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Abstract Psoriasis is a common chronic proliferative immune-mediated inflammatory condition which is well known for its relapsing nature. r (TRM) are non-circulating memory T cells, the inappropriate activation of which can be responsible for local recurrence of psoriatic lesions which have previously disappeared after a successful therapy. Objective: This work aimed at evaluating Tissue resident memory T cell (CD103+, CD69+ and CD49a-) in psoriatic patients before and after treatment with conventional, biological therapy and phototherapy. Methods: One hundred and twenty psoriatic patients were included in this cohort study after signing written informed consents. All participants were subjected to full medical history taking, clinical examination, PASI scoring and laboratory investigations. Patients were divided into 3 groups as; group A (N=45) received conventional therapy (methotrexate, cyclosporine and acitretin), group B (N=60) received biological therapy including anti TNF-α (Infliximab, adalimumab and etanercept), anti-IL 17 (secukinumab), anti-IL- 12/23 (ustekinumab) and anti-IL-23 (guselkumab) and group C (N=15) received phototherapy (nb-UVB) for 3 months. Two skin biopsies were taken from the perilesional skin, one before starting treatment and the second 3 months after treatment.Tissue levels of (CD103, CD49a- amd CD69) TRM markers were measured by flow cytometry technique. Results: CD103 expression was significantly increased (P=0.01) in group A remained unchanged in the other groups. CD49a- expression remained unchanged within the 3 study groups. CD69 expression was significantly II decreased in group B (P <0.001), significantly increased in group C (P =0,001) and remained unchanged in group A. Conclusion: Variable therapeutic modalities for psoriasis exert variable effects on TRM, None of the studied therapeutic modalities was capable of totally eliminating TRM in the studied patients |