 - 2493.
[Abstract] [Full Text] [PDF]


Home page
J. Immunol.Home page
C. Meagher, Q. Tang, B. T. Fife, H. Bour-Jordan, J. Wu, C. Pardoux, M. Bi, K. Melli, and J. A. Bluestone
Spontaneous Development of a Pancreatic Exocrine Disease in CD28-Deficient NOD Mice
J. Immunol., June 15, 2008; 180(12): 7793 - 7803.
[Abstract] [Full Text] [PDF]


Home page
J. Immunol.Home page
D. M. Turley and S. D. Miller
Peripheral Tolerance Induction Using Ethylenecarbodiimide-Fixed APCs Uses both Direct and Indirect Mechanisms of Antigen Presentation for Prevention of Experimental Autoimmune Encephalomyelitis
J. Immunol., February 15, 2007; 178(4): 2212 - 2220.
[Abstract] [Full Text] [PDF]


Home page
J. Immunol.Home page
T. N. Eagar, D. M. Turley, J. Padilla, N. J. Karandikar, L. Tan, J. A. Bluestone, and S. D. Miller
CTLA-4 Regulates Expansion and Differentiation of Th1 Cells Following Induction of Peripheral T Cell Tolerance
J. Immunol., June 15, 2004; 172(12): 7442 - 7450.
[Abstract] [Full Text] [PDF]


Home page
J. Immunol.Home page
J. S. Leon, K. Wang, and D. M. Engman
Myosin Autoimmunity Is Not Essential for Cardiac Inflammation in Acute Chagas' Disease
J. Immunol., October 15, 2003; 171(8): 4271 - 4277.
[Abstract] [Full Text] [PDF]


Home page
J. Immunol.Home page
G.-X. Zhang, H. Xu, M. Kishi, D. Calida, and A. Rostami
The Role of IL-12 in the Induction of Intravenous Tolerance in Experimental Autoimmune Encephalomyelitis
J. Immunol., March 1, 2002; 168(5): 2501 - 2507.
[Abstract] [Full Text] [PDF]


Home page
CirculationHome page
L. M. Godsel, K. Wang, B. A. Schodin, J. S. Leon, S. D. Miller, and D. M. Engman
Prevention of Autoimmune Myocarditis Through the Induction of Antigen-Specific Peripheral Immune Tolerance
Circulation, March 27, 2001; 103(12): 1709 - 1714.
[Abstract] [Full Text] [PDF]


Home page
Mult SclerHome page
Materials and Methods
Multiple Sclerosis, February 1, 1999; 5(1): 003 - 9.
[PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
This Website Copyright © 1988 by The American Association of Immunologists, Inc. All rights reserved.
All Contents Copyright © 1988 by The American Association of Immunologists, Inc. All rights reserved.