Puva Puede Alterar Los Linfocitos Circulantes o Intradérmicos y Su Función Inmunológica o Al Provocar Cambios en Los Vasos de La Superficie Cutánea Tanto in Vivo Como in Vitro
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Puva puede alterar los linfocitos circulantes o intradérmicos y su función inmunológica o al provocar cambios en los vasos de la superficie cutánea tanto in vivo como in vitro.docx
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Puva Puede Alterar Los Linfocitos Circulantes o Intradérmicos y Su Función Inmunológica o Al Provocar Cambios en Los Vasos de La Superficie Cutánea Tanto in Vivo Como in Vitro
Puva puede alterar los linfocitos circulantes o intradrmicos y su funcin
inmunolgica o al provocar cambios en los vasos de la superficie cutnea
tanto in vivo como in vitro. The exact mechanism of UVB for phototherapeutic utility for PL is unknown, and yet the immunomodulating effects of UV radiation do serve an important function. Both BB-UVB phototherapy (290320 nm) (1214), psoralen plus UVA (320400 nm) photochemotherapy (18, 19) and UVA-1 (340400 nm) (21) have been reported previously as effective treatments for PLEVA and PLC. All of these therapies modulate the inflammatory and immunologic activities of the skin through unique photobiologic mechanisms of action that are different from each other (22). NB-UVB is about five to 10- fold less potent than BB-UVB for erythema induction, hyperplasia, edema, sunburn cell formation and Langerhans cell depletion from the skin. By contrast, NB-UVB appears to have relatively more suppressive effects than BB-UVB on systemic immune response, including lymphoproliferation (22 24). Interestingly, Ozawa et al. (25) have demonstrated that NB-UVB causes greater depletion of T cells in inflammated skin lesions than BB-UVB, and has direct cytotoxic actions on T cells infiltrating skin lesions. Their in vivo results have been paralleled by in vitro experiments Table 3. Results of UVB phototherapy in PL compared with the literature Study Disease subtype and number of patients Type of UVB phototherapy Number of treatments or weeks (mean) Total cumulative dose (J/cm2 , mean) Clinic response and follow up LeVine (12) PLK (11) BB-UVB 29 (1059) 9.24 (0.80637.077) CR in all patients Follow-up data are not stated Tham (13) PLEVA (1) PLC (17) BB- UVB 33.2 (1577) 0.20.5 mW/cm2 Cumulative dose is not reported CR % 82.4 NR; 3 patients Relapse in two patients within 6 months2 years) Tay et al. (14) PLEVA (3) PLC (2) BB-UVB 11 weeks 4.2 CR in all patients Relapse in two patients within 79 months Pasic et al. (15) PLEVA (3) PLC (6) NB-UVB 19 (1424) 6.5 (3.02311.8) PR: 3 PLC: CR: 3 PLC (33.3%) NR: 3 PLEVA Follow-up data are not stated Pavlotsky et al. (16) PLEVA (10) PLC (3) Overlap (1) BB-UVB 11 weeks 3.6 CR: 93.3% Relapse free: 71% (mean follow up 58 months) PLEVA (10) PLC (2) Overlap (3) NB-UVB 9 weeks 15 CR: 92.9% Relapse free: 75% (mean follow up 34 months) Khachemoune and Blyumin (17) PLK (1) NB-UVB 20 NS Relapse free: 100% (at follow up 1 year) This study PLEVA (23) NB-UVB 33.85 (3053) 16.3 (8.243) CR: 65.2% Relapse free 86% (at follow up 612 months) PR: 34.8% PLK (8) NB-UVB 32.4 (2560) 13.7 (7.127.1) CR: 87.5% Relapse free: 71.4% (at follow up 612 months) PR: 12.5% Clinical diagnosis. CR, complete response; PR, partial response; NR, no response; PLEVA, pityriasis lichenoides et varioliformis acuta; PLC, pityriasis lichenoides chronica; NS, not stated; NB-UVB, narrowband UVB; BB-UVB, broadband UVB. 131 r 2008 The Authors Journal compilation r 2008 Blackwell Munksgaard Photodermatology, Photoimmunology & Photomedicine 24, 128133 Phototherapy for pityriasis lichenoides where exposure of T cells to moderate doses of NB-UVB induced rapid apoptosis. The greater capacity of NB-UVB in depletion of dermal T cells is probably related to the somewhat deeper penetration of this wavelength in dermis compared with BB-UVB and the ability to administer a higher dosage with NB-UVB sources because of its less burning potency (22 25). Recent studies have demonstrated that UVB suppresses the alloactivating and antigen-presenting capacity of epidermal Langerhans cells and enhances (or modulates) interleukin-1 (IL-1), IL-6, IL-8, IL-10, IL-12 and tumor necrosis factor a production by human keratinocytes (26). The modulation of circulating cytokines accounts for systemic NB-UVB-induced immunosuppression in human subjects (22, 26). Intercellular adhesion molecule 1 (ICAM-1) is observed on cells in inflammatory skin diseases (including PLEVA) that can cause pruritus (2729). UVB irradiation has been found to suppress the expression of ICAM-1 in cultured human keratinocytes (29). UVB has been reported to decrease the release of histamine from mast cells. UVB phototherapy given two to three times a week for 4 weeks decreased the itch response of the skin when histamine was injected, or when a mast cell degranulator, compound (48/80), was injected (30). Duthie et al. (31) concluded that UVB light possibly suppresses the function of neoplastic clonal T-cell populations in the skin and so serves as an immune up-regulator. These UVB-induced alterations may partly account for its immunotherapeutic role in preventing the progression of the disease.
Puva Puede Alterar Los Linfocitos Circulantes o Intradérmicos y Su Función Inmunológica o Al Provocar Cambios en Los Vasos de La Superficie Cutánea Tanto in Vivo Como in Vitro