2014
DOI: 10.3390/v6062416
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Vaccination against δ-Retroviruses: The Bovine Leukemia Virus Paradigm

Abstract: Bovine leukemia virus (BLV) and human T-lymphotropic virus type 1 (HTLV-1) are closely related δ-retroviruses that induce hematological diseases. HTLV-1 infects about 15 million people worldwide, mainly in subtropical areas. HTLV-1 induces a wide spectrum of diseases (e.g., HTLV-associated myelopathy/tropical spastic paraparesis) and leukemia/lymphoma (adult T-cell leukemia). Bovine leukemia virus is a major pathogen of cattle, causing important economic losses due to a reduction in production, export limitati… Show more

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Cited by 61 publications
(64 citation statements)
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“…-understand the mechanisms of innate and acquired anti-HTLV immunity, response to vaccines (Gutierrez et al, 2014) and immune escape of infected T cells;…”
Section: Develop Preventive and Therapeutic Vaccinesmentioning
confidence: 99%
“…-understand the mechanisms of innate and acquired anti-HTLV immunity, response to vaccines (Gutierrez et al, 2014) and immune escape of infected T cells;…”
Section: Develop Preventive and Therapeutic Vaccinesmentioning
confidence: 99%
“…Animals with an increase in white cell count of three standard deviations above the median and with similar counts for a period of not less than two months can be considered to have PL [21]. Over the last decade, major studies involving infected animals have allowed a more thorough classification [2,11,15,16]. Within the PL group, all animals carry a high proviral load and develop a strong immune response against the major antigenic proteins of the viral particle, p24 and gp51, and these are called the high proviral load (HPL) group.…”
Section: Introductionmentioning
confidence: 99%
“…Many attemps have been made to develop an efficient vaccine. Nevertheless, none of them seems to be fully effective for inducing an immune response strong enough to protect the host against infection [11].…”
Section: Introductionmentioning
confidence: 99%
“…119 It is likely that this recombinant provirus is both mutated on the immunoreceptor tyrosine activation motifs cytoplasmic tail of the BLV-gp30 glycoprotein gene and has the G4 and R3 genes deleted. 115 However, no proof of concept has been shown, nor has preliminary data been published concerning the identity of the provirus mutated/deleted genes, the immune protection conferred to the vaccinated animals in the long term, the safety assessment of the vaccine, and the proposed strategy to be used to differentiate vaccinated from infected animals.…”
Section: -101mentioning
confidence: 99%