Clinical features of HTLV-1-associated myelopathy/tropical spastic paraparesis (HAM/TSP) in northeast Iran

2013 ◽  
Vol 113 (4) ◽  
pp. 427-433 ◽  
Author(s):  
Ali Shoeibi ◽  
Houshang Rafatpanah ◽  
Amir Azarpazhooh ◽  
Naghme Mokhber ◽  
Mohammad Reza Hedayati-Moghaddam ◽  
...  
1996 ◽  
Vol 2 (2) ◽  
pp. 88-90 ◽  
Author(s):  
Fidias E Leon-S ◽  
Kimiyoshi Arimura ◽  
Mitsuhiro Osame

Multiple sclerosis (MS) and HTLV-I associated myelopathy/tropical spastic paraparesis (HAM/TSP) can overlap in their clinical features and thereby cause difficulties for clinicians in relation to diagnosis and therapy. However, epidemiological biochemical, immunological, virological and radiological studies point to a number of significant differences. Recent comparative neurophysiological data, induding blink reflex studies, obtained in these disorders, is briefly reviewed here and provides additional evidence of difference. The abnormal blink reflex in patients with MS consist of prolonged latencies and absences of R1 and R2 responses and are mainly due to demyelinating lesions around the pons. In contrast, in HAM/TSP the blink reflex abnormalities frequently include an unusual early response, R/k, which is probably a consequence of interneuronal hyperexcitability around the brainstem. Thus these findings provide further support for our contention that HAM/TSP and multiple sclerosis are distinctly different both as clinical entities and in their underlying pathomechanisms.


1999 ◽  
Vol 73 (6) ◽  
pp. 4575-4581 ◽  
Author(s):  
Masahiko Makino ◽  
Satoshi Shimokubo ◽  
Shin-Ichi Wakamatsu ◽  
Shuji Izumo ◽  
Masanori Baba

ABSTRACT The development of human T-lymphotropic virus type 1 (HTLV-1)-associated myelopathy/tropical spastic paraparesis (HAM/TSP) is closely associated with the activation of T cells which are HTLV-1 specific but may cross-react with neural antigens (Ags). Immature dendritic cells (DCs), differentiated from normal donor monocytes by using recombinant granulocyte-macrophage colony-stimulating factor and recombinant interleukin-4, were pulsed with HTLV-1 in vitro. The pulsed DCs contained HTLV-1 proviral DNA and expressed HTLV-1 Gag Ag on their surface 6 days after infection. The DCs matured by lipopolysaccharides stimulated autologous CD4+ T cells and CD8+ T cells in a viral dose-dependent manner. However, the proliferation level of CD4+ T cells was five- to sixfold higher than that of CD8+ T cells. In contrast to virus-infected DCs, DCs pulsed with heat-inactivated virions activated only CD4+ T cells. To clarify the role of DCs in HAM/TSP development, monocytes from patients were cultured for 4 days in the presence of the cytokines. The expression of CD86 Ag on DCs was higher and that of CD1a Ag was more down-regulated than in DCs generated from normal monocytes. DCs from two of five patients expressed HTLV-1 Gag Ag. Furthermore, both CD4+ and CD8+ T cells from the patients were greatly stimulated by contact with autologous DCs pulsed with inactivated viral Ag as well as HTLV-1-infected DCs. These results suggest that DCs are susceptible to HTLV-1 infection and that their cognate interaction with T cells may contribute to the development of HAM/TSP.


2021 ◽  
Vol 9 (7) ◽  
Author(s):  
Hiroshi Mori ◽  
Eiji Shibata ◽  
Tomoichiro Kuwazuru ◽  
Takayuki Uchimura ◽  
Emi Kondo ◽  
...  

2010 ◽  
Vol 82 (8) ◽  
pp. 1438-1441 ◽  
Author(s):  
Alena Mayo Iñiguez ◽  
René Gastaldello ◽  
Koko Otsuki ◽  
Marcos Balangero ◽  
Filipe Carvalho Costa ◽  
...  

1989 ◽  
Vol 160 (3) ◽  
pp. 371-379 ◽  
Author(s):  
G. McKhann ◽  
C. J. Gibbs ◽  
C. A. Mora ◽  
P. E. Rodgers-Jobnson ◽  
P. P. Liberski ◽  
...  

Lupus ◽  
1995 ◽  
Vol 4 (2) ◽  
pp. 138-141 ◽  
Author(s):  
Wendell A Wilson ◽  
Owen St. C Morgan ◽  
EN Barton ◽  
M. Smikle ◽  
B. Hanchard ◽  
...  

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