Shi et al, 2013[18]
|
China |
90 participants (42 T2D and 48 controls) |
Not reported |
51.46 ± 10.68 |
CD4+CD28–
|
The expression of PD-1 on CD4+CD28- T-cell subset was increased in T2D patients when compared to healthy controls. Moreover, the upregulation of PD-1 on these T-cells was associated with the development of atherosclerotic macrovascular diseases. |
Fujisawa et al, 2015[28]
|
Japan |
48 participants (19 T2D and 29 controls) |
24 (50) |
49 ± 11.82 |
CD4+
|
The levels of PD-1 expression on T-helper cells were comparable between individuals with T2D versus healthy controls. |
Jia et al, 2016[9]
|
China |
130 participants (80 T2D and 50 controls) |
70 (54) |
61 ± 4.10 |
CD4+ and CD8+
|
The expression of PD-1 on both CD4+ and CD8+ was increased in T2D when compared with healthy controls. In addition, the upregulation of PD-1 on T-cells positively correlated with the levels of C-reactive protein (CRP), an inflammation marker. |
Nyambuya et al, 2018[29]
|
South Africa |
69 participants (34 T2D and 35 controls) |
10 (14) |
54.48 ± 4.45 |
CD4+
|
There was no difference in the expression of PD-1 on T-cells in T2D patients and healthy controls. Moreover, there was no correlation between the expression of PD-1 on T-cell and glucose metabolic profile. However, T2D patients had increased levels of inflammation. |
Sun et al, 2019[19]
|
China |
43 participants (23 T2D and 20 controls) |
20 (47) |
57.47 ± 9.03 |
CD4+ and CD8+
|
CD4+ and CD8+ T-cells from individuals with T2D expressed lower levels of PD-1 when compared with healthy controls. However, no correlation was found between PD-1 expression and glucose metabolic profiles. |