Figure 2.
Evaluation of immune profiles at day 100 in patients who went on to develop late aGVHD or cGVHD. Volcano plots showing significant markers that meet all 3 criteria of a (1) P ≤ .05 (y-axis), (2) ROC AUC of ≥0.60 (circle, ≥0.60; cross, <0.6), and (3) effect ratio ≥1.3 or ≤0.75 (x-axis). The subfigures correspond to (A) cGVHD compared with no-cGVHD controls; (B) late aGVHD compared with no-cGVHD controls, and (C) cGVHD compared with late aGVHD. Cell population are identified by color, with dark blue representing B cells, orange myeloid populations, yellow NK cells, purple NKreg cells, green T cells, light blue Treg cells, and dark red plasma cytokines. We note the following clinical variables were modeled as confounding factors in the logistic regression model: (1) prophylaxis or treatment with either alemtuzumab or ATG, (2) prophylaxis or treatment with rituximab, (3) recipient age, (4) the use of a peripheral blood donor product or not, and (5) whether the donor was HLA identical or not.

Evaluation of immune profiles at day 100 in patients who went on to develop late aGVHD or cGVHD. Volcano plots showing significant markers that meet all 3 criteria of a (1) P ≤ .05 (y-axis), (2) ROC AUC of ≥0.60 (circle, ≥0.60; cross, <0.6), and (3) effect ratio ≥1.3 or ≤0.75 (x-axis). The subfigures correspond to (A) cGVHD compared with no-cGVHD controls; (B) late aGVHD compared with no-cGVHD controls, and (C) cGVHD compared with late aGVHD. Cell population are identified by color, with dark blue representing B cells, orange myeloid populations, yellow NK cells, purple NKreg cells, green T cells, light blue Treg cells, and dark red plasma cytokines. We note the following clinical variables were modeled as confounding factors in the logistic regression model: (1) prophylaxis or treatment with either alemtuzumab or ATG, (2) prophylaxis or treatment with rituximab, (3) recipient age, (4) the use of a peripheral blood donor product or not, and (5) whether the donor was HLA identical or not.

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