Correlation between profile of circulating mononuclear cells and clinical manifestations in patients with pemphigus vulgaris

Autoimmunity. 2000 Sep;32(2):115-28. doi: 10.3109/08916930008994081.

Abstract

Phenotypes of 38 samples of mononuclear (PBMC) cells from 11 different patients with pemphigus vulgaris (PV) at different stages of the disease were explored looking for a possible relationship between cell immunity, mucocutaneous or mucosal lesion intensity and capacity of serum autoantibodies to elicit the disease in mice. PBMC from 5 patients with mucocutaneous lesions and sera with IgG capable of inducing the disease in neonatal mice had a high proportion of mature monocytes with CD14low DRhigh, and co-expressing CD16 and CD11b. In addition, a high proportion of CD19+CD5+ activated B cells and a very low proportion of naive CD4+CD45RA+ and CD8+CD11b+ T lymphocytes was observed. Monocytes from these patients expressed inducible nitric oxide synthase (iNOS). In contrast, PBMC from 6 patients, with lesions restricted to mucosal membranes and IgG lacking the capacity to induce the disease in mice, contained a high proportion of CD14high DRlow co-expressing CD16 circulating macrophages, CD8+CD11b+ T cells, and a low proportion of activated B lymphocytes. The results suggest a possible association between proportion of different antigen presenting cells (monocytes with high HLA-DR and low CD14 expression and activated B lymphocytes, or differentiated monocytes/macrophages), type of PV and capacity of serum autoantibodies to elicit the disease in mice.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acantholysis / etiology
  • Acantholysis / immunology
  • Acantholysis / pathology
  • Animals
  • Animals, Newborn
  • Autoantibodies / administration & dosage
  • Autoantibodies / blood
  • Disease Models, Animal
  • HLA-DR Antigens / blood
  • Humans
  • Immunization, Passive
  • Immunoglobulin G / administration & dosage
  • Immunoglobulin G / blood
  • Immunophenotyping
  • Leukocytes, Mononuclear / enzymology
  • Leukocytes, Mononuclear / immunology*
  • Lipopolysaccharide Receptors / blood
  • Mice
  • Mice, Inbred BALB C
  • Monocytes / classification
  • Monocytes / enzymology
  • Monocytes / immunology
  • Nitric Oxide Synthase / blood
  • Nitric Oxide Synthase Type II
  • Pemphigus / enzymology
  • Pemphigus / immunology*
  • Pemphigus / pathology

Substances

  • Autoantibodies
  • HLA-DR Antigens
  • Immunoglobulin G
  • Lipopolysaccharide Receptors
  • NOS2 protein, human
  • Nitric Oxide Synthase
  • Nitric Oxide Synthase Type II
  • Nos2 protein, mouse