Induced pluripotent stem cells in autism research: a review of current advances and future directions

Abstract Background Autism spectrum disorder (ASD) is a complex neurodevelopmental condition affecting millions of people worldwide, with limited therapeutic options and significant heterogeneity in presentation and underlying pathophysiology. This review comprehensively examines the current state of induced pluripotent stem cell (iPSC) applications in ASD research, evaluates recent advances, identifies key limitations, and outlines future directions for clinical translation. Methods We conducted a narrative review of peer-reviewed literature examining iPSCs applications in ASD research, including disease modeling, drug discovery, and therapeutic development, with a particular focus on recent technological advances and clinical translation challenges. Results iPSC applications in ASD research have shown significant promise through personalized cellular models that have uncovered key mechanisms underlying synaptic defects, neuronal network changes, and neurotransmitter disruptions. Advanced three-dimensional organoid systems derived from patient-derived iPSCs offer enhanced physiological relevance for studying brain development and ASD pathogenesis. Nevertheless, critical obstacles remain, particularly safety risks, including tumor formation from incompletely differentiated cells, genetic alterations in cell lines, and marked inconsistency in laboratory protocols. Furthermore, the absence of standardized manufacturing guidelines and prohibitive treatment costs present substantial challenges to widespread clinical implementation and patient access. Conclusions Although iPSCs offer transformative potential for ASD research and therapy, significant obstacles must be overcome to achieve clinical success. Critical needs include enhanced safety measures, uniform manufacturing standards, improved cell viability, and robust regulatory oversight. Achieving clinical translation will depend on ongoing partnerships among scientists, healthcare providers, regulatory bodies, and autism communities to ensure that research breakthroughs result in safe, effective, and equitable treatments.

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Publication Details

Journal
Egyptian Journal of Medical Human Genetics
Published
2026-02-24
DOI
https://doi.org/10.1186/s43042-026-00850-8
Primary Topic
Pluripotent Stem Cells Research
Type
article
Field-Weighted Citation Impact
0.00

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article

Induced pluripotent stem cells in autism research: a review of current advances and future directions

Forough Azam Sayahpour, Abolfazl Lotfi, Arsh Haj Mohamad Ebrahim Ketabforoush, Saeid Abediankenari et al.
Egyptian Journal of Medical Human Genetics
Pluripotent Stem Cells Research
article

Induced pluripotent stem cells in autism research: a review of current advances and future directions

Forough Azam Sayahpour, Abolfazl Lotfi, Arsh Haj Mohamad Ebrahim Ketabforoush, Saeid Abediankenari, Faezeh Faghihi, Shirin Barati, Armin Ariaei, Sanaz Bordbar
article en

Abstract

Abstract Background Autism spectrum disorder (ASD) is a complex neurodevelopmental condition affecting millions of people worldwide, with limited therapeutic options and significant heterogeneity in presentation and underlying pathophysiology. This review comprehensively examines the current state of induced pluripotent stem cell (iPSC) applications in ASD research, evaluates recent advances, identifies key limitations, and outlines future directions for clinical translation. Methods We conducted a narrative review of peer-reviewed literature examining iPSCs applications in ASD research, including disease modeling, drug discovery, and therapeutic development, with a particular focus on recent technological advances and clinical translation challenges. Results iPSC applications in ASD research have shown significant promise through personalized cellular models that have uncovered key mechanisms underlying synaptic defects, neuronal network changes, and neurotransmitter disruptions. Advanced three-dimensional organoid systems derived from patient-derived iPSCs offer enhanced physiological relevance for studying brain development and ASD pathogenesis. Nevertheless, critical obstacles remain, particularly safety risks, including tumor formation from incompletely differentiated cells, genetic alterations in cell lines, and marked inconsistency in laboratory protocols. Furthermore, the absence of standardized manufacturing guidelines and prohibitive treatment costs present substantial challenges to widespread clinical implementation and patient access. Conclusions Although iPSCs offer transformative potential for ASD research and therapy, significant obstacles must be overcome to achieve clinical success. Critical needs include enhanced safety measures, uniform manufacturing standards, improved cell viability, and robust regulatory oversight. Achieving clinical translation will depend on ongoing partnerships among scientists, healthcare providers, regulatory bodies, and autism communities to ensure that research breakthroughs result in safe, effective, and equitable treatments.

Egyptian Journal of Medical Human GeneticsVol. 27(1)
Iran University of Medical Sciences (IR), Medical College of Wisconsin (US), Technical and Vocational University (IR), Saveh University of Medical Sciences (IR), Tehran University of Medical Sciences (IR), University of Missouri (US), Mazandaran University of Medical Sciences (IR)
Iran University of Medical Sciences
Openalex Percentile: Top 44%
Pluripotent Stem Cells Research
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