Author/Authors :
El Husseiny, Noha Mohamed Faculty of Medicine - Cairo University - Cairo , El Fattah Attya Elkak, Walaa Abd Faculty of Medicine - Cairo University - Cairo , El Ansary, Mervat Said Faculty of Medicine - Cairo University - Cairo , El Aziz El Khateeb, Engy Mohamed Abd Faculty of Medicine - Cairo University - Cairo , Mattar, Mervat Wagih Faculty of Medicine - Cairo University - Cairo , El Demerdash, Doaa Mohamed Faculty of Medicine - Cairo University - Cairo
Abstract :
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-1β) 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: The effect of MPLA in DC maturation is
comparable with traditional DC maturation cocktail.