
pmid: 21960413
Recently, there has been an increase of interest in the use of biological or immune-based therapies for patients with malignancies. This has been informed by the deeper understanding of the crosstalk between the host immune system and malignant tumours, as well as the potential advantages of immunotherapy-high specificity and less toxicity compared to standard approaches. The particular emphasis of this article is on the role of the complement system in tumour growth and antibody-based cancer immunotherapy. The functional consequences from overexpression of complement regulators by tumours and the development of strategies for overcoming this are discussed in detail. This review discusses these issues with a view to inspiring the development of new agents that could be useful for the treatment of cancer.
CD55 Antigens, Antibodies, Neoplasm, Antibody-Dependent Cell Cytotoxicity, Antibodies, Monoclonal, CD59 Antigens, Membrane Cofactor Protein, Mice, Adjuvants, Immunologic, Neoplasms, Models, Animal, Animals, Humans, Immunotherapy, Complement Activation, Transcription Factors
CD55 Antigens, Antibodies, Neoplasm, Antibody-Dependent Cell Cytotoxicity, Antibodies, Monoclonal, CD59 Antigens, Membrane Cofactor Protein, Mice, Adjuvants, Immunologic, Neoplasms, Models, Animal, Animals, Humans, Immunotherapy, Complement Activation, Transcription Factors
| citations This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically). | 59 | |
| popularity This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network. | Top 10% | |
| influence This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically). | Top 10% | |
| impulse This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network. | Top 10% |
