GS‐443902 concentrations in peripheral blood mononuclear cells and dried blood spots among pregnant and non‐pregnant women receiving remdesivir for COVID‐19 treatment
2 Background: Activation of remdesivir (RDV) has typically been assessed by measuring concentrations of GS-443902 (active triphosphate) in peripheral blood mononuclear cells (PBMC). We previously showed concentrations of RDV, and its major plasma metabolites were similar between pregnant and non-pregnant women with COVID-19, while those of GS-443902 in PBMC were ~50% lower in pregnancy. Dried blood spots (DBS) provide a simpler alternative to PBMC collection and may serve as another surrogate measure of cellular drug activation, but pregnancy status and inflammation due to COVID-19 may impact these measures. Here, we evaluated factors that affect GS-443902 in DBS and PBMC and relationships between cell types in pregnant and non-pregnant women with COVID-19. Methods: IMPAACT 2032 (NCT04582266) was a Phase IV prospective, open label, non-randomized, opportunistic study of hospitalized pregnant and non-pregnant women receiving intravenous RDV as part of clinical care for COVID-19. DBS and PBMC were isolated pre-dose and/or 23-h post-dose on infusion Days 3, 4 and 5. GS-443902 concentrations in each cell type were quantified using LC–MS/MS methods from 2 × 7 mm punches (DBS) or cell pellets (PBMCs). Generalized linear mixed effects modelling (1) evaluated the effect of pregnancy and baseline covariates on log-transformed GS-443902 in DBS and PBMC using forward selection (p < 0.2) and backwards elimination (p < 0.1) after adjusting for infusion number and (2) assessed relationships between GS-443902 in DBS vs. PBMC. Results: About 76 dB and PBMC observations were available from 51 participants (25 pregnant, 26 non-pregnant). Median (interquartile range) GS-443902 concentrations in DBS were 1807 (1395, 2292) and 1633 (1267, 2412) fmol/punch and in PBMC were 2.96 (0.79, 6.89) and 5.15 (3.22, 8.77) μM for pregnant and non-pregnant participants, respectively. In DBS, GS-443902 concentrations were 19% lower (90% CI −33, −2.5%) during pregnancy, increases in SBP (per 10 mmHg) were associated with an 8.1% decrease (90% CI −11.4%, −4.7%) and increases in ALP (per 10 U/L) and platelet count (per 50x109 cells/L) were associated with a 1.4% (90% CI 0.3%, 1.8%) and 5.3% (90% CI 0.8%, 13.4%) increase, respectively. In PBMC, GS-443902 concentrations were 45% lower (90% CI −19.4%, −61.8%) in pregnant vs. non-pregnant participants with each additional infusion. Increases in ALP and ALT (per 10 U/L) were associated with a 4.2% decrease (90% CI −7.7%, −0.6%) and 11.4% decrease (90% CI −18.8%, −3.4%) in GS-443902 concentrations in PBMC, respectively. For DBS vs. PBMC comparisons, GS-443902 concentrations in PBMCs increased by 7.7% (90% CI 4.0%, 11.6%) for every 100 fmol/punch increase in DBS for non-pregnant women; however, in pregnant women, there was a 4.4% decrease (90% CI −7.9%, −0.8%) for GS-443902 in PBMC for every 100 fmol/punch increase in DBS. Conclusions: Cellular disposition of GS-443902 between DBS and PBMCs differed by pregnancy status and other clinical factors associated with COVID-19 disease severity. The mechanisms and clinical significance of these differences are unknown. Further investigation into how pregnancy and other disease-specific factors affect cellular concentrations is warranted.
Authors
- Elizabeth Greene (ORCID: https://orcid.org/0000-0002-4952-6834)
- Frederic Bone
- Kathryn Kersey
- Daniel S. Shapiro
- Patrick Jean‐Philippe
- Sharon Nachman (ORCID: https://orcid.org/0000-0003-1665-7253)
- Diana F. Clarke
- Kelly A Brooks (ORCID: https://orcid.org/0000-0002-2698-5392)
- Ahizechukwu Chigoziem Eke (ORCID: https://orcid.org/0000-0002-0070-9840)
- Edmund V. Capparelli (ORCID: https://orcid.org/0000-0002-1630-0505)
- Andrew Dunbar (ORCID: https://orcid.org/0000-0003-0339-4220)
- Jeremiah D. Momper (ORCID: https://orcid.org/0000-0002-3154-6685)
- Kathleen M. Powis (ORCID: https://orcid.org/0000-0002-4478-4471)
- Nahida Chakhtoura
- Kathy George
- Brookie M. Best (ORCID: https://orcid.org/0000-0001-8569-2293)
- Lane R. Bushman
- Laura Roon (ORCID: https://orcid.org/0009-0000-4975-3343)
- Kristin Baltrusaitis (ORCID: https://orcid.org/0000-0003-2090-9513)
- Di Yin (ORCID: https://orcid.org/0000-0003-4456-9867)
- Alice Marie Stek
- Mark Mirochnick
Institutions
- Boston University (US)
- University of Southern California (US)
- Boston Medical Center (US)
- National Institutes of Health (US)
- Harvard University (US)
- Johns Hopkins University (US)
- Johns Hopkins Medicine (US)
- University of California San Diego (US)
- Rady Children's Hospital-San Diego (US)
- Massachusetts General Hospital (US)
- National Institute of Child Health (HU)
- National Institute of Allergy and Infectious Diseases (US)
- Frontier Science & Technology Research Foundation, Inc. (US)
- Gilead Sciences (United States) (US)
- National Institute of Child Health (PK)
- Eunice Kennedy Shriver National Institute of Child Health and Human Development (US)
- Stony Brook Children's Hospital (US)
- Impact (CA)
- Health and Human Development (2HD) Research Network (CM)
- University of Colorado Anschutz Medical Campus (US)
- University of Montana (US)
Publication Details
- Journal
- British Journal of Clinical Pharmacology
- Published
- 2025-09-01
- DOI
- https://doi.org/10.1002/bcp.70206
- Primary Topic
- COVID-19 Impact on Reproduction
- Type
- article
- Field-Weighted Citation Impact
- 0.00