Current Cancer Treatment - Novel Beyond Conventional Approaches 2011
DOI: 10.5772/23671
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Xenovaccinotherapy for Cancer

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Cited by 5 publications
(3 citation statements)
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“…In particular, has shown the development of prolonged anticancer response in mice with melanoma В-16 vaccinated with human melanoma cells SK-MEL-1 at the background of increased CTL activity. Activation of specific chain of cell immunity has been also documented in clinical studies when the patients with uveal melanoma were vaccinated with xenogeneic vaccine containing mouse melanoma В-16 cells transplanted into conjunctive tissue capsule [17,18], or when the patients with metastatic skin melanoma were vaccinated with polyantigen cellular vaccine on the basis of В-16 melanoma cells and mouse Lewis lung carcinoma cells [16]. Antimetastatic efficacy of xenogeneic anticancer vaccine developed on the basis of embryonal proteins and products of bacterial origin (B. subtilis) is mostly exerted via activation of effectors of unspecific immunity (PM and NK).…”
Section: Resultsmentioning
confidence: 99%
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“…In particular, has shown the development of prolonged anticancer response in mice with melanoma В-16 vaccinated with human melanoma cells SK-MEL-1 at the background of increased CTL activity. Activation of specific chain of cell immunity has been also documented in clinical studies when the patients with uveal melanoma were vaccinated with xenogeneic vaccine containing mouse melanoma В-16 cells transplanted into conjunctive tissue capsule [17,18], or when the patients with metastatic skin melanoma were vaccinated with polyantigen cellular vaccine on the basis of В-16 melanoma cells and mouse Lewis lung carcinoma cells [16]. Antimetastatic efficacy of xenogeneic anticancer vaccine developed on the basis of embryonal proteins and products of bacterial origin (B. subtilis) is mostly exerted via activation of effectors of unspecific immunity (PM and NK).…”
Section: Resultsmentioning
confidence: 99%
“…An induction of specific cellular and humoral immune response against self tumor antigens in the case of use of xenogeneic vaccines relies on high homology between tumor-associated antigens of man and animals [10][11][12], in particular those of man and mouse [13,14]. The presence of such homology was utilized in some experimental and clinical stu dies where for melanoma treatment tumor antigens of mouse were used as xenogeneic ones in humans, and vice versa [15,16]. In particular, xenovaccination with the use of transplantable human melanoma SK-MEL-28 cells or primary human melanoma cell culture performed at prophylactic regimen with following removal of primary tumor node, resulted in significant suppression of syngeneic melanoma В-16 in mice and reduced lung metastasis.…”
mentioning
confidence: 99%
“…Some XAV successfully passed I-II phases of clinical trials. Their safety and ability to induce immune response without autoimmune complications have been proven [4][5][6][7][8]. Among others, genes and proteins of chicken origin which share homology with human counterparts are exploited in the XAV construction [9][10][11][12][13][14].…”
mentioning
confidence: 99%