R. Jones, Eckart M. D. D. De Bie, Nina Deliu, Anthony YKC Ng, Benjamin J. Dunmore, Stefan Gräf, Christophe Guignabert, Marc Humbert, Laurent Savale, L Tu, Athénäis Boucly, Joseph Newman, Gary Polwarth, Paul D. Upton, Allan Lawrie, C J Rhodes, M R Wilkins, S Binmahfooz, Alexander M. K. Rothman, anna hemnes, Sofía S. Villar, J D West, M Toshner, Nicholas W. Morrell, Charles Elliot, Athanasios Charalampopulos, Ian Sabroe, Abdul Hameed, I Armstrong, Stephen J. Wort, Luke S. Howard, Andrew J. Swift, James M. Wild, Dennis Wang, David G. Kiely, Robin Condliffe, Amanda Creaser-Myers, Sara I. Walker, Stephen Roney, Roger Thompson, Joanna Pepke-Zaba, Katherine Bunclark, Jim Lordan, Colin Church, Shahin Moledina, Lynsay MacDonald, Eleni Tamvaki, Anabelle Barnes, Victoria Cookson, Latifa Chentouf, Rosa DaCosta, Joy Pinguel, Natalie Dormand, Alice Parker, Della Stokes, Laura Price, Dipa Ghedia, Yvonne Tan, Tanaka Ngcozana, Ivy Wanjiku, Gerry Coghlan, Rob V. Mackenzie Ross, Jay Suntharalingam, Mark Grover, Ali Kirby, Ali Grove, Katie White, A Seatter, Joanna Pepke-Zaba, Katherine Bunclark, Stephen J. Wort, Luke S. Howard, Rachel Davies, Roger Thompson, Robin Condliffe, F. Varian, Andrew J. Swift, David G. Kiely, Val Irvine, Colin Church, Rob V. Mackenzie Ross, Jay Suntharalingam, Zandile Maseko, Shahin Moledina, Gerry Coghlan, Dan Knight, Colm McCabe
Pulmonary arterial hypertension (PAH) is a rare, life-limiting disease where imbalances in the transforming growth factor-β (TGF-β) and bone morphogenetic protein receptor type II (BMPR-II) superfamily pathways have causal roles in hereditary and idiopathic forms of the disease. These pathways are emerging attractive candidates for therapeutic intervention, but there is an unmet need for clinically relevant and practical biomarkers that can measure target engagement, partly because of the inaccessibility of lung tissue in disease for molecular profiling. Here, we explored the surrogate capacity of peripheral blood bone morphogenetic protein (BMP) pathway-specific markers using samples collected in the StratosPHere 1 study using both cell surface assessment of BMPR-II receptor levels and quantitative PCR for the assessment of downstream target engagement. Downstream BMPR-II canonical and noncanonical signaling was measurable and altered in whole blood in both discovery and international replication cohorts, and transcriptomic signatures were clustered by discrete gene modules that associated with clinical outcomes and mortality. We derived a transcriptomic biomarker panel that was repeatable, reproducible, and longitudinally stable for use in early phase, target engagement clinical trials. The biomarker panel was used in a pilot study of nine sotatercept-treated patients with PAH to test the effect of the therapy on the BMP pathway; analysis suggested that sotatercept did not rebalance or increase BMPR-II pathway signaling but rather led to a reduction, possibly due to depletion of circulating BMP9 and BMP10.