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Long term follow up study and prevention of ATL occurrence among HTLV-1 carriers : a nationwide cohort study

Long term follow up study and prevention of ATL occurrence among HTLV-1 carriers : a nationwide cohort study
HTLV-1携带者中ATL发生的长期随访研究和预防:一项全国性队列研究
批准号:
17015047
负责人:
山口 一成
金额:
$58.75万
依托单位国家:
日本
项目类别:
Grant-in-Aid for Scientific Research on Priority Areas
财政年份:
2005
资助国家:
日本
项目状态:
已结题
起止时间:
2005 至 2009

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项目成果

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中文摘要
翻译
目前日本仍有100万HTLV-1运载火箭。携带者状态导致ATL发展的危险因素尚不清楚。研究HTLV-1携带者发生ATL的病毒和宿主特异性决定因素。一项针对HTLV-1携带者的全国性队列研究名为ATL发展诱发因素联合研究(JSPFAD),由41个机构组成。参与者是HTLV-1携带者,他们提供了书面知情同意书。每年检测HTLV-1前病毒载量(VL)和sIL-2R。每年还收集人口统计学特征和临床数据。我们评估了1218 HTLV-1携带者(426名男性和792名女性),他们在2002 - 2008年期间入组。入组时,男性的VL显著高于女性40 - 49岁和50 - 59岁组的平均拷贝数分别为2.10和1.39拷贝/100个PBMC。40岁(P值分别为0.02和0.007),且有ATL家族史者明显高于无ATL家族史者(中位数,2.32 vs 1.33拷贝/100 PBMC)(P = 0.005)。在截至2009年9月的随访期间,14名参与者进展为明显的ATL。他们的基线VL高(范围,4。17 - 28.58拷贝/100PBMC)。基线VL <4拷贝/100 PBMC者无一例发生ATL。多变量考克斯分析表明,不仅VL较高,而且高龄、ATL家族史和在治疗其他疾病期间首次进行HTLV-1检测的机会也是ATL从携带者状态进展的独立危险因素
英文摘要
There are still 1.0 million HTLV-1 carriers in Japan. Definitive risk factors for ATL development from carrier status remain unclear. To investigate viral- and host-specific determinants of the development of ATL among HTLV-1 carriers. A nationwide cohort study for HTLV-1 carriers named the Joint Study on Predisposing Factors of ATL Development (JSPFAD) comprising of 41 institutions. Participants were HTLV-1 carriers who provided written informed consent. HTLV-1 proviral load (VL) and sIL-2R were measured annually. Demographic characteristics and clinical data were also collected annually. We evaluated 1218 HTLV-1 carriers (426 males and 792 females) who were enrolled during 2002-2008. VL at enrollment was significantly higher in males than females (median, 2.10 vs 1.39 copies/100PBMC), in those aged 40-49 and 50-59 yrs than that of those aged &lt ; 40 yrs (P=0.02 and 0.007, respectively), and in those with a family history of ATL than those without the history (median, 2.32 vs 1.33 copies/100PBMC) (P=0.005). During follow-up as of September 2009, 14 participants progressed to overt ATL. Their baseline VL was high (range, 4. 17-28.58 copies/100PBMC). None developed ATL among those with a baseline VL lower than &lt ; 4 copies/100PBMC. Multivariate Cox analyses indicated that not only a higher VL but also advanced age, family history of ATL, and first opportunity for HTLV-1 testing during treatment for other diseases were independent risk factors for progression of ATL from carrier status
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会议论文
Engraftment of peripheral blood mononuclear cells from human T-lymphotropic virus type 1 carriers in NOD/SCID/gammac(null)(NOD) mice.
将人嗜 T 淋巴细胞病毒 1 型携带者的外周血单核细胞移植到 NOD/SCID/gamma(null)(NOD) 小鼠中。
DOI: --
发表时间: 2007
期刊: Int J Cancer 121(10)
影响因子: --
作者: [Takajo I, Umeki K, Morishita K, Yamamoto I, Kubuki Y, Hatakeyama K, Kataoka H, Okayama A.]
通讯作者: Okayama A.
In vitro and in vivo antitumor activity of the NF-kB inhibitor DHMEQ in the human T-cell leukemia virus type I-transformed cell line, HUT-102
NF-kB 抑制剂 DHMEQ 在人 T 细胞白血病病毒 I 型转化细胞系 HUT-102 中的体外和体内抗肿瘤活性
DOI: --
发表时间: 2006
期刊: Leuk Res 30
影响因子: --
作者: [Matsuura N, Miyamae Y, et al., Ohsugi T et al.]
通讯作者: Ohsugi T et al.
Down-regulation of CDKN1A in adult T cell leukemia/lymphoma despite overexpression of CDKN1A in HTLV-1-infected cell lines.
尽管在 HTLV-1 感染的细胞系中 CDKN1A 过度表达,但成人 T 细胞白血病/淋巴瘤中 CDKN1A 下调。
DOI: --
发表时间: 2010
期刊: J Virol
影响因子: 5.4
作者: [Watanabe M, Nakahata S, Hamasaki M, Saito Y, Kawano Y, Hidaka T, Yamashita K, Umeki K, Taki T, Taniwaki M, Okayama A, Mori shita K]
通讯作者: Mori shita K
DOI: 10.1182/blood-2009-09-242347
发表时间: 2010-06-03
期刊: BLOOD
影响因子: 20.3
作者: [Takasaki, Yumi, Iwanaga, Masako, Tsukasaki, Kunihiro]
通讯作者: Tsukasaki, Kunihiro
46
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