Article

Clinical experience with α-galactosylceramide (KRN7000) in patients with advanced cancer and chronic hepatitis B/C infection.

Department of Medical Oncology, VU University Medical Center, De Boelelaan 1117, 1081 HV Amsterdam, The Netherlands.
Clinical Immunology (impact factor: 4.05). 12/2010; 140(2):130-41. DOI:10.1016/j.clim.2010.11.010 pp.130-41
Source: PubMed

ABSTRACT 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 α-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 α-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 α-galactosylceramide in these patient groups.

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Keywords

activation
 
antiviral effector cell properties
 
chronic hepatitis B/C
 
conserved T lymphocyte lineage
 
effective therapeutic approaches
 
hepatitis immunotherapeutic strategies
 
immune system
 
immunosurveillance
 
long-lasting Th1
 
multiple tumor-metastasis
 
own clinical experience
 
patient groups
 
preclinical data
 
proinflammatory immune response
 
subsequent clinical trials
 
viral infection models
 
viruses