Indication for a role of regulatory T cells for the advent of influenza A (H1N1)-related pneumonia

Clin Exp Immunol. 2010 Sep;161(3):576-83. doi: 10.1111/j.1365-2249.2010.04208.x.

Abstract

Regulatory T cells (T(regs) ) have an anti-inflammatory role. A former study in a limited number of patients found that absolute counts of T(regs) increase when infection by the new influenza H1N1 virus is complicated with pneumonia. These results generate the question if H1N1-related pneumonia is associated with a state of hypo-inflammation. A total of 135 patients were enrolled with blood sampling within less than 24 h from diagnosis; 23 with flu-like syndrome; 69 with uncomplicated H1N1-infection; seven with bacterial pneumonia; and 36 with H1N1-related pneumonia. T(regs) and CD14/HLA-DR co-expression were estimated by flow cytometry; concentrations of tumour necrosis factor-alpha (TNF-α), of interleukin (IL)-6 and of soluble triggering receptor expressed on myeloid cells-1 (sTREM-1) by an enzyme immunoassay; those of procalcitonin (PCT) by immuno-time-resolved amplified cryptate technology assay. Expression of human leucocyte antigen D-related (HLA-DR) on monocytes was similar between groups; absolute T(reg) counts were greater among patients with H1N1-related pneumonia than flu-like syndrome or H1N1-uncomplicated infection. Serum TNF-α of patients with bacterial pneumonia was greater than those of other groups, but IL-10 was similar between groups. Serum PCT was greater among patients with H1N1-related pneumonia and sTREM-1 among those with H1N1-related pneumonia. Regression analysis revealed that the most important factors related with the advent of pneumonia were the existence of underlying illnesses (P = 0·006) and of T(regs) equal to or above 16 mm(3) (P = 0·013). It is concluded that the advent of H1N1-related pneumonia is related to an early increase of the absolute T(reg) counts. This increase is probably not part of a hypo-inflammatory state of the host.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Aged
  • Female
  • Flow Cytometry
  • HLA-DR Antigens / metabolism
  • Humans
  • Immunophenotyping
  • Influenza A Virus, H1N1 Subtype / immunology*
  • Influenza, Human / blood
  • Influenza, Human / complications
  • Influenza, Human / immunology*
  • Interleukin-6 / blood
  • Lipopolysaccharide Receptors / metabolism
  • Male
  • Membrane Glycoproteins / blood
  • Middle Aged
  • Pneumonia, Bacterial / blood
  • Pneumonia, Bacterial / complications
  • Pneumonia, Bacterial / immunology*
  • Receptors, Immunologic / blood
  • T-Lymphocytes, Regulatory / immunology*
  • T-Lymphocytes, Regulatory / metabolism
  • Triggering Receptor Expressed on Myeloid Cells-1
  • Tumor Necrosis Factor-alpha / blood
  • Young Adult

Substances

  • HLA-DR Antigens
  • Interleukin-6
  • Lipopolysaccharide Receptors
  • Membrane Glycoproteins
  • Receptors, Immunologic
  • TREM1 protein, human
  • Triggering Receptor Expressed on Myeloid Cells-1
  • Tumor Necrosis Factor-alpha