Local secretion/shedding of tumor-derived CD83 molecules as a novel tumor escape mechanism [Letter] (2008)
- Authors:
- USP affiliated author: BARBUTO, JOSE ALEXANDRE MARZAGAO - ICB
- School: ICB
- Subject: IMUNOLOGIA
- Language: Inglês
- Imprenta:
- Source:
- Título do periódico: Molecular Immunology
- ISSN: 0161-5890
- Volume/Número/Paginação/Ano: v. 45, n. 12, p. 3502-3504, 2008
-
ABNT
BALEEIRO, R. B.; BARBUTO, José Alexandre Marzagão. Local secretion/shedding of tumor-derived CD83 molecules as a novel tumor escape mechanism [Letter]. Molecular Immunology[S.l: s.n.], 2008. -
APA
Baleeiro, R. B., & Barbuto, J. A. M. (2008). Local secretion/shedding of tumor-derived CD83 molecules as a novel tumor escape mechanism [Letter]. Molecular Immunology. Oxford. -
NLM
Baleeiro RB, Barbuto JAM. Local secretion/shedding of tumor-derived CD83 molecules as a novel tumor escape mechanism [Letter]. Molecular Immunology. 2008 ; 45( 12): 3502-3504. -
Vancouver
Baleeiro RB, Barbuto JAM. Local secretion/shedding of tumor-derived CD83 molecules as a novel tumor escape mechanism [Letter]. Molecular Immunology. 2008 ; 45( 12): 3502-3504. - Dendritic cells derived from metastatic cancer patients vaccinated with allogenic dendritic cell-autologous tumor cell hybrids express more CD86 and induce higher levels of interferon-gamma in mixed lymphocyte reactions
- High frequency of immature dendritic cells and altered in situ production of interleukin-4 and tumor necrosis factor-'alfa' in lung cancer
- Altered phenotype and function of dendritic cells in individuals with chronic periodontitis
- Use of transformed t cell lines for clonal expansion of human b cells from peripheral blood, spleen, and tumor-infiltrating lymphocytes
- Immunopharmacology
- Human monoclonal antimelanoma single-chain fv antibody derived from tumor-infiltrating lymphocytes
- Analise do comportamento de marcadores tumorais isoladamente e em diferentes associacoes
- Immunopharmacology
- Controvérsias e perspectivas da imunoterapia em tumores do pulmão
- Tumor cell stimulation of nitric oxide release by BCG-activated mouse peritoneal cells
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