Ionizable Lipid Nanoparticles for In Vivo mRNA Delivery to the Placenta during Pregnancy

被引:75
|
作者
Mitchell, Michael J. [1 ,2 ,3 ,4 ]
Swingle, Kelsey L. [1 ]
Safford, Hannah C. [1 ]
Geisler, Hannah C. [1 ]
Hamilton, Alex G. [1 ]
Thatte, Ajay S. [1 ]
Billingsley, Margaret M. [1 ]
Joseph, Ryann A. [1 ]
Mrksich, Kaitlin [1 ]
Padilla, Marshall S. [1 ]
Ghalsasi, Aditi A. [1 ]
Alameh, Mohamad-Gabriel [4 ,5 ]
Weissman, Drew [4 ,5 ]
机构
[1] Univ Penn, Dept Bioengn, Philadelphia, PA 19104 USA
[2] Univ Penn, Inst Immunol, Cardiovasc Inst,Perelman Sch Med, Inst Regenerat Med,Abramson Canc Ctr, Philadelphia, PA 19104 USA
[3] Univ Penn, Inst Regenerat Med, Perelman Sch Med, Philadelphia, PA 19104 USA
[4] Univ Penn, Penn Inst RNA Innovat, Perelman Sch Med, Philadelphia, PA 19104 USA
[5] Univ Penn, Dept Med, Philadelphia, PA 19104 USA
关键词
GENE-THERAPY; TRANSTROPHOBLASTIC CHANNELS; ANIMAL-MODELS; SIRNA; FORMULATIONS; POTENCY;
D O I
10.1021/jacs.2c12893
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Ionizable lipid nanoparticles (LNPs) are the most clinically advanced nonviral platform for mRNA delivery. While they have been explored for applications including vaccines and gene editing, LNPs have not been investigated for placental insufficiency during pregnancy. Placental insufficiency is caused by inadequate blood flow in the placenta, which results in increased maternal blood pressure and restricted fetal growth. Therefore, improving vasodilation in the placenta can benefit both maternal and fetal health. Here, we engineered ionizable LNPs for mRNA delivery to the placenta with applications in mediating placental vasodilation. We designed a library of ionizable lipids to formulate LNPs for mRNA delivery to placental cells and identified a lead LNP that enables in vivo mRNA delivery to trophoblasts, endothelial cells, and immune cells in the placenta. Delivery of this top LNP formulation encapsulated with VEGF-A mRNA engendered placental vasodilation, demonstrating the potential of mRNA LNPs for protein replacement therapy during pregnancy to treat placental disorders.
引用
收藏
页码:4691 / 4706
页数:16
相关论文
共 50 条
  • [21] Efficient in vitro and in vivo mRNA and CRISPR delivery with lipid nanoparticles
    Olsen, A. L.
    Petersen, J. L.
    Askou, A.
    Russ, K.
    Sorensen, J.
    Brandt, C. B.
    Jensen, N.
    Willen, K.
    Volbracht, C.
    Stummann, T.
    Boysen, A.
    Curci, B.
    Olesen, E. B. R.
    Zhou, Y.
    Rasmussen, R.
    Jakobsen, T.
    Petersen, T. S.
    Pena, I.
    Rio, P.
    Nejsum, P.
    Ludvigsen, M.
    Lin, L.
    Etzerodt, A.
    Fog, K.
    Jensen, P.
    Corydon, T.
    Luo, Y.
    HUMAN GENE THERAPY, 2024, 35 (3-4) : A334 - A334
  • [22] Systematic development of ionizable lipid nanoparticles for placental mRNA delivery using a design of experiments approach
    Young, Rachel E.
    Nelson, Katherine M.
    Hofbauer, Samuel I.
    Vijayakumar, Tara
    Alameh, Mohamad-Gabriel
    Weissman, Drew
    Papachristou, Charalampos
    Gleghorn, Jason P.
    Riley, Rachel S.
    BIOACTIVE MATERIALS, 2024, 34 : 125 - 137
  • [23] Nonclinical safety evaluation of a novel ionizable lipid for mRNA delivery
    Broudic, Karine
    Amberg, Alexander
    Schaefer, Markus
    Spirkl, Hans-Peter
    Bernard, Marie- Clotilde
    Desert, Paul
    TOXICOLOGY AND APPLIED PHARMACOLOGY, 2022, 451
  • [24] Chemical Design Strategy of Ionizable Lipids for In Vivo mRNA Delivery
    He, Zepeng
    Liu, Zhijia
    Chen, Yongming
    CHEMMEDCHEM, 2024, 19 (16)
  • [25] Lipid nanoparticles for mRNA delivery
    Xucheng Hou
    Tal Zaks
    Robert Langer
    Yizhou Dong
    Nature Reviews Materials, 2021, 6 : 1078 - 1094
  • [26] Lipid nanoparticles for mRNA delivery
    Hou, Xucheng
    Zaks, Tal
    Langer, Robert
    Dong, Yizhou
    NATURE REVIEWS MATERIALS, 2021, 6 (12) : 1078 - 1094
  • [27] Minimizing the ratio of ionizable lipid in lipid nanoparticles for in vivo base editing
    Chen, Qiubing
    Wang, Xuebin
    Zhang, Yizhou
    Tian, Ming
    Duan, Junyi
    Zhang, Ying
    Yin, Hao
    NATIONAL SCIENCE REVIEW, 2024, 11 (06)
  • [28] Minimizing the ratio of ionizable lipid in lipid nanoparticles for in vivo base editing
    Qiubing Chen
    Xuebin Wang
    Yizhou Zhang
    Ming Tian
    Junyi Duan
    Ying Zhang
    Hao Yin
    National Science Review, 2024, 11 (06) : 285 - 293
  • [29] In Vivo mRNA CAR T Cell Engineering via Targeted Ionizable Lipid Nanoparticles with Extrahepatic Tropism
    Billingsley, Margaret M.
    Gong, Ningqiang
    Mukalel, Alvin J.
    Thatte, Ajay S.
    El-Mayta, Rakan
    Patel, Savan K.
    Metzloff, Ann E.
    Swingle, Kelsey L.
    Han, Xuexiang
    Xue, Lulu
    Hamilton, Alex G.
    Safford, Hannah C.
    Alameh, Mohamad-Gabriel
    Papp, Tyler E.
    Parhiz, Hamideh
    Weissman, Drew
    Mitchell, Michael J.
    SMALL, 2024, 20 (11)
  • [30] Efficient delivery of VEGF-A mRNA for promoting diabetic wound healing via ionizable lipid nanoparticles
    Zha, Wenhui
    Wang, Ji
    Guo, Zongke
    Zhang, Yanhao
    Wang, Yang
    Dong, Shuo
    Liu, Chao
    Xing, Hanlei
    Li, Xinsong
    INTERNATIONAL JOURNAL OF PHARMACEUTICS, 2023, 632