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Iran J Immunol ; 14(1): 1-12, 2017 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-28341814

RESUMO

BACKGROUND: Generation of monocyte-derived dendritic cells (MDDC) is induced in the presence of GM-CSF and IL-4, and a maturation stimulus is added to the monocyte culture to obtain mature Dendritic Cells (DCs) suitable for therapy. TNF-α is the most common cytokine used for activating DCs and generating mature MDDC either alone or in combination with other cytokines. OBJECTIVE: To compare effects of traditional cytokine cocktail (TNF-α + IL-1ß) versus TLR4-agonist monophosphoryl lipid A on the viability, phenotype, cytokine profile and functionality of MDDC. METHODS: The study included 32 individuals; twenty Acute Myeloid Leukaemia (AML) cases in complete remission and 12 healthy volunteers. They were divided into 3 groups: Group 1: control group: 12 subjects to measure the baseline levels of all markers in the monocytic preparation. Group 2: cytokine cocktail (TNF-α) group, which included 10 AML subjects. Group 3: MPLA group which included 10 AML subjects. RESULTS: TNF-α group showed higher expression of CD83 than MPLA group indicating higher capacity to induce DC maturation but both were similar in CD86, CCR7 and IL-10 expression. Preparation of dendritic cells from AML cases in remission and loading them with tumor peptides was successful. CONCLUSION: MPLA effect in DC maturation is comparable with traditional DC maturation cocktail.


Assuntos
Células Dendríticas/efeitos dos fármacos , Imunoterapia Adotiva/métodos , Leucemia Mieloide Aguda/terapia , Lipídeo A/análogos & derivados , Receptor 4 Toll-Like/agonistas , Antígenos de Neoplasias/imunologia , Antígeno B7-2/metabolismo , Diferenciação Celular/efeitos dos fármacos , Células Cultivadas , Células Dendríticas/imunologia , Células Dendríticas/transplante , Humanos , Interleucina-10 , Interleucina-1beta/imunologia , Leucemia Mieloide Aguda/imunologia , Lipídeo A/farmacologia , Fragmentos de Peptídeos/imunologia , Receptores CCR7/metabolismo , Fator de Necrose Tumoral alfa/imunologia
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