Evidence map›Paper›PMID 42703805›Full record

ArticleInternational journal of fertility & sterility2026

Innovative Xenotransplantation of Reconstructed Human Artificial Ovary Using 3D-Printed Scaffolds and Umbilical Cord Mesenchymal Stem Cells.

Mohammad Ayoubipour, Hussein Eimani, Rouhollah Fathi, Abdolhossien Shahverdi, Morteza Zarrabi, Mohammad Kazemi Ashtiani, Somayeh Tavana, Seyed Akbar Moosavi, Leila Sadat Tahaei, Zeinab Ghezelayagh and 4 more

Abstract read
In one paragraph

Article in International journal of fertility & sterility, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

14 authors.

Mohammad AyoubipourDepartment of Developmental Biology, Faculty of Basic Sciences and Advanced Technologies in Biology, University of Science and Culture, ACECR, Tehran, Iran.ORCID 0009-0001-7187-6785
Hussein EimaniDepartment of Embryology, Reproductive Biomedicine Research Center, Royan Institute for Reproductive Biomedicine, ACECR, Tehran, Iran. Email: eimanih@royaninstitute.org.ORCID 0000-0002-5771-806X
Rouhollah FathiDepartment of Embryology, Reproductive Biomedicine Research Center, Royan Institute for Reproductive Biomedicine, ACECR, Tehran, Iran.ORCID 0000-0003-3871-5207
Abdolhossien ShahverdiDepartment of Embryology, Reproductive Biomedicine Research Center, Royan Institute for Reproductive Biomedicine, ACECR, Tehran, Iran.
Morteza ZarrabiDepartment of Regenerative Medicine, Cell Science Research Center, Royan Institute for Stem Cell Biology and Technology, ACECR, Tehran, Iran.
Mohammad Kazemi AshtianiDepartment of Cell Engineering, Cell Science Research Center, Royan Institute for Stem Cell Biology and Technology, ACECR, Tehran, Iran.
Somayeh TavanaDepartment of Embryology, Reproductive Biomedicine Research Center, Royan Institute for Reproductive Biomedicine, ACECR, Tehran, Iran.
Seyed Akbar MoosaviIran University of Medical Sciences, Allied Health Department, Tehran, Iran.ORCID 0000-0002-5813-359X
Leila Sadat TahaeiDepartment of Embryology, Reproductive Biomedicine Research Center, Royan Institute for Reproductive Biomedicine, ACECR, Tehran, Iran.ORCID 0009-0007-7635-8366
Zeinab GhezelayaghDepartment of Embryology, Reproductive Biomedicine Research Center, Royan Institute for Reproductive Biomedicine, ACECR, Tehran, Iran.
Majid HalvaeiDepartment of Cell Engineering, Cell Science Research Center, Royan Institute for Stem Cell Biology and Technology, ACECR, Tehran, Iran.
Masoumeh NouriDepartment of Regenerative Medicine, Cell Science Research Center, Royan Institute for Stem Cell Biology and Technology, ACECR, Tehran, Iran.
Parviz Golmohammadi GerdkohiDepartment of Embryology, Reproductive Biomedicine Research Center, Royan Institute for Reproductive Biomedicine, ACECR, Tehran, Iran.
Ashraf MoeiniDepartment of Embryology, Reproductive Biomedicine Research Center, Royan Institute for Reproductive Biomedicine, ACECR, Tehran, Iran.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Objective: The primary objective of this study was to develop an artificial ovary made of polylactic acid (PLA) material, which could potentially be used for fertility preservation. This scaffold was used to carry umbilical cord mesenchymal stem cells (UCMSCs) for xenotransplantation to study follicular growth, viability, and angiogenesis. Materials and Methods: The experimental study involved transplanting human ovarian cortical pieces into 3Dprinted baskets, with or without human UCMSCs. Four groups were considered as control: vitrified-warmed ovarian tissue (OT), OT transplantation without 3D-printed baskets without UCMSCs, OT+D; OT transplantation with 3D-printed baskets and without UCMSCs, and OT+D+C; OT transplantation with 3D-printed baskets and UCMSCs. Eighteen rats were divided into three transplantation groups, with grafts implanted into their back muscles. After one week, comparisons were made between OT, OT+D, and OT+D+C with control groups. Histological evaluations and gene expression analyses, including Results: The results revealed that OT+D had the highest follicular growth (99.3%) and transition rate (74.08%). OT+D+C indicated increased follicular survival, reduced mortality (P<0.0001), and a higher percentage of primordial follicles (59.1%) compared to OT and OT+D groups. UCMSCs' paracrine secretions likely preserved the follicular reserve. Additionally, OT+D+C exhibited significantly increased blood vessel number and diameter (P<0.0001) compared to other groups. Conclusion: This study underscores the significance of utilizing a three-dimensional basket scaffold to enhance the development of ovarian follicles and facilitate angiogenesis. The integration of stem cells with the scaffold demonstrated a noteworthy synergistic effect, resulting in improved preservation and viability of the follicles and Reduced fibrosis. These findings illuminate the promising potential of scaffold-based strategies in advancing reproductive therapies and tissue engineering, thereby offering prospects for innovative treatments in the future.

Indexed as

ArtificialFolliculogenesisOvaryXenotransplantation

Identifiers

PMID42703805
PMCPMC13535265

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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.