Early pregnancy factor suppresses the infiltration of lymphocytes and macrophages in the spinal cord of rats during experimental autoimmune encephalomyelitis but has no effect on apoptosis


Autoria(s): Athanasas-Platsis, S.; Zhang, B.; Hillyard, N. C.; Cavanagh, A. C.; Csurhes, P. A.; Morton, H.; McCombe, P. A.
Contribuinte(s)

R. A. Lewis

R. P. Lisak

Data(s)

01/01/2003

Resumo

Early pregnancy factor (EPF) is a secreted protein with immunosuppressive and growth factor properties that has been shown to suppress acute experimental autoimmune encephalomyelitis (EAE) induced with myelin basic protein (MBP) in Lewis rats. EAE is associated with infiltration of the central nervous system (CNS) with inflammatory cells. Spontaneous recovery involves the loss of T lymphocytes from the CNS and the selective apoptosis of Vbeta8.2(+) cells. In the present study, T cell, macrophage (CD11b/c(+)) and B cell (CD45RA(+)) populations in spinal cord and popliteal lymph nodes (LN) of Lewis rats with EAE were quantitated and apoptosis was studied. Rats were treated with EPF or vehicle. Following treatment on day 14 after inoculation with MBP, neither 1 x 100 mug nor 2 x 100 mug doses of EPF affected the total number of cells infiltrating the spinal cord on day 15, although the higher dose caused a decrease in the number of CD5(+) and CD11b/c(+) cells. Treatment with 2 x 100 mug/day from days 10 to 14 decreased the total number of infiltrating cells, and the numbers of CD5(+), CD11b/c(+) and CD45RA(+) cells. Apoptosis was unaffected. No alteration on the number or type of inflammatory cells in the popliteal LN was observed after treatment on days 10-14. However, treatment with EPF from days 0 to 11 increased the total number of T and B cells and CD5(+) T cells found on day 12 in the LN. Similarly, there was an increase in the frequency of MBP-reactive cells in the LN as determined by limiting dilution analysis. These results suggest that EPF treatment reduces the numbers of lymphocytes and macrophages in the CNS, possibly through an effect on cell trafficking. (C) 2003 Elsevier B.V. All rights reserved.

Identificador

http://espace.library.uq.edu.au/view/UQ:65343

Idioma(s)

eng

Publicador

Elsevier BV

Palavras-Chave #Neurosciences #Apoptosis #Early Pregnancy Factor #Experimental Autoimmune Encephalomyelitis #Lymphocytes #Macrophages #Multiple Sclerosis #Spinal Cord #Myelin Basic-protein #Experimental Allergic Encephalomyelitis #Central-nervous-system #Cell Apoptosis #Embryonic-development #V-beta-8.2(+) Cells #Multiple-sclerosis #Sjl/j Mice #Lewis Rats #T-cells #Clinical Neurology #C1 #320207 Autoimmunity #730102 Immune system and allergy
Tipo

Journal Article