Monitoring of Peripheral Blood Leukocytes and Plasma Samples: A Pilot Study to Examine Treatment Response to Leflunomide in Rheumatoid Arthritis.
João F S RodriguesLiziane C M da SilvaLeia Cardoso-SousaDouglas Carvalho CaixetaDébora Denardin LückemeyerAlisson S HenriqueJaqueline P PontesLycia M G da SilvaJuliana S S MacedoPedro S Carvalho JúniorCristiane Silva E SilvaMahiba M R S MartinsValério Monteiro-NetoMarcos Augusto Grigolin GrisottoAnita M R FernandesJuliano FerreiraJoão B CalixtoRobinson Sabino SilvaElizabeth Soares FernandesPublished in: Pharmaceuticals (Basel, Switzerland) (2021)
Rheumatoid arthritis (RA) is a painful inflammatory disease of the joints which affects a considerable proportion of the world population, mostly women. If not adequately treated, RA patients can become permanently disabled. Importantly, not all the patients respond to the available anti-rheumatic therapies, which also present diverse side effects. In this context, monitoring of treatment response is pivotal to avoid unnecessary side effects and costs towards an ineffective therapy. Herein, we performed a pilot study to investigate the potential use of flow cytometry and attenuated total reflection-Fourier transform infrared (ATR-FTIR) spectroscopy as measures to identify responders and non-responders to leflunomide, a disease-modifying drug used in the treatment of RA patients. The evaluation of peripheral blood CD62L+ polymorphonuclear cell numbers and ATR-FTIR vibrational modes in plasma were able to discriminate responders to leflunomide (LFN) three-months after therapy has started. Overall, the results indicate that both flow cytometry and ATR-FTIR can potentially be employed as additional measures to monitor early treatment response to LFN in RA patients.
Keyphrases
- rheumatoid arthritis
- end stage renal disease
- peripheral blood
- newly diagnosed
- ejection fraction
- chronic kidney disease
- prognostic factors
- disease activity
- type diabetes
- adipose tissue
- risk assessment
- metabolic syndrome
- dna damage
- pregnant women
- density functional theory
- replacement therapy
- systemic sclerosis
- adverse drug
- dna damage response