Base Editing (ABE8e) for ADA c.632G>A (p.Arg211His) in Adenosine deaminase-deficient severe combined immunodeficiency

Base Editing (ABE8e) via RNP electroporation (ex vivo) delivery is a rationale-driven therapeutic strategy for Adenosine deaminase-deficient severe combined immunodeficiency targeting the ADA c.632G>A (p.Arg211His) variant (Pathogenic, missense variant, non-coding transcript variant, intron variant). The editing system (ABE8e-nSpCas9 (adenine base editor)) converts the pathogenic A back to G on the target strand, restoring the wild-type codon. Target tissue: Blood/HSC. Therapeutic goal: Correct pathogenic ADA loss-of-function variants in autologous hematopoietic stem cells at the ADA locus to restore sufficient ADA activity, clear toxic purine metabolites, and achieve durable immune . Risk profile: off-target Medium (bystander bases in editing window), delivery complexity Medium, immunogenicity Low.

1. Molecular basis: ADA NM_000022.4(ADA):c.632G>A (p.Arg211His) is classified as Pathogenic (ClinVar variation ID 1957). Molecular consequence: missense variant, non-coding transcript variant, intron variant. Protein change: R211H, R76H. 2. Epidemiology: ADA-SCID is an ultra-rare primary immunodeficiency with estimated incidence between roughly 1 in 200,000 and 1 in 1,000,000 live births. Classic disease presents in early infancy with severe, recurrent opportunistic infections, failure to thrive, and non-immune manifestations; without definitive tre 3. Standard of care: Consensus guidelines recommend initiating polyethylene glycol–modified bovine ADA enzyme replacement therapy (ERT) at diagnosis, then proceeding to definitive therapy with either allogeneic hematopoietic stem cell transplantation (HSCT) from an HLA-matched sibling/family donor or autologous hematopo 4. Pipeline: Multiple Phase I/II and Phase II trials of ex vivo ADA HSC gene therapy using gammaretroviral or lentiviral vectors have demonstrated stable multilineage engraftment, sustained ADA expression, metabolic correction, and long-term immune reconstitution, with patients remaining free from severe infecti 5. ABE clinical validation: ABE8e (Richter et al. 2020, Nat Biotechnol) achieves ~1.7x higher editing efficiency than ABE7.10. VERVE-101 demonstrated first-in-human LNP-ABE liver editing with 55-66% PCSK9 reduction (Raal et al. 2025, NEJM). Beam Therapeutics is advancing multiple ABE programs.

1. No published data specifically correcting ADA c.632G>A (p.Arg211His) with Base Editing (ABE8e); strategy is based on general principles and must be validated preclinically.
2. PAM availability and bystander base analysis for the specific genomic context have not been performed. If no canonical NGG PAM positions the target within the editing window, PAM-flexible variants (SpRY) may be needed.
3. Long-term durability, off-target genome-wide effects, and immunogenicity in the target patient population require thorough preclinical and clinical evaluation.