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Tacrolimus Ointment (Protopic)

Revolutionary steroid-free topical immunomodulator selectively suppressing T-cells

Duration
1 days2 sessions topical (改善後は weeks2 sessions維持)
Downtime
なし (初期灼熱感あり)
Sessions
急性期2-4 weeks間 → 維持療法 (保険適用)

About This Treatment

Tacrolimus ointment (Protopic 0.1%/0.03%) is an insurance-covered topical calcineurin inhibitor. Selectively suppresses T-cell activation without causing steroid side effects (skin atrophy, telangiectasia). Particularly useful for facial/neck atopic dermatitis. First-choice for steroid-problematic areas (face, eyelids, groin). Also used for vitiligo in aesthetic dermatology.

Mechanism of Action

Tacrolimus binds cytoplasmic FKBP-12, and the complex inhibits calcineurin (calcium/calmodulin-dependent phosphatase). This prevents NFAT dephosphorylation/nuclear translocation, suppressing T-cell cytokine production (IL-2, IL-4, IL-5, IFN-γ). Unlike steroids, does not inhibit collagen synthesis - no skin atrophy. Large molecular weight (822Da) limits absorption to barrier-damaged inflamed skin only.

Indications

General indication (see detailed description)

Expected Results

Significant inflammation improvement at 1-2 weeks. Clinical trials: >67% of patients achieve >50% improvement. Rapid reduction of facial erythema and pruritus. No skin atrophy or telangiectasia with long-term use (>1 year). Proactive therapy (twice weekly maintenance) significantly reduces relapse.

Clinical Evidence

Ruzicka T, et al. (1997)
A short-term trial of tacrolimus ointment for atopic dermatitis. N Engl J Med
Clinical improvement was reported in this study (see original paper for details).
Wollenberg A, et al. (2008)
Proactive treatment of atopic dermatitis in adults with 0.1% tacrolimus ointment. Allergy
Clinical improvement was reported in this study (see original paper for details).
Ashcroft DM, et al. (2005)
Efficacy and tolerability of topical pimecrolimus and tacrolimus in the treatment of atopic dermatitis. BMJ
Clinical improvement was reported in this study (see original paper for details).

Risks & Side Effects

Initial burning/stinging at application site (40-50%) usually subsides in days to 1 week. Theoretical infection risk from immunosuppression (HSV). FDA black box warning (lymphoma risk) but no causation established after 20+ years of post-marketing surveillance. Alcohol-induced facial flushing may occur. Sun protection recommended. Only 0.03% for children under 2.

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