# Exosomes in Skin of Color: Dermatological Insights, Therapeutic Potential, and Clinical Realities in India

**Authors:** Kajomi Shingala, Dipesh Nariya

PMC · DOI: 10.7759/cureus.102145 · 2026-01-23

## TL;DR

Exosomes are tiny cell messengers with potential in skin treatments, but more research and regulation are needed, especially for skin of color in India.

## Contribution

This review highlights the therapeutic potential and challenges of exosome-based dermatology in the Indian context, emphasizing skin-of-color considerations.

## Key findings

- Exosomes may help with pigmentation, scarring, hair loss, and wound healing in dermatology.
- Current clinical data on exosomes are limited, with small studies and inconsistent protocols.
- India faces challenges in standardizing exosome therapies and ensuring safety for diverse skin types.

## Abstract

Exosomes are nanosized extracellular vesicles that mediate intercellular communication by transferring proteins, lipids, and nucleic acids, and growing experimental evidence indicates their involvement in key cutaneous processes such as inflammation, melanogenesis, wound repair, angiogenesis, fibroblast activation, and hair follicle cycling. These biological properties have generated substantial interest in the use of exosome-based therapies in regenerative and aesthetic dermatology, although clinical adoption has often outpaced the strength of supporting evidence and regulatory oversight - particularly in India, where skin-of-color considerations, high disease burden, and rapid commercialization converge.

This narrative review synthesizes current understanding of exosome biology, therapeutic potential, clinical evidence, and safety considerations in dermatology, with emphasis on pigmentary disorders, acne scarring, hair disorders, wound healing, and inflammatory dermatoses relevant to Indian practice. Preclinical studies suggest that mesenchymal stem cell- and skin-derived exosomes can modulate immune signaling, melanocyte function, angiogenesis, and extracellular matrix remodeling, while early clinical reports indicate possible benefits in pigmentation, scar modulation, hair loss, and tissue repair. However, available human data are largely derived from small, uncontrolled studies employing heterogeneous products and protocols, with limited representation of skin-of-color populations and insufficient long-term safety data. In the Indian context, gaps in product standardization, quality control, regulatory clarity, and informed consent further complicate clinical translation. While exosomes represent a promising frontier in dermatology, their use should presently be considered investigational and approached with caution, transparency, and robust ethical safeguards, until standardized manufacturing processes, population-specific trials, and comprehensive safety data become available.

## Full-text entities

- **Genes:** PIK3CB (phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit beta) [NCBI Gene 5291] {aka P110BETA, PI3K, PI3KBETA, PIK3C1}, TGFB1 (transforming growth factor beta 1) [NCBI Gene 7040] {aka CAEND1, CED, DPD1, IBDIMDE, LAP, TGF-beta1}, CTNNB1 (catenin beta 1) [NCBI Gene 1499] {aka CTNNB, EVR7, MRD19, NEDSDV, armadillo}, TYR (tyrosinase) [NCBI Gene 7299] {aka ATN, CMM8, OCA1, OCA1A, OCAIA, SHEP3}, VEGFA (vascular endothelial growth factor A) [NCBI Gene 7422] {aka L-VEGF, MVCD1, VEGF, VPF}, AKT1 (AKT serine/threonine kinase 1) [NCBI Gene 207] {aka AKT, PKB, PKB-ALPHA, PRKBA, RAC, RAC-ALPHA}, MITF (melanocyte inducing transcription factor) [NCBI Gene 4286] {aka CMM8, COMMAD, MI, MITF-A, WS2, WS2A}
- **Diseases:** atopic dermatitis (MESH:D003876), acne (MESH:D000152), alopecia areata (MESH:D000506), inflammatory and aesthetic skin disorders (MESH:D012868), hypertrophic scarring (MESH:D017439), melasma (MESH:D008548), eczema (MESH:D004485), keloid (MESH:D007627), infection (MESH:D007239), Fitzpatrick skin types IV-VI (MESH:C000631847), Dermatologic (MESH:D000168), Hair Disorders (MESH:D006201), Hair loss disorders (MESH:D000505), Scarring (MESH:D002921), Pigmentary Disorders (MESH:C535508), psoriasis (MESH:D011565), Fibrosis (MESH:D005355), inflammation (MESH:D007249), trauma (MESH:D014947), Inflammatory Dermatoses (MESH:D012871), hypopigmentation (MESH:D017496), hyperpigmentation (MESH:D017495), pigmentation (MESH:D010859)
- **Chemicals:** lipid (MESH:D008055)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Figures

3 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12925381/full.md

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Source: https://tomesphere.com/paper/PMC12925381