# Sotatercept analog suppresses inflammation to reverse experimental pulmonary arterial hypertension

**Authors:** Sachindra R. Joshi, Jun Liu, Troy Bloom, Elif Karaca Atabay, Tzu-Hsing Kuo, Michael Lee, Elitza Belcheva, Matthew Spaits, Rosa Grenha, Michelle C. Maguire, Jeffrey L. Frost, Kathryn Wang, Steven D. Briscoe, Mark J. Alexander, Brantley R. Herrin, Roselyne Castonguay, R. Scott Pearsall, Patrick Andre, Paul B. Yu, Ravindra Kumar, Gang Li

PMC · DOI: 10.1038/s41598-022-11435-x · 2022-05-12

## TL;DR

A drug called sotatercept reduces inflammation and improves lung and heart function in a rat model of pulmonary arterial hypertension.

## Contribution

The study reveals that sotatercept's anti-inflammatory effects, in addition to its known anti-proliferative actions, contribute to its therapeutic benefits in PAH.

## Key findings

- ActRIIA-Fc reversed proinflammatory gene expression and macrophage infiltration in PAH rat lungs.
- ActRIIA-Fc corrected cardiopulmonary structure and function in a genetic model of heritable PAH.
- Neutralizing ActRIIA-Fc ligands produced similar benefits to ActRIIA-Fc treatment in PAH rats.

## Abstract

Sotatercept is an activin receptor type IIA-Fc (ActRIIA-Fc) fusion protein that improves cardiopulmonary function in patients with pulmonary arterial hypertension (PAH) by selectively trapping activins and growth differentiation factors. However, the cellular and molecular mechanisms of ActRIIA-Fc action are incompletely understood. Here, we determined through genome-wide expression profiling that inflammatory and immune responses are prominently upregulated in the lungs of a Sugen-hypoxia rat model of severe angio-obliterative PAH, concordant with profiles observed in PAH patients. Therapeutic treatment with ActRIIA-Fc—but not with a vasodilator—strikingly reversed proinflammatory and proliferative gene expression profiles and normalized macrophage infiltration in diseased rodent lungs. Furthermore, ActRIIA-Fc normalized pulmonary macrophage infiltration and corrected cardiopulmonary structure and function in Bmpr2 haploinsufficient mice subjected to hypoxia, a model of heritable PAH. Three high-affinity ligands of ActRIIA-Fc each induced macrophage activation in vitro, and their combined immunoneutralization in PAH rats produced cardiopulmonary benefits comparable to those elicited by ActRIIA-Fc. Our results in complementary experimental and genetic models of PAH reveal therapeutic anti-inflammatory activities of ActRIIA-Fc that, together with its known anti-proliferative effects on vascular cell types, could underlie clinical activity of sotatercept as either monotherapy or add-on to current PAH therapies.

## Linked entities

- **Genes:** BMPR2 (bone morphogenetic protein receptor type 2) [NCBI Gene 659]
- **Diseases:** Pulmonary arterial hypertension (MONDO:0015924), PAH (MONDO:0015924)
- **Species:** Mus musculus (taxon 10090), Rattus norvegicus (taxon 10116)

## Full-text entities

- **Genes:** MAPK1 (mitogen-activated protein kinase 1) [NCBI Gene 5594] {aka ERK, ERK-2, ERK2, ERT1, MAPK2, NS13}, P2ry2 (purinergic receptor P2Y2) [NCBI Gene 29597] {aka P2Y2}, BMP1 (bone morphogenetic protein 1) [NCBI Gene 649] {aka OI13, PCOLC, PCP, TLD}, Bmpr2 (bone morphogenetic protein receptor type 2) [NCBI Gene 12168] {aka 2610024H22Rik, BMP-2, BMPR-2, BMPR-II, BMPRII, BRK-3}, Acvr2a (activin A receptor type 2A) [NCBI Gene 29263] {aka Acvr2, rActR-II}, Ighv1-9 (immunoglobulin heavy variable 1-9) [NCBI Gene 668478] {aka Gm16697, Igg2a}, BMP10 (bone morphogenetic protein 10) [NCBI Gene 27302], EPHB1 (EPH receptor B1) [NCBI Gene 2047] {aka ELK, EPHT2, Hek6, NET}, CCL2 (C-C motif chemokine ligand 2) [NCBI Gene 6347] {aka GDCF-2, HC11, HSMCR30, MCAF, MCP-1, MCP1}, Havcr2 (hepatitis A virus cellular receptor 2) [NCBI Gene 171285] {aka TIM-3, Tim3, Timd3}, Gpbar1 (G protein-coupled bile acid receptor 1) [NCBI Gene 338443] {aka M-BAR, Tgr5}, BMPR2 (bone morphogenetic protein receptor type 2) [NCBI Gene 659] {aka BMPR-II, BMPR3, BMR2, BRK-3, POVD1, PPH1}, F2 (coagulation factor II, thrombin) [NCBI Gene 29251], Tgfb1 (transforming growth factor, beta 1) [NCBI Gene 59086] {aka Tgfb}, Dnase1 (deoxyribonuclease 1) [NCBI Gene 25633], Il10 (interleukin 10) [NCBI Gene 16153] {aka CSIF, If2a, Il-10}, Smad9 (SMAD family member 9) [NCBI Gene 85435] {aka Madh9, Smad8}, Gapdh (glyceraldehyde-3-phosphate dehydrogenase) [NCBI Gene 24383] {aka BARS-38, Gapd}, MAP2K1 (mitogen-activated protein kinase kinase 1) [NCBI Gene 5604] {aka CFC3, MAPKK1, MEK1, MEL, MKK1, PRKMK1}, Eng (endoglin) [NCBI Gene 497010], Tgfbr1 (transforming growth factor, beta receptor 1) [NCBI Gene 29591] {aka Alk5, Skr4, Tgfr-1, tbetaR-I}, Tgfb1 (transforming growth factor, beta 1) [NCBI Gene 21803] {aka TGF-beta1, TGFbeta1, Tgfb, Tgfb-1}, Ccl2 (C-C motif chemokine ligand 2) [NCBI Gene 24770] {aka MCP-1, MCP1, Scya2, Sigje}, Acvrl1 (activin A receptor like type 1) [NCBI Gene 25237] {aka Alk1, R-3, R3, SETHKIR}, Map2k1 (mitogen activated protein kinase kinase 1) [NCBI Gene 170851] {aka Mek1}, INHBE (inhibin subunit beta E) [NCBI Gene 83729], Mstn (myostatin) [NCBI Gene 17700] {aka Cmpt, Gdf8}, Il6 (interleukin 6) [NCBI Gene 24498] {aka ILg6, Ifnb2}, VCAN (versican) [NCBI Gene 1462] {aka CSPG2, ERVR, GHAP, PG-M, WGN, WGN1}, Myh6 (myosin heavy chain 6) [NCBI Gene 29556] {aka MyHC-beta, MyHC-slow, Myh7, Myhca, Myosin-7}, IL1B (interleukin 1 beta) [NCBI Gene 3553] {aka IL-1, IL1-BETA, IL1F2, IL1beta}, GDF11 (growth differentiation factor 11) [NCBI Gene 10220] {aka BMP-11, BMP11, VHO}, TSC2 (TSC complex subunit 2) [NCBI Gene 7249] {aka LAM, PPP1R160, TSC4}, Sele (selectin, endothelial cell) [NCBI Gene 20339] {aka CD62E, E-selectin, ELAM-1, Elam, LECAM2}, Inhba (inhibin subunit beta A) [NCBI Gene 29200], Smad3 (SMAD family member 3) [NCBI Gene 25631] {aka Madh3, Smad 3, mad3}, MSTN (myostatin) [NCBI Gene 2660] {aka GDF8, MSLHP}, Myh7 (myosin heavy chain 7) [NCBI Gene 29557] {aka Bmyo, Myhcb, myHC-beta, myHC-slow}, Gdf11 (growth differentiation factor 11) [NCBI Gene 29454] {aka BMP-11}, Nfat5 (nuclear factor of activated T-cells 5) [NCBI Gene 307820] {aka NF-AT5, Nfat, TonEBP}, Gdf11 (growth differentiation factor 11) [NCBI Gene 14561] {aka BMP-11, Bmp11}, EGLN1 (egl-9 family hypoxia inducible factor 1) [NCBI Gene 54583] {aka C1orf12, ECYT3, HALAH, HIF-PH2, HIFPH2, HPH-2}, VCAM1 (vascular cell adhesion molecule 1) [NCBI Gene 7412] {aka CD106, INCAM-100}, Inhbb (inhibin subunit beta B) [NCBI Gene 25196], Bmpr2 (bone morphogenetic protein receptor type 2) [NCBI Gene 140590] {aka Bmpr-II}, TGFBR2 (transforming growth factor beta receptor 2) [NCBI Gene 7048] {aka AAT3, FAA3, LDS1B, LDS2, LDS2B, MFS2}, Nfatc2 (nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 2) [NCBI Gene 18019] {aka NF-ATc2, NF-ATp, NFAT1, NFAT1-D, Nfatp}, Grem1 (gremlin 1, DAN family BMP antagonist) [NCBI Gene 50566] {aka Cktsf1b1, drm}, Itgam (integrin subunit alpha M) [NCBI Gene 25021] {aka Cd11b}, GREM1 (gremlin 1, DAN family BMP antagonist) [NCBI Gene 26585] {aka C15DUPq, CKTSF1B1, CRAC1, CRCS4, DAND2, DRM}, Tnf (tumor necrosis factor) [NCBI Gene 21926] {aka DIF, TNF-a, TNF-alpha, TNFSF2, TNFalpha, Tnfa}, IL6 (interleukin 6) [NCBI Gene 3569] {aka BSF-2, BSF2, CDF, HGF, HSF, IFN-beta-2}, TNF (tumor necrosis factor) [NCBI Gene 7124] {aka DIF, IMD127, TNF-alpha, TNFA, TNFSF2, TNLG1F}, Grem1 (gremlin 1, DAN family BMP antagonist) [NCBI Gene 23892] {aka Cktsf1b1, Drm, Grem, ld}, Hist1h3b (histone cluster 1, H3b) [NCBI Gene 680498], Itgam (integrin alpha M) [NCBI Gene 16409] {aka CD11b/CD18, CR3, CR3A, Cd11b, F730045J24Rik, Ly-40}, GDF2 (growth differentiation factor 2) [NCBI Gene 2658] {aka BMP-9, BMP9, HHT5}, Ifng (interferon gamma) [NCBI Gene 25712] {aka IFNG2, If2f}, Gna14 (G protein subunit alpha 14) [NCBI Gene 309242] {aka Hg1i, Tieg3}, Col2a1 (collagen type II alpha 1 chain) [NCBI Gene 25412] {aka CG2A1A, COLLII}
- **Diseases:** immune dysregulation (OMIM:614878), Inflammation (MESH:D007249), Complement (MESH:D007153), pulmonary vascular disease (MESH:D014652), abnormalities in pulmonary artery (MESH:D000071079), lung (MESH:D008171), Osteoarthritis (MESH:D010003), occlusive arteriopathy (MESH:C537440), heart failure (MESH:D006333), vascular pathology (MESH:D005598), Hypoxia (MESH:D000860), RV dilatation (MESH:C535682), Cardiac remodeling (MESH:D020257), pulmonary vascular remodeling (MESH:D066253), luminal occlusion (MESH:D001157), cardiac dysfunction (MESH:D006331), fibrosis (MESH:D005355), vascular occlusion (MESH:D008641), PAH (MESH:D000081029), congenital heart disease (MESH:D006330), pulmonary inflammation (MESH:D011014), rheumatoid arthritis (MESH:D001172), pulmonary vascular resistance (MESH:D057772), RV hypertrophy (MESH:D017380), and vessel injury (MESH:C536223), cardiopulmonary impairments (MESH:D006323), premature death (MESH:D003643), structural (MESH:D020914), cardiovascular phenotypes (MESH:D002318), hypoxic (MESH:D002534), systemic-to-pulmonary shunts (MESH:C562451), EndMT (MESH:D008579), Hepatic fibrosis (MESH:D008103), functional abnormalities (MESH:D000014), Cardiac hypertrophy (MESH:D006332),  (MESH:D004195),  (MESH:D065627),  (MESH:D006976)
- **Chemicals:** streptomycin (MESH:D013307), HEPES (MESH:D006531), penicillin (MESH:D010406), SU5416 (MESH:C116890), Sildenafil (MESH:D000068677), paraffin (MESH:D010232), isoflurane (MESH:D007530), RPMI 1640 (-), formalin (MESH:D005557), nitrogen (MESH:D009584), H&amp;E (MESH:D006371), 2-mercaptoethanol (MESH:D008623), PBS (MESH:D007854), amphotericin B (MESH:D000666), propidium iodide (MESH:D011419), tocilizumab (MESH:C502936), monocrotaline (MESH:D016686), MCT (MESH:C000709826)
- **Species:** Mus musculus (house mouse, species) [taxon 10090], Homo sapiens (human, species) [taxon 9606], Bacteria Latreille et al. 1825 (Bacteria stick insect, genus) [taxon 629395], Rattus norvegicus (brown rat, species) [taxon 10116]
- **Mutations:** R899X
- **Cell lines:** THP-1 — Homo sapiens (Human), Childhood acute monocytic leukemia, Cancer cell line (CVCL_0006)

## Figures

6 figures with captions in the complete paper: https://tomesphere.com/paper/PMC9098455/full.md

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Source: https://tomesphere.com/paper/PMC9098455