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Clinical experience with α-galactosylceramide (KRN7000) in patients with advanced cancer and chronic hepatitis B/C infection
被引:80
|作者:
Schneiders, Famke L.
[1
]
Scheper, Rik J.
[1
,2
]
von Blomberg, B. Mary E.
[2
]
Woltman, Andrea M.
[3
]
Janssen, Harry L. A.
[3
]
van den Eertwegh, Alfons J. M.
[1
]
Verheul, Henk M. W.
[1
]
de Gruijl, Tanja D.
[1
]
van der Vliet, Hans J.
[1
]
机构:
[1] Vrije Univ Amsterdam, Med Ctr, Dept Med Oncol, NL-1081 HV Amsterdam, Netherlands
[2] Vrije Univ Amsterdam, Med Ctr, Dept Pathol, NL-1081 HV Amsterdam, Netherlands
[3] Erasmus MC Univ Med Ctr Rotterdam, Dept Gastroenterol & Hepatol, NL-3000 CA Rotterdam, Netherlands
关键词:
iNKT cells;
alpha-Galactosylceramide;
KRN7000;
Cancer;
Chronic hepatitis B/C infection;
KILLER-T-CELLS;
V-ALPHA-24(+)V-BETA-11(+) NKT CELLS;
ANTIGEN-PRESENTING CELLS;
PHASE I/II TRIAL;
DENDRITIC CELLS;
FUNCTIONALLY DISTINCT;
GLYCOLIPID ANTIGENS;
CD1D EXPRESSION;
RECURRENT HEAD;
IFN-GAMMA;
D O I:
10.1016/j.clim.2010.11.010
中图分类号:
R392 [医学免疫学];
Q939.91 [免疫学];
学科分类号:
100102 ;
摘要:
For over a century, research has sought ways to boost the immune system in order to eradicate tumors and viruses that exist after escaping immunosurveillance. For the treatment of cancer and hepatitis immunotherapeutic strategies have overall had limited clinical success. An urgent need exists therefore to introduce more effective therapeutic approaches. Invariant (i)NKT cells constitute a conserved T lymphocyte lineage with dominant immunoregulatory, antitumor and antiviral effector cell properties. iNKT specifically recognize the glycolipid alpha-galactosylceramide in the context of CD1d resulting in their activation. Activated iNKT can promote the development of a long-lasting Th1 biased proinflammatory immune response as demonstrated in multiple tumor-metastasis and viral infection models. Here, we will provide a brief overview of the preclinical data of alpha-galactosylceramide that formed the basis for subsequent clinical trials in patients with advanced cancer and chronic hepatitis B/C, and elaborate on our own clinical experience with alpha-galactosylceramide in these patient groups. (C) 2010 Elsevier Inc. All rights reserved.
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页码:130 / 141
页数:12
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