Repigmentation in vitiligo using the Janus kinase inhibitor tofacitinib may require concomitant light exposure
Vitiligo is an autoimmune disease in which cutaneous depigmentation occurs. Existing therapies are often inadequate. Prior reports have shown benefit of the Janus kinase (JAK) inhibitors. To evaluate the efficacy of the JAK 1/3 inhibitor tofacitinib in the treatment of vitiligo. This is a retrospect...
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Veröffentlicht in: | Journal of the American Academy of Dermatology 2017-10, Vol.77 (4), p.675-682.e1 |
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creator | Liu, Lucy Y. Strassner, James P. Refat, Maggi A. Harris, John E. King, Brett A. |
description | Vitiligo is an autoimmune disease in which cutaneous depigmentation occurs. Existing therapies are often inadequate. Prior reports have shown benefit of the Janus kinase (JAK) inhibitors.
To evaluate the efficacy of the JAK 1/3 inhibitor tofacitinib in the treatment of vitiligo.
This is a retrospective case series of 10 consecutive patients with vitiligo treated with tofacitinib. Severity of disease was assessed by body surface area of depigmentation.
Ten consecutive patients were treated with tofacitinib. Five patients achieved some repigmentation at sites of either sunlight exposure or low-dose narrowband ultraviolet B phototherapy. Suction blister sampling revealed that the autoimmune response was inhibited during treatment in both responding and nonresponding lesions, suggesting that light rather than immunosuppression was primarily required for melanocyte regeneration.
Limitations include the small size of the study population, retrospective nature of the study, and lack of a control group.
Treatment of vitiligo with JAK inhibitors appears to require light exposure. In contrast to treatment with phototherapy alone, repigmentation during treatment with JAK inhibitors may require only low-level light. Maintenance of repigmentation may be achieved with JAK inhibitor monotherapy. These results support a model wherein JAK inhibitors suppress T cell mediators of vitiligo and light exposure is necessary for stimulation of melanocyte regeneration. |
doi_str_mv | 10.1016/j.jaad.2017.05.043 |
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To evaluate the efficacy of the JAK 1/3 inhibitor tofacitinib in the treatment of vitiligo.
This is a retrospective case series of 10 consecutive patients with vitiligo treated with tofacitinib. Severity of disease was assessed by body surface area of depigmentation.
Ten consecutive patients were treated with tofacitinib. Five patients achieved some repigmentation at sites of either sunlight exposure or low-dose narrowband ultraviolet B phototherapy. Suction blister sampling revealed that the autoimmune response was inhibited during treatment in both responding and nonresponding lesions, suggesting that light rather than immunosuppression was primarily required for melanocyte regeneration.
Limitations include the small size of the study population, retrospective nature of the study, and lack of a control group.
Treatment of vitiligo with JAK inhibitors appears to require light exposure. In contrast to treatment with phototherapy alone, repigmentation during treatment with JAK inhibitors may require only low-level light. Maintenance of repigmentation may be achieved with JAK inhibitor monotherapy. These results support a model wherein JAK inhibitors suppress T cell mediators of vitiligo and light exposure is necessary for stimulation of melanocyte regeneration.</description><identifier>ISSN: 0190-9622</identifier><identifier>EISSN: 1097-6787</identifier><identifier>DOI: 10.1016/j.jaad.2017.05.043</identifier><identifier>PMID: 28823882</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Adult ; Aged ; Autoimmunity ; Chemokine CXCL10 - metabolism ; Chemokine CXCL9 - metabolism ; Combined Modality Therapy ; Female ; Humans ; JAK ; Janus kinase ; Janus Kinase 1 - antagonists & inhibitors ; Janus Kinase 3 - antagonists & inhibitors ; Male ; Middle Aged ; narrowband ultraviolet B ; nbUVB ; phototherapy ; Piperidines - therapeutic use ; Protein Kinase Inhibitors - therapeutic use ; Pyrimidines - therapeutic use ; Pyrroles - therapeutic use ; Retrospective Studies ; ruxolitinib ; Severity of Illness Index ; Skin Pigmentation ; tofacitinib ; Ultraviolet Therapy ; vitiligo ; Vitiligo - immunology ; Vitiligo - metabolism ; Vitiligo - therapy</subject><ispartof>Journal of the American Academy of Dermatology, 2017-10, Vol.77 (4), p.675-682.e1</ispartof><rights>2017 American Academy of Dermatology, Inc.</rights><rights>Copyright © 2017 American Academy of Dermatology, Inc. Published by Elsevier Inc. All rights reserved.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c521t-c93c238b74b28c29a66aea1649bf224e47326e5fd2613ee597e0d170e90570dc3</citedby><cites>FETCH-LOGICAL-c521t-c93c238b74b28c29a66aea1649bf224e47326e5fd2613ee597e0d170e90570dc3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.jaad.2017.05.043$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>230,315,782,786,887,3552,27931,27932,46002</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/28823882$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Liu, Lucy Y.</creatorcontrib><creatorcontrib>Strassner, James P.</creatorcontrib><creatorcontrib>Refat, Maggi A.</creatorcontrib><creatorcontrib>Harris, John E.</creatorcontrib><creatorcontrib>King, Brett A.</creatorcontrib><title>Repigmentation in vitiligo using the Janus kinase inhibitor tofacitinib may require concomitant light exposure</title><title>Journal of the American Academy of Dermatology</title><addtitle>J Am Acad Dermatol</addtitle><description>Vitiligo is an autoimmune disease in which cutaneous depigmentation occurs. Existing therapies are often inadequate. Prior reports have shown benefit of the Janus kinase (JAK) inhibitors.
To evaluate the efficacy of the JAK 1/3 inhibitor tofacitinib in the treatment of vitiligo.
This is a retrospective case series of 10 consecutive patients with vitiligo treated with tofacitinib. Severity of disease was assessed by body surface area of depigmentation.
Ten consecutive patients were treated with tofacitinib. Five patients achieved some repigmentation at sites of either sunlight exposure or low-dose narrowband ultraviolet B phototherapy. Suction blister sampling revealed that the autoimmune response was inhibited during treatment in both responding and nonresponding lesions, suggesting that light rather than immunosuppression was primarily required for melanocyte regeneration.
Limitations include the small size of the study population, retrospective nature of the study, and lack of a control group.
Treatment of vitiligo with JAK inhibitors appears to require light exposure. In contrast to treatment with phototherapy alone, repigmentation during treatment with JAK inhibitors may require only low-level light. Maintenance of repigmentation may be achieved with JAK inhibitor monotherapy. These results support a model wherein JAK inhibitors suppress T cell mediators of vitiligo and light exposure is necessary for stimulation of melanocyte regeneration.</description><subject>Adult</subject><subject>Aged</subject><subject>Autoimmunity</subject><subject>Chemokine CXCL10 - metabolism</subject><subject>Chemokine CXCL9 - metabolism</subject><subject>Combined Modality Therapy</subject><subject>Female</subject><subject>Humans</subject><subject>JAK</subject><subject>Janus kinase</subject><subject>Janus Kinase 1 - antagonists & inhibitors</subject><subject>Janus Kinase 3 - antagonists & inhibitors</subject><subject>Male</subject><subject>Middle Aged</subject><subject>narrowband ultraviolet B</subject><subject>nbUVB</subject><subject>phototherapy</subject><subject>Piperidines - therapeutic use</subject><subject>Protein Kinase Inhibitors - therapeutic use</subject><subject>Pyrimidines - therapeutic use</subject><subject>Pyrroles - therapeutic use</subject><subject>Retrospective Studies</subject><subject>ruxolitinib</subject><subject>Severity of Illness Index</subject><subject>Skin Pigmentation</subject><subject>tofacitinib</subject><subject>Ultraviolet Therapy</subject><subject>vitiligo</subject><subject>Vitiligo - immunology</subject><subject>Vitiligo - metabolism</subject><subject>Vitiligo - therapy</subject><issn>0190-9622</issn><issn>1097-6787</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kU2LFDEQhhtR3HH1D3iQHL10m4_upAMiyOInC4LoOaTT1TM1diezSXrY_fdmmHXRi4eQQ556U1VPVb1ktGGUyTf7Zm_t2HDKVEO7hrbiUbVhVKtaql49rjaUaVpryflF9SylPaVUt0I9rS5433NRzqby3-GA2wV8thmDJ-jJETPOuA1kTei3JO-AfLV-TeQXepugIDscMIdIcpisK7THgSz2jkS4WTECccG7sGC2PpOStMsEbg8hrRGeV08mOyd4cX9fVj8_fvhx9bm-_vbpy9X769p1nOXaaeFKg4NqB947rq2UFiyTrR4mzltoleASumnkkgmATiugI1MUNO0UHZ24rN6dcw_rsMDoynzRzuYQcbHxzgSL5t8XjzuzDUcjuRC9kiXg9X1ADDcrpGwWTA7m2XoIazJMC6qF7GlfUH5GXQwpRZgevmHUnESZvTmJMidRhnamiCpFr_5u8KHkj5kCvD0DUNZ0RIgmOQTvYCwbdtmMAf-X_xumaqfz</recordid><startdate>20171001</startdate><enddate>20171001</enddate><creator>Liu, Lucy Y.</creator><creator>Strassner, James P.</creator><creator>Refat, Maggi A.</creator><creator>Harris, John E.</creator><creator>King, Brett A.</creator><general>Elsevier Inc</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20171001</creationdate><title>Repigmentation in vitiligo using the Janus kinase inhibitor tofacitinib may require concomitant light exposure</title><author>Liu, Lucy Y. ; Strassner, James P. ; Refat, Maggi A. ; Harris, John E. ; King, Brett A.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c521t-c93c238b74b28c29a66aea1649bf224e47326e5fd2613ee597e0d170e90570dc3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><topic>Adult</topic><topic>Aged</topic><topic>Autoimmunity</topic><topic>Chemokine CXCL10 - metabolism</topic><topic>Chemokine CXCL9 - metabolism</topic><topic>Combined Modality Therapy</topic><topic>Female</topic><topic>Humans</topic><topic>JAK</topic><topic>Janus kinase</topic><topic>Janus Kinase 1 - antagonists & inhibitors</topic><topic>Janus Kinase 3 - antagonists & inhibitors</topic><topic>Male</topic><topic>Middle Aged</topic><topic>narrowband ultraviolet B</topic><topic>nbUVB</topic><topic>phototherapy</topic><topic>Piperidines - therapeutic use</topic><topic>Protein Kinase Inhibitors - therapeutic use</topic><topic>Pyrimidines - therapeutic use</topic><topic>Pyrroles - therapeutic use</topic><topic>Retrospective Studies</topic><topic>ruxolitinib</topic><topic>Severity of Illness Index</topic><topic>Skin Pigmentation</topic><topic>tofacitinib</topic><topic>Ultraviolet Therapy</topic><topic>vitiligo</topic><topic>Vitiligo - immunology</topic><topic>Vitiligo - metabolism</topic><topic>Vitiligo - therapy</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Liu, Lucy Y.</creatorcontrib><creatorcontrib>Strassner, James P.</creatorcontrib><creatorcontrib>Refat, Maggi A.</creatorcontrib><creatorcontrib>Harris, John E.</creatorcontrib><creatorcontrib>King, Brett A.</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Journal of the American Academy of Dermatology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Liu, Lucy Y.</au><au>Strassner, James P.</au><au>Refat, Maggi A.</au><au>Harris, John E.</au><au>King, Brett A.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Repigmentation in vitiligo using the Janus kinase inhibitor tofacitinib may require concomitant light exposure</atitle><jtitle>Journal of the American Academy of Dermatology</jtitle><addtitle>J Am Acad Dermatol</addtitle><date>2017-10-01</date><risdate>2017</risdate><volume>77</volume><issue>4</issue><spage>675</spage><epage>682.e1</epage><pages>675-682.e1</pages><issn>0190-9622</issn><eissn>1097-6787</eissn><abstract>Vitiligo is an autoimmune disease in which cutaneous depigmentation occurs. Existing therapies are often inadequate. Prior reports have shown benefit of the Janus kinase (JAK) inhibitors.
To evaluate the efficacy of the JAK 1/3 inhibitor tofacitinib in the treatment of vitiligo.
This is a retrospective case series of 10 consecutive patients with vitiligo treated with tofacitinib. Severity of disease was assessed by body surface area of depigmentation.
Ten consecutive patients were treated with tofacitinib. Five patients achieved some repigmentation at sites of either sunlight exposure or low-dose narrowband ultraviolet B phototherapy. Suction blister sampling revealed that the autoimmune response was inhibited during treatment in both responding and nonresponding lesions, suggesting that light rather than immunosuppression was primarily required for melanocyte regeneration.
Limitations include the small size of the study population, retrospective nature of the study, and lack of a control group.
Treatment of vitiligo with JAK inhibitors appears to require light exposure. In contrast to treatment with phototherapy alone, repigmentation during treatment with JAK inhibitors may require only low-level light. Maintenance of repigmentation may be achieved with JAK inhibitor monotherapy. These results support a model wherein JAK inhibitors suppress T cell mediators of vitiligo and light exposure is necessary for stimulation of melanocyte regeneration.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>28823882</pmid><doi>10.1016/j.jaad.2017.05.043</doi><oa>free_for_read</oa></addata></record> |
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subjects | Adult Aged Autoimmunity Chemokine CXCL10 - metabolism Chemokine CXCL9 - metabolism Combined Modality Therapy Female Humans JAK Janus kinase Janus Kinase 1 - antagonists & inhibitors Janus Kinase 3 - antagonists & inhibitors Male Middle Aged narrowband ultraviolet B nbUVB phototherapy Piperidines - therapeutic use Protein Kinase Inhibitors - therapeutic use Pyrimidines - therapeutic use Pyrroles - therapeutic use Retrospective Studies ruxolitinib Severity of Illness Index Skin Pigmentation tofacitinib Ultraviolet Therapy vitiligo Vitiligo - immunology Vitiligo - metabolism Vitiligo - therapy |
title | Repigmentation in vitiligo using the Janus kinase inhibitor tofacitinib may require concomitant light exposure |
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