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