Evidence map›Paper›PMID 40495292›Full record

ReviewPrenatal diagnosis2025

Hemophilia A: An Ideal Disease for Prenatal Therapy.

Christopher D Porada, Anthony Atala, Graça Almeida-Porada

Abstract readReview
In one paragraph

Review in Prenatal diagnosis, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

  1. Article
  2. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

3 authors.

Christopher D PoradaWake Forest Institute for Regenerative Medicine, Winston-Salem, North Carolina, USA.ORCID https://orcid.org/0000-0002-7321-7556
Anthony AtalaWake Forest Institute for Regenerative Medicine, Winston-Salem, North Carolina, USA.
Graça Almeida-PoradaWake Forest Institute for Regenerative Medicine, Winston-Salem, North Carolina, USA.

Funding

CTSA UM1 Program at Wake ForestUM1TR004929 · NCATS · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI Jamy D Ard, KRISTIE L FOLEY · 2024 to 2026
$11.9M
Prenatal Cell and Gene Therapy for Hemophilia AR01HL135853 · NHLBI · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI ALMEIDA-PORADA, GRACA DUARTE, PORADA, CHRISTOPHER D · 2017 to 2020
$2.8M
Defining the therapeutic efficacy, tolerogenic potential, and genotoxicity of liver-targeted AAV gene therapy for hemophilia AR01HL161290 · NHLBI · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI ALMEIDA-PORADA, GRACA DUARTE, PORADA, CHRISTOPHER D · 2022 to 2025
$2.7M
Postnatal Cell-Based Therapies for Hemophilia AR01HL130856 · NHLBI · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI ALMEIDA-PORADA, GRACA DUARTE, PORADA, CHRISTOPHER D · 2016 to 2019
$2.5M
cGMP Manufacture Of FVIII-Expressing Placental Cells For Hemophilia AU01HL148681 · NHLBI · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI Graca Duarte Almeida-Porada · 2019 to 2026
$1.6M
NCATS NIH HHS UM1 TR004929NHLBI NIH HHS R01 HL130856NHLBI NIH HHS R01 HL135853NHLBI NIH HHS R01 HL161290NHLBI NIH HHS U01 HL148681NIH HHS R01 HL130856NIH HHS R01 HL135853NIH HHS R01 HL148681NIH HHS R01 HL161290
6 · The paper itself

Abstract

Hemophilia A (HA) is the most common inherited coagulation defect. Current state-of-the-art treatment consists of frequent administration of prophylactic infusions of coagulation factor VIII (FVIII) protein or bispecific antibodies that replace the cofactor function of FVIIIa to maintain hemostasis. However, these treatments are far from ideal, due to their high cost, the need for lifelong treatment, the fact that they are unavailable to a large percentage of the world's persons with hemophilia A (PWHA), and the high risk of treatment failure due to immune response to the infused FVIII protein. Thus, there is a need for novel treatments, such as those using gene therapy and/or cell transplantation, that can promise long-term correction or permanent cure. In the present review, we discuss the clinical feasibility and unique advantages a prenatal approach to HA treatment could offer, placing special emphasis on a sheep model of HA we developed and on using mesenchymal cells (MSC) as cellular delivery vehicles for the FVIII gene to achieve a single treatment cure for HA prior to birth.

Indexed as

fetal interventionhemophiliaimmune tolerancein utero gene therapyin utero transplantationmesenchymal stromal cellssheep model

Identifiers

PMID40495292
PMCPMC12288728

What OpenQuestion holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.