Natalie Eaton, Helene Cabanas, Cassandra Balinas, Anne Klein, Donald Staines and Sonya Marshall-Gradisnik
Griffith University, Australia
Scientific Tracks Abstracts: Clin Exp Pharmacol
It outlines the toxicological effect Rituximab has on the cytotoxic activity of NK cells isolated from CFS/ME patients. CFS/ ME is a multifactorial disorder commonly characterized by reduced NK cell cytotoxicity. A total of 8 CFS/ME patients (48.63±15.69 years) and 9 Non-Fatigued Controls (NFC) (37.56±11.06 years) were included using the Fukuda case definition. Apoptotic function, lytic proteins (granzyme A and granzyme B) and degranulation markers (CD107a and CD107b) were measured on NK cells using flow cytometric analysis prior to and following overnight incubation with Rituximab at 10 µg/ ml and 100 µg/ml. We reported a significant reduction in NK cell lysis of target K562 cells in CFS/ME patients compared to NFC following incubation with 100 µg/ml of Rituximab (p<0.05). Conversely, no significant difference was reported for NFC following incubation with Rituximab. There was also a significant decrease in granzyme B in CFS/ME patients compared to NFC with 100 µg/ml of Rituximab prior to K562 cells stimulation (p<0.05). Moreover, a significant increase in CD107a (p<0.05) and CD107b (p<0.01) expression was observed in NFC after stimulation with K562 cells prior to incubation with Rituximab. There was a significant increase in CD107b expression in CFS/ME patients before and after overnight incubation with 100 µg/ml of Rituximab prior to K562 cells stimulation (p<0.01). This study showed that Rituximab can have significant impairment on NK cell activity and finally the toxicological effects may worsen patientsâ?? symptoms.
Natalie Eaton has completed her Bachelor of Health Science degree with a major in Biomedical Science at the University of Southern Queensland, Australia