Evidence-Based
Psoriasis plaque and immune pathway visualization

Psoriasis

Immune Modulation Protocol

Investigational regenerative protocol for psoriasis using umbilical cord mesenchymal stem cells as core therapy, integrated with physical medicine and nutritional support. Minimally invasive techniques. No claim of cure – objective, verifiable information.

Investigational
Status
1-2
Treatment Sessions
Ongoing
Conventional Care
Adjunctive
Approach

Clinical Rationale

Umbilical cord mesenchymal stem cells exert immunomodulatory effects and secrete paracrine factors that may help regulate aberrant T-cell activity and reduce pro-inflammatory cytokines involved in psoriatic inflammation. The protocol is strictly adjunctive; conventional dermatologic care remains mandatory. Physical therapy addresses joint stiffness and mobility; nutritional medicine focuses on anti‑inflammatory patterns. All techniques are minimally invasive (intradermal or subcutaneous microinjections). Peer‑reviewed investigations focus on safety and preliminary efficacy.

Protocol Components

Umbilical cord MSC
Physical therapy
Nutritional medicine
Minimally invasive
Immunomodulation
Adjunctive only

Comprehensive candidacy review

telemedicine or in‑person consultation

Best candidates & eligibility

This protocol is appropriate for a defined patient subset. Objective criteria:

  • Moderate to severe plaque psoriasis (BSA ≥10%)
  • Inadequate response or intolerance to ≥1 conventional systemic therapy
  • No active malignancy or untreated infection
  • Age 18–75, no pregnancy/lactation
  • Willing to maintain concomitant dermatologic care

Full eligibility determined via multidisciplinary intake and review of medical records. Not a replacement for first‑line treatment.

Minimally invasive delivery

Cellular administrations are performed using precise intradermal or subcutaneous microinjections with fine-gauge needles. No surgical incisions, no general anesthesia. Procedure time: approximately 30 minutes. Patients resume normal activities within 24‑48 hours. This approach reduces mechanical trauma and supports cellular retention.

Verifiable technique – utilized in registered clinical studies (NCT identifiers available on request).

Microinjection technique

precision, minimal discomfort