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. 2018 Jul 30;9:1608. doi: 10.3389/fmicb.2018.01608

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Copyright © 2018 Gomes, de Araújo, Vitelli-Avelar, Sathler-Avelar, Lage, Wendling, do Vale, Dias, Elói-Santos, Teixeira-Carvalho and Martins-Filho.

This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

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Expression of Fc-γR by phagocytes, NK-cells, and B-lymphocytes. The analysis of Fc-γR expression by neutrophils, monocytes, NK-cells, and B-cells were performed in whole blood samples collected from indeterminate (IND, = 8) and cardiac (CARD, = 13) Chagas disease patients and non-infected subjects (NI, = 11). The profile of CD16, CD32, and CD64 was characterized at ex vivo (A) and upon Trypanosoma cruzi-antigen recall in vitro (B). Data are displayed in box plot format (median with minimum and maximum values) as mean fluorescence intensity (MFI) for each Fc-γR. Significant differences at p < 0.05 are underscored by connecting lines and p-values provided in the figure.

Inline graphic — Expression of Fc-γR by phagocytes, NK-cells, and B-lymphocytes. The analysis of Fc-γR expression by neutrophils, monocytes, NK-cells, and B-cells were performed in whole blood samples collected from indeterminate (IND, = 8) and cardiac (CARD, = 13) Chagas disease patients and non-infected subjects (NI, = 11). The profile of CD16, CD32, and CD64 was characterized at ex vivo (A) and upon Trypanosoma cruzi-antigen recall in vitro (B). Data are displayed in box plot format (median with minimum and maximum values) as mean fluorescence intensity (MFI) for each Fc-γR. Significant differences at p < 0.05 are underscored by connecting lines and p-values provided in the figure.