2009
DOI: 10.1016/j.micinf.2009.06.007
|View full text |Cite
|
Sign up to set email alerts
|

Functional analysis of Foxp3 and CTLA-4 expressing HTLV-1-infected cells in a rat model

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
2
1

Citation Types

0
4
0

Year Published

2012
2012
2015
2015

Publication Types

Select...
5

Relationship

1
4

Authors

Journals

citations
Cited by 5 publications
(4 citation statements)
references
References 30 publications
(25 reference statements)
0
4
0
Order By: Relevance
“…The presence of CTLA-4 on CD4 + CD25 + Foxp3 + T cells has been regarded as an explanation for immunosuppression during disease progression in infections with HIV, SIV, HCV, and Trypanosoma and in B cell non-Hodgkin lymphoma (Boasso et al, 2007;Graefe et al, 2004;Kaufmann and Walker, 2009;Leng et al, 2002;Nakamoto et al, 2009;Yang et al, 2006;Zaunders et al, 2006;Zhang et al, 2010). In the model of HTLV-I-related BLV, Foxp3-and CTLA-4-expressing HTLV-I-infected cells suppressed the proliferation of naïve T cells that were stimulated with anti-CD3 antibody (Takayanagi et al, 2009). In the present study, bovine CTLA-4 mRNA was predominantly expressed in CD4 + T cells among cell populations from BLV-infected cattle (data not shown), and the expression of CTLA-4 in CD4 + cells was positively correlated with Foxp3, the most reliable marker for Treg, suggesting that CTLA-4 was expressed by Tregs.…”
Section: Discussionmentioning
confidence: 99%
“…The presence of CTLA-4 on CD4 + CD25 + Foxp3 + T cells has been regarded as an explanation for immunosuppression during disease progression in infections with HIV, SIV, HCV, and Trypanosoma and in B cell non-Hodgkin lymphoma (Boasso et al, 2007;Graefe et al, 2004;Kaufmann and Walker, 2009;Leng et al, 2002;Nakamoto et al, 2009;Yang et al, 2006;Zaunders et al, 2006;Zhang et al, 2010). In the model of HTLV-I-related BLV, Foxp3-and CTLA-4-expressing HTLV-I-infected cells suppressed the proliferation of naïve T cells that were stimulated with anti-CD3 antibody (Takayanagi et al, 2009). In the present study, bovine CTLA-4 mRNA was predominantly expressed in CD4 + T cells among cell populations from BLV-infected cattle (data not shown), and the expression of CTLA-4 in CD4 + cells was positively correlated with Foxp3, the most reliable marker for Treg, suggesting that CTLA-4 was expressed by Tregs.…”
Section: Discussionmentioning
confidence: 99%
“…Our findings of reduced Tregs in skin of patients with ID, an inflammatory condition similar to HAM/TSP, are in agreement with that observation. The reported relationship between FoxP3 expression and ATLL progression [33] may be explained by acquisition of Treg like function of ATLL cells or HTLV-1 infected cells expressing FoxP3, which would impair cellular immune responses perpetuating and exacerbating HTLV-1-associated diseases [33].…”
Section: Discussionmentioning
confidence: 99%
“…As an alternative hypothesis, Treg suppresses immune responses through direct cell–cell contact in a process that is dependent on signaling via CTLA‐4 . Indeed, Foxp3 + CTLA‐4 + expressing HTLV‐1‐infected cells suppressed proliferation of naïve T cells that were stimulated with anti‐CD3 antibody . However, there is no information about bovine CTLA‐4 and its associations with disease.…”
mentioning
confidence: 99%