Immuno-engineering and Cellular Therapies
Laura Fusco, n/a
Marie Curie Postdoctoral Fellow
University of Padua
Padua, Veneto, Italy
Arianna Gazzi, n/a
University of Trieste
Trieste, Friuli-Venezia Giulia, Italy
Christopher E. Shuck, n/a
Drexel University
Philadelphia, Pennsylvania, United States
Darawan Rinchai, n/a
Postdoctoral Fellow
Sidra Medicine
Doha, Ar Rayyan, Qatar
Eiman Ahmed, n/a
Sidra Medicine
Doha, Ar Rayyan, Qatar
Jean-Charles Grivel, n/a
Sidra Medicine
Doha, Ar Rayyan, Qatar
Davide Bedognetti, n/a
Sidra Medicine
Doha, Ar Rayyan, Qatar
Yury Gogotsi, n/a
Drexel University
Doha, Pennsylvania, United States
Lucia Gemma Delogu, n/a
University of Padua
Padua, Veneto, Italy
Two-dimensional (2D) transition metal carbides/carbonitrides (MXenes) are rapidly growing as nanoplatforms in biomedicine. Considering the central importance of the immune response for any clinical translation of nanomaterials, we evaluated the effects on human peripheral blood mononuclear cells (PBMCs) of three MXenes: Mo2Ti2C3, Nb4C3, and Ta4C3.
We assessed immune cell functionality by measuring 40 cytokines by Luminex technology. The materials exhibited only a slight modulation on the inflammatory mediators analyzed. Next, we investigated their effects on PBMC by mRNA sequencing. By performing principal component analysis on all analyzed transcripts (N=19,959), we found that MXene-treated samples clustered close to the controls, and separately from concanavalin A (ConA)- and lipopolysaccharide (LPS)-treated samples, thus indicating that only minimal perturbations were induced by the materials. Overall, we did not observe genome-wide changes induced by MXenes. All materials showed modest effects on PBMCs, modulating the expression of fewer genes than the positive controls ConA and LPS. In particular, even if all materials had similar effects on gene expression modulation, Ta4C3 had slightly greater effects than Mo2Ti2C3 and Nb4C3. The expression of 142, 46, and 83 genes was modulated by Ta4C3, Mo2Ti2C3, and Nb4C3, respectively, whereas the positive controls ConA and LPS modulated the expression of 4,340 and 710 genes, respectively. Furthermore, pathway-enrichment analyses on genes coherently modulated by the materials showed only modest enrichment of immune-related pathways without a clear indication of activation or inhibition.
Our results provide a compendium of knowledge on the biocompatibility of MXenes for the safe development of nanosystems in biomedicine.