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- W2129972783 abstract "African trypanosomiasis causes devastating effects on human populations and livestock herds in large parts of sub-Saharan Africa. Control of the disease is hampered by the lack of any efficient vaccination results in a field setting, and the severe side effects of current drug therapies. In addition, with the exception of Trypanosoma brucei gambiense infections, the diagnosis of trypanosomiasis has to rely on microscopic analysis of blood samples, as other specific tools are nonexistent. However, new developments in biotechnology, which include loop-mediated isothermal amplification as an adaptation to conventional PCR, as well as the antibody engineering that has allowed the development of Nanobody ® technology, offer new perspectives in both the detection and treatment of trypanosomiasis. In addition, recent data on parasite-induced B-cell memory destruction offer new insights into mechanisms of vaccine failure, and should lead us towards new strategies to overcome trypanosome defenses operating against the host immune system." @default.
- W2129972783 created "2016-06-24" @default.
- W2129972783 creator A5035905258 @default.
- W2129972783 creator A5085358954 @default.
- W2129972783 date "2009-10-01" @default.
- W2129972783 modified "2023-10-14" @default.
- W2129972783 title "African trypanosomiasis and antibodies: implications for vaccination, therapy and diagnosis" @default.
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- W2129972783 doi "https://doi.org/10.2217/fmb.09.65" @default.
- W2129972783 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/19824795" @default.
- W2129972783 hasPublicationYear "2009" @default.
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