PLoS ONE (Jan 2016)

Mucorales-Specific T Cells in Patients with Hematologic Malignancies.

  • Leonardo Potenza,
  • Daniela Vallerini,
  • Patrizia Barozzi,
  • Giovanni Riva,
  • Andrea Gilioli,
  • Fabio Forghieri,
  • Anna Candoni,
  • Simone Cesaro,
  • Chiara Quadrelli,
  • Johan Maertens,
  • Giulio Rossi,
  • Giulio Rossi,
  • Monica Morselli,
  • Mauro Codeluppi,
  • Cristina Mussini,
  • Elisabetta Colaci,
  • Andrea Messerotti,
  • Ambra Paolini,
  • Monica Maccaferri,
  • Valeria Fantuzzi,
  • Cinzia Del Giovane,
  • Alessandro Stefani,
  • Uliano Morandi,
  • Rossana Maffei,
  • Roberto Marasca,
  • Franco Narni,
  • Renato Fanin,
  • Patrizia Comoli,
  • Luigina Romani,
  • Anne Beauvais,
  • Pier Luigi Viale,
  • Jean Paul Latgè,
  • Russell E Lewis,
  • Mario Luppi

DOI
https://doi.org/10.1371/journal.pone.0149108
Journal volume & issue
Vol. 11, no. 2
p. e0149108

Abstract

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BACKGROUND:Invasive mucormycosis (IM) is an emerging life-threatening fungal infection. It is difficult to obtain a definite diagnosis and to initiate timely intervention. Mucorales-specific T cells occur during the course of IM and are involved in the clearance of the infection. We have evaluated the feasibility of detecting Mucorales-specific T cells in hematological patients at risk for IM, and have correlated the detection of such cells with the clinical conditions of the patients. METHODS AND FINDINGS:By using an enzyme linked immunospot assay, the presence of Mucorales-specific T cells in peripheral blood (PB) samples has been investigated at three time points during high-dose chemotherapy for hematologic malignancies. Mucorales-specific T cells producing interferon-γ, interleukin-10 and interleukin-4 were analysed in order to detect a correlation between the immune response and the clinical picture. Twenty-one (10.3%) of 204 patients, accounting for 32 (5.3%) of 598 PB samples, tested positive for Mucorales-specific T cells. Two groups could be identified. Group 1, including 15 patients without signs or symptoms of invasive fungal diseases (IFD), showed a predominance of Mucorales-specific T cells producing interferon-gamma. Group 2 included 6 patients with a clinical picture consistent with invasive fungal disease (IFD): 2 cases of proven IM and 4 cases of possible IFD. The proven patients had significantly higher number of Mucorales-specific T cells producing interleukin-10 and interleukin-4 and higher rates of positive samples by using derived diagnostic cut-offs when compared with the 15 patients without IFD. CONCLUSIONS:Mucorales-specific T cells can be detected and monitored in patients with hematologic malignancies at risk for IM. Mucorales-specific T cells polarized to the production of T helper type 2 cytokines are associated with proven IM and may be evaluated as a surrogate diagnostic marker for IM.