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This project aims to understand the molecular biology underlying the improvement of surgical scars treated by ablative fractional photothermolysis (FP). Previous human studies at MGH have shown that FP significantly improves the appearance and functionality of surgical and burn scars. At the Wellman Center, we have conducted a randomized, controlled study on linear surgical scars demonstrating the efficacy of FP to decrease the volume of hypertrophic scars, and to improve the appearance and texture of scars. However, the underlying mechanism of this therapeutic effect is unknown. It is clear that FP induces wound healing and remodeling of the normal skin surrounding microthermal zones (MTZs). Furthermore, other researchers have employed animal models using transgenic zebrafish and the mouse eye, and found that laser treatments induce changes in gene expression in specific cells. We propose to determine whether the effect of FP on scar improvement occurs via changes in patterns of local gene expression within the skin, specifically dermal fibroblasts. By characterizing these changes, we may be able to identify molecular mechanisms that both explain and contribute to the beneficial effects of FP in the surgical and traumatic scar. The molecular insights into the therapeutic effects of fractional laser photothermolysis may provide a basis for future therapeutic strategies to improve scar remodeling.

A prospective, open-label study in 10 healthy adults, ages 18-50, with abdominal scars will be pursued at the Clinical Research Unit at Wellman Center for Photomedicine (MGH). A side-by-side comparison of untreated vs. one topical treatment of ablative fractional photothermolysis in qualifying subjects will be made. Ten subjects will receive treatment on randomly-assigned portions of their scars, in addition to non-treated control sites. The primary measures of efficacy are (a) blinded evaluation of scar improvement from standard digital photographs taken before and after the treatments, (b) changes in scar volume (measured by 3D Image system) and/or scar width, and (c) a quantitative characterization of gene expression measured by mRNA expression levels from treated and untreated scars and control sites. The primary measures of side effects are inflammatory and pigmentary outcomes assessed by blind evaluation of digital photographs taken before and after the treatments. Another study endpoint includes histopathological examination and comparison of treated and untreated scars.

An FDA-approved 10600 nm Fractional laser source will be used for laser exposures performed 2 months prior to 2 skin biopsies (each 24 mm x 4 mm) of treated and untreated scar sites. A control site, with no treatment will also be left for clinical, histological and molecular examination.

Inclusion Criteria:

1. Subjects who are healthy with ages between 18 and 50 years.
2. Subjects who have had their most recent abdominal procedure at least 2 years prior to enrollment in study.
3. Subjects with surgical scars with a length greater than 10 cm or 4 inches.
4. Subjects whose scars are either hypertrophic or atrophic but enlarged.
5. Subjects who are willing to participate in the study.
6. Subjects who are willing to receive laser treatment.
7. Subjects who are willing to receive skin biopsies.
8. Subjects who agree and sign an informed consent relating to study procedures.
9. Subjects who are willing to follow the treatment schedule and post-treatment care requirements.
10. Subjects who had not received any topical treatment for scars in the past month, including corticosteroid injections, topical fluorinated corticosteroids or any other laser treatment.
11. Subjects who are willing to avoid topical or systemic scar treatment, including topical over-the-counter (OTC) corticosteroids, during the study period.

Exclusion Criteria:

1. Subjects with underlying skin or other medical conditions that could have an adverse effect on wound healing.

2. Subjects with evidence of infection on area to be treated or elsewhere on body.

3. Subjects with presence of suntan in the area to be treated.

4. Subjects who have had topical/Injected corticosteroids within 1 month of entering the study.

5. Subjects with known anticoagulation or thromboembolic condition.

6. Subjects who are immunosuppressed.

7. Subjects who are unable to comply with treatment, home care, or follow-up visits.

8. Subjects who are pregnant or breast-feeding.

9. Subjects with known autoimmune disease.

10. Subjects who are enrolled in any other clinical trial using systemic medication; or any other treatment that might interfere with this study.

11. Subjects with known diabetes mellitus

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