Experimental Autoimmune Encephalomyelitis Develops in CC Chemokine Receptor 7-deficient Mice with Altered T-cell Responses

Autor: Peter Hevezi, Sandra M. Lechner, Anil Pahuja, A. Chen, Richard B. Roth, David G. Alleva, Albert Zlotnik, Gail M. Verge, Richard A. Maki
Rok vydání: 2006
Předmět:
Zdroj: Scandinavian Journal of Immunology. 64:361-369
ISSN: 1365-3083
0300-9475
DOI: 10.1111/j.1365-3083.2006.01787.x
Popis: CC chemokine receptor 7 (CCR7) is involved in the initiation of immune responses by mediating the migration of naive T cells and mature dendritic cells to T-cell-rich zones of secondary lymphoid organs where antigen presen- tation occurs. To address whether CCR7 plays a role in the development of autoimmunity, we induced experimental autoimmune encephalomyelitis in CCR7-deficient mice on a C57BL/6 background (CCR7 )/) ) using the neuroan- tigen, myelin oligodendrocyte glycoprotein 35-55 amino acid peptide (MOG(35)55)) and Bordetella pertussis toxin (PTX). CCR7 )/) mice acquired dis- ease with an intensity similar to wild-type littermates. MOG(35)55)-specific lymphocyte responses were dominant in the spleen of CCR7 )/) mice, rather than in lymph nodes as observed in wild-type mice. These results indicate that effective immune responses (with altered kinetics) can develop in the absence of CCR7 but develop in the spleen rather than lymph nodes as CCR7 is neces- sary for T and dendritic cells to enter lymph nodes.
Databáze: OpenAIRE