Post-therapeutic relapse of psoriasis after CD11a blockade is associated with T cells and inflammatory myeloid DCs. Academic Article uri icon

Overview

abstract

  • UNLABELLED: To understand the development of new psoriasis lesions, we studied a group of moderate-to-severe psoriasis patients who experienced a relapse after ceasing efalizumab (anti-CD11a, Raptiva, Genentech). There were increased CD3(+) T cells, neutrophils, CD11c(+) and CD83(+) myeloid dendritic cells (DCs), but no increase in CD1c(+) resident myeloid DCs. In relapsed lesions, there were many CD11c(+)CD1c(-), inflammatory myeloid DCs identified by TNFSF10/TRAIL, TNF, and iNOS. CD11c(+) cells in relapsed lesions co-expressed CD14 and CD16 in situ. Efalizumab induced an improvement in many psoriasis genes, and during relapse, the majority of these genes reversed back to a lesional state. Gene Set Enrichment Analysis (GSEA) of the transcriptome of relapsed tissue showed that many of the gene sets known to be present in psoriasis were also highly enriched in relapse. Hence, on ceasing efalizumab, T cells and myeloid cells rapidly enter the skin to cause classic psoriasis. TRIAL REGISTRATION: Clinicaltrials.gov NCT00115076.

publication date

  • February 10, 2012

Research

keywords

  • Antibodies, Monoclonal
  • CD11a Antigen
  • Dendritic Cells
  • Psoriasis
  • T-Lymphocytes

Identity

PubMed Central ID

  • PMC3277585

Scopus Document Identifier

  • 84856797945

Digital Object Identifier (DOI)

  • 10.1371/journal.pone.0030308

PubMed ID

  • 22348003

Additional Document Info

volume

  • 7

issue

  • 2