Drug pipeline
Full profile accessExplore the programs pursuing this target and their development progress.
- Drug candidates
- Developers
- Development stage
Target intelligence / Profile preview
Autologous CD34+ hematopoietic stem and progenitor cells (HSPCs) are a population of multipotent cells harvested from a patient's own bone marrow or mobilized peripheral blood [1, 2]. These cells are defined by the expression of the CD34 surface glycoprotein, a sialomucin that facilitates cell adhesion and homing to the bone marrow niche [3, 4]. CD34+ HSPCs are essential for hematopoiesis, as they possess the unique ability to self-renew and differentiate into all mature blood cell types, including erythrocytes, leukocytes, and platelets [5]. In the context of advanced therapeutics, these cells serve as the primary substrate for ex vivo gene therapies and genome editing [6]. The therapeutic process involves the isolation of CD34+ cells, followed by genetic modification—such as the insertion of a functional gene via lentiviral vectors or the precise editing of genomic loci using CRISPR/Cas9—and subsequent reinfusion into the patient [1, 7]. This approach is currently utilized to provide potentially curative treatments for a range of genetic disorders, including sickle cell disease, beta-thalassemia, and various primary immunodeficiencies [8, 9]. References: [1] FDA (2023) Casgevy Approval; [2] FDA (2023) Lyfgenia Approval; [3] NIH (2023) CD34 Protein Function; [4] PubMed (2017) CD34 Homing; [5] StatPearls (2023) Hematopoiesis; [6] NIH (2024) Gene Therapy Overview; [7] NEJM (2021) CRISPR-Cas9 Gene Editing for SCD; [8] FDA (2022) Zynteglo Approval; [9] NIH (2022) SCID Gene Therapy.
Ex vivo genetic modification via gene addition (lentiviral vectors) or gene editing (CRISPR/Cas9) followed by autologous transplantation to restore or correct hematopoietic function [1, 2]. Mobilization from bone marrow to peripheral blood for collection [6, 7]. Myeloablative conditioning to create space for engraftment [8].
7 more in the full profile.
Beyond the preview
Explore the evidence, development activity, and competitive landscape with Gosset’s full data platform.
Explore the programs pursuing this target and their development progress.
Follow the clinical studies evaluating therapies directed at this target.
Compare approaches across drug candidates, modalities, and indications.
Investigate the research and source evidence behind target biology and development.
Explore patent activity around therapies and technologies addressing this target.
Connect target biology, drug development, and emerging evidence in your research.
See how Gosset can support your research on Autologous CD34+ hematopoietic stem and progenitor cells (CD34+ HSPCs).