{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,4,16]],"date-time":"2026-04-16T18:25:06Z","timestamp":1776363906672,"version":"3.51.2"},"reference-count":113,"publisher":"Oxford University Press (OUP)","issue":"1","license":[{"start":{"date-parts":[[2019,1,1]],"date-time":"2019-01-01T00:00:00Z","timestamp":1546300800000},"content-version":"vor","delay-in-days":0,"URL":"https:\/\/academic.oup.com\/pages\/standard-publication-reuse-rights"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":[],"published-print":{"date-parts":[[2019,1,1]]},"abstract":"<jats:title>Abstract<\/jats:title>\n               <jats:p>Perivascular accumulation of lymphocytes can be a prominent histopathologic feature of various human inflammatory skin diseases. Select examples include systemic sclerosis, spongiotic dermatitis, and cutaneous lupus. Although a large body of work has described various aspects of the endothelial and vascular smooth muscle layers in these diseases, the outer adventitial compartment is poorly explored. The goal of the current study was to characterize perivascular adventitial fibroblast states in inflammatory human skin diseases and relate these states to perivascular lymphocyte accumulation. In normal skin, adventitial fibroblasts are distinguished by CD90 expression, and dense perivascular lymphocytic infiltrates are uncommon. In systemic sclerosis, this compartment expands, but lymphocyte infiltrates remain sparse. In contrast, perivascular adventitial fibroblast expression of VCAM1 is upregulated in spongiotic dermatitis and lupus and is associated with a dense perivascular T cell infiltrate. VCAM1 expression marks transitioned fibroblasts that show some resemblance to the reticular stromal cells in secondary lymphoid organs. Expanded adventitial compartments with perivascular infiltrates similar to the human settings were not seen in the inflamed murine dermis. This species difference may hinder the dissection of aspects of perivascular adventitial pathology. The altered perivascular adventitial compartment and its associated reticular network form a niche for lymphocytes and appear to be fundamental in the development of an inflammatory pattern.<\/jats:p>","DOI":"10.4049\/jimmunol.1801209","type":"journal-article","created":{"date-parts":[[2018,12,3]],"date-time":"2018-12-03T21:09:17Z","timestamp":1543871357000},"page":"56-68","source":"Crossref","is-referenced-by-count":21,"title":["Perivascular Adventitial Fibroblast Specialization Accompanies T Cell Retention in the Inflamed Human Dermis"],"prefix":"10.1093","volume":"202","author":[{"ORCID":"https:\/\/orcid.org\/0000-0001-5962-553X","authenticated-orcid":false,"given":"Alexander M S","family":"Barron","sequence":"first","affiliation":[{"name":"Department of Microbiology, Boston University School of Medicine , Boston, MA 02118"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Julio C","family":"Mantero","sequence":"additional","affiliation":[{"name":"Department of Microbiology, Boston University School of Medicine , Boston, MA 02118"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"ORCID":"https:\/\/orcid.org\/0000-0002-8752-8769","authenticated-orcid":false,"given":"Jonathan D","family":"Ho","sequence":"additional","affiliation":[{"name":"Department of Dermatology, Boston University School of Medicine , Boston, MA 02118"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Banafsheh","family":"Nazari","sequence":"additional","affiliation":[{"name":"Section of Rheumatology, Boston University School of Medicine , Boston, MA 02118"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Katharine L","family":"Horback","sequence":"additional","affiliation":[{"name":"Department of Pathology, Brigham and Women\u2019s Hospital and Harvard Medical School , Boston, MA 02115"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"ORCID":"https:\/\/orcid.org\/0000-0001-9264-7300","authenticated-orcid":false,"given":"Jag","family":"Bhawan","sequence":"additional","affiliation":[{"name":"Department of Dermatology, Boston University School of Medicine , Boston, MA 02118"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Robert","family":"Lafyatis","sequence":"additional","affiliation":[{"name":"Section of Rheumatology, Boston University School of Medicine , Boston, MA 02118"},{"name":"Division of Rheumatology and Clinical Immunology, University of Pittsburgh Medical Center , Pittsburgh, PA 15213"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"ORCID":"https:\/\/orcid.org\/0000-0002-4761-5163","authenticated-orcid":false,"given":"Christina","family":"Lam","sequence":"additional","affiliation":[{"name":"Department of Dermatology, Boston University School of Medicine , Boston, MA 02118"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"ORCID":"https:\/\/orcid.org\/0000-0001-9168-5233","authenticated-orcid":false,"given":"Jeffrey L","family":"Browning","sequence":"additional","affiliation":[{"name":"Department of Microbiology, Boston University School of Medicine , Boston, MA 02118"},{"name":"Section of Rheumatology, Boston University School of Medicine , Boston, MA 02118"}],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"286","published-online":{"date-parts":[[2019,1,1]]},"reference":[{"key":"2025030417555798300_r1","doi-asserted-by":"crossref","first-page":"349","DOI":"10.4103\/0378-6323.110780","article-title":"Interface dermatitis","volume":"79","author":"Joshi","year":"2013","journal-title":"Indian J. 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