The success of immunotherapy against infectious diseases has shown us the powerful potential that such a treatment offers, and substantial work has been done to apply this strategy in the fight against cancer. Cancer is however a fiercer opponent than pathogen-caused diseases due to natural tolerance towards tumour associated antigens and tumour-induced immunosuppression. Recent gene therapy clinical trials with viral vectors have shown clinical efficacy in the correction of genetic diseases, HIV and cancer. The first successful gene therapy clinical trials were carried out with onco(g-)retroviral vectors but oncogenesis by insertional mutagenesis appeared as a serious complication. Lentiviral vectors have emerged as a potentially safer str...
Lentiviral vectors (LVs) play an important role in gene therapy and have proven successful in clinic...
Delivery of tumour-associated antigens (TAA) in a way that induces effective, specific immunity is a...
Gene transfer into B cells by lentivectors can provide an alternative approach to managing B lymphoc...
The success of immunotherapy against infectious diseases has shown us the powerful potential that su...
Vectors based on lentivirus backbones have revolutionized our ability to transfer genesinto many cel...
Lentiviral vectors are promising tools for the development of gene therapy since they can transduce ...
Gene therapy involves the transfer of genetic information to a target cell to facilitate the product...
Lentiviral vectors are the most frequently used tool to stably transfer and express genes in the con...
Gene therapy is the introduction or alteration of genetic material with the intention to treat disea...
The past 3 years have witnessed the spectacular irruption of lentiviral vectors into the limelight o...
Lentiviral vectors have played a critical role in the emergence of gene-modified cell therapies, spe...
Applications of viral vectors have found an encouraging new beginning in gene therapy in recent year...
Glioblastoma (GBM) has the worst prognosis among brain tumors, hence basic biology, preclinical, and...
Gene therapy has recently attracted attention as a novel therapeutic strategy and several methods fo...
Gene therapy has been considered as one of the optimal treatments. Although, at the beginning of thi...
Lentiviral vectors (LVs) play an important role in gene therapy and have proven successful in clinic...
Delivery of tumour-associated antigens (TAA) in a way that induces effective, specific immunity is a...
Gene transfer into B cells by lentivectors can provide an alternative approach to managing B lymphoc...
The success of immunotherapy against infectious diseases has shown us the powerful potential that su...
Vectors based on lentivirus backbones have revolutionized our ability to transfer genesinto many cel...
Lentiviral vectors are promising tools for the development of gene therapy since they can transduce ...
Gene therapy involves the transfer of genetic information to a target cell to facilitate the product...
Lentiviral vectors are the most frequently used tool to stably transfer and express genes in the con...
Gene therapy is the introduction or alteration of genetic material with the intention to treat disea...
The past 3 years have witnessed the spectacular irruption of lentiviral vectors into the limelight o...
Lentiviral vectors have played a critical role in the emergence of gene-modified cell therapies, spe...
Applications of viral vectors have found an encouraging new beginning in gene therapy in recent year...
Glioblastoma (GBM) has the worst prognosis among brain tumors, hence basic biology, preclinical, and...
Gene therapy has recently attracted attention as a novel therapeutic strategy and several methods fo...
Gene therapy has been considered as one of the optimal treatments. Although, at the beginning of thi...
Lentiviral vectors (LVs) play an important role in gene therapy and have proven successful in clinic...
Delivery of tumour-associated antigens (TAA) in a way that induces effective, specific immunity is a...
Gene transfer into B cells by lentivectors can provide an alternative approach to managing B lymphoc...